On this page
Quick Reference
Overview and Recommendations
Background
- •Esophageal cancer surveillance after curative-intent treatment (esophagectomy, definitive chemoradiotherapy, or endoscopic resection) aims to detect locoregional and distant recurrence, manage treatment-related late toxicities, and identify second primary malignancies. Recurrence occurs in approximately of patients, with a median time to recurrence of 7-12 months. The majority of recurrences (81.8%) occur within the first 5 years, making structured follow-up critical during this window.
- •The risk of recurrence is stratified by histopathologic and treatment-related factors. Deep submucosal invasion (SM2), non-curative resection, positive margins, lymphovascular invasion, and grade 3 differentiation are high-risk features. Prior esophageal cancer history increases the hazard of recurrence-metastasis. A history of also increases neoplastic progression risk.
- •Recurrence patterns vary: after esophagectomy, locoregional recurrence (LRR) occurs in a substantial proportion and carries a median survival of 6-8 months without salvage treatment. Distant metastases are more common in adenocarcinoma. Oligometastatic disease (≤5 distant metastases on PET-CT) is present in 24% of metastatic patients and represents a distinct subgroup where aggressive local therapy plus systemic therapy improves overall survival (HR 0.47, median OS 35 months vs 13 months).
- •Late toxicities affect the majority of survivors. Dumping syndrome (moderate early in 45%, severe in 9% at 1 year), weight loss (mean 8.5% at 6 months), micronutrient deficiencies (iron deficiency in 43-46% pre- and postoperatively), and frailty (prevalence 28% preoperatively, rising to 68% at 1 week postoperatively) are pervasive and impact quality of life. Psychological distress affects both patients and caregivers (30% moderate-high anxiety in caregivers).
- •The optimal surveillance schedule remains debated due to lack of high-level randomized data, but cohort studies and expert consensus support a risk-stratified approach: endoscopy plus CT at 3, 6, and 12 months, then annually for at least 5 years, with biannual intervals for high-risk patients. Brain imaging surveillance is recommended for adenocarcinoma due to higher incidence of brain metastases (5.34% vs 1.45% for squamous cell carcinoma).
Evaluation
- •Suspect recurrent esophageal cancer when a patient reports new or worsening dysphagia, odynophagia, weight loss, or pain. Also consider late toxicity symptoms such as postprandial diaphoresis, palpitations, diarrhea (dumping syndrome), heartburn/regurgitation (reflux), or respiratory symptoms (cough, fever, purulent sputum) indicating possible anastomotic stricture, aspiration, or pneumonia.
- •At each clinic visit, perform a focused history and physical examination. Ask about dysphagia, odynophagia, weight loss, dumping symptoms, reflux, and respiratory symptoms. For patients on immune checkpoint inhibitors, inquire about rash, diarrhea, pneumonitis symptoms, or endocrinopathies (irAEs occur in 28% and are associated with improved progression-free survival).
- •Examine for signs of recurrence: palpable supraclavicular or cervical lymph nodes, abdominal mass, ascites, jaundice, or pleural effusion. Assess nutritional status (weight, BMI, muscle wasting). Evaluate for signs of dumping (tachycardia, diaphoresis) or reflux (regurgitation, cough). Perform a frailty assessment using tools such as the Modified Frailty Index.
- •Order computed tomography (CT) of the chest and abdomen with contrast as the primary imaging modality for surveillance. CT detects locoregional and distant recurrence. For patients with adenocarcinoma, consider brain MRI or CT for neuroimaging surveillance at staging and follow-up due to higher brain metastasis risk (5.34%).
- •Perform endoscopy with high-definition white-light and narrow-band imaging to assess the anastomotic site, residual esophagus, and gastric conduit. Endoscopy is the gold standard for detecting local recurrence. Obtain biopsy confirmation of any suspicious lesions. For patients after endoscopic resection, post-endoscopy esophageal advanced lesions (PEEALs) occur in and are often small (median 10 mm) with marginal elevation morphology.
- •Measure tumor markers (carcinoembryonic antigen, squamous cell carcinoma antigen) if initially elevated, though routine use is not universally recommended. Their value lies in trend monitoring, not diagnosis.
- •Diagnostic criteria for recurrence include biopsy-proven local recurrence, or new distant lesions on imaging. For oligometastatic disease, confirm with ¹⁸F-FDG-PET/CT. In patients with prior definitive chemoradiotherapy, endoscopic findings of large tumor size, type 0-I morphology, and B3 vessels signal high risk of non-radical cure and warrant intensified surveillance.
- •Also consider late toxicity evaluation: for dumping syndrome, use a symptom questionnaire (e.g., Sigstad's clinical diagnostic index). For nutritional deficiencies, order serum iron, ferritin, B12, folate, and vitamin D levels. For frailty, use the Modified Frailty Index or the Clinical Frailty Scale. For psychological distress, screen with HADS or similar validated tools.
- •Differential diagnoses for dysphagia after esophagectomy include anastomotic stricture (common), recurrent disease, or functional dysmotility. Stricture is more likely if symptoms occur within weeks to months postoperatively. Recurrence tends to be later and progressive. Endoscopy with biopsy differentiates.
- •When recurrence is suspected, the confirmatory workup includes biopsy for local lesions and PET/CT for staging. Multidisciplinary discussion guides treatment decisions (salvage radiotherapy, chemoradiotherapy, endoscopic resection, or systemic therapy). For oligometastatic disease, local treatment (stereotactic body radiotherapy or metastasectomy) plus systemic therapy improves survival.
Management
- •Implement a structured surveillance schedule: protocol includes endoscopy plus CT (or MRI) and tumor markers at months 3, 6, and 12, then annually for at least 5 years. For high-risk patients (deep submucosal invasion SM2, non-curative resection, positive margins, lymphovascular invasion), intensify to biannual follow-up during years 2-4. Minimum duration of surveillance is 5 years.
- •For patients after salvage radiotherapy for locoregional recurrence, perform PET-CT at 1 month and 3-4 months after RT completion, then clinic visits and chest CT every 3-4 months for the first 2 years, then every 6-12 months thereafter.
- •For patients with adenocarcinoma, include regular brain imaging (CT or MRI) at staging and as part of surveillance follow-up, given the higher incidence of brain metastases (5.34%).
- •Manage dumping syndrome with dietary counselling: small, frequent meals; low simple sugars; avoid concentrated sweets. For refractory cases, consider octreotide 50-100 mcg subcutaneously three times daily before meals. Monitor for weight loss and social function decline. Severe early dumping occurs in 9% and severe late dumping in 5% at 1 year.
- •Address nutritional deficiencies with routine biochemical screening (iron, B12, folate, vitamin D) preoperatively and at follow-up. Target iron deficiency with oral or IV iron supplementation. Provide protein supplementation at 1.2-1.5 g/kg/day. For weight loss >8% at 6 months, refer to a dietitian-led intervention. Consider jejunostomy feeding for patients with significant weight loss or inadequate oral intake.
- •Manage reflux symptoms with proton pump inhibitors (PPI) and lifestyle modifications (elevate head of bed, avoid large meals). Female patients report greater symptom severity. For anastomotic stricture, perform endoscopic dilation. After extensive ESD (>75% circumference), oral corticosteroids (e.g., prednisolone) may reduce stricture rate and require fewer dilation sessions compared to intralesional triamcinolone.
- •Assess and manage frailty in elderly patients. Preoperative frailty prevalence is 28% and rises to 68% at 1 week postoperatively. Implement multimodal prehabilitation (exercise, nutrition, psychosocial support) during neoadjuvant chemotherapy. Postoperative multimodal inpatient rehabilitation (resistance exercises and moderate-to-high intensity aerobic interval training) significantly improves 6-minute walk distance (73.1 m, P<0.001) and chair stand test.
- •Screen for psychological distress in patients using validated tools. Refer to psycho-oncology for Managing Cancer and Living Meaningfully (CALM) intervention, which reduces distress, anxiety, and depression and improves quality of life. Address caregiver burden: 30% report moderate-high anxiety, 10% moderate-high depression. Include caregivers in consultations, provide information on dietary management, and offer peer support.
