# Pattern of disease recurrence and outcomes after progression of high-risk renal cell carcinoma (RCC) patients treated with adjuvant immunotherapy

**Authors:** Chiara Ciccarese, Denis Occhipinti, Daniela Arduini, Davide Di Leo, Alessio Neri, Luigi Roca, Gloria Messina, Paola Troisi, Romina Rose Pedone, Maria Antonia Fucile, Rachele Belletto, Valeria Sardaro, Chiara Ligato, Rexhina Ajdhoni, Fabiana Caliciotti, Chiara Sighinolfi, Luca Tagliaferri, Bernardo Rocco, Giampaolo Tortora, Roberto Iacovelli

PMC · DOI: 10.1007/s00262-026-04331-0 · Cancer Immunology, Immunotherapy : CII · 2026-02-25

## TL;DR

High-risk kidney cancer patients treated with immunotherapy after surgery often relapse with limited metastases, but can have good outcomes with targeted treatments.

## Contribution

Identifies recurrence patterns and treatment outcomes in RCC patients post-adjuvant immunotherapy, advocating for metastasis-directed strategies.

## Key findings

- 21% of high-risk RCC patients treated with adjuvant immunotherapy experienced recurrence.
- Oligometastatic disease was common at recurrence, primarily in the lungs and lymph nodes.
- Post-progression survival was excellent with loco-regional treatments, suggesting a multidisciplinary approach.

## Abstract

Radical or partial nephrectomy followed by adjuvant pembrolizumab is the standard of care for high-risk localized renal cell carcinoma (RCC), yet around 40% of patients relapse within 5 years. We investigated patterns of disease recurrence and the clinical management of RCC patients treated with adjuvant immunotherapy.

We collected patients with high-risk RCC who received adjuvant immunotherapy after radical surgery in our Institution. The primary endpoint was the rate and pattern of disease recurrence. Secondary endpoints were disease-free survival (DFS), overall survival (OS), post-progression survival (OS2) and treatments at recurrence.

From March 2018 to September 2025, 70 patients were included, most received adjuvant pembrolizumab (71%), followed by nivolumab + ipilimumab (16%), and nivolumab monotherapy (13%). 15 patients (21%) experienced recurrence, including 7 (10%) who relapsed on adjuvant treatment. Oligometastatic disease was observed in 10 cases (67%), mainly involving lung (60%), lymph nodes (33%) and renal bed (13%). At recurrence, 9 patients (60%) started first-line therapy, while 5 patients (33%) received loco-regional treatments. After a median follow-up of 30.2 months, 30-month DFS and OS rates were 74% and 94%, respectively, in the overall population. Among patients who progressed, the 24-month OS2 rate was 100% after local therapy alone and 86% with systemic therapy.

High-risk RCC patients treated with adjuvant immunotherapy remain at considerable risk of relapse, frequently with oligometastatic disease. Excellent post-progression outcomes after loco-regional treatment support a multidisciplinary, metastasis-directed approach to recurrence after adjuvant immunotherapy.

## Linked entities

- **Diseases:** renal cell carcinoma (MONDO:0005086), RCC (MONDO:0005086)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, MATN3 (matrilin 3) [NCBI Gene 4148] {aka DIPOA, EDM5, HOA, OADIP, OS2, SEMDBCD}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, EPAS1 (endothelial PAS domain protein 1) [NCBI Gene 2034] {aka ECYT4, HIF2A, HLF, MOP2, PASD2, bHLHe73}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, HAVCR1 (hepatitis A virus cellular receptor 1) [NCBI Gene 26762] {aka CD365, HAVCR, HAVCR-1, KIM-1, KIM1, TIM}
- **Diseases:** cancers (MESH:D009369), metastatic disease (MESH:D000092182), toxicity (MESH:D064420), Metastasis (MESH:D009362), disease (MESH:D004194), death (MESH:D003643), kidney cancer (MESH:D007680), stages I-III) (MESH:D062706), RCC (MESH:D002292)
- **Chemicals:** pembrolizumab (MESH:C582435), Immune checkpoint (-), nivolumab (MESH:D000077594), ipilimumab (MESH:D000074324), tremelimumab (MESH:C520704), belzutifan (MESH:C000720612), sunitinib (MESH:D000077210), durvalumab (MESH:C000613593), lenvatinib (MESH:C531958)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12936213