Clinico-Pathological Features Influencing the Prognostic Role of Body Mass Index in Patients With Advanced Renal Cell Carcinoma Treated by Immuno-Oncology Combinations (ARON-1)
Obesity has been associated with improved response to immunotherapy in cancer patients. We investigated the role of body mass index (BMI) in patients from the ARON-1 study (NCT05287464) treated by dual immuno-oncology agents (IO+IO) or a combination of immuno-oncology drug and a tyrosine kinase inhi...
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creator | Santoni, Matteo Massari, Francesco Myint, Zin W. Iacovelli, Roberto Pichler, Martin Basso, Umberto Kopecky, Jindrich Kucharz, Jakub Buti, Sebastiano Salfi, Alessia Büttner, Thomas De Giorgi, Ugo Kanesvaran, Ravindran Fiala, Ondřej Grande, Enrique Zucali, Paolo Andrea Fornarini, Giuseppe Bourlon, Maria T Scagliarini, Sarah Molina-Cerrillo, Javier Aurilio, Gaetano Matrana, Marc R Pichler, Renate Cattrini, Carlo Büchler, Tomas Seront, Emmanuel Calabrò, Fabio Pinto, Alvaro Berardi, Rossana Zgura, Anca Mammone, Giulia Ansari, Jawaher Atzori, Francesco Chiari, Rita Zakopoulou, Roubini Caffo, Orazio Procopio, Giuseppe Bassanelli, Maria Zampiva, Ilaria Messina, Carlo Küronya, Zsófia Mosca, Alessandra Bhuva, Dipen Vau, Nuno Incorvaia, Lorena Rebuzzi, Sara Elena Roviello, Giandomenico Zabalza, Ignacio Ortego Rizzo, Alessandro Mollica, Veronica Catalini, Ilaria Monteiro, Fernando Sabino M. Montironi, Rodolfo Battelli, Nicola Rizzo, Mimma Porta, Camillo |
description | Obesity has been associated with improved response to immunotherapy in cancer patients. We investigated the role of body mass index (BMI) in patients from the ARON-1 study (NCT05287464) treated by dual immuno-oncology agents (IO+IO) or a combination of immuno-oncology drug and a tyrosine kinase inhibitors (TKI) as first-line therapy for metastatic renal cell carcinoma (mRCC).
Medical records of patients with documented mRCC treated by immuno-oncology combinations were reviewed at 47 institutions from 16 countries. Patients were assessed for overall survival (OS), progression-free survival (OS), and overall clinical benefit (OCB), defined as the sum of the rate of partial/complete responses and stable disease. Univariate and multivariate analyses were used to explore the association of variables of interest with survival.
A total of 675 patients were included; BMI was >25 kg/m2 in 345 patients (51%) and was associated with improved OS (55.7 vs. 28.4 months, P < .001). The OCB of patients with BMI >25 kg/m2 versus those with BMI ≤25 kg/m2 was significantly higher only in patients with nonclear cell histology (81% vs. 65%, P = .011), and patients with liver metastases (76% vs. 58%, P = .007), Neutrophil to lymphocyte ratio >4 (77% vs 62%, P = .022) or treated by nivolumab plus ipilimumab (77% vs. 64%, P = .044). In the BMI ≤25 kg/m2 subgroup, significant differences were found between patients with NLR >4 versus ≤4 (62% vs. 82%, P = .002) and patients treated by IO+IO versus IO+TKIs combinations (64% vs. 83%, P = .002).
Our study suggests that the prognostic significance and the association of BMI with treatment outcome varies across clinico-pathological mRCC subgroups.