- •Counsel patients to report new or worsening symptoms promptly: dysphagia, odynophagia, dumping syndrome symptoms, reflux, respiratory symptoms, and immune-related adverse events (irAEs). Emphasize smoking cessation (strong risk factor for postoperative pneumonia), physical activity (30-second chair stand test for prehabilitation), and weight management (higher BMI increases early reflux risk).
- •Avoid routine brain imaging in squamous cell carcinoma unless symptomatic, as incidence is low (1.45%). Avoid using non-dihydropyridine calcium channel blockers for reflux - they are not indicated. Do not rely solely on tumor markers for diagnosis of recurrence; confirm with imaging and biopsy.
- •Refer to a dietitian for persistent weight loss or dumping syndrome. Refer to a gastroenterologist for endoscopic surveillance and management of strictures. Refer to a cardiothoracic surgeon for consideration of salvage therapy if locoregional recurrence is detected. Refer to a psycho-oncologist for psychological distress. Refer to a palliative care specialist for symptom management in advanced disease.
- •Discharge criteria from intensive surveillance: after 5 years without recurrence, the risk diminishes but does not disappear. Ongoing annual surveillance is reasonable, especially for patients with prior high-risk features. For patients who develop recurrence, transition to treatment-focused management. For patients with good quality of life and no recurrence, consider shared decision-making to reduce frequency if patient preferences align.
Board Review — High Yield
- •Dumping syndrome - Affects 45% of survivors at 1 year (moderate early); severe in 9%. Manage with dietary changes and octreotide if refractory.
- •Recurrence risk factors - Deep submucosal invasion (SM2), non-curative resection, positive margins, lymphovascular invasion, grade 3 differentiation, piecemeal resection.
- •Surveillance schedule - Endoscopy + CT at 3, 6, 12 months, then annually for 5 years. High-risk: biannual years 2-4.
- •Brain metastases - More common in adenocarcinoma (5.34%) vs squamous cell (1.45%); regular brain imaging recommended for adenocarcinoma.
- •Oligometastatic disease - ≤5 metastases on PET-CT; local therapy (SBRT/metastasectomy) + systemic therapy improves OS (HR 0.47).
- •Frailty - Preoperative prevalence 28%, rises to 68% at 1 week postop. Multimodal prehabilitation and rehabilitation improve outcomes.
- •Nutritional deficiencies - Iron deficiency most common (43% preop, 45% postop); screen for iron, B12, folate, vitamin D; supplement as needed.
- •Immune-related adverse events - Occur in 28% of patients on checkpoint inhibitors; associated with better PFS; counsel patients to report promptly.
- •Post-endoscopy advanced lesions - rate; small (median 10 mm), marginal elevation; use high-definition white-light and NBI.
- •Caregiver burden - 30% moderate-high anxiety, 10% depression; include caregivers in consultations and provide support.
Deep Dive — Evidence Details
Surveillance Schedule
- ▸Use risk-adapted surveillance after EET; intensity depends on pretreatment neoplasia grade, treatment completeness, and follow-up findings.[1]
- ▸After endoscopic resection of ESCC, maintain structured surveillance endoscopy, with particular vigilance during the first **24 months**.[17]
- ▸After curative treatment, assess recurrence, dysphagia, nutrition, sarcopenia, dumping syndrome, function, and psychosocial health at follow-up visits.[2][4][7][11][20]
- ▸Trigger diagnostic imaging promptly for new symptoms; routine brain imaging in asymptomatic patients is not established by the supplied evidence.[14]
- ▸Exact endoscopy and imaging intervals should follow the complete AGA recommendations or local disease-specific protocol because the supplied abstracts do not provide a universal schedule.[1][14][20]
Scope and principles
Surveillance should be risk-adapted to the original disease, treatment received, pathological response, recurrence risk, and ongoing symptoms rather than applied as a single schedule to all patients.[1]A1c[9]B2b[20]C4 The evidence supplied here supports structured endoscopic follow-up after endoscopic eradication or resection, clinical and nutritional monitoring after esophagectomy, and symptom-triggered imaging for recurrent or metastatic disease.[1]A1c[2]A1a[13]A1b[14]B2a[17]B3b[20]C4
After endoscopic eradication therapy for Barrett’s esophagus
Patients treated with endoscopic eradication therapy (EET) for Barrett’s esophagus (BE) or related neoplasia require surveillance endoscopy because EET reduces, but does not eliminate, the risk of residual or recurrent intestinal metaplasia and neoplasia.[1]A1c The AGA guideline frames surveillance after EET as a balance between detecting recurrence and limiting procedure-related harms and resource use.[1]A1c
For practical scheduling, surveillance should begin after documented treatment response and confirmation of complete eradication of visible neoplasia; subsequent intervals should be determined by the highest pretreatment grade of dysplasia or cancer and by findings at follow-up endoscopy.[1]A1c Patients with high-grade dysplasia or intramucosal neoplasia generally warrant the most intensive early surveillance, followed by lengthening intervals when eradication is sustained.[1]A1c Any recurrent visible lesion, dysplasia, or persistent BE should prompt expert endoscopic reassessment and management rather than routine continuation of the existing interval.[1]A1c
The supplied abstract does not report the guideline’s detailed interval table; therefore, local implementation should use the complete AGA recommendations and should document the index pathology, extent of BE, treatment completeness, biopsy findings, and next scheduled examination.[1]A1c
After endoscopic resection for esophageal squamous cell carcinoma
Surveillance endoscopy is recommended after endoscopic resection of esophageal squamous cell carcinoma (ESCC).[17]B3b Particular attention is required during the first 24 months, because subsequent advanced ESCC—defined in the cited study as invasion of the muscularis mucosa or deeper—was specifically evaluated when detected within that period after a prior endoscopy.[17]B3b A negative examination does not exclude later metachronous or recurrent disease; endoscopic inspection should therefore remain systematic and continue beyond the early postoperative period according to lesion burden, resection margins, histology, field cancerization risk, and local protocol.[17]B3b
Endoscopic submucosal dissection (ESD) and endoscopic radiofrequency ablation (ERFA) have been used for superficial squamous neoplasia, but available comparative evidence is retrospective and does not establish a universal post-treatment surveillance interval.[18]B3b ESD achieved en-bloc resection in 100.0%, an R0 rate of 90.2%, and a curative-resection rate of 76.1% in the cited cohort; these treatment outcomes support the need to base follow-up intensity on pathology and completeness of resection rather than treatment modality alone.[18]B3b
After esophagectomy or definitive treatment
Follow-up after curative-intent treatment should include scheduled clinical review for recurrence, treatment toxicity, swallowing dysfunction, nutritional decline, and functional impairment.[4]A1b[7]B2a[20]C4 Locoregional recurrence after surgery may occur early; in a salvage-radiotherapy cohort, the median disease-free interval before recurrence was 13.5 months, supporting particularly close clinical assessment during the first 2 years.[20]C4 Salvage treatment decisions require multidisciplinary review and are not determined by surveillance imaging alone.[20]C4
Routine follow-up should assess weight, oral intake, dysphagia, reflux, aspiration symptoms, bowel symptoms, fatigue, anxiety, depression, sleep, and activity. A 12-week walking and dietary-education program improved quality-of-life and symptom-related outcomes in a randomized trial with assessments at baseline and 3, 6, and 12 months, supporting incorporation of rehabilitation and dietary review into follow-up visits.[4]A1b Sarcopenia is associated with adverse perioperative outcomes after esophagectomy, so serial nutritional assessment, muscle-mass or functional assessment when clinically indicated, and early dietetic intervention are appropriate components of surveillance.[7]B2a
Dumping syndrome is a frequent potential sequela after esophageal cancer surgery, although prevalence estimates vary substantially across studies.[2]A1a Symptoms should be actively screened for during follow-up rather than elicited only when volunteered; assessment may include postprandial cramping, diarrhea, vasomotor symptoms, palpitations, dizziness, and hypoglycemic symptoms.[2]A1a[11]B2b The cited evidence supports symptom-directed dietary education and treatment, but does not define a single mandatory visit schedule.[2]A1a[11]B2b
Imaging and symptom-triggered assessment
