A Prospective Cohort Study of Biomarkers in Squamous Cell Carcinoma of the Anal Canal (SCCAC) and their Influence on Treatment Outcomes
Background: Although Chemoradiation (CRT) is the curative treatment for SCCAC, many patients present primary resistance. Since it is a rare tumor, response predictors remain unknown. Methods: We performed a prospective cohort study to evaluate biomarkers associated with CRT response, progression-fre...
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creator | Moniz, Camila Motta Venchiarutti Riechelmann, Rachel Pimenta Oliveira, Suilane Coelho Ribeiro Bariani, Giovanni Mendonça Rivelli, Thomas Giollo Ortega, Cintia Pereira, Allan Andresson Lima Meireles, Sibele Inácio Franco, Rejane Chen, Andre Bonadio, Renata Colombo Nahas, Caio Sabbaga, Jorge Coudry, Renata Almeida Braghiroli, Maria Ignez Hoff, Paulo Marcelo |
description | Background: Although Chemoradiation (CRT) is the curative treatment for SCCAC, many patients present primary resistance. Since it is a rare tumor, response predictors remain unknown. Methods: We performed a prospective cohort study to evaluate biomarkers associated with CRT response, progression-free survival (PFS), and overall survival (OS). The primary endpoint was response at 6 months (m). Tumor DNA and HPV were analyzed by next-generation sequencing, while KI-67 and PD-L1 by immunohistochemistry in tumor tissue. Results: Seventy-eight patients were recruited between October/2011 and December/2015, and 75 were response evaluable. The median age was 57 years, 65% (n=49) were stage III and 12% (n=9) were HIV positive (HIV+). At 6m, 62.7% (n=47) presented CR. On multivariate analyses, stage II patients were 4.7 more likely to achieve response than stage III (OR, 4.70; 95%CI, 1.36-16.30; p=0.015). HIV+ was associated with a worse response (OR, 5.72; 95%CI, 2.5-13.0; p< 0.001). 5-year PFS and OS rates were 63.3% and 76.4%, respectively, with a median follow up of 66m. On multivariate analyses, older age (HR 1.06, p=0.022, 95%IC 1.01-1.11) and absence of CR at 6m (HR 3.36, p=0.007, 95%IC 1.39-8.09) were associated with inferior OS. The 5-year OS rate was 62.5% in HIV+ group compared to 78% among HIV- pts, although this difference was not statistically significant (p=0.4). PIK3CA, MET and TP53 mutations, HPV, Ki-67 expression, and PD-L1 expression, were not associated with PFS and OS. Conclusions: Clinical stage III and HIV+ were associated with worse response to CRT at 6m. The absence of CR was the main factor associated with poor 5-year OS. |
doi_str_mv | 10.7150/jca.57678 |
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Since it is a rare tumor, response predictors remain unknown. Methods: We performed a prospective cohort study to evaluate biomarkers associated with CRT response, progression-free survival (PFS), and overall survival (OS). The primary endpoint was response at 6 months (m). Tumor DNA and HPV were analyzed by next-generation sequencing, while KI-67 and PD-L1 by immunohistochemistry in tumor tissue. Results: Seventy-eight patients were recruited between October/2011 and December/2015, and 75 were response evaluable. The median age was 57 years, 65% (n=49) were stage III and 12% (n=9) were HIV positive (HIV+). At 6m, 62.7% (n=47) presented CR. On multivariate analyses, stage II patients were 4.7 more likely to achieve response than stage III (OR, 4.70; 95%CI, 1.36-16.30; p=0.015). HIV+ was associated with a worse response (OR, 5.72; 95%CI, 2.5-13.0; p< 0.001). 