Obesity is a well-known risk factor for the development of renal cell carcinoma (RCC), one of the most frequent malignant urogenital tumors. The development of immunotherapy (IO)-based combinations for the treatment of metastatic RCC (mRCC) has led to a marked improvement of patients’ outcomes and quality of life. The ARON-1 study (NCT05287464) was designed to globally analyze real-world treatment outcomes of mRCC patients receiving first-line immune-based combinations. In this sub-analysis, we investigated the role of body mass index (BMI) in patients treated by immuno-oncology combinations stratified by clinico-pathological features. According to our results, the prognostic significance and the association of BMI with treatment outcome may vary across clinico-pathological mRCC subgroups. |
doi_str_mv | 10.1016/j.clgc.2023.03.006 |
format | Article |
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Medical records of patients with documented mRCC treated by immuno-oncology combinations were reviewed at 47 institutions from 16 countries. Patients were assessed for overall survival (OS), progression-free survival (OS), and overall clinical benefit (OCB), defined as the sum of the rate of partial/complete responses and stable disease. Univariate and multivariate analyses were used to explore the association of variables of interest with survival.
A total of 675 patients were included; BMI was >25 kg/m2 in 345 patients (51%) and was associated with improved OS (55.7 vs. 28.4 months, P < .001). The OCB of patients with BMI >25 kg/m2 versus those with BMI ≤25 kg/m2 was significantly higher only in patients with nonclear cell histology (81% vs. 65%, P = .011), and patients with liver metastases (76% vs. 58%, P = .007), Neutrophil to lymphocyte ratio >4 (77% vs 62%, P = .022) or treated by nivolumab plus ipilimumab (77% vs. 64%, P = .044). In the BMI ≤25 kg/m2 subgroup, significant differences were found between patients with NLR >4 versus ≤4 (62% vs. 82%, P = .002) and patients treated by IO+IO versus IO+TKIs combinations (64% vs. 83%, P = .002).
Our study suggests that the prognostic significance and the association of BMI with treatment outcome varies across clinico-pathological mRCC subgroups.
Obesity is a well-known risk factor for the development of renal cell carcinoma (RCC), one of the most frequent malignant urogenital tumors. The development of immunotherapy (IO)-based combinations for the treatment of metastatic RCC (mRCC) has led to a marked improvement of patients’ outcomes and quality of life. The ARON-1 study (NCT05287464) was designed to globally analyze real-world treatment outcomes of mRCC patients receiving first-line immune-based combinations. In this sub-analysis, we investigated the role of body mass index (BMI) in patients treated by immuno-oncology combinations stratified by clinico-pathological features. According to our results, the prognostic significance and the association of BMI with treatment outcome may vary across clinico-pathological mRCC subgroups.</description><identifier>ISSN: 1558-7673</identifier><identifier>EISSN: 1938-0682</identifier><identifier>DOI: 10.1016/j.clgc.2023.03.006</identifier><identifier>PMID: 37062658</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Immunocombo ; Immunotherapy ; mRCC ; NCT05287464 ; Obesity ; Survival ; Tumor Response</subject><ispartof>Clinical genitourinary cancer, 2023-10, Vol.21 (5), p.e309-e319.e1</ispartof><rights>2023 Elsevier Inc.