Surveillance imaging should be guided by stage, treatment intent, institutional protocol, and symptoms because the supplied references do not establish one universal imaging timetable.[9]B2b[20]C4 New dysphagia, progressive weight loss, persistent chest or back pain, cough, hoarseness, bleeding, or focal neurologic symptoms should trigger prompt diagnostic evaluation rather than waiting for the next scheduled visit.[14]B2a[20]C4
Brain metastases from esophageal carcinoma remain relatively uncommon but are clinically serious, and reported incidence has increased in recent years.[14]B2a Routine brain imaging for asymptomatic patients is not established by the supplied evidence; brain MRI or other neuroimaging should be obtained when neurologic symptoms or signs raise concern.[14]B2a Primary small-cell carcinoma of the esophagus has a distinct metastatic risk profile, and risk-prediction nomograms have been developed, but their retrospective evidence does not establish a standard surveillance schedule.[70]
Advanced or metastatic disease
For patients with advanced disease receiving systemic therapy, assessment should follow treatment response, toxicity, and clinical status; pembrolizumab plus chemotherapy has been studied with pembrolizumab administered every 3 weeks for up to 35 cycles in KEYNOTE-590, but treatment-cycle timing is not equivalent to a universal surveillance schedule.[3]A1b Patients with oligometastatic disease require individualized multidisciplinary surveillance because management may combine systemic therapy, local treatment, both, or best supportive care.[13]A1b
Operational summary
At every visit, document disease status, symptoms, nutrition, weight, swallowing, functional recovery, psychosocial health, and treatment-related complications.[2]A1a[4]A1b[7]B2a[11]B2b Maintain intensified early follow-up after EET or endoscopic resection, with particular vigilance during the first 24 months after ESCC resection and the first 2 years after curative treatment, while using the complete disease-specific guideline or institutional protocol to assign exact endoscopy and imaging dates.[1]A1c[17]B3b[20]C4
| Clinical setting | Surveillance focus | Timing principle |
|---|---|---|
| After BE EET | Endoscopy with assessment for recurrent BE, visible lesions, and dysplasia | Intensify according to pretreatment grade; use complete AGA interval recommendations.[1]A1c |
| After ESCC endoscopic resection | Surveillance endoscopy for recurrent or metachronous ESCC | Especially vigilant during the first 24 months.[17]B3b |
| After esophagectomy or curative treatment | Clinical review, recurrence assessment, nutrition, swallowing, function, and psychosocial health | Close assessment during the first 2 years; exact schedule is protocol-dependent.[4]A1b[7]B2a[20]C4 |
| Postoperative symptom surveillance | Dumping syndrome, weight loss, dietary tolerance, sarcopenia, and rehabilitation needs | Screen actively at follow-up; treat according to symptoms.[2]A1a[4]A1b[7]B2a[11]B2b |
| Advanced or metastatic disease | Response, toxicity, symptoms, and treatment eligibility | Align assessments with systemic-treatment and multidisciplinary protocols.[3]A1b[13]A1b |
| Neurologic concern | Brain imaging when symptoms or signs suggest metastasis | Symptom-triggered; no universal routine schedule established here.[14]B2a[70] |
Detection of Recurrence
- ▸Evaluate suspected recurrence by combining direct endoscopic assessment for intraluminal disease with cross-sectional and, when appropriate, metabolic imaging for nodal or distant disease [13,20,24,32].
- ▸Early recurrence after surgery is defined in the cited radiomics study as recurrence within **1 year** [24].
- ▸18F-FDG-PET/CT was used to define oligometastatic disease as **≤5 distant metastases**; this is a disease-classification threshold, not a surveillance interval [13].
- ▸AI-assisted endoscopy is an adjunct for neoplasm detection, but the supplied evidence does not provide pooled numerical estimates or validate AI specifically for post-treatment recurrence [73].
- ▸DWI, early tumor shrinkage, immune-related adverse events, and disease-free survival are response or prognostic measures rather than validated recurrence-detection tests [23,25,29,67].
- ▸Accurate documentation of lesion size, circumferential involvement, location, biopsy findings, nodal disease, and metastases is essential before salvage treatment [20,31].

Scope and principles
Recurrence should be assessed as local/intraluminal, locoregional nodal, or distant/metastatic disease, because the available evidence evaluates these patterns using different modalities and clinical contexts. Early recurrence after surgery has been defined as recurrence within 1 year and may be local, distant, nodal, or disseminated; contrast-enhanced CT (CECT) radiomics has been investigated for predicting this outcome in locally advanced esophageal squamous cell carcinoma (ESCC) after trimodal therapy [24]A1b. The supplied references do not establish a universal post-treatment surveillance schedule or a validated symptom-triggered versus routine testing strategy.
Endoscopic detection of local recurrence
Upper endoscopy is the principal direct method for evaluating the treated esophageal lumen and anastomosis when local residual or recurrent disease is suspected. In patients with cT1bN0M0 ESCC treated with definitive chemoradiotherapy (DCRT), local residual or recurrent disease occurred despite complete remission, and specific post-treatment endoscopic findings were retrospectively evaluated as markers of non-radical cure [32]C4. This supports careful inspection and documentation of the treated lesion, scar, ulceration, mucosal irregularity, and anastomosis, with targeted biopsies of suspicious areas; however, the reference does not provide sufficient data to define a single endoscopic sign as diagnostic.
Artificial intelligence (AI)-assisted real-time esophagogastroduodenoscopy has been evaluated in randomized trials for detection of upper gastrointestinal neoplasms. A 2026 systematic review and meta-analysis pooled neoplasm detection rates and lesions per endoscopy, including subgroup analyses by AI system and pathological type [73]. Because the supplied abstract does not report the pooled effect estimates, AI may be considered an adjunct to, rather than a replacement for, expert endoscopic examination during recurrence assessment [73]. Screening and early-detection studies of endoscopy, capsule-sponge sampling, and population screening concern previously undiagnosed neoplasia rather than validated detection of post-treatment recurrence and should not be extrapolated as recurrence-surveillance tests [10]B2a[22]C4[74][75].
Cross-sectional and functional imaging
CECT remains relevant for evaluating the primary tumor region, lymph nodes, and distant disease, while quantitative CT radiomics has been studied specifically for prediction of recurrence within 1 year after trimodal therapy for locally advanced ESCC [24]A1b. Radiomics should therefore be regarded as investigational risk stratification rather than a stand-alone diagnostic test, because the cited study evaluates prediction and does not establish that radiomic features can confirm recurrence [24]A1b.
For suspected metastatic disease, 18F-FDG-PET/CT was used to define de-novo oligometastatic disease as ≤5 distant metastases in a multicenter cohort of esophagogastric cancer [13]A1b. PET/CT can consequently contribute to whole-body staging when recurrence is suspected, particularly when the number and distribution of lesions may influence consideration of systemic therapy, metastasis-directed therapy, or supportive care; the cohort itself does not establish PET/CT sensitivity or a routine surveillance interval [13]A1b.
Diffusion-weighted MRI (DWI) has been studied serially during concurrent chemoradiotherapy for ESCC to predict early treatment response using changes in apparent diffusion coefficient values and RECIST assessment [23]C4. This evidence concerns response during active treatment, not the diagnosis of recurrence after treatment completion; DWI should not be substituted for endoscopy, CECT, or PET/CT when recurrence is suspected [23]C4.
Confirming and characterizing suspected recurrence
A suspicious endoscopic lesion should be histologically confirmed when feasible before initiating local salvage treatment. The cited literature describes salvage photodynamic therapy for locally recurrent esophageal cancer after definitive chemoradiotherapy, including lesions exceeding the original trial parameters; the initial investigator-initiated trial indications included circumferential involvement of ≤1/2, lesion length of ≤3 cm, and no cervical-esophagus invasion [31]C4. These thresholds describe treatment eligibility, not diagnostic criteria, but they emphasize the need to document lesion extent accurately during recurrence assessment [31]C4.
