Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study
Purpose Uncertainty exists regarding comparative effectiveness of cetuximab versus bevacizumab in metastatic colorectal cancer (mCRC). We conducted a retrospective head-to-head multi-cohort study comparing clinical outcomes from both antibodies Methods Cohorts were defined by treatment line and subg...
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Veröffentlicht in: | Journal of cancer research and clinical oncology 2020-05, Vol.146 (5), p.1321-1334 |
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creator | Marques, Rui Pedro Godinho, Ana Rita Heudtlass, Peter Pais, Helena Luna Quintela, António Martins, Ana Paula |
description | Purpose
Uncertainty exists regarding comparative effectiveness of cetuximab versus bevacizumab in metastatic colorectal cancer (mCRC). We conducted a retrospective head-to-head multi-cohort study comparing clinical outcomes from both antibodies
Methods
Cohorts were defined by treatment line and subgroups by (K)RAS status and tumour sidedness. Among other outcomes, we estimated and compared response rates, progression-free (PFS) and overall survival (OS).
Results
Between January 2010 and April 2018, 311 patients were included. Except for (K)RAS mutation status, baseline characteristics were balanced across treatment groups. In the full analysis of first and second-line cohorts, PFS (first-line: HR = 0.85; 95% CI 0.64 to 1.13;
P
= 0.26; second-line: HR = 1.16; 95% CI 0.74 to 1.83;
P
= 0.51) and OS (first-line: HR = 0.83; 95% CI 0.61 to 1.15;
P
= 0.26; second-line: HR = 0.88; 95% CI 0.56 to 1.38;
P
= 0.58) were similar between bevacizumab and cetuximab arms. In subgroup analyses of first-line therapy, we found a survival difference favouring bevacizumab in right-sided tumours (PFS: HR = 0.52; 95% CI 0.29 to 0.93;
P
= 0.025; OS: HR = 0.60; 95% CI 0.32 to 1.12;
P
= 0.11), but not in left-sided (HR = 1.04; 95% CI 0.75 to 1.46;
P
= 0.81; OS: HR = 0.94; 95% CI 0.65 to 1.36;
P
= 0.74), or (K)RAS wild-type tumours (PFS: HR = 0.91; 95% CI 0.60 to 1.40;
P
= 0.67; OS: HR = 0.79; 95% CI 0.50 to 1.25;
P
= 0.31). Response rates were similar across treatment groups, except for the subgroup of patients bearing right-sided primaries, where bevacizumab performed substantially better.
Conclusion
This study provides evidence suggesting bevacizumab and cetuximab lead to similar effectiveness outcomes in mCRC, except for right-sided tumours, where cetuximab seemed to show considerably poorer outcomes. Further research is needed to confirm these results. |
doi_str_mv | 10.1007/s00432-020-03167-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2374351708</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2374351708</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-928fd9761e28e84ef7aaef6c35194f4987160bacc14385b9db167ff9e62900a03</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRS0EoqXwAyxQJDZsAmM7jhN2qOIlVWIDa8txxihVHsVOKsrX49ACEgtWtuce35m5hJxSuKQA8soDJJzFwCAGTlMZwx6Z0rFEORf7ZApU0lgwmk7IkfdLCG8h2SGZcEaTRHA-JWqO_fBeNbqI1uj84KMC19pUH8NYqtqowV77XveViUxXdw5Nr-vI6Nagu450KDYr7YK-xgitDXK4teh95Puh3ByTA6trjye7c0Ze7m6f5w_x4un-cX6ziA2Xoo9zltkylylFlmGWoJVao00NFzRPbJJnkqZQaGPCepko8rII-1qbY8pyAA18Ri62vivXvQ3oe9VU3mBd6xa7wSvGZRLMJGQBPf-DLrvBtWG6QGVSCEEFCxTbUsZ13ju0auVCTG6jKKgxfrWNX4X41Vf8apzibGc9FA2WP1--8w4A3wI-SO0rut_e_9h-AvPVkGE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2387555152</pqid></control><display><type>article</type><title>Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Marques, Rui Pedro ; Godinho, Ana Rita ; Heudtlass, Peter ; Pais, Helena Luna ; Quintela, António ; Martins, Ana Paula</creator><creatorcontrib>Marques, Rui Pedro ; Godinho, Ana Rita ; Heudtlass, Peter ; Pais, Helena Luna ; Quintela, António ; Martins, Ana Paula</creatorcontrib><description>Purpose
Uncertainty exists regarding comparative effectiveness of cetuximab versus bevacizumab in metastatic colorectal cancer (mCRC). We conducted a retrospective head-to-head multi-cohort study comparing clinical outcomes from both antibodies
Methods
Cohorts were defined by treatment line and subgroups by (K)RAS status and tumour sidedness. Among other outcomes, we estimated and compared response rates, progression-free (PFS) and overall survival (OS).