</rights><rights>Copyright © 2023 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-1a5ac9cf0ab89ca24bac6b00456fd8f15b61dd7c02b149351fd8fda7d0b7db693</citedby><cites>FETCH-LOGICAL-c356t-1a5ac9cf0ab89ca24bac6b00456fd8f15b61dd7c02b149351fd8fda7d0b7db693</cites><orcidid>0000-0003-0316-9621 ; 0000-0001-8589-2148 ; 0000-0003-0876-0226 ; 0000-0003-4858-3965 ; 0000-0003-0546-6304 ; 0000-0001-6476-6871 ; 0000-0001-5814-2296 ; 0000-0002-6621-8251 ; 0000-0003-4754-6572 ; 0000-0003-0111-7588 ; 0000-0003-2973-6065 ; 0000-0002-4756-0756 ; 0000-0001-6667-994X ; 0000-0001-7340-6173 ; 0000-0002-4719-053X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37062658$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Santoni, Matteo</creatorcontrib><creatorcontrib>Massari, Francesco</creatorcontrib><creatorcontrib>Myint, Zin W.</creatorcontrib><creatorcontrib>Iacovelli, Roberto</creatorcontrib><creatorcontrib>Pichler, Martin</creatorcontrib><creatorcontrib>Basso, Umberto</creatorcontrib><creatorcontrib>Kopecky, Jindrich</creatorcontrib><creatorcontrib>Kucharz, Jakub</creatorcontrib><creatorcontrib>Buti, Sebastiano</creatorcontrib><creatorcontrib>Salfi, Alessia</creatorcontrib><creatorcontrib>Büttner, Thomas</creatorcontrib><creatorcontrib>De Giorgi, Ugo</creatorcontrib><creatorcontrib>Kanesvaran, Ravindran</creatorcontrib><creatorcontrib>Fiala, Ondřej</creatorcontrib><creatorcontrib>Grande, Enrique</creatorcontrib><creatorcontrib>Zucali, Paolo Andrea</creatorcontrib><creatorcontrib>Fornarini, Giuseppe</creatorcontrib><creatorcontrib>Bourlon, Maria T</creatorcontrib><creatorcontrib>Scagliarini, Sarah</creatorcontrib><creatorcontrib>Molina-Cerrillo, Javier</creatorcontrib><creatorcontrib>Aurilio, Gaetano</creatorcontrib><creatorcontrib>Matrana, Marc R</creatorcontrib><creatorcontrib>Pichler, Renate</creatorcontrib><creatorcontrib>Cattrini, Carlo</creatorcontrib><creatorcontrib>Büchler, Tomas</creatorcontrib><creatorcontrib>Seront, Emmanuel</creatorcontrib><creatorcontrib>Calabrò, Fabio</creatorcontrib><creatorcontrib>Pinto, Alvaro</creatorcontrib><creatorcontrib>Berardi, Rossana</creatorcontrib><creatorcontrib>Zgura, Anca</creatorcontrib><creatorcontrib>Mammone, Giulia</creatorcontrib><creatorcontrib>Ansari, Jawaher</creatorcontrib><creatorcontrib>Atzori, Francesco</creatorcontrib><creatorcontrib>Chiari, Rita</creatorcontrib><creatorcontrib>Zakopoulou, Roubini</creatorcontrib><creatorcontrib>Caffo, Orazio</creatorcontrib><creatorcontrib>Procopio, Giuseppe</creatorcontrib><creatorcontrib>Bassanelli, Maria</creatorcontrib><creatorcontrib>Zampiva, Ilaria</creatorcontrib><creatorcontrib>Messina, Carlo</creatorcontrib><creatorcontrib>Küronya, Zsófia</creatorcontrib><creatorcontrib>Mosca, Alessandra</creatorcontrib><creatorcontrib>Bhuva, Dipen</creatorcontrib><creatorcontrib>Vau, Nuno</creatorcontrib><creatorcontrib>Incorvaia, Lorena</creatorcontrib><creatorcontrib>Rebuzzi, Sara Elena</creatorcontrib><creatorcontrib>Roviello, Giandomenico</creatorcontrib><creatorcontrib>Zabalza, Ignacio Ortego</creatorcontrib><creatorcontrib>Rizzo, Alessandro</creatorcontrib><creatorcontrib>Mollica, Veronica</creatorcontrib><creatorcontrib>Catalini, Ilaria</creatorcontrib><creatorcontrib>Monteiro, Fernando Sabino M.</creatorcontrib><creatorcontrib>Montironi, Rodolfo</creatorcontrib><creatorcontrib>Battelli, Nicola</creatorcontrib><creatorcontrib>Rizzo, Mimma</creatorcontrib><creatorcontrib>Porta, Camillo</creatorcontrib><title>Clinico-Pathological Features Influencing the Prognostic Role of Body Mass Index in Patients With Advanced Renal Cell Carcinoma Treated by Immuno-Oncology Combinations (ARON-1)</title><title>Clinical genitourinary cancer</title><addtitle>Clin Genitourin Cancer</addtitle><description>Obesity has been associated with improved response to immunotherapy in cancer patients. We investigated the role of body mass index (BMI) in patients from the ARON-1 study (NCT05287464) treated by dual immuno-oncology agents (IO+IO) or a combination of immuno-oncology drug and a tyrosine kinase inhibitors (TKI) as first-line therapy for metastatic renal cell carcinoma (mRCC).