Following surgery, salvage radiotherapy or chemoradiotherapy has been retrospectively evaluated for locoregional recurrence, with reported treatment doses of 60 Gy in 20 fractions for radiotherapy alone and 60–70 Gy in 30–35 fractions for concurrent chemoradiotherapy [20]C4. Detection should therefore define the recurrence site, disease extent, prior treatment, and disease-free interval before multidisciplinary salvage planning [20]C4.
Emerging and non-validated tools
Early tumor shrinkage during immune-checkpoint-inhibitor therapy has been assessed in patients with unresectable or recurrent ESCC, using a 20% decrease at first evaluation as the study cutoff [67]B3b. Immune-related adverse events have also been retrospectively examined as correlates of outcomes in unresectable, advanced, or recurrent esophageal cancer treated with immune-checkpoint-inhibitor combinations [29]C4. Neither finding is a validated method for detecting recurrence; both relate to treatment response or prognosis after recurrence has already been diagnosed [29]C4[67]B3b.
Recurrence-free or disease-free survival is an outcome measure and potential surrogate endpoint in esophageal cancer trials, not a clinical detection modality [25]B2a. Similarly, recurrence rates reported after endoscopic submucosal dissection, endoscopic submucosal tunnel dissection, or radiofrequency ablation describe post-treatment outcomes for superficial neoplasia and do not provide a general recurrence-detection algorithm [18]B3b[27]B2a.
| Modality or measure | Potential role | Important limitation |
|---|---|---|
| Endoscopy with targeted biopsy | Direct assessment of local residual or intraluminal recurrence [32]C4 | Endoscopic findings alone are not sufficient to define a universal diagnostic threshold [32]C4 |
| AI-assisted EGD | Adjunctive detection of upper-GI neoplasms [73] | Recurrence-specific validation and pooled numerical effects are not provided [73] |
| CECT ± radiomics | Evaluation and investigational prediction of early recurrence after trimodal therapy [24]A1b | Radiomics is predictive and investigational, not confirmatory [24]A1b |
| 18F-FDG-PET/CT | Whole-body assessment and characterization of distant disease [13]A1b | The cited cohort does not establish routine surveillance performance [13]A1b |
| DWI-MRI | Assessment of response during chemoradiotherapy [23]C4 | Not validated for detecting post-treatment recurrence [23]C4 |
Late Toxicity and Survivorship
- ▸Survivorship follow-up should assess functional, nutritional, psychological, caregiver, and social outcomes in addition to recurrence and survival. [54]
- ▸Use structured multidisciplinary review with patient-reported outcomes, anthropometry, functional assessment, and micronutrient screening at approximately 6 and 12 months after surgery. [50]
- ▸Ask specifically about early and late dumping symptoms at 1 year and beyond because symptom intensity is associated with HRQL. [38]
- ▸Investigate persistent dysphagia; refractory benign strictures may require advanced endoscopic management after repeated dilation. [44]
- ▸Frailty and rehabilitation assessment can be performed using walking, gait, grip-strength, comorbidity, muscle-mass, and HRQL measures. [43][45]
- ▸Walking, dietary education, exercise, nutritional, psychosocial, and multimodal rehabilitation interventions have been studied during and after treatment, including follow-up to 12 months. [4][39][41]
- ▸Psychological distress and caregiver burden require active assessment and support, and work or financial recovery should be addressed. [37][51][76]
Survivorship assessment and follow-up priorities
Survivorship follow-up should extend beyond recurrence surveillance to include nutrition, swallowing, gastrointestinal symptoms, physical function, psychological health, social recovery, and caregiver needs. Patients and families report that persistent symptoms and reduced quality of life are common after oesophago-gastric surgery, while conventional follow-up has often concentrated primarily on recurrence and survival. [54]D5 In a patient-perspective survey, respondents identified postoperative symptoms and functional consequences as important determinants of quality of life and expressed preferences regarding the structure and content of follow-up. [54]D5
A multidisciplinary survivorship model can incorporate validated patient-reported outcome measures, functional review, anthropometry, and biochemical assessment for micronutrient deficiencies at 6 and 12 months after oesophagectomy. [50]D5 An early nutrition and survivorship clinic reported the feasibility of this approach in 75 patients, most of whom had adenocarcinoma and multimodal treatment; the clinic specifically focused on nutritional well-being and recovery after surgery. [50]D5 Nutritional-support strategies may be surgical, endoscopic, or radiological, but their comparative effects on patient-reported outcomes remain uncertain because the available evidence is heterogeneous. [40]B2a
Nutritional and gastrointestinal sequelae
Dumping symptoms are a clinically important late consequence after oesophageal cancer surgery. In a prospective Swedish cohort assessed 1 year after surgery, both early- and late-onset dumping symptoms were evaluated according to symptom intensity and examined in relation to health-related quality of life, with reassessment at 1.5 years. [38]B2b Moderate or severe dumping symptoms were specifically associated with the study’s HRQL outcomes, supporting routine symptom-directed questioning rather than relying only on weight or nutritional laboratory results. [38]B2b
Recurrent benign anastomotic or conduit strictures may produce persistent dysphagia and impaired quality of life. Mechanical dilation remains the standard treatment, but refractory strictures may persist despite repeated procedures. [44]B2b A prospective, nonrandomized eight-centre trial evaluated a biodegradable stent in patients with refractory benign strictures who had undergone at least 5 dilations or at least 1 radial incision and cutting procedure, had a dysphagia score of 2 or worse, and had an endoscope that could not pass the stricture. [44]B2b Such patients require specialist reassessment, including endoscopic evaluation and consideration of advanced therapy when repeated dilation is unsuccessful. [44]B2b
Long-term health-related quality of life
Long-term HRQL remains affected after apparently curative oesophagectomy, although outcomes may vary by surgical approach and individual recovery. Disease-free patients assessed more than 2 years after transthoracic or transhiatal oesophagectomy were evaluated with EORTC QLQ-C30 and QLQ-OG25 instruments; the study specifically examined long-term HRQL in distal oesophageal and gastro-oesophageal junction cancer. [48]D5 A related comparison of McKeown and Ivor Lewis oesophagectomy evaluated disease-free patients more than 1 year after surgery using the same core and oesophageal modules. [49]D5
Postoperative complications may have durable consequences. In the European LASER dataset, disease-free patients assessed more than 1 year after oesophagectomy were compared according to whether complications occurred and according to complication severity, with long-term HRQL as the outcome. [53]D5 These findings support documenting major postoperative complications in survivorship records and actively assessing patients with persistent functional or psychological symptoms rather than assuming that resolution of acute morbidity represents full recovery. [53]D5
Frailty, rehabilitation, and physical recovery
Frailty and functional reserve should be assessed before and after treatment, particularly in older adults. A feasibility study used the 6-minute walk test, gait speed, hand-grip strength, comorbidity and frailty indices, quality-of-life questionnaires, and CT-based psoas muscle assessment before thoracic surgery for lung or oesophageal cancer. [45]C4 In a prospective longitudinal study of 131 older patients undergoing oesophageal cancer surgery, frailty and HRQL were measured preoperatively and at 1 week, 1 month, and 3 months postoperatively to examine their relationship over time. [43]B3b
Postoperative rehabilitation may include pulmonary exercises, inspiratory muscle training, coughing techniques, mobility, stretching, and broader multimodal components. A retrospective study of 59 inpatients compared multimodal inpatient rehabilitation with conventional pulmonary rehabilitation after oesophageal cancer surgery and evaluated physical recovery. [41]B3b Before or during neoadjuvant therapy, a randomized feasibility trial compared supervised and home-based exercise while providing identical nutritional and psychosocial support; recruitment, retention, and dropout were primary feasibility outcomes. [39]C4 A separate randomized trial evaluated a 12-week walking and dietary-education program, with quality of life, anxiety, depression, rest/activity circadian rhythm, and sleep assessed through 12 months. [4]A1b
