Adjuvant immunotherapy in renal cell carcinoma: a systematic review and meta‐analysis

Author:

Riveros Carlos1ORCID,Huang Emily1,Ranganathan Sanjana1,Klaassen Zachary2ORCID,Rini Brian3,Wallis Christopher J.D.456ORCID,Satkunasivam Raj1

Affiliation:

1. Department of Urology Houston Methodist Hospital Houston TX USA

2. Division of Urology, Medical College of Georgia Augusta University Augusta GA USA

3. Division of Hematology and Oncology Vanderbilt University Medical Center Nashville TN USA

4. Division of Urology and Surgical Oncology, Department of Surgery, Princess Margaret Cancer Centre University Health Network, University of Toronto Toronto ON Canada

5. Division of Urology University of Toronto Toronto ON Canada

6. Division of Urology Mount Sinai Hospital Toronto ON Canada

Abstract

ObjectivesTo synthesise available data regarding the disease‐free survival (DFS) benefit of adjuvant immune checkpoint inhibitors (ICIs) for patients with renal cell carcinoma (RCC) and evaluate the overall safety profile of ICIs in this setting.Materials and MethodsWe utilised PubMed, Embase, and relevant conference proceedings to identify phase III randomised controlled trials comparing adjuvant ICIs vs placebo/observation for RCC. The primary outcome of interest was DFS. Variables for subgroup analyses were programmed death‐ligand 1 (PD‐L1) expression, sarcomatoid features, nephrectomy type, and disease‐risk category. Secondary outcomes included Grade ≥3 adverse events (AEs), immune‐related AEs, and treatment discontinuation due to AEs. All outcomes were analysed using random‐effects models owing to inter‐study heterogeneity.ResultsAmong the four included studies, one demonstrated a significant DFS benefit. There was considerable clinical and statistical heterogeneity (I2 = 64%) due to differences in inclusion criteria and interventions. While pooled results across the four studies did not demonstrate a significant benefit in DFS overall (hazard ratio [HR] 0.85, 95% confidence interval [CI] 0.69–1.04) there was significant benefit among patients with positive PD‐L1 expression (HR 0.72, 95% CI 0.55–0.94) and sarcomatoid features (HR 0.59, 95% CI 0.38–0.91).ConclusionThe evidence base to date regarding ICIs as adjuvant therapy in RCC is mixed – conclusions are limited by considerable heterogeneity between studies. However, pooled analyses suggest that patients with positive PD‐L1 expression or sarcomatoid features are most likely to benefit from adjuvant immunotherapy.

Publisher

Wiley

Subject

Urology

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