Impact of deferred cytoreductive nephrectomy in the era of the immunotherapy in metastatic renal cell carcinoma: A multicenter retrospective study.

P Patricia Rioja (Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru) C Carolina Passarella (Hospital Universitario Austral, Buenos Aires, Argentina) M Martin Angel W Wbeimar Valderrama (Hospital Universitario Austral, Buenos Aires, Argentina) F Freya Bosma (Hospital de la Santa Creu i Sant Pau, Barcelona, Spain) G Georgia Anguera (Medical Oncology Department, Santa Creu i Sant Pau Hospital, Barcelona, Spain) V Victoria Gomez (Rush University, Chicago, IL) Álvaro Ruiz-Granados (Hospital Universitario Ramón y Cajal, Madrid, Spain) D David Plata (Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia) M Martin Ignacio Zapata Laguado (Instituto Nacional De Cancerologia (Colombia), Bogotá, Colombia) A Alberto Orta-Ruiz (Department of Medical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain) M Maria Natalia Gandur-Quiroga (Department of Medical Oncology, Genitourinary Tumors, Institute of Oncology Angel H Roffo, Buenos Aires, Argentina) M Maria T. Bourlon (Urologic Oncology Clinic, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico) E Enrique Grande R Ray Manneh (Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia) J Javier Molina-Cerrillo P Pablo Maroto-Rey (Hospital de la Santa Creu i Sant Pau, Barcelona, Spain) J Juan Pablo Sade D Daniel Castellano (Hospital Universitario 12 de Octubre, Madrid)

Abstract

502 Background: Deferred cytoreductive nephrectomy (dCN) is an emerging, strategy in the management of metastatic renal cell carcinoma (mRCC), applied selectively to patients who demonstrate a favorable response to initial systemic therapy. This study aimed to assess the clinical impact of dCN within the context of sequential treatment management. Methods: A multi-institutional retrospective evaluation. The descriptive analysis was performed to examine the demographic and clinical characteristics. Progression-free survival (PFS) and overall survival (OS) were analyzed by the Kaplan-Meier method. A level of p < 0.05 was considered significant. Results: With a median follow-up of 19 months (1-174 months), 50 patients were divided into three groups: 46% received IO+TKI, 24% received IO+IO, and 30% received TKI. Of the cohort, 66% were male, with median age of 60.6 years. All had clear cell histology, and 76% were intermediate IMDC risk. The most common metastatic sites were lungs (50%), lymph nodes (36%), and bone (32%). The median time from systemic therapy to cytoreductive nephrectomy (CN) was 6 months. Notably, 26% did not restart treatment post-CN, and 6% discontinued pre-CN (two due to toxicity, one due to progression). Median PFS was 36 months, with a 5-year PFS rate of 40%. Analysis by IMDC risk and type of treatment showed no significant differences. However, patients with a Karnofsky score (KS) ≤80% had a lower risk of progression than those with KS >80% [HR: 0.31, 95% CI (0.13-0.75), p=0.01] and those achieving complete response had a significantly lower risk of progression [HR: 8.59, 95% CI (1.1-67), p=0.042]. Median OS was 91 months, with no significant differences between groups. Conclusions: This study demonstrates that dCN can offer a therapeutic advantage especially in selected patients who achieve favorable responses to upfront systemic therapy. Careful patient selection is crucial to maximize the potential benefits of delayed surgery, reduce perioperative risks and improve oncological outcomes. Larger patient cohorts and well-designed prospective clinical trials are essential to solidify these findings and establish evidence-based guidelines.

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
Pages 502-502
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (19)

P

Patricia Rioja

Instituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru

C

Carolina Passarella

Hospital Universitario Austral, Buenos Aires, Argentina

M

Martin Angel

W

Wbeimar Valderrama

Hospital Universitario Austral, Buenos Aires, Argentina

F

Freya Bosma

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

G

Georgia Anguera

Medical Oncology Department, Santa Creu i Sant Pau Hospital, Barcelona, Spain

V

Victoria Gomez

Rush University, Chicago, IL

Álvaro Ruiz-Granados

Hospital Universitario Ramón y Cajal, Madrid, Spain

D

David Plata

Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia

M

Martin Ignacio Zapata Laguado

Instituto Nacional De Cancerologia (Colombia), Bogotá, Colombia

A

Alberto Orta-Ruiz

Department of Medical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain

M

Maria Natalia Gandur-Quiroga

Department of Medical Oncology, Genitourinary Tumors, Institute of Oncology Angel H Roffo, Buenos Aires, Argentina

M

Maria T. Bourlon

Urologic Oncology Clinic, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

E

Enrique Grande

R

Ray Manneh

Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia

J

Javier Molina-Cerrillo

P

Pablo Maroto-Rey

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

J

Juan Pablo Sade

D

Daniel Castellano

Hospital Universitario 12 de Octubre, Madrid