5-year PFS and OS rates were 63.3% and 76.4%, respectively, with a median follow up of 66m. On multivariate analyses, older age (HR 1.06, p=0.022, 95%IC 1.01-1.11) and absence of CR at 6m (HR 3.36, p=0.007, 95%IC 1.39-8.09) were associated with inferior OS. The 5-year OS rate was 62.5% in HIV+ group compared to 78% among HIV- pts, although this difference was not statistically significant (p=0.4). PIK3CA, MET and TP53 mutations, HPV, Ki-67 expression, and PD-L1 expression, were not associated with PFS and OS. Conclusions: Clinical stage III and HIV+ were associated with worse response to CRT at 6m. The absence of CR was the main factor associated with poor 5-year OS.</description><identifier>ISSN: 1837-9664</identifier><identifier>EISSN: 1837-9664</identifier><identifier>DOI: 10.7150/jca.57678</identifier><identifier>PMID: 34729104</identifier><language>eng</language><publisher>Wyoming: Ivyspring International Publisher Pty Ltd</publisher><subject>Age ; Anal cancer ; Anus ; Biomarkers ; Cloning ; Cohort analysis ; Colorectal cancer ; Drug dosages ; Human papillomavirus ; Medical prognosis ; Medical screening ; Metastasis ; Mutation ; Radiation therapy ; Research Paper ; Response rates ; Squamous cell carcinoma ; Systematic review ; Tumors</subject><ispartof>Journal of Cancer, 2021-01, Vol.12 (23), p.7018-7025</ispartof><rights>2021. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-e054567aa07d46429275ea032f4e09942a3c6f277b67db172efbd800edd93ca83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558650/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558650/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids></links><search><creatorcontrib>Moniz, Camila Motta Venchiarutti</creatorcontrib><creatorcontrib>Riechelmann, Rachel Pimenta</creatorcontrib><creatorcontrib>Oliveira, Suilane Coelho Ribeiro</creatorcontrib><creatorcontrib>Bariani, Giovanni Mendonça</creatorcontrib><creatorcontrib>Rivelli, Thomas Giollo</creatorcontrib><creatorcontrib>Ortega, Cintia</creatorcontrib><creatorcontrib>Pereira, Allan Andresson Lima</creatorcontrib><creatorcontrib>Meireles, Sibele Inácio</creatorcontrib><creatorcontrib>Franco, Rejane</creatorcontrib><creatorcontrib>Chen, Andre</creatorcontrib><creatorcontrib>Bonadio, Renata Colombo</creatorcontrib><creatorcontrib>Nahas, Caio</creatorcontrib><creatorcontrib>Sabbaga, Jorge</creatorcontrib><creatorcontrib>Coudry, Renata Almeida</creatorcontrib><creatorcontrib>Braghiroli, Maria Ignez</creatorcontrib><creatorcontrib>Hoff, Paulo Marcelo</creatorcontrib><title>A Prospective Cohort Study of Biomarkers in Squamous Cell Carcinoma of the Anal Canal (SCCAC) and their Influence on Treatment Outcomes</title><title>Journal of Cancer</title><description>Background: Although Chemoradiation (CRT) is the curative treatment for SCCAC, many patients present primary resistance. Since it is a rare tumor, response predictors remain unknown. Methods: We performed a prospective cohort study to evaluate biomarkers associated with CRT response, progression-free survival (PFS), and overall survival (OS). The primary endpoint was response at 6 months (m). Tumor DNA and HPV were analyzed by next-generation sequencing, while KI-67 and PD-L1 by immunohistochemistry in tumor tissue. Results: Seventy-eight patients were recruited between October/2011 and December/2015, and 75 were response evaluable. The median age was 57 years, 65% (n=49) were stage III and 12% (n=9) were HIV positive (HIV+). At 6m, 62.7% (n=47) presented CR. On multivariate analyses, stage II patients were 4.7 more likely to achieve response than stage III (OR, 4.70; 95%CI, 1.36-16.30; p=0.015). HIV+ was associated with a worse response (OR, 5.72; 95%CI, 2.5-13.0; p< 0.001). 5-year PFS and OS rates were 63.3% and 76.4%, respectively, with a median follow up of 66m. On multivariate analyses, older age (HR 1.06, p=0.022, 95%IC 1.01-1.11) and absence of CR at 6m (HR 3.36, p=0.007, 95%IC 1.39-8.09) were associated with inferior OS. The 5-year OS rate was 62.5% in HIV+ group compared to 78% among HIV- pts, although this difference was not statistically significant (p=0.4). PIK3CA, MET and TP53 mutations, HPV, Ki-67 expression, and PD-L1 expression, were not associated with PFS and OS. Conclusions: Clinical stage III and HIV+ were associated with worse response to CRT at 6m. The absence of CR was the main factor associated with poor 5-year OS.