Results
Between January 2010 and April 2018, 311 patients were included. Except for (K)RAS mutation status, baseline characteristics were balanced across treatment groups. In the full analysis of first and second-line cohorts, PFS (first-line: HR = 0.85; 95% CI 0.64 to 1.13;
P
= 0.26; second-line: HR = 1.16; 95% CI 0.74 to 1.83;
P
= 0.51) and OS (first-line: HR = 0.83; 95% CI 0.61 to 1.15;
P
= 0.26; second-line: HR = 0.88; 95% CI 0.56 to 1.38;
P
= 0.58) were similar between bevacizumab and cetuximab arms. In subgroup analyses of first-line therapy, we found a survival difference favouring bevacizumab in right-sided tumours (PFS: HR = 0.52; 95% CI 0.29 to 0.93;
P
= 0.025; OS: HR = 0.60; 95% CI 0.32 to 1.12;
P
= 0.11), but not in left-sided (HR = 1.04; 95% CI 0.75 to 1.46;
P
= 0.81; OS: HR = 0.94; 95% CI 0.65 to 1.36;
P
= 0.74), or (K)RAS wild-type tumours (PFS: HR = 0.91; 95% CI 0.60 to 1.40;
P
= 0.67; OS: HR = 0.79; 95% CI 0.50 to 1.25;
P
= 0.31). Response rates were similar across treatment groups, except for the subgroup of patients bearing right-sided primaries, where bevacizumab performed substantially better.
Conclusion
This study provides evidence suggesting bevacizumab and cetuximab lead to similar effectiveness outcomes in mCRC, except for right-sided tumours, where cetuximab seemed to show considerably poorer outcomes. Further research is needed to confirm these results.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-020-03167-0</identifier><identifier>PMID: 32144533</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aged ; Antineoplastic Agents, Immunological - administration & dosage ; Antineoplastic Agents, Immunological - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bevacizumab ; Bevacizumab - administration & dosage ; Bevacizumab - therapeutic use ; Cancer Research ; Cetuximab - administration & dosage ; Cetuximab - therapeutic use ; Cohort Studies ; Colonic Neoplasms - drug therapy ; Colonic Neoplasms - genetics ; Colonic Neoplasms - pathology ; Colorectal cancer ; Colorectal carcinoma ; Female ; Hematology ; Humans ; Immunotherapy ; Internal Medicine ; Male ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Middle Aged ; Monoclonal antibodies ; Mutation ; Neoplasm Staging ; Oncology ; Original Article – Clinical Oncology ; Patients ; Proto-Oncogene Proteins p21(ras) - genetics ; Rectal Neoplasms - drug therapy ; Rectal Neoplasms - genetics ; Rectal Neoplasms - pathology ; Response rates ; Retrospective Studies ; Survival ; Targeted cancer therapy ; Tumors</subject><ispartof>Journal of cancer research and clinical oncology, 2020-05, Vol.146 (5), p.1321-1334</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-928fd9761e28e84ef7aaef6c35194f4987160bacc14385b9db167ff9e62900a03</citedby><cites>FETCH-LOGICAL-c375t-928fd9761e28e84ef7aaef6c35194f4987160bacc14385b9db167ff9e62900a03</cites><orcidid>0000-0002-7880-4506</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00432-020-03167-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00432-020-03167-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32144533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marques, Rui Pedro</creatorcontrib><creatorcontrib>Godinho, Ana Rita</creatorcontrib><creatorcontrib>Heudtlass, Peter</creatorcontrib><creatorcontrib>Pais, Helena Luna</creatorcontrib><creatorcontrib>Quintela, António</creatorcontrib><creatorcontrib>Martins, Ana Paula</creatorcontrib><title>Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Purpose
Uncertainty exists regarding comparative effectiveness of cetuximab versus bevacizumab in metastatic colorectal cancer (mCRC). We conducted a retrospective head-to-head multi-cohort study comparing clinical outcomes from both antibodies
Methods
Cohorts were defined by treatment line and subgroups by (K)RAS status and tumour sidedness. Among other outcomes, we estimated and compared response rates, progression-free (PFS) and overall survival (OS).
