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Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)

PURPOSE: We hypothesized that two-tier re-classification of the “M” (metastasis) domain of the Tumor-Node-Metastasis (TNM) staging of Renal Cell Carcinoma (RCC) may improve staging accuracy than the current monolithic classification, as advancements in the understanding of tumor biology have led to...

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Autores principales: Meagher, Margaret F., Mir, Maria C., Minervini, Andrea, Kriegmair, Maximilian, Heck, Matthias, Porpiglia, Francesco, Van Bruwaene, Siska, Linares, Estefania, Hevia, Vital, D’Anna, Maurizio, Veccia, Alessandro, Roussel, Eduard, Claps, Francesco, Palumbo, Carlotta, Marchioni, Michele, Afari, Jonathan, Saitta, Cesare, Liu, Franklin, Rubio, Jose, Campi, Riccardo, Mari, Andrea, Amiel, Thomas, Checcucci, Enrico, Musquera, Mireia, Guruli, Georgi, Pavan, Nicola, Albersen, Maarten, Antonelli, Alessandro, Klatte, Tobias, Autorino, Riccardo, McKay, Rana R., Derweesh, Ithaar H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092360/
https://www.ncbi.nlm.nih.gov/pubmed/37064092
http://dx.doi.org/10.3389/fonc.2023.1113246
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author Meagher, Margaret F.
Mir, Maria C.
Minervini, Andrea
Kriegmair, Maximilian
Heck, Matthias
Porpiglia, Francesco
Van Bruwaene, Siska
Linares, Estefania
Hevia, Vital
D’Anna, Maurizio
Veccia, Alessandro
Roussel, Eduard
Claps, Francesco
Palumbo, Carlotta
Marchioni, Michele
Afari, Jonathan
Saitta, Cesare
Liu, Franklin
Rubio, Jose
Campi, Riccardo
Mari, Andrea
Amiel, Thomas
Checcucci, Enrico
Musquera, Mireia
Guruli, Georgi
Pavan, Nicola
Albersen, Maarten
Antonelli, Alessandro
Klatte, Tobias
Autorino, Riccardo
McKay, Rana R.
Derweesh, Ithaar H.
author_facet Meagher, Margaret F.
Mir, Maria C.
Minervini, Andrea
Kriegmair, Maximilian
Heck, Matthias
Porpiglia, Francesco
Van Bruwaene, Siska
Linares, Estefania
Hevia, Vital
D’Anna, Maurizio
Veccia, Alessandro
Roussel, Eduard
Claps, Francesco
Palumbo, Carlotta
Marchioni, Michele
Afari, Jonathan
Saitta, Cesare
Liu, Franklin
Rubio, Jose
Campi, Riccardo
Mari, Andrea
Amiel, Thomas
Checcucci, Enrico
Musquera, Mireia
Guruli, Georgi
Pavan, Nicola
Albersen, Maarten
Antonelli, Alessandro
Klatte, Tobias
Autorino, Riccardo
McKay, Rana R.
Derweesh, Ithaar H.
author_sort Meagher, Margaret F.
collection PubMed
description PURPOSE: We hypothesized that two-tier re-classification of the “M” (metastasis) domain of the Tumor-Node-Metastasis (TNM) staging of Renal Cell Carcinoma (RCC) may improve staging accuracy than the current monolithic classification, as advancements in the understanding of tumor biology have led to increased recognition of the heterogeneous potential of metastatic RCC (mRCC). METHODS: Multicenter retrospective analysis of patients from the REMARCC (REgistry of MetAstatic RCC) database. Patients were stratified by number of metastases into two groups, M1 (≤3, “Oligometastatic”) and M2 (>3, “Polymetastatic”). Primary outcome was overall survival (OS). Secondary outcomes were cancer-specific survival (CSS). Cox-regression and Kaplan-Meier (KMA) analysis were utilized for outcomes, and receiver operating characteristic analysis (ROC) was utilized to assess diagnostic accuracy compared to current “M” staging. RESULTS: 429 patients were stratified into proposed M1 and M2 groups (M1 = 286/M2 = 143; median follow-up 19.2 months). Cox-regression revealed M2 classification as an independent risk factor for worsened all-cause mortality (HR=1.67, p=0.001) and cancer-specific mortality (HR=1.74, p<0.001). Comparing M1-oligometastatic vs. M2-polymetastatic groups, KMA revealed significantly higher 5-year OS (36% vs. 21%, p<0.001) and 5-year CSS (39% vs. 17%, p<0.001). ROC analyses comparing OS and CSS, for M1/M2 reclassification versus unitary M designation currently in use demonstrated improved c-index for OS (M1/M2 0.635 vs. unitary M 0.500) and CSS (M1/M2 0.627 vs. unitary M 0.500). CONCLUSION: Subclassification of Stage “M” domain of mRCC into two clinical substage categories based on metastatic burden corresponds to distinctive tumor groups whose oncological potential varies significantly and result in improved predictive capability compared to current staging.