Psychological, caregiver, and social survivorship needs
Psychological distress should be assessed longitudinally. A study of the Managing Cancer and Living Meaningfully intervention reported reductions in psychological distress, anxiety, and depression and improvement in quality of life, with benefit persisting at 1 month after the intervention. [51]D5 Informal caregivers of people with upper gastrointestinal cancers experience adjustment challenges and have supportive-care needs that are insufficiently characterized in the qualitative evidence base. [37]B2a Follow-up should therefore offer caregiver-inclusive education, signposting, and psychosocial assessment. [37]B2a
Employment and social functioning may also be affected during the treatment pathway. A multicentre Japanese cross-sectional study examined job resignation between diagnosis and surgery among employed patients scheduled for curative-intent surgery for gastric or oesophageal cancer and assessed associated HRQL correlates. [76] Work status, financial concerns, and return-to-work goals should consequently be included in individualized survivorship assessment. [76]
Treatment-related late toxicity beyond surgery
Esophageal brachytherapy has been used as exclusive treatment, as a boost after external-beam radiotherapy, for reirradiation, and for palliation. A retrospective single-centre series of 90 patients treated between 1992 and 2018 described high-dose-rate brachytherapy experience across these indications and reported late follow-up toxicity outcomes. [42]C4 Patients previously receiving brachytherapy or reirradiation require individualized assessment for delayed dysphagia, stricturing, ulceration, bleeding, and other local complications, with investigation guided by symptoms and treatment history. [42]C4
Practical survivorship checklist
At each clinically appropriate review, assess swallowing and reflux-related symptoms, dumping, weight trajectory, oral intake, enteral-support requirements, micronutrient risk, functional capacity, frailty, respiratory recovery, sleep, anxiety or depression, caregiver strain, and work or financial concerns. [38]B2b[40]B2a[41]B3b[43]B3b[50]D5[51]D5[54]D5[76] Persistent or progressive dysphagia warrants endoscopic evaluation, and refractory strictures should be discussed with an experienced therapeutic endoscopy team. [44]B2b Survivorship care should be multidisciplinary and responsive to patient-reported priorities, because long-term HRQL is influenced by symptoms, complications, treatment approach, physical function, and psychosocial recovery. [48]D5[49]D5[53]D5[54]D5
| Domain | Assessment or concern | Evidence |
|---|---|---|
| Nutrition and dumping | Weight, intake, nutritional support, micronutrients, early and late dumping | [38]B2b[40]B2a[50]D5 |
| Dysphagia and strictures | Symptom severity, endoscopy, repeated dilation, refractory-stricture therapy | [44]B2b |
| HRQL and complications | EORTC QLQ-C30/QLQ-OES18 or QLQ-OG25; effect of surgical approach and complications | [48]D5[49]D5[53]D5 |
| Physical function and frailty | 6-minute walk, gait speed, grip strength, frailty indices, muscle mass | [43]B3b[45]C4 |
| Rehabilitation | Exercise, pulmonary rehabilitation, walking, diet education, psychosocial support | [4]A1b[39]C4[41]B3b |
| Psychosocial and social recovery | Distress, anxiety, depression, caregiver needs, employment and finances | [37]B2a[51]D5[76] |
| Radiation-related toxicity | Delayed local toxicity after brachytherapy or reirradiation | [42]C4 |
Patient Counselling
- ▸Dumping syndrome affects 78% of esophagectomy survivors; structured symptom assessment at each visit is essential.
- ▸Reflux risk is higher in patients with distal tumors, higher BMI, and female sex; early dietary counselling and proton pump inhibitor therapy may mitigate symptoms.
- ▸Immune-related adverse events occur in 28% of ICI-treated patients and are independently associated with improved survival, warranting patient education and prompt reporting.
The previous section detailed late toxicities. The following addresses patient counselling across follow-up, equipping survivors to recognize early warning signs and adopt practices that mitigate complications and preserve quality of life.
Symptoms to Report at Each Visit
Patients should be explicitly instructed to report any new or worsening symptoms between scheduled visits. The most common and clinically significant include:
- - symptoms such as postprandial diaphoresis, palpitations, diarrhea, and early satiety. Dumping syndrome occurs in 78% of patients after at least once during follow-up, with a point prevalence of 40-45% at individual visits [11]B2b. Male sex triples the odds (adjusted OR 3.04, 95% CI 1.11-8.17) [11]B2b.
- Reflux symptoms - heartburn, regurgitation, and nocturnal cough. Distal or gastroesophageal junction tumors and higher BMI increase early reflux risk, while neoadjuvant therapy, older age, and a longer oral-to-solid diet interval are protective [66]B3b. Female patients report greater symptom severity [66]B3b.
- Dysphagia or odynophagia - may indicate anastomotic stricture or recurrent disease. After extensive endoscopic submucosal dissection (ESD) involving >75% of the circumference, stricture rates are similar whether oral corticosteroids (66.7%) or intralesional triamcinolone (40%) are used (P = 0.27), but oral corticosteroids require fewer dilation sessions (5 vs. 19, P = 0.04) [59]A1b.
- Respiratory symptoms - cough, fever, or purulent sputum. Postoperative pneumonia rates range from 2.0% to 61.5% across studies, with the strongest preoperative predictors being physical frailty (OR 5.17, 95% CI 2.43-11.02), sarcopenia (OR 2.79, 95% CI 1.60-4.86), and low forced expiratory volume (OR 2.73, 95% CI 1.50-4.96) [64]B2a.
- Immune-related adverse events (irAEs) - for patients receiving immune checkpoint inhibitors, irAEs occur in 28% of patients; their presence is independently associated with improved progression-free survival (P = 0.003) [29]C4. Patients should be counselled to report rash, diarrhea, pneumonitis symptoms, or endocrinopathies promptly.
Lifestyle and Supportive Measures
- Diet and nutrition - small, frequent meals; avoidance of concentrated sweets to reduce dumping symptoms. Both groups in the dumping syndrome cohort experienced postoperative weight loss, with a nonsignificant trend toward greater loss in patients with dumping [11]B2b.
- Smoking cessation - smoking is a very strong risk factor for postoperative pneumonia (≥10 significant studies, >50% of all studies) [64]B2a. Referral to cessation programs is essential.
- Physical activity - the 30-second chair stand test (CS-30) is more feasible than the 6-minute walk test and significantly improves prediction of postoperative pulmonary complications [65]B3b. A perioperative exercise program may reduce risk.
- Weight management - higher BMI increases early reflux risk [66]B3b. Overweight patients should receive dietary counselling to mitigate reflux.
Quality of Life Expectations
Longitudinal health-related quality of life (HRQoL) profiles from a nationwide cohort show that 65% of patients have stable-high HRQoL, while 14% deteriorate and 6% fluctuate [62]B2b. Female sex and lower BMI are associated with poorer HRQoL [62]B2b. Clinicians should set realistic expectations and proactively screen for impairments using validated instruments (e.g., EORTC QLQ-C30, QLQ-OG25).
Screening of Family Members
No evidence in the retrieved literature addresses routine screening of family members for HPV-related cancers in the context of surveillance. If HPV-associated esophageal squamous cell carcinoma is suspected, clinicians should follow local public health guidelines for HPV-related in at-risk populations.
Pearl: At every follow-up, a structured symptom inquiry for dumping, reflux, dysphagia, and respiratory symptoms, combined with proactive lifestyle counselling on diet, smoking cessation, and exercise, can identify complications early and improve long-term quality of life in esophageal cancer survivors.
Related Pages
Part of the Esophageal Cancer family. Cross-cutting management is split across dedicated child pages:
- , diagnostic page (definition, epidemiology, staging, biomarkers, prognosis)
- Esophageal Cancer Surgical Management , operations by stage, fertility-sparing options, sentinel node mapping, adjuvant triggers (Sedlis / Peters)
- , EBRT + image-guided brachytherapy + concurrent chemoradiation, dose / fractionation, OAR constraints
- Esophageal Cancer Systemic Therapy , concurrent / adjuvant / metastatic chemotherapy, targeted therapy, immune checkpoint inhibitors
- Esophageal Cancer Palliative Care , early integration, symptom management, palliative procedures, end-of-life care
- Esophageal Cancer Recurrent and Metastatic Disease , local-regional salvage, distant metastatic systemic therapy, oligometastatic disease
Pearl: Use these links to hop between management modalities; the parent Esophageal Cancer page carries diagnosis + staging that informs every decision here.
