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Cancer Risk in Kidney Transplant Recipients on Belatacept Versus Calcineurin Inhibitors: A Systematic Review and Meta-Analysis

In brief

Cancer risk similar for belatacept and calcineurin inhibitors in kidney transplant patients

A meta-analysis of 13 studies (3,070 recipients) found no overall increase in skin cancer or any cancer with belatacept versus calcineurin inhibitors. However, patients switched from calcineurin inhibitors to belatacept showed a trend toward higher cancer rates, highlighting the need for larger trials focused on cancer outcomes after conversion.

Journal
Transplantation (Q1)
Published
27 August 2026
Study design
Systematic review / meta-analysis of RCTs
Evidence level
Level 1, High (CEBM 1a)
Authors
Zein Alabdin Hannouneh, Muhsen Issa, Hiroki Mizuno, Naoka Murakami
PMID
42649552
DOI
10.1097/TP.0000000000005856

Why clinicians should know about it

  • Picked for Nephrology (paper of the day, 29 August 2026): Cancer risk in kidney transplant recipients on belatacept vs CNI
  • Picked for Epidemiology (paper of the day, 29 August 2026): Belatacept vs CNI cancer risk meta‑analysis

Abstract

BACKGROUND: Belatacept has been increasingly used as a maintenance immunosuppression in kidney transplant recipients since its approval in 2011, due to favorable renal and cardiovascular profiles compared with calcineurin inhibitors (CNIs). However, the long-term risk of cancers associated with beletacept, particularly skin cancer, remains incompletely characterized. METHODS: We conducted a systematic review and meta-analysis of clinical studies comparing cancer risk in kidney transplant recipients receiving belatacept-based regimens versus CNI-based regimens. Thirteen studies were included, comprising 3,070 patients from 10 randomized controlled trials and 3 observational cohort studies. Pooled risk estimates were calculated for skin cancers and other cancers. Subgroup analyses were performed to compare patients converted from CNIs to belatacept to those receiving de novo belatacept. RESULTS: Across all included studies, there was no statistically significant difference in the risk of skin cancer (odds ratio [OR], 1.01; 95% confidence interval [CI], 0.67-1.52) or all cancers (OR, 1.14; 95% CI, 0.69-1.88) between belatacept-based and CNI-based regimens. However, in subgroup analyses, patients converted from CNIs to belatacept demonstrated a trend toward increased risk of both skin cancers (OR, 1.82; 95% CI, 0.43-7.63) and all cancers (OR, 1.83; 95% CI, 0.99-3.39) compared with those receiving de novo belatacept (skin cancer: OR 0.85; 95% CI, 0.68-1.06, all cancers: OR, 0.92; 95% CI, 0.41-2.09). CONCLUSIONS: Overall, belatacept-based immunosuppression was not associated with a significantly increased risk of skin or other cancers compared with CNI-based regimens. Larger, adequately powered studies with cancer outcomes as primary endpoints are needed to better define cancer risk associated with belatacept conversion in kidney transplant recipients.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.