Microsatellite Instability in Patients With Stage III Colon Cancer Receiving Fluoropyrimidine With or Without Oxaliplatin: An ACCENT Pooled Analysis of 12 Adjuvant Trials
In patients with stage III colon cancer (CC) whose tumors demonstrate microsatellite instability (MSI), the efficacy of adjuvant fluoropyrimidine (FP) with or without oxaliplatin has not been clearly demonstrated and the prognostic value of MSI remains uncertain. Individual patient data from the ACC...
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Veröffentlicht in: | Journal of clinical oncology 2021-02, Vol.39 (6), p.642-651 |
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creator | Cohen, Romain Taieb, Julien Fiskum, Jack Yothers, Greg Goldberg, Richard Yoshino, Takayuki Alberts, Steven Allegra, Carmen de Gramont, Aimery Seitz, Jean-Francois O'Connell, Michael Haller, Daniel Wolmark, Norman Erlichman, Charles Zaniboni, Alberto Lonardi, Sara Kerr, Rachel Grothey, Axel Sinicrope, Frank A André, Thierry Shi, Qian |
description | In patients with stage III colon cancer (CC) whose tumors demonstrate microsatellite instability (MSI), the efficacy of adjuvant fluoropyrimidine (FP) with or without oxaliplatin has not been clearly demonstrated and the prognostic value of MSI remains uncertain.
Individual patient data from the ACCENT database were used to evaluate the effect of FP with or without oxaliplatin on disease-free survival (DFS) and overall survival (OS) among patients with MSI stage III CC and the prognostic value of MSI in patients treated with FP plus oxaliplatin, by stratified Cox models adjusted for demographic and clinicopathological factors.
MSI status was available for 5,457 patients (609 MSI, 11.2%; 4848 microsatellite stable [MSS], 88.8%) from 12 randomized clinical trials (RCTs). Oxaliplatin significantly improved OS of MSI patients from the two RCTs testing FP with or without oxaliplatin (n = 185; adjusted hazard ratio [aHR] = 0.52, 95% CI, 0.28 to 0.93). Among the 4,250 patients treated with FP plus oxaliplatin (461 MSI and 3789 MSS), MSI was associated with better OS in the N1 group compared with MSS (aHR = 0.66; 95% CI, 0.46 to 0.95) but similar survival in the N2 population (aHR = 1.13; 95% CI, 0.86 to 1.48;
interaction = .029). The main independent prognosticators of MSI patients treated with FP plus oxaliplatin were T stage (aHR = 2.09; 95% CI, 1.29 to 3.38) and N stage (aHR = 3.57; 95% CI, 2.32 to 5.48). Similar results were observed for DFS in all analyses.
Adding oxaliplatin to FP improves OS and DFS in patients with MSI stage III CC. Compared with MSS, MSI patients experienced better outcomes in the N1 group but similar survival in the N2 group. |
doi_str_mv | 10.1200/JCO.20.01600 |
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Individual patient data from the ACCENT database were used to evaluate the effect of FP with or without oxaliplatin on disease-free survival (DFS) and overall survival (OS) among patients with MSI stage III CC and the prognostic value of MSI in patients treated with FP plus oxaliplatin, by stratified Cox models adjusted for demographic and clinicopathological factors.
MSI status was available for 5,457 patients (609 MSI, 11.2%; 4848 microsatellite stable [MSS], 88.8%) from 12 randomized clinical trials (RCTs). Oxaliplatin significantly improved OS of MSI patients from the two RCTs testing FP with or without oxaliplatin (n = 185; adjusted hazard ratio [aHR] = 0.52, 95% CI, 0.28 to 0.93). Among the 4,250 patients treated with FP plus oxaliplatin (461 MSI and 3789 MSS), MSI was associated with better OS in the N1 group compared with MSS (aHR = 0.66; 95% CI, 0.46 to 0.95) but similar survival in the N2 population (aHR = 1.13; 95% CI, 0.86 to 1.48;
interaction = .029). The main independent prognosticators of MSI patients treated with FP plus oxaliplatin were T stage (aHR = 2.09; 95% CI, 1.29 to 3.38) and N stage (aHR = 3.57; 95% CI, 2.32 to 5.48). Similar results were observed for DFS in all analyses.