</description><subject>Age</subject><subject>Anal cancer</subject><subject>Anus</subject><subject>Biomarkers</subject><subject>Cloning</subject><subject>Cohort analysis</subject><subject>Colorectal cancer</subject><subject>Drug dosages</subject><subject>Human papillomavirus</subject><subject>Medical prognosis</subject><subject>Medical screening</subject><subject>Metastasis</subject><subject>Mutation</subject><subject>Radiation therapy</subject><subject>Research Paper</subject><subject>Response rates</subject><subject>Squamous cell carcinoma</subject><subject>Systematic review</subject><subject>Tumors</subject><issn>1837-9664</issn><issn>1837-9664</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpVUctKxDAUDaKojC78g4AbXYymzavdCGPxBYLCjOuQSW-djm0yJqngF_jbpiqid5F7yTmcm5OD0FFGzmTGyfna6DMuhSy20H5WUDkthWDbf-Y9dBjCmqSiZS4Z3UV7lMm8zAjbRx8z_Ohd2ICJ7Rvgyq2cj3geh_oduwZftq7X_gV8wK3F89dB924IuIKuw5X2prUJH4lxBXhm9Xg7nifzqppVp1jbeoRaj-9s0w1gDWBn8cKDjj3YiB-GaFwP4QDtNLoLcPjTJ-jp-mpR3U7vH27uqtn91LBMxikQzriQWhNZM8HyZIiDJjRvGJCyZLmmRjS5lEsh62Umc2iWdUEI1HVJjS7oBF18626GZQ-1SW_wulMb3yaf78rpVv1HbLtSz-5NFZwXgpMkcPwj4N3rACGqtRt88hxUzksuhMxKmlin3yyTPjd4aH43ZESNsakUm_qKjX4C0XiJoA</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Moniz, Camila Motta Venchiarutti</creator><creator>Riechelmann, Rachel Pimenta</creator><creator>Oliveira, Suilane Coelho Ribeiro</creator><creator>Bariani, Giovanni Mendonça</creator><creator>Rivelli, Thomas Giollo</creator><creator>Ortega, Cintia</creator><creator>Pereira, Allan Andresson Lima</creator><creator>Meireles, Sibele Inácio</creator><creator>Franco, Rejane</creator><creator>Chen, Andre</creator><creator>Bonadio, Renata Colombo</creator><creator>Nahas, Caio</creator><creator>Sabbaga, Jorge</creator><creator>Coudry, Renata Almeida</creator><creator>Braghiroli, Maria Ignez</creator><creator>Hoff, Paulo Marcelo</creator><general>Ivyspring International Publisher Pty Ltd</general><general>Ivyspring International Publisher</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20210101</creationdate><title>A Prospective Cohort Study of Biomarkers in Squamous Cell Carcinoma of the Anal Canal (SCCAC) and their Influence on Treatment Outcomes</title><author>Moniz, Camila Motta Venchiarutti ; Riechelmann, Rachel Pimenta ; Oliveira, Suilane Coelho Ribeiro ; Bariani, Giovanni Mendonça ; Rivelli, Thomas Giollo ; Ortega, Cintia ; Pereira, Allan Andresson Lima ; Meireles, Sibele Inácio ; Franco, Rejane ; Chen, Andre ; Bonadio, Renata Colombo ; Nahas, Caio ; Sabbaga, Jorge ; Coudry, Renata Almeida ; Braghiroli, Maria Ignez ; Hoff, Paulo Marcelo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-e054567aa07d46429275ea032f4e09942a3c6f277b67db172efbd800edd93ca83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Age</topic><topic>Anal cancer</topic><topic>Anus</topic><topic>Biomarkers</topic><topic>Cloning</topic><topic>Cohort analysis</topic><topic>Colorectal cancer</topic><topic>Drug dosages</topic><topic>Human papillomavirus</topic><topic>Medical prognosis</topic><topic>Medical screening</topic><topic>Metastasis</topic><topic>Mutation</topic><topic>Radiation therapy</topic><topic>Research Paper</topic><topic>Response rates</topic><topic>Squamous cell carcinoma</topic><topic>Systematic review</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moniz, Camila Motta Venchiarutti</creatorcontrib><creatorcontrib>Riechelmann, Rachel Pimenta</creatorcontrib><creatorcontrib>Oliveira, Suilane Coelho Ribeiro</creatorcontrib><creatorcontrib>Bariani, Giovanni Mendonça</creatorcontrib><creatorcontrib>Rivelli, Thomas