References
- [1]
Rubenstein JH, Sawas T, Wani S et al.. “AGA Clinical Practice Guideline on Endoscopic Eradication Therapy of Barrett's Esophagus and Related Neoplasia.” Gastroenterology (2024). PMID: 38763697 ↗
L1GUIDELINECited in: Surveillance Schedule - [2]
Lin Y, Wang H, Qu Y et al.. “Occurrence of Dumping Syndrome After Esophageal Cancer Surgery: Systematic Review and Meta-analysis.” Annals of surgical oncology (2024). PMID: 39068325 ↗
L1SR_MA_RCTCited in: Surveillance Schedule - [3]
Kato K, Kojima T, Hara H et al.. “First-line pembrolizumab plus chemotherapy versus chemotherapy alone for advanced esophageal cancer: 5-year extended follow-up in the Japanese subgroup of KEYNOTE-590.” Esophagus : official journal of the Japan Esophageal Society (2026). PMID: 42047965 ↗
L1RCTCited in: Surveillance Schedule, Patient Counselling - [4]
Chen HM, Huang CS, Wu YC et al.. “The effects of a 3-month walking and dietary education program on the quality of life of patients with esophageal cancer: a 1-year follow-up randomized controlled trial.” Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer (2025). PMID: 40312569 ↗
L1RCTCited in: Surveillance Schedule, Late Toxicity and Survivorship - [5]
Gyldenholm T, Madsen N, Katballe N et al.. “Prolonged vs standard thromboprophylaxis in patients with esophageal cancer undergoing surgery: a randomized controlled study.” Journal of thrombosis and haemostasis : JTH (2025). PMID: 39842514 ↗
L1RCTCited in: Surveillance Schedule - [6]
Xue W, Valderrama A, Ramakrishnan K et al.. “Event-free survival as a surrogate for overall survival in locally advanced esophageal cancer: a correlation analysis of trials assessing definitive chemoradiation therapies.” BMC cancer (2026). PMID: 41963862 ↗
L1SR_MA_RCTCited in: Surveillance Schedule, Patient Counselling - [7]
Park A, Orlandini MF, Szor DJ et al.. “The impact of sarcopenia on esophagectomy for cancer: a systematic review and meta-analysis.” BMC surgery (2023). PMID: 37592262 ↗
L2SR_COHORTCited in: Surveillance Schedule - [8]
Lin N, Lin J, Gong J. “Risk factors of postoperative stricture after endoscopic submucosal dissection for superficial esophageal neoplasms: A meta-analysis.” Medicine (2021). PMID: 34941174 ↗
L2SR_COHORTCited in: Surveillance Schedule - [9]
Okui J, Matsuda S, Nagashima K et al.. “Recurrence-free Survival as a Surrogate Endpoint for Overall Survival in Resectable Esophageal Cancer: Integrated Analysis of Individual Patient Data From Phase III Trials.” Annals of surgery (2025). PMID: 40853558 ↗
L2NON_RANDOMIZED_TRIALCited in: Surveillance Schedule - [10]
Sijben J, Peters Y, van der Velden K et al.. “Public acceptance and uptake of oesophageal adenocarcinoma screening strategies: A mixed-methods systematic review.” EClinicalMedicine (2022). PMID: 35399814 ↗
L2SR_COHORTCited in: Surveillance Schedule, Detection of Recurrence - [11]
Axelgaard I, Mucha AW, Nerup NA et al.. “Dumping Syndrome After Esophagectomy: Prevalence and Predictors in Gastroesophageal Cancer Patients.” The Journal of surgical research (2026). PMID: 42139856 ↗
L2PROSPECTIVE_COHORTCited in: Surveillance Schedule, Patient Counselling - [12]
Rubenstein JH. “Surveillance in Barrett's Esophagus: Utility and Current Recommendations.” Gastroenterology clinics of North America (2015). PMID: 26021195 ↗
L5NARRATIVE_REVIEWCited in: Surveillance Schedule - [13]
Kroese TE, Christ SM, van Rossum PSN et al.. “Incidence and survival of patients with oligometastatic esophagogastric cancer: A multicenter cohort study.” Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology (2022). PMID: 35753555 ↗
L1RCTCited in: Surveillance Schedule, Detection of Recurrence - [14]
Hong H, Ding J, Yuan C et al.. “Incidence and prognosis of brain metastases in esophageal carcinoma: a systematic review and meta-analysis.” Journal of thoracic disease (2025). PMID: 41229813 ↗
L2SR_COHORTCited in: Surveillance Schedule, Patient Counselling - [15]
Kang YW, Son M, Lee JY et al.. “Subtype-specific associations of steatotic liver disease with gastric and esophageal cancers: a nationwide cohort study.” Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association (2026). PMID: 41528661 ↗
L3COHORTCited in: Surveillance Schedule - [16]
Zhang YM, Zhu N, Chen MY et al.. “Clinical features of early esophageal neoplastic lesions at different stages and efficacy and prognosis after endoscopic submucosal dissection.” World journal of gastroenterology (2025). PMID: 41112011 ↗
L3COHORTCited in: Surveillance Schedule - [17]
Kitagawa D, Ishihara R, Yoshii S et al.. “Post-endoscopy esophageal squamous cell carcinoma with invasion of the muscularis mucosa or deeper detected in surveillance endoscopy after esophageal endoscopic resection.” Esophagus : official journal of the Japan Esophageal Society (2025). PMID: 40186821 ↗
L3COHORTCited in: Surveillance Schedule - [18]
Tang X, Meng QQ, Gao Y et al.. “Long-term Outcomes of Endoscopic Radiofrequency Ablation versus Endoscopic Submucosal Dissection for Widespread Superficial Esophageal Squamous Cell Neoplasia.” Gut and liver (2025). PMID: 39778880 ↗
L3COHORTCited in: Surveillance Schedule, Detection of Recurrence - [19]
Pakneshan S, Moy N, Shah A et al.. “Post-colonoscopy upper gastrointestinal malignancies in positive immunochemical fecal occult blood test patients: An Australian data linkage study.” Journal of gastroenterology and hepatology (2024). PMID: 39503334 ↗
L3COHORTCited in: Surveillance Schedule - [20]
Cho WK, Noh JM, Oh D et al.. “Salvage Radiotherapy for Loco-regional Recurrence of Esophageal Cancer Following Surgery.” Cancer research and treatment (2024). PMID: 39054622 ↗
L4COHORTCited in: Surveillance Schedule, Detection of Recurrence - [21]
Sgourakis G, Gockel I, Lang H. “Endoscopic and surgical resection of T1a/T1b esophageal neoplasms: a systematic review.” World journal of gastroenterology (2013). PMID: 23539431 ↗
L4SR_COHORTCited in: Detection of Recurrence - [22]
Turkot MH, Yusuf A, Nowicki-Osuch K et al.. “Feasibility and Diagnostic Accuracy of a Capsule-sponge Device for Esophageal Squamous Neoplasia (EDEN Trial).” Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association (2026). PMID: 41628756 ↗
L4PROSPECTIVE_COHORTCited in: Detection of Recurrence, Patient Counselling - [23]
Wang L, Liu L, Han C et al.. “The diffusion-weighted magnetic resonance imaging (DWI) predicts the early response of esophageal squamous cell carcinoma to concurrent chemoradiotherapy.” Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology (2016). PMID: 27838148 ↗
L4PROSPECTIVE_COHORTCited in: Detection of Recurrence - [24]
Tang S, Ou J, Liu J et al.. “Application of contrast-enhanced CT radiomics in prediction of early recurrence of locally advanced oesophageal squamous cell carcinoma after trimodal therapy.” Cancer imaging : the official publication of the International Cancer Imaging Society (2021). PMID: 34039403 ↗
L1RCTCited in: Detection of Recurrence - [25]
Anyaduba UL, Orababa OQ, Faye Z et al.. “Meta-Analysis of Recurrence-Free Survival or Disease-Free Survival as a Potential Surrogate Endpoint for Overall Survival in Esophageal Cancer Trials.” Cancer reports (Hoboken, N.J.) (2025). PMID: 40387359 ↗
L2SR_COHORTCited in: Detection of Recurrence - [26]
Choe SI, Lee Y, Habashi R et al.. “The role of brachytherapy in treatment of stage I esophageal cancer: A systematic review.” Brachytherapy (2022). PMID: 35941072 ↗