Adding oxaliplatin to FP improves OS and DFS in patients with MSI stage III CC. Compared with MSS, MSI patients experienced better outcomes in the N1 group but similar survival in the N2 group.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.20.01600</identifier><identifier>PMID: 33356421</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>Colonic Neoplasms - genetics ; Female ; Fluorouracil - pharmacology ; Fluorouracil - therapeutic use ; Humans ; Male ; Microsatellite Instability ; Neoplasm Staging ; ORIGINAL REPORTS ; Oxaliplatin - pharmacology ; Oxaliplatin - therapeutic use ; Prognosis</subject><ispartof>Journal of clinical oncology, 2021-02, Vol.39 (6), p.642-651</ispartof><rights>2020 by American Society of Clinical Oncology 2020 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-28a30f332b2322682f140c63f97950bb52956ea5174356464308fe30363340073</citedby><cites>FETCH-LOGICAL-c427t-28a30f332b2322682f140c63f97950bb52956ea5174356464308fe30363340073</cites><orcidid>0000-0002-4640-8832 ; 0000-0002-5835-4122 ; 0000-0002-5103-7095 ; 0000-0001-9602-5162 ; 0000-0002-9955-4753 ; 0000-0003-0308-8223 ; 0000-0002-7593-8138 ; 0000-0002-2907-1000 ; 0000-0002-0489-4756</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33356421$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cohen, Romain</creatorcontrib><creatorcontrib>Taieb, Julien</creatorcontrib><creatorcontrib>Fiskum, Jack</creatorcontrib><creatorcontrib>Yothers, Greg</creatorcontrib><creatorcontrib>Goldberg, Richard</creatorcontrib><creatorcontrib>Yoshino, Takayuki</creatorcontrib><creatorcontrib>Alberts, Steven</creatorcontrib><creatorcontrib>Allegra, Carmen</creatorcontrib><creatorcontrib>de Gramont, Aimery</creatorcontrib><creatorcontrib>Seitz, Jean-Francois</creatorcontrib><creatorcontrib>O'Connell, Michael</creatorcontrib><creatorcontrib>Haller, Daniel</creatorcontrib><creatorcontrib>Wolmark, Norman</creatorcontrib><creatorcontrib>Erlichman, Charles</creatorcontrib><creatorcontrib>Zaniboni, Alberto</creatorcontrib><creatorcontrib>Lonardi, Sara</creatorcontrib><creatorcontrib>Kerr, Rachel</creatorcontrib><creatorcontrib>Grothey, Axel</creatorcontrib><creatorcontrib>Sinicrope, Frank A</creatorcontrib><creatorcontrib>André, Thierry</creatorcontrib><creatorcontrib>Shi, Qian</creatorcontrib><title>Microsatellite Instability in Patients With Stage III Colon Cancer Receiving Fluoropyrimidine With or Without Oxaliplatin: An ACCENT Pooled Analysis of 12 Adjuvant Trials</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>In patients with stage III colon cancer (CC) whose tumors demonstrate microsatellite instability (MSI), the efficacy of adjuvant fluoropyrimidine (FP) with or without oxaliplatin has not been clearly demonstrated and the prognostic value of MSI remains uncertain.
Individual patient data from the ACCENT database were used to evaluate the effect of FP with or without oxaliplatin on disease-free survival (DFS) and overall survival (OS) among patients with MSI stage III CC and the prognostic value of MSI in patients treated with FP plus oxaliplatin, by stratified Cox models adjusted for demographic and clinicopathological factors.
MSI status was available for 5,457 patients (609 MSI, 11.2%; 4848 microsatellite stable [MSS], 88.8%) from 12 randomized clinical trials (RCTs). Oxaliplatin significantly improved OS of MSI patients from the two RCTs testing FP with or without oxaliplatin (n = 185; adjusted hazard ratio [aHR] = 0.52, 95% CI, 0.28 to 0.93). Among the 4,250 patients treated with FP plus oxaliplatin (461 MSI and 3789 MSS), MSI was associated with better OS in the N1 group compared with MSS (aHR = 0.66; 95% CI, 0.46 to 0.95) but similar survival in the N2 population (aHR = 1.13; 95% CI, 0.86 to 1.48;
interaction = .029). The main independent prognosticators of MSI patients treated with FP plus oxaliplatin were T stage (aHR = 2.09; 95% CI, 1.29 to 3.38) and N stage (aHR = 3.57; 95% CI, 2.32 to 5.48). Similar results were observed for DFS in all analyses.