Results
Between January 2010 and April 2018, 311 patients were included. Except for (K)RAS mutation status, baseline characteristics were balanced across treatment groups. In the full analysis of first and second-line cohorts, PFS (first-line: HR = 0.85; 95% CI 0.64 to 1.13;
P
= 0.26; second-line: HR = 1.16; 95% CI 0.74 to 1.83;
P
= 0.51) and OS (first-line: HR = 0.83; 95% CI 0.61 to 1.15;
P
= 0.26; second-line: HR = 0.88; 95% CI 0.56 to 1.38;
P
= 0.58) were similar between bevacizumab and cetuximab arms. In subgroup analyses of first-line therapy, we found a survival difference favouring bevacizumab in right-sided tumours (PFS: HR = 0.52; 95% CI 0.29 to 0.93;
P
= 0.025; OS: HR = 0.60; 95% CI 0.32 to 1.12;
P
= 0.11), but not in left-sided (HR = 1.04; 95% CI 0.75 to 1.46;
P
= 0.81; OS: HR = 0.94; 95% CI 0.65 to 1.36;
P
= 0.74), or (K)RAS wild-type tumours (PFS: HR = 0.91; 95% CI 0.60 to 1.40;
P
= 0.67; OS: HR = 0.79; 95% CI 0.50 to 1.25;
P
= 0.31). Response rates were similar across treatment groups, except for the subgroup of patients bearing right-sided primaries, where bevacizumab performed substantially better.
Conclusion
This study provides evidence suggesting bevacizumab and cetuximab lead to similar effectiveness outcomes in mCRC, except for right-sided tumours, where cetuximab seemed to show considerably poorer outcomes. Further research is needed to confirm these results.</description><subject>Aged</subject><subject>Antineoplastic Agents, Immunological - administration & dosage</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bevacizumab</subject><subject>Bevacizumab - administration & dosage</subject><subject>Bevacizumab - therapeutic use</subject><subject>Cancer Research</subject><subject>Cetuximab - administration & dosage</subject><subject>Cetuximab - therapeutic use</subject><subject>Cohort Studies</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>Colonic Neoplasms - genetics</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Female</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Mutation</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Original Article – Clinical Oncology</subject><subject>Patients</subject><subject>Proto-Oncogene Proteins p21(ras) - genetics</subject><subject>Rectal Neoplasms - drug therapy</subject><subject>Rectal Neoplasms - genetics</subject><subject>Rectal Neoplasms - pathology</subject><subject>Response rates</subject><subject>Retrospective Studies</subject><subject>Survival</subject><subject>Targeted cancer therapy</subject><subject>Tumors</subject><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwAyxQJDZsAmM7jhN2qOIlVWIDa8txxihVHsVOKsrX49ACEgtWtuce35m5hJxSuKQA8soDJJzFwCAGTlMZwx6Z0rFEORf7ZApU0lgwmk7IkfdLCG8h2SGZcEaTRHA-JWqO_fBeNbqI1uj84KMC19pUH8NYqtqowV77XveViUxXdw5Nr-vI6Nagu450KDYr7YK-xgitDXK4teh95Puh3ByTA6trjye7c0Ze7m6f5w_x4un-cX6ziA2Xoo9zltkylylFlmGWoJVao00NFzRPbJJnkqZQaGPCepko8rII-1qbY8pyAA18Ri62vivXvQ3oe9VU3mBd6xa7wSvGZRLMJGQBPf-DLrvBtWG6QGVSCEEFCxTbUsZ13ju0auVCTG6jKKgxfrWNX4X41Vf8apzibGc9FA2WP1--8w4A3wI-SO0rut_e_9h-AvPVkGE</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Marques, Rui Pedro</creator><creator>Godinho, Ana Rita</creator><creator>Heudtlass, Peter</creator><creator>Pais, Helena Luna</creator><creator>Quintela, António</creator><creator>Martins, Ana Paula</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7880-4506</orcidid></search><sort><creationdate>20200501</creationdate><title>Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study</title><author>Marques, Rui Pedro ; Godinho, Ana Rita ; Heudtlass, Peter ; Pais, Helena Luna ; Quintela, António ; Martins, Ana Paula</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-928fd9761e28e84ef7aaef6c35194f4987160bacc14385b9db167ff9e62900a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Antineoplastic Agents, Immunological - administration & dosage</topic><topic>Antineoplastic Agents, Immunological - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Bevacizumab</topic><topic>Bevacizumab - administration & dosage</topic><topic>Bevacizumab - therapeutic use</topic><topic>Cancer Research</topic><topic>Cetuximab - administration & dosage</topic><topic>Cetuximab - therapeutic use</topic><topic>Cohort Studies</topic><topic>Colonic Neoplasms - drug therapy</topic><topic>Colonic Neoplasms - genetics</topic><topic>Colonic Neoplasms - pathology</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Female</topic><topic>Hematology</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Monoclonal antibodies</topic><topic>Mutation</topic><topic>Neoplasm Staging</topic><topic>Oncology</topic><topic>Original Article – Clinical Oncology</topic><topic>Patients</topic><topic>Proto-Oncogene Proteins p21(ras) - genetics</topic><topic>Rectal Neoplasms - drug therapy</topic><topic>Rectal Neoplasms - genetics</topic><topic>Rectal Neoplasms - pathology</topic><topic>Response rates</topic><topic>Retrospective Studies</topic><topic>Survival</topic><topic>Targeted cancer therapy</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marques, Rui Pedro</creatorcontrib><creatorcontrib>Godinho, Ana Rita</creatorcontrib><creatorcontrib>Heudtlass, Peter</creatorcontrib><creatorcontrib>Pais, Helena Luna</creatorcontrib><creatorcontrib>Quintela, António</creatorcontrib><creatorcontrib>Martins, Ana Paula</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</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 Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cancer research and clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marques, Rui Pedro</au><au>Godinho, Ana Rita</au><au>Heudtlass, Peter</au><au>Pais, Helena Luna</au><au>Quintela, António</au><au>Martins, Ana Paula</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><stitle>J Cancer Res Clin Oncol</stitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>2020-05-01</date><risdate>2020</risdate><volume>146</volume><issue>5</issue><spage>1321</spage><epage>1334</epage><pages>1321-1334</pages><issn>0171-5216</issn><eissn>1432-1335</eissn><abstract>Purpose
Uncertainty exists regarding comparative effectiveness of cetuximab versus bevacizumab in metastatic colorectal cancer (mCRC). We conducted a retrospective head-to-head multi-cohort study comparing clinical outcomes from both antibodies
Methods
Cohorts were defined by treatment line and subgroups by (K)RAS status and tumour sidedness. Among other outcomes, we estimated and compared response rates, progression-free (PFS) and overall survival (OS).
Results
Between January 2010 and April 2018, 311 patients were included. Except for (K)RAS mutation status, baseline characteristics were balanced across treatment groups. In the full analysis of first and second-line cohorts, PFS (first-line: HR = 0.85; 95% CI 0.64 to 1.13;
P
= 0.26; second-line: HR = 1.16; 95% CI 0.74 to 1.83;
P
= 0.51) and OS (first-line: HR = 0.83; 95% CI 0.61 to 1.15;
P
= 0.26; second-line: HR = 0.88; 95% CI 0.56 to 1.38;
P
= 0.58) were similar between bevacizumab and cetuximab arms. In subgroup analyses of first-line therapy, we found a survival difference favouring bevacizumab in right-sided tumours (PFS: HR = 0.52; 95% CI 0.29 to 0.93;
P
= 0.025; OS: HR = 0.60; 95% CI 0.32 to 1.12;
P
= 0.11), but not in left-sided (HR = 1.04; 95% CI 0.75 to 1.46;
P
= 0.81; OS: HR = 0.94; 95% CI 0.65 to 1.36;
P
= 0.74), or (K)RAS wild-type tumours (PFS: HR = 0.91; 95% CI 0.60 to 1.40;
P
= 0.67; OS: HR = 0.79; 95% CI 0.50 to 1.25;
P
= 0.31). Response rates were similar across treatment groups, except for the subgroup of patients bearing right-sided primaries, where bevacizumab performed substantially better.
Conclusion
This study provides evidence suggesting bevacizumab and cetuximab lead to similar effectiveness outcomes in mCRC, except for right-sided tumours, where cetuximab seemed to show considerably poorer outcomes. Further research is needed to confirm these results.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32144533</pmid><doi>10.1007/s00432-020-03167-0</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-7880-4506</orcidid></addata></record> |
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subjects | Aged Antineoplastic Agents, Immunological - administration & dosage Antineoplastic Agents, Immunological - therapeutic use Antineoplastic Combined Chemotherapy Protocols - therapeutic use Bevacizumab Bevacizumab - administration & dosage Bevacizumab - therapeutic use Cancer Research Cetuximab - administration & dosage Cetuximab - therapeutic use Cohort Studies Colonic Neoplasms - drug therapy Colonic Neoplasms - genetics Colonic Neoplasms - pathology Colorectal cancer Colorectal carcinoma Female Hematology Humans Immunotherapy Internal Medicine Male Medicine Medicine & Public Health Metastases Metastasis Middle Aged Monoclonal antibodies Mutation Neoplasm Staging Oncology Original Article – Clinical Oncology Patients Proto-Oncogene Proteins p21(ras) - genetics Rectal Neoplasms - drug therapy Rectal Neoplasms - genetics Rectal Neoplasms - pathology Response rates Retrospective Studies Survival Targeted cancer therapy Tumors |
title | Cetuximab versus bevacizumab in metastatic colorectal cancer: a comparative effectiveness study |
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