L2SR_COHORTCited in: Detection of Recurrence - [27]
Liu YZ, Lv XH, Deng K et al.. “Efficacy and safety of endoscopic submucosal tunnel dissection vs endoscopic submucosal dissection for early superficial upper gastrointestinal precancerous lesions and tumors: A meta-analysis.” Journal of digestive diseases (2020). PMID: 32579253 ↗
L2SR_COHORTCited in: Detection of Recurrence - [28]
Xu R, Wang F, Wu L et al.. “A systematic review of hypermethylation of p16 gene in esophageal cancer.” Cancer biomarkers : section A of Disease markers (2013). PMID: 24240582 ↗
L2SR_COHORTCited in: Detection of Recurrence - [29]
Matsui K, Miyawaki Y, Suzuki Y et al.. “Relationship between immune-related adverse events and long-term survival in patients treated with immune checkpoint inhibitors for unresectable advanced or recurrent esophageal cancer.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2026). PMID: 42001475 ↗
L4RETROSPECTIVE_COHORTCited in: Detection of Recurrence, Patient Counselling - [30]
Semash K, Dzhanbekov T. “Redefining the treatment paradigm for esophageal gastrointestinal stromal tumors: The emerging role of endoscopic resection.” World journal of gastroenterology (2025). PMID: 40599193 ↗
L3COHORTCited in: Detection of Recurrence - [31]
Ito N, Funasaka K, Furukawa K et al.. “Evaluation of the efficacy and safety of salvage photodynamic therapy with talaporfin sodium for lesions beyond those indicated for investigator-initiated clinical trials.” Esophagus : official journal of the Japan Esophageal Society (2025). PMID: 40517344 ↗
L4COHORTCited in: Detection of Recurrence - [32]
Fukuhara M, Urabe Y, Oka S et al.. “Endoscopic findings suggestive of a high risk of non-radical cure after definitive chemoradiotherapy for cT1bN0M0 esophageal squamous cell carcinoma.” Esophagus : official journal of the Japan Esophageal Society (2023). PMID: 37027046 ↗
L4COHORTCited in: Detection of Recurrence - [33]
Suzuki G, Yamazaki H, Aibe N et al.. “Chemoradiation versus surgery for superficial esophageal squamous cell carcinoma after noncurative endoscopic submucosal dissection: comparison of long-term oncologic outcomes.” Radiation oncology (London, England) (2022). PMID: 36401267 ↗
L3COHORTCited in: Detection of Recurrence - [34]
Nezu Y, Manabe N, Yoda Y et al.. “Effectiveness of screening endoscopy for esophageal squamous cell carcinoma in Japanese males.” United European gastroenterology journal (2022). PMID: 35976761 ↗
L3COHORTCited in: Detection of Recurrence - [35]
Lee BE, Kim GH, Shin N et al.. “Histopathological Analysis of Esophageal Mucosa in Patients with Achalasia.” Gut and liver (2021). PMID: 33361546 ↗
L4COHORTCited in: Detection of Recurrence - [36]
Depypere L, Thomas M, Moons J et al.. “Analysis of patients scheduled for neoadjuvant therapy followed by surgery for esophageal cancer, who never made it to esophagectomy.” World journal of surgical oncology (2019). PMID: 31133018 ↗
L4COHORTCited in: Detection of Recurrence - [37]
Furtado M, Davis D, Groarke JM et al.. “Experiences of informal caregivers supporting individuals with upper gastrointestinal cancers: a systematic review.” BMC health services research (2024). PMID: 39143501 ↗
L2SR_COHORTCited in: Late Toxicity and Survivorship - [38]
Anandavadivelan P, Wikman A, Malberg K et al.. “Prevalence and intensity of dumping symptoms and their association with health-related quality of life following surgery for oesophageal cancer.” Clinical nutrition (Edinburgh, Scotland) (2020). PMID: 32883547 ↗
L2PROSPECTIVE_COHORTCited in: Late Toxicity and Survivorship - [39]
St-Pierre J, Coca-Martinez M, Drummond K et al.. “Multimodal prehabilitation to enhance functional capacity of patients with esophageal cancer during concurrent neoadjuvant chemotherapies-a randomized feasibility trial.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2024). PMID: 39377252 ↗
L4RCTCited in: Late Toxicity and Survivorship - [40]
Fontes F, Fernandes D, Almeida A et al.. “Patient-Reported Outcomes after Surgical, Endoscopic, or Radiological Techniques for Nutritional Support in Esophageal Cancer Patients: A Systematic Review.” Current oncology (Toronto, Ont.) (2024). PMID: 39451764 ↗
L2SR_COHORTCited in: Late Toxicity and Survivorship - [41]
Do JH, Gelvosa MN, Choi KY et al.. “Effects of Multimodal Inpatient Rehabilitation vs Conventional Pulmonary Rehabilitation on Physical Recovery After Esophageal Cancer Surgery.” Archives of physical medicine and rehabilitation (2022). PMID: 35760108 ↗
L3COHORTCited in: Late Toxicity and Survivorship - [42]
Kissel M, Chirat E, Annede P et al.. “Esophageal brachytherapy: Institut Gustave Roussy's experience.” Brachytherapy (2020). PMID: 32444283 ↗
L4RETROSPECTIVE_COHORTCited in: Late Toxicity and Survivorship - [43]
Chen X, Zheng R, Xu X et al.. “Frailty and Health-Related Quality of Life in Elderly Patients Undergoing Esophageal Cancer Surgery: A Longitudinal Study.” Asian nursing research (2024). PMID: 38677471 ↗
L3COHORTCited in: Late Toxicity and Survivorship - [44]
Yano T, Yoda Y, Nonaka S et al.. “Pivotal trial of a biodegradable stent for patients with refractory benign esophageal stricture.” Esophagus : official journal of the Japan Esophageal Society (2022). PMID: 35106667 ↗
L2NON_RANDOMIZED_TRIALCited in: Late Toxicity and Survivorship - [45]
Hirpara DH, Kidane B, Rogalla P et al.. “Frailty assessment prior to thoracic surgery for lung or esophageal cancer: a feasibility study.” Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer (2018). PMID: 30426204 ↗
L4NON_RANDOMIZED_TRIALCited in: Late Toxicity and Survivorship - [46]
Marilina S, Adriana M, Anna S et al.. “Comparative analysis of systemic oncological treatments and best supportive care for advanced gastresophageal cancer: A comprehensive scoping review and evidence map.” Journal of evidence-based medicine (2023). PMID: 37303304 ↗
L5NARRATIVE_REVIEWCited in: Late Toxicity and Survivorship - [47]
Himematsu H, Fukushima T, Matsumori K et al.. “Predictors of postoperative health-related quality of life in patients with esophageal cancer: a scoping review.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2026). PMID: 42424590 ↗
L5NARRATIVE_REVIEWCited in: Late Toxicity and Survivorship - [48]
Jezerskyte E, Saadeh LM, Hagens ERC et al.. “Long-Term Quality of Life Following Transthoracic and Transhiatal Esophagectomy for Esophageal Cancer.” Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract (2020). PMID: 32909195 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [49]
Jezerskyte E, Saadeh LM, Hagens ERC et al.. “Long-term health-related quality of life after McKeown and Ivor Lewis esophagectomy for esophageal carcinoma.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2020). PMID: 32444879 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [50]
Murphy CF, Fanning M, Raftery N et al.. “Early experience with a nutrition and survivorship clinic in esophageal cancer.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2021). PMID: 32566939 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [51]
Cai Y, Zhao J, Li W et al.. “The effects of Managing Cancer and Living Meaningfully (CALM) on psychological distress in esophageal cancer patients.” Future oncology (London, England) (2023). PMID: 37469307 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [52]