Adding oxaliplatin to FP improves OS and DFS in patients with MSI stage III CC. Compared with MSS, MSI patients experienced better outcomes in the N1 group but similar survival in the N2 group.</description><subject>Colonic Neoplasms - genetics</subject><subject>Female</subject><subject>Fluorouracil - pharmacology</subject><subject>Fluorouracil - therapeutic use</subject><subject>Humans</subject><subject>Male</subject><subject>Microsatellite Instability</subject><subject>Neoplasm Staging</subject><subject>ORIGINAL REPORTS</subject><subject>Oxaliplatin - pharmacology</subject><subject>Oxaliplatin - therapeutic use</subject><subject>Prognosis</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1vEzEQtRCIhsKNM_KRAxvGH-vdcECKVi1N1ZIKguBmeTfe1JVjp7Y3In-pv7JO01Zwetb4zZuZ9xB6T2BMKMDn82Y-pjAGIgBeoBEpaVVUVVm-RCOoGC1Izf4coTcx3gAQXrPyNTpijJWCUzJCd5emCz6qpK01SeOZi0m1Jr932Dh8pZLRLkX826Rr_DOpVabMZrjx1jvcKNfpgH_oTputcSt8agcf_GYXzNosjdOHNh8e0A8Jz_8qazY2q7oveOrwtGlOvi_wlfdWL3NB2V00EfseE4qny5thq1zCi2CUjW_Rqz6DfveIx-jX6cmiOSsu5t9mzfSi6DitUkFrxaBnjLaUUSpq2hMOnWD9pJqU0LYlnZRCq5JUfG-C4AzqXjNggjEO2bJj9PWguxnatV52-f6grNzko1TYSa-M_P_HmWu58ltZk3oigGeBj48Cwd8OOia5NrHLBiun_RAl5VWeRKiATP10oO5DiEH3z2MIyH28MscrKciHeDP9w7-rPZOf8mT3unWgmg</recordid><startdate>20210220</startdate><enddate>20210220</enddate><creator>Cohen, Romain</creator><creator>Taieb, Julien</creator><creator>Fiskum, Jack</creator><creator>Yothers, Greg</creator><creator>Goldberg, Richard</creator><creator>Yoshino, Takayuki</creator><creator>Alberts, Steven</creator><creator>Allegra, Carmen</creator><creator>de Gramont, Aimery</creator><creator>Seitz, Jean-Francois</creator><creator>O'Connell, Michael</creator><creator>Haller, Daniel</creator><creator>Wolmark, Norman</creator><creator>Erlichman, Charles</creator><creator>Zaniboni, Alberto</creator><creator>Lonardi, Sara</creator><creator>Kerr, Rachel</creator><creator>Grothey, Axel</creator><creator>Sinicrope, Frank A</creator><creator>André, Thierry</creator><creator>Shi, Qian</creator><general>American Society of Clinical Oncology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4640-8832</orcidid><orcidid>https://orcid.org/0000-0002-5835-4122</orcidid><orcidid>https://orcid.org/0000-0002-5103-7095</orcidid><orcidid>https://orcid.org/0000-0001-9602-5162</orcidid><orcidid>https://orcid.org/0000-0002-9955-4753</orcidid><orcidid>https://orcid.org/0000-0003-0308-8223</orcidid><orcidid>https://orcid.org/0000-0002-7593-8138</orcidid><orcidid>https://orcid.org/0000-0002-2907-1000</orcidid><orcidid>https://orcid.org/0000-0002-0489-4756</orcidid></search><sort><creationdate>20210220</creationdate><title>Microsatellite Instability in Patients With Stage III Colon Cancer Receiving Fluoropyrimidine With or Without Oxaliplatin: An ACCENT Pooled Analysis of 12 Adjuvant Trials</title><author>Cohen, Romain ; Taieb, Julien ; Fiskum, Jack ; Yothers, Greg ; Goldberg, Richard ; Yoshino, Takayuki ; Alberts, Steven ; Allegra, Carmen ; de Gramont, Aimery ; Seitz, Jean-Francois ; O'Connell, Michael ; Haller, Daniel ; Wolmark, Norman ; Erlichman, Charles ; Zaniboni, Alberto ; Lonardi, Sara ; Kerr, Rachel ; Grothey, Axel ; Sinicrope, Frank A ; André, Thierry ; Shi, Qian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-28a30f332b2322682f140c63f97950bb52956ea5174356464308fe30363340073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Colonic Neoplasms - genetics</topic><topic>Female</topic><topic>Fluorouracil - pharmacology</topic><topic>Fluorouracil - therapeutic use</topic><topic>Humans</topic><topic>Male</topic><topic>Microsatellite Instability</topic><topic>Neoplasm Staging</topic><topic>ORIGINAL REPORTS</topic><topic>Oxaliplatin - pharmacology</topic><topic>Oxaliplatin - therapeutic use</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cohen, Romain</creatorcontrib><creatorcontrib>Taieb, Julien</creatorcontrib><creatorcontrib>Fiskum, Jack</creatorcontrib><creatorcontrib>Yothers, Greg</creatorcontrib><creatorcontrib>Goldberg, Richard</creatorcontrib><creatorcontrib>Yoshino, Takayuki</creatorcontrib><creatorcontrib>Alberts, Steven</creatorcontrib><creatorcontrib>Allegra, Carmen</creatorcontrib><creatorcontrib>de