Medical records of patients with documented mRCC treated by immuno-oncology combinations were reviewed at 47 institutions from 16 countries. Patients were assessed for overall survival (OS), progression-free survival (OS), and overall clinical benefit (OCB), defined as the sum of the rate of partial/complete responses and stable disease. Univariate and multivariate analyses were used to explore the association of variables of interest with survival.
A total of 675 patients were included; BMI was >25 kg/m2 in 345 patients (51%) and was associated with improved OS (55.7 vs. 28.4 months, P < .001). The OCB of patients with BMI >25 kg/m2 versus those with BMI ≤25 kg/m2 was significantly higher only in patients with nonclear cell histology (81% vs. 65%, P = .011), and patients with liver metastases (76% vs. 58%, P = .007), Neutrophil to lymphocyte ratio >4 (77% vs 62%, P = .022) or treated by nivolumab plus ipilimumab (77% vs. 64%, P = .044). In the BMI ≤25 kg/m2 subgroup, significant differences were found between patients with NLR >4 versus ≤4 (62% vs. 82%, P = .002) and patients treated by IO+IO versus IO+TKIs combinations (64% vs. 83%, P = .002).
Our study suggests that the prognostic significance and the association of BMI with treatment outcome varies across clinico-pathological mRCC subgroups.
Obesity is a well-known risk factor for the development of renal cell carcinoma (RCC), one of the most frequent malignant urogenital tumors. The development of immunotherapy (IO)-based combinations for the treatment of metastatic RCC (mRCC) has led to a marked improvement of patients’ outcomes and quality of life. The ARON-1 study (NCT05287464) was designed to globally analyze real-world treatment outcomes of mRCC patients receiving first-line immune-based combinations. In this sub-analysis, we investigated the role of body mass index (BMI) in patients treated by immuno-oncology combinations stratified by clinico-pathological features. According to our results, the prognostic significance and the association of BMI with treatment outcome may vary across clinico-pathological mRCC subgroups.</description><subject>Immunocombo</subject><subject>Immunotherapy</subject><subject>mRCC</subject><subject>NCT05287464</subject><subject>Obesity</subject><subject>Survival</subject><subject>Tumor 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Features Influencing the Prognostic Role of Body Mass Index in Patients With Advanced Renal Cell Carcinoma Treated by Immuno-Oncology Combinations (ARON-1)</title><author>Santoni, Matteo ; Massari, Francesco ; Myint, Zin W. ; Iacovelli, Roberto ; Pichler, Martin ; Basso, Umberto ; Kopecky, Jindrich ; Kucharz, Jakub ; Buti, Sebastiano ; Salfi, Alessia ; Büttner, Thomas ; De Giorgi, Ugo ; Kanesvaran, Ravindran ; Fiala, Ondřej ; Grande, Enrique ; Zucali, Paolo Andrea ; Fornarini, Giuseppe ; Bourlon, Maria T ; Scagliarini, Sarah ; Molina-Cerrillo, Javier ; Aurilio, Gaetano ; Matrana, Marc R ; Pichler, Renate ; Cattrini, Carlo ; Büchler, Tomas ; Seront, Emmanuel ; Calabrò, Fabio ; Pinto, Alvaro ; Berardi, Rossana ; Zgura, Anca ; Mammone, Giulia ; Ansari, Jawaher ; Atzori, Francesco ; Chiari, Rita ; Zakopoulou, Roubini ; Caffo, Orazio ; Procopio, Giuseppe ; Bassanelli, Maria ; Zampiva, Ilaria ; Messina, Carlo ; Küronya, Zsófia ; Mosca, Alessandra ; Bhuva, Dipen ; Vau, Nuno ; Incorvaia, Lorena ; Rebuzzi, Sara Elena ; Roviello, Giandomenico ; Zabalza, Ignacio Ortego ; Rizzo, Alessandro ; Mollica, Veronica ; Catalini, Ilaria ; Monteiro, Fernando Sabino M. ; Montironi, Rodolfo ; Battelli, Nicola ; Rizzo, Mimma ; Porta, Camillo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-1a5ac9cf0ab89ca24bac6b00456fd8f15b61dd7c02b149351fd8fda7d0b7db693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Immunocombo</topic><topic>Immunotherapy</topic><topic>mRCC</topic><topic>NCT05287464</topic><topic>Obesity</topic><topic>Survival</topic><topic>Tumor Response</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santoni, Matteo</creatorcontrib><creatorcontrib>Massari, Francesco</creatorcontrib><creatorcontrib>Myint, Zin W.</creatorcontrib><creatorcontrib>Iacovelli, Roberto</creatorcontrib><creatorcontrib>Pichler, Martin</creatorcontrib><creatorcontrib>Basso, Umberto</creatorcontrib><creatorcontrib>Kopecky, Jindrich</creatorcontrib><creatorcontrib>Kucharz, Jakub</creatorcontrib><creatorcontrib>Buti, Sebastiano</creatorcontrib><creatorcontrib>Salfi, Alessia</creatorcontrib><creatorcontrib>Büttner, Thomas</creatorcontrib><creatorcontrib>De Giorgi, Ugo</creatorcontrib><creatorcontrib>Kanesvaran, Ravindran</creatorcontrib><creatorcontrib>Fiala, Ondřej</creatorcontrib><creatorcontrib>Grande, Enrique</creatorcontrib><creatorcontrib>Zucali, Paolo Andrea</creatorcontrib><creatorcontrib>Fornarini, Giuseppe</creatorcontrib><creatorcontrib>Bourlon, Maria T</creatorcontrib><creatorcontrib>Scagliarini, Sarah</creatorcontrib><creatorcontrib>Molina-Cerrillo, Javier</creatorcontrib><creatorcontrib>Aurilio, Gaetano</creatorcontrib><creatorcontrib>Matrana, Marc R</creatorcontrib><creatorcontrib>Pichler, Renate</creatorcontrib><creatorcontrib>Cattrini, Carlo</creatorcontrib><creatorcontrib>Büchler, Tomas</creatorcontrib><creatorcontrib>Seront, Emmanuel</creatorcontrib><creatorcontrib>Calabrò, Fabio</creatorcontrib><creatorcontrib>Pinto, Alvaro</creatorcontrib><creatorcontrib>Berardi, Rossana</creatorcontrib><creatorcontrib>Zgura, Anca</creatorcontrib><creatorcontrib>Mammone, Giulia</creatorcontrib><creatorcontrib>Ansari, Jawaher</creatorcontrib><creatorcontrib>Atzori, Francesco</creatorcontrib><creatorcontrib>Chiari, Rita</creatorcontrib><creatorcontrib>Zakopoulou, Roubini</creatorcontrib><creatorcontrib>Caffo, Orazio</creatorcontrib><creatorcontrib>Procopio, Giuseppe</creatorcontrib><creatorcontrib>Bassanelli, Maria</creatorcontrib><creatorcontrib>Zampiva, Ilaria</creatorcontrib><creatorcontrib>Messina, Carlo</creatorcontrib><creatorcontrib>Küronya, Zsófia</creatorcontrib><creatorcontrib>Mosca, Alessandra</creatorcontrib><creatorcontrib>Bhuva, Dipen</creatorcontrib><creatorcontrib>Vau, Nuno</creatorcontrib><creatorcontrib>Incorvaia, Lorena</creatorcontrib><creatorcontrib>Rebuzzi, Sara Elena</creatorcontrib><creatorcontrib>Roviello, Giandomenico</creatorcontrib><creatorcontrib>Zabalza, Ignacio Ortego</creatorcontrib><creatorcontrib>Rizzo, Alessandro</creatorcontrib><creatorcontrib>Mollica, Veronica</creatorcontrib><creatorcontrib>Catalini, Ilaria</creatorcontrib><creatorcontrib>Monteiro, Fernando Sabino M.