Outcomes of delayed cytoreductive nephrectomy in patients with metastatic clear cell renal cell carcinoma treated with immune checkpoint inhibitor therapy.

M Mohamed Soufi (CancerCare Manitoba, University of Manitoba, Winnipeg, MB, Canada) S Sunita Ghosh N Naveen S. Basappa C Camilla Tajzler (McGill University Health Center- Research Institute/Center for Innovative Medicine, Montréal, QC, Canada) D Dominick Bosse (University of Ottawa, Ottawa, ON, Canada) G Georg A. Bjarnason (Sunnybrook Odette Cancer Centre, Toronto, ON, Canada) D Daniel Yick Chin Heng (Department of Medical Oncology, Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada) L Lori Wood (Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, NS, Canada) R Rodney H. Breau (University of Ottawa, Ottawa) B Bimal Bhindi (Southern Alberta Institute of Urology, Calgary, AB, Canada) R Ramy Saleh (Department of Medicine, McGill University Health Centre, Montréal, QC, Canada) C Christian K. Kollmannsberger (BC Cancer Vancouver Center, University of British Columbia, Vancouver, BC, Canada) Z Zineb Hamilou (Centre Hospitalier de l’Université de Montréal, Montreal, QC, Canada) S Simon Tanguay (McGill University Health Centre, Montréal, QC, Canada) V Vincent Castonguay (Hotel Dieu de Quebec, Quebec, QC, Canada) F Frederic Pouliot (CHU de Québec-Université Laval Research Center, Quebec City, QC, Canada) A Antonio Finelli (University of Toronto, Toronto, ON, Canada) A Aly-Khan A. Lalani (Juravinski Cancer Centre, McMaster University, Hamilton, ON, Canada) J Jeffrey Graham (Intermountain Medical Center, Salt Lake City, Utah, United States)

Abstract

462 Background: The role of cytoreductive nephrectomy (CN) in metastatic renal cell carcinoma (mRCC) has evolved in the immune checkpoint inhibitor (ICI) era. We evaluated outcomes of patients with clear cell mRCC treated with first-line ICI therapy who subsequently underwent delayed CN. Methods: Using the Canadian Kidney Cancer information system (CKCis), a multi-institutional database, we retrospectively identified patients with clear cell mRCC treated with first-line ICI-based therapy who subsequently underwent CN. Clinical characteristics, treatment details, use of metastasis-directed therapy, and survival outcomes were collected. Descriptive statistics were applied and Kaplan–Meier methods were used to estimate progression-free survival (PFS) and overall survival (OS). Results: A total of 61 patients underwent delayed CN from January 2017 to June 2024 from a cohort of 1560 patients. Median age at CN was 64 years; 84% were male. All patients had intermediate (47%) or poor-risk (53%) by IMDC criteria. Sarcomatoid features were present in 22%. Lung (77%), lymph node (48%), and bone (18%) were the most common metastatic sites. Most patients had less than 3 sites of disease (65.6%). The most common ICI regime was ipilimumab + nivolumab (85%). Median time from ICI therapy initiation to CN was 11.5 months. A total of 38 patients (62%) who received first-line ICI therapy have discontinued treatment and remain alive, with only 20% (N = 12) requiring second-line therapy. With a median follow-up of 44 months, median OS was not reached; 2- and 5-year OS rates were 88% and 74%, respectively. Median PFS was 35 months, with 2- and 3-year PFS of 61% and 50%. Conclusions: In this retrospective series, delayed CN following ICI therapy in carefully selected patients was associated with durable disease control and encouraging long-term survival. Future analyses will explore pathologic response. These results highlight the need for randomized trials of deferred CN in the ICI era. Characteristic (N=61) Value Ipilimumab + Nivolumab 52 (85%) Pembrolizumab + Axitinib 9 (15%) Metastasis Directed Therapy  Radiation therapy 18 (30%)  Metastasectomy 12 (20%) Complete Response pre-CN 8 (13%) Discontinuation of systemic therapy 38 (62%) 5-year OS 74% 5-year PFS 50%

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 462-462
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (19)

M

Mohamed Soufi

CancerCare Manitoba, University of Manitoba, Winnipeg, MB, Canada

S

Sunita Ghosh

N

Naveen S. Basappa

C

Camilla Tajzler

McGill University Health Center- Research Institute/Center for Innovative Medicine, Montréal, QC, Canada

D

Dominick Bosse

University of Ottawa, Ottawa, ON, Canada

G

Georg A. Bjarnason

Sunnybrook Odette Cancer Centre, Toronto, ON, Canada

D

Daniel Yick Chin Heng

Department of Medical Oncology, Arthur JE Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB, Canada

L

Lori Wood

Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, NS, Canada

R

Rodney H. Breau

University of Ottawa, Ottawa

B

Bimal Bhindi

Southern Alberta Institute of Urology, Calgary, AB, Canada

R

Ramy Saleh

Department of Medicine, McGill University Health Centre, Montréal, QC, Canada

C

Christian K. Kollmannsberger

BC Cancer Vancouver Center, University of British Columbia, Vancouver, BC, Canada

Z

Zineb Hamilou

Centre Hospitalier de l’Université de Montréal, Montreal, QC, Canada

S

Simon Tanguay

McGill University Health Centre, Montréal, QC, Canada

V

Vincent Castonguay

Hotel Dieu de Quebec, Quebec, QC, Canada

F

Frederic Pouliot

CHU de Québec-Université Laval Research Center, Quebec City, QC, Canada

A

Antonio Finelli

University of Toronto, Toronto, ON, Canada

A

Aly-Khan A. Lalani

Juravinski Cancer Centre, McMaster University, Hamilton, ON, Canada

J

Jeffrey Graham

Intermountain Medical Center, Salt Lake City, Utah, United States