Giollo</creatorcontrib><creatorcontrib>Ortega, Cintia</creatorcontrib><creatorcontrib>Pereira, Allan Andresson Lima</creatorcontrib><creatorcontrib>Meireles, Sibele Inácio</creatorcontrib><creatorcontrib>Franco, Rejane</creatorcontrib><creatorcontrib>Chen, Andre</creatorcontrib><creatorcontrib>Bonadio, Renata Colombo</creatorcontrib><creatorcontrib>Nahas, Caio</creatorcontrib><creatorcontrib>Sabbaga, Jorge</creatorcontrib><creatorcontrib>Coudry, Renata Almeida</creatorcontrib><creatorcontrib>Braghiroli, Maria Ignez</creatorcontrib><creatorcontrib>Hoff, Paulo Marcelo</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moniz, Camila Motta Venchiarutti</au><au>Riechelmann, Rachel Pimenta</au><au>Oliveira, Suilane Coelho Ribeiro</au><au>Bariani, Giovanni Mendonça</au><au>Rivelli, Thomas Giollo</au><au>Ortega, Cintia</au><au>Pereira, Allan Andresson Lima</au><au>Meireles, Sibele Inácio</au><au>Franco, Rejane</au><au>Chen, Andre</au><au>Bonadio, Renata Colombo</au><au>Nahas, Caio</au><au>Sabbaga, Jorge</au><au>Coudry, Renata Almeida</au><au>Braghiroli, Maria Ignez</au><au>Hoff, Paulo Marcelo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Prospective Cohort Study of Biomarkers in Squamous Cell Carcinoma of the Anal Canal (SCCAC) and their Influence on Treatment Outcomes</atitle><jtitle>Journal of Cancer</jtitle><date>2021-01-01</date><risdate>2021</risdate><volume>12</volume><issue>23</issue><spage>7018</spage><epage>7025</epage><pages>7018-7025</pages><issn>1837-9664</issn><eissn>1837-9664</eissn><abstract>Background: Although Chemoradiation (CRT) is the curative treatment for SCCAC, many patients present primary resistance. Since it is a rare tumor, response predictors remain unknown. Methods: We performed a prospective cohort study to evaluate biomarkers associated with CRT response, progression-free survival (PFS), and overall survival (OS). The primary endpoint was response at 6 months (m). Tumor DNA and HPV were analyzed by next-generation sequencing, while KI-67 and PD-L1 by immunohistochemistry in tumor tissue. Results: Seventy-eight patients were recruited between October/2011 and December/2015, and 75 were response evaluable. The median age was 57 years, 65% (n=49) were stage III and 12% (n=9) were HIV positive (HIV+). At 6m, 62.7% (n=47) presented CR. On multivariate analyses, stage II patients were 4.7 more likely to achieve response than stage III (OR, 4.70; 95%CI, 1.36-16.30; p=0.015). HIV+ was associated with a worse response (OR, 5.72; 95%CI, 2.5-13.0; p< 0.001). 5-year PFS and OS rates were 63.3% and 76.4%, respectively, with a median follow up of 66m. On multivariate analyses, older age (HR 1.06, p=0.022, 95%IC 1.01-1.11) and absence of CR at 6m (HR 3.36, p=0.007, 95%IC 1.39-8.09) were associated with inferior OS. The 5-year OS rate was 62.5% in HIV+ group compared to 78% among HIV- pts, although this difference was not statistically significant (p=0.4). PIK3CA, MET and TP53 mutations, HPV, Ki-67 expression, and PD-L1 expression, were not associated with PFS and OS. Conclusions: Clinical stage III and HIV+ were associated with worse response to CRT at 6m. The absence of CR was the main factor associated with poor 5-year OS.</abstract><cop>Wyoming</cop><pub>Ivyspring International Publisher Pty Ltd</pub><pmid>34729104</pmid><doi>10.7150/jca.57678</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Anal cancer Anus Biomarkers Cloning Cohort analysis Colorectal cancer Drug dosages Human papillomavirus Medical prognosis Medical screening Metastasis Mutation Radiation therapy Research Paper Response rates Squamous cell carcinoma Systematic review Tumors |
title | A Prospective Cohort Study of Biomarkers in Squamous Cell Carcinoma of the Anal Canal (SCCAC) and their Influence on Treatment Outcomes |
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