</creatorcontrib><creatorcontrib>Montironi, Rodolfo</creatorcontrib><creatorcontrib>Battelli, Nicola</creatorcontrib><creatorcontrib>Rizzo, Mimma</creatorcontrib><creatorcontrib>Porta, Camillo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical genitourinary cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santoni, Matteo</au><au>Massari, Francesco</au><au>Myint, Zin W.</au><au>Iacovelli, Roberto</au><au>Pichler, Martin</au><au>Basso, Umberto</au><au>Kopecky, Jindrich</au><au>Kucharz, Jakub</au><au>Buti, Sebastiano</au><au>Salfi, Alessia</au><au>Büttner, Thomas</au><au>De Giorgi, Ugo</au><au>Kanesvaran, Ravindran</au><au>Fiala, Ondřej</au><au>Grande, Enrique</au><au>Zucali, Paolo Andrea</au><au>Fornarini, Giuseppe</au><au>Bourlon, Maria T</au><au>Scagliarini, Sarah</au><au>Molina-Cerrillo, Javier</au><au>Aurilio, Gaetano</au><au>Matrana, Marc R</au><au>Pichler, Renate</au><au>Cattrini, Carlo</au><au>Büchler, Tomas</au><au>Seront, Emmanuel</au><au>Calabrò, Fabio</au><au>Pinto, Alvaro</au><au>Berardi, Rossana</au><au>Zgura, Anca</au><au>Mammone, Giulia</au><au>Ansari, Jawaher</au><au>Atzori, Francesco</au><au>Chiari, Rita</au><au>Zakopoulou, Roubini</au><au>Caffo, Orazio</au><au>Procopio, Giuseppe</au><au>Bassanelli, Maria</au><au>Zampiva, Ilaria</au><au>Messina, Carlo</au><au>Küronya, Zsófia</au><au>Mosca, Alessandra</au><au>Bhuva, Dipen</au><au>Vau, Nuno</au><au>Incorvaia, Lorena</au><au>Rebuzzi, Sara Elena</au><au>Roviello, Giandomenico</au><au>Zabalza, Ignacio Ortego</au><au>Rizzo, Alessandro</au><au>Mollica, Veronica</au><au>Catalini, Ilaria</au><au>Monteiro, Fernando Sabino M.</au><au>Montironi, Rodolfo</au><au>Battelli, Nicola</au><au>Rizzo, Mimma</au><au>Porta, Camillo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinico-Pathological Features Influencing the Prognostic Role of Body Mass Index in Patients With Advanced Renal Cell Carcinoma Treated by Immuno-Oncology Combinations (ARON-1)</atitle><jtitle>Clinical genitourinary cancer</jtitle><addtitle>Clin Genitourin Cancer</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>21</volume><issue>5</issue><spage>e309</spage><epage>e319.e1</epage><pages>e309-e319.e1</pages><issn>1558-7673</issn><eissn>1938-0682</eissn><abstract>Obesity has been associated with improved response to immunotherapy in cancer patients. We investigated the role of body mass index (BMI) in patients from the ARON-1 study (NCT05287464) treated by dual immuno-oncology agents (IO+IO) or a combination of immuno-oncology drug and a tyrosine kinase inhibitors (TKI) as first-line therapy for metastatic renal cell carcinoma (mRCC).
