Impact of Metastasectomy on Cancer Specific and Overall Survival in Metastatic Renal Cell Carcinoma: Analysis of the REMARCC Registry.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
08 2022
Historique:
received: 19 10 2020
revised: 27 11 2021
accepted: 21 03 2022
pubmed: 19 5 2022
medline: 27 7 2022
entrez: 18 5 2022
Statut: ppublish

Résumé

Treatment paradigms for management of metastatic renal cell carcinoma (mRCC) are evolving. We examined impact of surgical metastasectomy on survival across in mRCC stratified by risk-group. Multicenter retrospective analysis from the Registry of Metastatic RCC database. The cohort was subdivided utilizing Motzer criteria (favorable-, intermediate-, high-risk). Primary outcome was all-cause mortality (ACM)/overall survival (OS); secondary outcome was cancer-specific mortality (CSM)/cancer-specific survival (CSS). Impact of metastasectomy was analyzed via Cox-Regression analysis adjusting for potential prognostic variables and Kaplan-Meier analysis (KMA) within each risk-group. Four hundred thirty-one patients (59 favorable-risk, 274 intermediate-risk, 98 high-risk; median follow-up 27.2 months) were analyzed. Metastasectomy was performed in 22 (37%), 66 (24%), and 32 (16%) of favorable-, intermediate- and high-risk groups (P = .012). Median number of metastases at diagnosis differed significantly (favorable-risk 2, intermediate-risk 3.4, high-risk 5.1, P < .001). On Cox-regression, high-risk (HR = 1.72, P = .002) was associated with worsened ACM, while metastasectomy was associated with improved ACM (HR = 0.56, P = .005). On KMA, median OS (months) was longer with metastasectomy in favorable- (92.7 vs. 25.8, P = .003) and intermediate-risk (26.3 vs. 20.1, P = .038), but not high-risk (P = .911) groups. Metastasectomy was associated with longer CSS in favorable- (76.1 vs. 32.8, P = .004) but not intermediate- (P = .06) and high-risk (P = .595) groups. Metastasectomy was independently associated with improved ACM and CSM, as well as improved CSS and OS in favorable- and intermediate-risk mRCC patients. Metastasectomy may be considered as component of multimodal management strategy in favorable and intermediate-risk subgroups. In high-risk patients, metastasectomy should be deferred except in select circumstances.

Sections du résumé

BACKGROUND
Treatment paradigms for management of metastatic renal cell carcinoma (mRCC) are evolving. We examined impact of surgical metastasectomy on survival across in mRCC stratified by risk-group.
METHODS
Multicenter retrospective analysis from the Registry of Metastatic RCC database. The cohort was subdivided utilizing Motzer criteria (favorable-, intermediate-, high-risk). Primary outcome was all-cause mortality (ACM)/overall survival (OS); secondary outcome was cancer-specific mortality (CSM)/cancer-specific survival (CSS). Impact of metastasectomy was analyzed via Cox-Regression analysis adjusting for potential prognostic variables and Kaplan-Meier analysis (KMA) within each risk-group.
RESULTS
Four hundred thirty-one patients (59 favorable-risk, 274 intermediate-risk, 98 high-risk; median follow-up 27.2 months) were analyzed. Metastasectomy was performed in 22 (37%), 66 (24%), and 32 (16%) of favorable-, intermediate- and high-risk groups (P = .012). Median number of metastases at diagnosis differed significantly (favorable-risk 2, intermediate-risk 3.4, high-risk 5.1, P < .001). On Cox-regression, high-risk (HR = 1.72, P = .002) was associated with worsened ACM, while metastasectomy was associated with improved ACM (HR = 0.56, P = .005). On KMA, median OS (months) was longer with metastasectomy in favorable- (92.7 vs. 25.8, P = .003) and intermediate-risk (26.3 vs. 20.1, P = .038), but not high-risk (P = .911) groups. Metastasectomy was associated with longer CSS in favorable- (76.1 vs. 32.8, P = .004) but not intermediate- (P = .06) and high-risk (P = .595) groups.
CONCLUSIONS
Metastasectomy was independently associated with improved ACM and CSM, as well as improved CSS and OS in favorable- and intermediate-risk mRCC patients. Metastasectomy may be considered as component of multimodal management strategy in favorable and intermediate-risk subgroups. In high-risk patients, metastasectomy should be deferred except in select circumstances.

Identifiants

pubmed: 35585014
pii: S1558-7673(22)00076-3
doi: 10.1016/j.clgc.2022.03.013
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

326-333

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Margaret F Meagher (MF)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA.

Maria C Mir (MC)

Department of Urology, Fundacion Instituto Valenciano Oncologia Valencia, Spain.

Riccardo Autorino (R)

Department of Urology, Virginia Commonwealth University Medical Center, Richmond, VA.

Andrea Minervini (A)

Department of Urology, University of Florence, Careggi Hospital, Florence, Italy.

Maximilian Kriegmair (M)

Department of Urology, University Medical Centre Mannheim, Mannheim, Germany.

Tobias Maurer (T)

Department of Urology, Technical University of Munich, Munich, Germany.

Francesco Porpiglia (F)

Department of Urology, University of Turin-San Luigi Gonzaga Hospital, Orbassano, Italy.

Siska Van Bruwaene (S)

Department of Urology, AZ Groeninge, Kortrijk, Belgium.

Estefania Linares (E)

Department of Urology, Hospital 12 de Octubre, Madrid, Spain.

Vital Hevia (V)

Department of Urology, Hospital Ramon y Cajal, Madrid, Spain.

Mireia Musquera (M)

Department of Urology, Hospital Clinic, Carrer de Villarroel, Barcelona, Spain.

Eduard Roussel (E)

Department of Urology, UK Leuven, Leuven, Belgium.

Nicola Pavan (N)

Department of Urology, University of Trieste, Trieste, Italy.

Alessandro Antonelli (A)

Department of Urology, Spedali Civili Hospital, University of Brescia, Brescia, Italy.

Shudong Zhang (S)

Department of Urology, Peking University Third Hospital, Beijing, PRC.

Fady Ghali (F)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA.

Devin Patel (D)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA.

Juan Javier-Desloges (J)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA.

Aaron Bradshaw (A)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA.

Jose Rubio (J)

Department of Urology, Fundacion Instituto Valenciano Oncologia Valencia, Spain.

Georgi Guruli (G)

Department of Urology, Virginia Commonwealth University Medical Center, Richmond, VA.

Andrew Tracey (A)

Department of Urology, Virginia Commonwealth University Medical Center, Richmond, VA.

Riccardo Campi (R)

Department of Urology, University of Florence, Careggi Hospital, Florence, Italy.

Maarten Albersen (M)

Department of Urology, UK Leuven, Leuven, Belgium.

Maria Furlan (M)

Department of Urology, Spedali Civili Hospital, University of Brescia, Brescia, Italy.

Rana R McKay (RR)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA.

Ithaar H Derweesh (IH)

Department of Urology, UC San Diego School of Medicine, La Jolla, CA. Electronic address: iderweesh@gmail.com.

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