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
Hauptverfasser: Marques, Rui Pedro, Godinho, Ana Rita, Heudtlass, Peter, Pais, Helena Luna, Quintela, António, Martins, Ana Paula
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container_end_page 1334
container_issue 5
container_start_page 1321
container_title Journal of cancer research and clinical oncology
container_volume 146
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
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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 &amp; dosage ; Antineoplastic Agents, Immunological - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bevacizumab ; Bevacizumab - administration &amp; dosage ; Bevacizumab - therapeutic use ; Cancer Research ; Cetuximab - administration &amp; 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 &amp; 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 &amp; dosage</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bevacizumab</subject><subject>Bevacizumab - administration &amp; dosage</subject><subject>Bevacizumab - therapeutic use</subject><subject>Cancer Research</subject><subject>Cetuximab - administration &amp; 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 &amp; 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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 &amp; 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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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