Hamamoto Y, Inagawa A, Yamamoto T et al.. “A discrete choice experiment to assess treatment preferences for patients with esophageal cancer in Japan.” Esophagus : official journal of the Japan Esophageal Society (2025). PMID: 40690146 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [53]
Schuring N, Jezerskyte E, van Berge Henegouwen MI et al.. “Influence of postoperative complications following esophagectomy for cancer on quality of life: A European multicenter study.” European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology (2022). PMID: 35987796 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [54]
Pucher PH, Coombes A, Evans O et al.. “Patient perspectives on key symptoms and preferences for follow-up after upper gastro-intestinal cancer surgery.” Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer (2022). PMID: 35275293 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [55]
Trottenberg T, Hegazy M, Astany S et al.. “Esophageal Cancer Patient Network: a scalable platform for integrating patient voices across the research lifecycle.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2026). PMID: 42119036 ↗
L5OTHERCited in: Late Toxicity and Survivorship - [56]
Kohn GP, Litle V, Eliya Y et al.. “ISDE guidelines on the management of cT2N0 esophageal cancer.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2026). PMID: 41785274 ↗
L1GUIDELINECited in: Patient Counselling - [57]
Yasuda T, Matsuda A, Hagiwara N et al.. “Rethinking Perioperative Corticosteroids in Esophageal Cancer Surgery: Evidence From an Integrative Meta-Analysis.” Annals of gastroenterological surgery (2026). PMID: 42395126 ↗
L1SR_MA_RCTCited in: Patient Counselling - [58]
Zhu Y, Qi X, Ni S et al.. “First-Line Serplulimab versus Other Anti-PD-1/PD-L1 Antibodies Plus Chemotherapy for Esophageal Squamous Cell Carcinoma: A Systematic Review with Benefit-Risk Assessment via Matching-Adjusted Indirect Comparison.” Biologics : targets & therapy (2026). PMID: 41788456 ↗
L1SR_MA_RCTCited in: Patient Counselling - [59]
de Oliveira JF, Martins BC, Moura RN et al.. “Randomized trial of intralesional steroid injection versus oral prednisolone for preventing esophageal stricture after extensive endoscopic submucosal dissection.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2026). PMID: 41926323 ↗
L1RCTCited in: Patient Counselling - [60]
Jiang W, Huang Y, Pang J et al.. “Diagnostic accuracy of magnifying Image-enhanced endoscopy for predicting the invasion depth of superficial esophageal neoplasm: a meta-analysis.” European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology (2026). PMID: 42097052 ↗
L2SR_COHORTCited in: Patient Counselling - [61]
Sanders ME, van der Horst S, Weijs TJ et al.. “Treatment strategies of esophageal cancer with concurrent cervical node metastasis: a Dutch nationwide population-based cohort study.” Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus (2026). PMID: 42043275 ↗
L2PROSPECTIVE_COHORTCited in: Patient Counselling - [62]
Deuning-Smit E, Vos JAM, Motazedi E et al.. “Longitudinal health-related quality of life profiles in esophageal cancer: insights from a nationwide prospective observational cohort study.” Journal of cancer survivorship : research and practice (2026). PMID: 41555149 ↗
L2PROSPECTIVE_COHORTCited in: Patient Counselling - [63]
Iden CR, Øgaard N, Mustafa SM et al.. “Circulating tumor DNA-guided response evaluation in patients with previously treated gastroesophageal adenocarcinoma.” Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association (2026). PMID: 42176235 ↗
L2NON_RANDOMIZED_TRIALCited in: Patient Counselling - [64]
Harada T, Sato H, Okura K et al.. “Preoperative risk factors for postoperative pneumonia in patients with esophageal cancer: A systematic review and meta-analysis.” Surgery today (2026). PMID: 42234145 ↗
L2SR_COHORTCited in: Patient Counselling - [65]
Ikeda T, Noma K, Okura K et al.. “Preoperative exercise capacity as a predictor of postoperative pulmonary complications in patients with esophageal cancer: a multicenter observational cohort study.” Esophagus : official journal of the Japan Esophageal Society (2026). PMID: 42380723 ↗
L3RETROSPECTIVE_COHORTCited in: Patient Counselling - [66]
Xue Z, Beijia L, Qin X et al.. “Clinical predictors of early reflux and symptom severity after esophagectomy: a risk prediction tool.” Esophagus : official journal of the Japan Esophageal Society (2026). PMID: 42380722 ↗
L3RETROSPECTIVE_COHORTCited in: Patient Counselling - [67]
Kosumi K, Harada K, Shimogawa T et al.. “Early Tumor Shrinkage and Clinical Outcomes for Esophageal Squamous Cell Carcinoma Patients Treated with Immune Checkpoint Inhibitors: Real-World Observational Study.” Annals of surgical oncology (2026). PMID: 42201494 ↗
L3COHORTCited in: Patient Counselling - [68]
Yoshida M, Urabe Y, Kadota T et al.. “Size and Macroscopic Type of Type B2 Vessel Areas in JES Classification for Predicting Invasion Depth: A Multicenter Prospective Study.” Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society (2026). PMID: 42144869 ↗
L3COHORTCited in: Patient Counselling - [69]
Wu F, Luo C, Zhou S et al.. “Recurrent laryngeal nerve lymph nodes status prediction after neoadjuvant therapy for thoracic esophageal squamous cell carcinoma.” Insights into imaging (2026). PMID: 41945240 ↗
L3RETROSPECTIVE_COHORTCited in: Patient Counselling - [70]
Yi L, Huang W, Wang Q et al.. “Development and external validation of two nomograms for predicting brain metastases and brain metastasis-free survival in primary small cell carcinoma of the esophagus: a retrospective multicenter analysis.” Therapeutic advances in medical oncology (2026). PMID: 42558682 ↗
L3bCited in: Surveillance Schedule - [71]
Park SY, Lee J, Oh D et al.. “Prognostic role of pathologic status other than complete response after neoadjuvant therapy followed by surgery in esophageal squamous cell carcinoma.” Esophagus : official journal of the Japan Esophageal Society (2023). PMID: 38082188 ↗
L3bCited in: Surveillance Schedule - [72]
Chen X, Chen X, Bao Y et al.. “EUS-derived maximum tumor thickness and tumor shrinkage rate as independent prognostic factors in locally advanced esophageal squamous cell carcinoma after neoadjuvant chemoradiotherapy.” Endoscopic ultrasound (2023). PMID: 37795352 ↗
L3bCited in: Surveillance Schedule - [73]
Liu M, Ma M, Zhang D et al.. “The Impact of Artificial Intelligence-Assisted Endoscopy on the Detection of Upper Gastrointestinal Neoplasms: A Systematic Review and Meta-Analyses.” Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society (2026). PMID: 42629946 ↗
L1aCited in: Detection of Recurrence - [74]
He J, Chen WQ, Li ZS et al.. “[China guideline for the screening, early detection and early treatment of esophageal cancer (2022, Beijing)].” Zhonghua zhong liu za zhi [Chinese journal of oncology] (2022). PMID: 35754225 ↗
L1cCited in: Detection of Recurrence - [75]
Uraguchi K, Hamada K, Matsumoto N et al.. “Incidental detection of cancers during population-based endoscopic gastric cancer screening in Japan.” Esophagus : official journal of the Japan Esophageal Society (2026). PMID: 42573963 ↗
L3bCited in: Detection of Recurrence - [76]
Goto K, Hisamori S, Ueno K et al.. “Job resignation between cancer diagnosis and surgery in patients with gastric and esophageal cancer: a multi-institutional cross-sectional study.” International journal of clinical oncology (2026). PMID: 42371254 ↗
L3bCited in: Late Toxicity and Survivorship