Gramont, Aimery</creatorcontrib><creatorcontrib>Seitz, Jean-Francois</creatorcontrib><creatorcontrib>O'Connell, Michael</creatorcontrib><creatorcontrib>Haller, Daniel</creatorcontrib><creatorcontrib>Wolmark, Norman</creatorcontrib><creatorcontrib>Erlichman, Charles</creatorcontrib><creatorcontrib>Zaniboni, Alberto</creatorcontrib><creatorcontrib>Lonardi, Sara</creatorcontrib><creatorcontrib>Kerr, Rachel</creatorcontrib><creatorcontrib>Grothey, Axel</creatorcontrib><creatorcontrib>Sinicrope, Frank A</creatorcontrib><creatorcontrib>André, Thierry</creatorcontrib><creatorcontrib>Shi, Qian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, Romain</au><au>Taieb, Julien</au><au>Fiskum, Jack</au><au>Yothers, Greg</au><au>Goldberg, Richard</au><au>Yoshino, Takayuki</au><au>Alberts, Steven</au><au>Allegra, Carmen</au><au>de Gramont, Aimery</au><au>Seitz, Jean-Francois</au><au>O'Connell, Michael</au><au>Haller, Daniel</au><au>Wolmark, Norman</au><au>Erlichman, Charles</au><au>Zaniboni, Alberto</au><au>Lonardi, Sara</au><au>Kerr, Rachel</au><au>Grothey, Axel</au><au>Sinicrope, Frank A</au><au>André, Thierry</au><au>Shi, Qian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microsatellite Instability in Patients With Stage III Colon Cancer Receiving Fluoropyrimidine With or Without Oxaliplatin: An ACCENT Pooled Analysis of 12 Adjuvant Trials</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2021-02-20</date><risdate>2021</risdate><volume>39</volume><issue>6</issue><spage>642</spage><epage>651</epage><pages>642-651</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>In patients with stage III colon cancer (CC) whose tumors demonstrate microsatellite instability (MSI), the efficacy of adjuvant fluoropyrimidine (FP) with or without oxaliplatin has not been clearly demonstrated and the prognostic value of MSI remains uncertain.
Individual patient data from the ACCENT database were used to evaluate the effect of FP with or without oxaliplatin on disease-free survival (DFS) and overall survival (OS) among patients with MSI stage III CC and the prognostic value of MSI in patients treated with FP plus oxaliplatin, by stratified Cox models adjusted for demographic and clinicopathological factors.
MSI status was available for 5,457 patients (609 MSI, 11.2%; 4848 microsatellite stable [MSS], 88.8%) from 12 randomized clinical trials (RCTs). Oxaliplatin significantly improved OS of MSI patients from the two RCTs testing FP with or without oxaliplatin (n = 185; adjusted hazard ratio [aHR] = 0.52, 95% CI, 0.28 to 0.93). Among the 4,250 patients treated with FP plus oxaliplatin (461 MSI and 3789 MSS), MSI was associated with better OS in the N1 group compared with MSS (aHR = 0.66; 95% CI, 0.46 to 0.95) but similar survival in the N2 population (aHR = 1.13; 95% CI, 0.86 to 1.48;
interaction = .029). The main independent prognosticators of MSI patients treated with FP plus oxaliplatin were T stage (aHR = 2.09; 95% CI, 1.29 to 3.38) and N stage (aHR = 3.57; 95% CI, 2.32 to 5.48). Similar results were observed for DFS in all analyses.
Adding oxaliplatin to FP improves OS and DFS in patients with MSI stage III CC. Compared with MSS, MSI patients experienced better outcomes in the N1 group but similar survival in the N2 group.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>33356421</pmid><doi>10.1200/JCO.20.01600</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-4640-8832</orcidid><orcidid>https://orcid.org/0000-0002-5835-4122</orcidid><orcidid>https://orcid.org/0000-0002-5103-7095</orcidid><orcidid>https://orcid.org/0000-0001-9602-5162</orcidid><orcidid>https://orcid.org/0000-0002-9955-4753</orcidid><orcidid>https://orcid.org/0000-0003-0308-8223</orcidid><orcidid>https://orcid.org/0000-0002-7593-8138</orcidid><orcidid>https://orcid.org/0000-0002-2907-1000</orcidid><orcidid>https://orcid.org/0000-0002-0489-4756</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Colonic Neoplasms - genetics Female Fluorouracil - pharmacology Fluorouracil - therapeutic use Humans Male Microsatellite Instability Neoplasm Staging ORIGINAL REPORTS Oxaliplatin - pharmacology Oxaliplatin - therapeutic use Prognosis |
title | Microsatellite Instability in Patients With Stage III Colon Cancer Receiving Fluoropyrimidine With or Without Oxaliplatin: An ACCENT Pooled Analysis of 12 Adjuvant Trials |
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