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spelling pubmed-100923602023-04-13 Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC) Meagher, Margaret F. Mir, Maria C. Minervini, Andrea Kriegmair, Maximilian Heck, Matthias Porpiglia, Francesco Van Bruwaene, Siska Linares, Estefania Hevia, Vital D’Anna, Maurizio Veccia, Alessandro Roussel, Eduard Claps, Francesco Palumbo, Carlotta Marchioni, Michele Afari, Jonathan Saitta, Cesare Liu, Franklin Rubio, Jose Campi, Riccardo Mari, Andrea Amiel, Thomas Checcucci, Enrico Musquera, Mireia Guruli, Georgi Pavan, Nicola Albersen, Maarten Antonelli, Alessandro Klatte, Tobias Autorino, Riccardo McKay, Rana R. Derweesh, Ithaar H. Front Oncol Oncology PURPOSE: We hypothesized that two-tier re-classification of the “M” (metastasis) domain of the Tumor-Node-Metastasis (TNM) staging of Renal Cell Carcinoma (RCC) may improve staging accuracy than the current monolithic classification, as advancements in the understanding of tumor biology have led to increased recognition of the heterogeneous potential of metastatic RCC (mRCC). METHODS: Multicenter retrospective analysis of patients from the REMARCC (REgistry of MetAstatic RCC) database. Patients were stratified by number of metastases into two groups, M1 (≤3, “Oligometastatic”) and M2 (>3, “Polymetastatic”). Primary outcome was overall survival (OS). Secondary outcomes were cancer-specific survival (CSS). Cox-regression and Kaplan-Meier (KMA) analysis were utilized for outcomes, and receiver operating characteristic analysis (ROC) was utilized to assess diagnostic accuracy compared to current “M” staging. RESULTS: 429 patients were stratified into proposed M1 and M2 groups (M1 = 286/M2 = 143; median follow-up 19.2 months). Cox-regression revealed M2 classification as an independent risk factor for worsened all-cause mortality (HR=1.67, p=0.001) and cancer-specific mortality (HR=1.74, p<0.001). Comparing M1-oligometastatic vs. M2-polymetastatic groups, KMA revealed significantly higher 5-year OS (36% vs. 21%, p<0.001) and 5-year CSS (39% vs. 17%, p<0.001). ROC analyses comparing OS and CSS, for M1/M2 reclassification versus unitary M designation currently in use demonstrated improved c-index for OS (M1/M2 0.635 vs. unitary M 0.500) and CSS (M1/M2 0.627 vs. unitary M 0.500). CONCLUSION: Subclassification of Stage “M” domain of mRCC into two clinical substage categories based on metastatic burden corresponds to distinctive tumor groups whose oncological potential varies significantly and result in improved predictive capability compared to current staging. Frontiers Media S.A. 2023-03-29 /pmc/articles/PMC10092360/ /pubmed/37064092 http://dx.doi.org/10.3389/fonc.2023.1113246 Text en Copyright © 2023 Meagher, Mir, Minervini, Kriegmair, Heck, Porpiglia, Van Bruwaene, Linares, Hevia, D’Anna, Veccia, Roussel, Claps, Palumbo, Marchioni, Afari, Saitta, Liu, Rubio, Campi, Mari, Amiel, Checcucci, Musquera, Guruli, Pavan, Albersen, Antonelli, Klatte, Autorino, McKay and Derweesh https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Meagher, Margaret F.
Mir, Maria C.
Minervini, Andrea
Kriegmair, Maximilian
Heck, Matthias
Porpiglia, Francesco
Van Bruwaene, Siska
Linares, Estefania
Hevia, Vital
D’Anna, Maurizio
Veccia, Alessandro
Roussel, Eduard
Claps, Francesco
Palumbo, Carlotta
Marchioni, Michele
Afari, Jonathan
Saitta, Cesare
Liu, Franklin
Rubio, Jose
Campi, Riccardo
Mari, Andrea
Amiel, Thomas
Checcucci, Enrico
Musquera, Mireia
Guruli, Georgi
Pavan, Nicola
Albersen, Maarten
Antonelli, Alessandro
Klatte, Tobias
Autorino, Riccardo
McKay, Rana R.
Derweesh, Ithaar H.
Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)
title Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)
title_full Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)
title_fullStr Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)
title_full_unstemmed Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)
title_short Proposal for a Two-Tier Re-classification of Stage IV/M1 domain of Renal Cell Carcinoma into M1 (“Oligometastatic”) and M2 (“Polymetastatic”) subdomains: Analysis of the Registry for Metastatic Renal Cell Carcinoma (REMARCC)
title_sort proposal for a two-tier re-classification of stage iv/m1 domain of renal cell carcinoma into m1 (“oligometastatic”) and m2 (“polymetastatic”) subdomains: analysis of the registry for metastatic renal cell carcinoma (remarcc)
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092360/
https://www.ncbi.nlm.nih.gov/pubmed/37064092
http://dx.doi.org/10.3389/fonc.2023.1113246
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