Medical records of patients with documented mRCC treated by immuno-oncology combinations were reviewed at 47 institutions from 16 countries. Patients were assessed for overall survival (OS), progression-free survival (OS), and overall clinical benefit (OCB), defined as the sum of the rate of partial/complete responses and stable disease. Univariate and multivariate analyses were used to explore the association of variables of interest with survival.
A total of 675 patients were included; BMI was >25 kg/m2 in 345 patients (51%) and was associated with improved OS (55.7 vs. 28.4 months, P < .001). The OCB of patients with BMI >25 kg/m2 versus those with BMI ≤25 kg/m2 was significantly higher only in patients with nonclear cell histology (81% vs. 65%, P = .011), and patients with liver metastases (76% vs. 58%, P = .007), Neutrophil to lymphocyte ratio >4 (77% vs 62%, P = .022) or treated by nivolumab plus ipilimumab (77% vs. 64%, P = .044). In the BMI ≤25 kg/m2 subgroup, significant differences were found between patients with NLR >4 versus ≤4 (62% vs. 82%, P = .002) and patients treated by IO+IO versus IO+TKIs combinations (64% vs. 83%, P = .002).
Our study suggests that the prognostic significance and the association of BMI with treatment outcome varies across clinico-pathological mRCC subgroups.
Obesity is a well-known risk factor for the development of renal cell carcinoma (RCC), one of the most frequent malignant urogenital tumors. The development of immunotherapy (IO)-based combinations for the treatment of metastatic RCC (mRCC) has led to a marked improvement of patients’ outcomes and quality of life. The ARON-1 study (NCT05287464) was designed to globally analyze real-world treatment outcomes of mRCC patients receiving first-line immune-based combinations. In this sub-analysis, we investigated the role of body mass index (BMI) in patients treated by immuno-oncology combinations stratified by clinico-pathological features. According to our results, the prognostic significance and the association of BMI with treatment outcome may vary across clinico-pathological mRCC subgroups.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37062658</pmid><doi>10.1016/j.clgc.2023.03.006</doi><orcidid>https://orcid.org/0000-0003-0316-9621</orcidid><orcidid>https://orcid.org/0000-0001-8589-2148</orcidid><orcidid>https://orcid.org/0000-0003-0876-0226</orcidid><orcidid>https://orcid.org/0000-0003-4858-3965</orcidid><orcidid>https://orcid.org/0000-0003-0546-6304</orcidid><orcidid>https://orcid.org/0000-0001-6476-6871</orcidid><orcidid>https://orcid.org/0000-0001-5814-2296</orcidid><orcidid>https://orcid.org/0000-0002-6621-8251</orcidid><orcidid>https://orcid.org/0000-0003-4754-6572</orcidid><orcidid>https://orcid.org/0000-0003-0111-7588</orcidid><orcidid>https://orcid.org/0000-0003-2973-6065</orcidid><orcidid>https://orcid.org/0000-0002-4756-0756</orcidid><orcidid>https://orcid.org/0000-0001-6667-994X</orcidid><orcidid>https://orcid.org/0000-0001-7340-6173</orcidid><orcidid>https://orcid.org/0000-0002-4719-053X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1558-7673 |
ispartof | Clinical genitourinary cancer, 2023-10, Vol.21 (5), p.e309-e319.e1 |
issn | 1558-7673 1938-0682 |
language | eng |
recordid | cdi_proquest_miscellaneous_2802426276 |
source | Alma/SFX Local Collection |
subjects | Immunocombo Immunotherapy mRCC NCT05287464 Obesity Survival Tumor Response |
title | Clinico-Pathological Features Influencing the Prognostic Role of Body Mass Index in Patients With Advanced Renal Cell Carcinoma Treated by Immuno-Oncology Combinations (ARON-1) |
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