Comparative Effectiveness and Safety of Monoclonal Antibodies (Bevacizumab, Cetuximab, and Panitumumab) in Combination with Chemotherapy for Metastatic Colorectal Cancer: A Systematic Review and Meta-Analysis

Background The last decade has seen the increasing use of biological medicines in combination with chemotherapy containing 5-fluorouracil/oxaliplatin or irinotecan for the treatment of metastatic colorectal cancer (mCRC). These combinations have resulted in increased progression-free survival (PFS)...

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Veröffentlicht in:BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy biopharmaceuticals, and gene therapy, 2018-12, Vol.32 (6), p.585-606
Hauptverfasser: da Silva, Wânia Cristina, de Araujo, Vânia Eloisa, Lima, Ellias Magalhães e Abreu, dos Santos, Jessica Barreto Ribeiro, Silva, Michael Ruberson Ribeiro da, Almeida, Paulo Henrique Ribeiro Fernandes, de Assis Acurcio, Francisco, Godman, Brian, Kurdi, Amanj, Cherchiglia, Mariângela Leal, Andrade, Eli Iola Gurgel
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container_end_page 606
container_issue 6
container_start_page 585
container_title BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy
container_volume 32
creator da Silva, Wânia Cristina
de Araujo, Vânia Eloisa
Lima, Ellias Magalhães e Abreu
dos Santos, Jessica Barreto Ribeiro
Silva, Michael Ruberson Ribeiro da
Almeida, Paulo Henrique Ribeiro Fernandes
de Assis Acurcio, Francisco
Godman, Brian
Kurdi, Amanj
Cherchiglia, Mariângela Leal
Andrade, Eli Iola Gurgel
description Background The last decade has seen the increasing use of biological medicines in combination with chemotherapy containing 5-fluorouracil/oxaliplatin or irinotecan for the treatment of metastatic colorectal cancer (mCRC). These combinations have resulted in increased progression-free survival (PFS) in patients with mCRC; however, there are remaining concerns over the extent of their effect on overall survival (OS). Published studies to date suggest no major differences between the three currently available monoclonal antibodies (MoAbs); however, there are differences in costs. In addition, there is rising litigation in Brazil in order to access these medicines as they are currently not reimbursed. Objective The aim was to investigate the comparative effectiveness and safety of three MoAbs (bevacizumab, cetuximab and panitumumab) associated with fluoropyrimidine-based chemotherapy regimens and compared to fluoropyrimidine-based chemotherapy alone in patients with mCRC, through an updated systematic review and meta-analysis of concurrent or non-concurrent observational cohort studies, to guide authorities and the judiciary. Method A systematic review and meta-analysis was performed based on cohort studies published in databases up to November 2017. Effectiveness measures included OS, PFS, post-progression survival (PPS), Response Evaluation Criteria In Solid Tumors (RECIST), response rate, metastasectomy and safety. The methodological quality of the studies was also evaluated. Results A total of 21 observational cohort studies were included. There were statistically significant and clinically relevant benefits in patients treated with bevacizumab versus no bevacizumab mainly around OS, PFS, PPS and the metastasectomy rate, but not for the disease control rates. However, there was an increase in treatment-related toxicities and concerns with the heterogeneity of the studies. Conclusion The results pointed to an advantage in favor of bevacizumab for OS, PFS, PPS, and metastasectomy. Although this advantage may be considered clinically modest, bevacizumab represents a hope for increased survival and a chance of metastasectomy for patients with mCRC. However, there are serious adverse events associated with its use, especially severe hypertension and gastrointestinal perforation, that need to be considered.
doi_str_mv 10.1007/s40259-018-0322-1
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These combinations have resulted in increased progression-free survival (PFS) in patients with mCRC; however, there are remaining concerns over the extent of their effect on overall survival (OS). Published studies to date suggest no major differences between the three currently available monoclonal antibodies (MoAbs); however, there are differences in costs. In addition, there is rising litigation in Brazil in order to access these medicines as they are currently not reimbursed. Objective The aim was to investigate the comparative effectiveness and safety of three MoAbs (bevacizumab, cetuximab and panitumumab) associated with fluoropyrimidine-based chemotherapy regimens and compared to fluoropyrimidine-based chemotherapy alone in patients with mCRC, through an updated systematic review and meta-analysis of concurrent or non-concurrent observational cohort studies, to guide authorities and the judiciary. Method A systematic review and meta-analysis was performed based on cohort studies published in databases up to November 2017. Effectiveness measures included OS, PFS, post-progression survival (PPS), Response Evaluation Criteria In Solid Tumors (RECIST), response rate, metastasectomy and safety. The methodological quality of the studies was also evaluated. Results A total of 21 observational cohort studies were included. There were statistically significant and clinically relevant benefits in patients treated with bevacizumab versus no bevacizumab mainly around OS, PFS, PPS and the metastasectomy rate, but not for the disease control rates. However, there was an increase in treatment-related toxicities and concerns with the heterogeneity of the studies. Conclusion The results pointed to an advantage in favor of bevacizumab for OS, PFS, PPS, and metastasectomy. Although this advantage may be considered clinically modest, bevacizumab represents a hope for increased survival and a chance of metastasectomy for patients with mCRC. However, there are serious adverse events associated with its use, especially severe hypertension and gastrointestinal perforation, that need to be considered.</description><identifier>ISSN: 1173-8804</identifier><identifier>EISSN: 1179-190X</identifier><identifier>DOI: 10.1007/s40259-018-0322-1</identifier><identifier>PMID: 30499082</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>5-Fluorouracil ; Acids ; Antibodies ; Antineoplastic Combined Chemotherapy Protocols - economics ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bevacizumab ; Bevacizumab - economics ; Bevacizumab - therapeutic use ; Biomedical and Life Sciences ; Biomedicine ; Brazil ; Cancer Research ; Cancer therapies ; Cetuximab - economics ; Cetuximab - therapeutic use ; Chemotherapy ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - mortality ; Cost-Benefit Analysis ; Disease control ; Disease-Free Survival ; Drug resistance ; Fees, Pharmaceutical ; Fluorouracil - economics ; Fluorouracil - therapeutic use ; Growth factors ; Humans ; Hypertension - chemically induced ; Hypertension - epidemiology ; Immunoglobulins ; Immunotherapy ; Incidence ; Internet ; Intestinal Perforation - chemically induced ; Intestinal Perforation - epidemiology ; Irinotecan ; Irinotecan - economics ; Irinotecan - therapeutic use ; Meta-analysis ; Metastases ; Metastasis ; Molecular Medicine ; Monoclonal antibodies ; Oxaliplatin ; Oxaliplatin - economics ; Oxaliplatin - therapeutic use ; Panitumumab - economics ; Panitumumab - therapeutic use ; Patients ; Pharmaceutical industry ; Pharmacotherapy ; Reimbursement Mechanisms - legislation &amp; jurisprudence ; Response Evaluation Criteria in Solid Tumors ; Safety ; Solid tumors ; Statistical analysis ; Studies ; Survival ; Systematic Review ; Targeted cancer therapy</subject><ispartof>BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy, 2018-12, Vol.32 (6), p.585-606</ispartof><rights>The Author(s) 2018</rights><rights>Copyright Springer Nature B.V. 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These combinations have resulted in increased progression-free survival (PFS) in patients with mCRC; however, there are remaining concerns over the extent of their effect on overall survival (OS). Published studies to date suggest no major differences between the three currently available monoclonal antibodies (MoAbs); however, there are differences in costs. In addition, there is rising litigation in Brazil in order to access these medicines as they are currently not reimbursed. Objective The aim was to investigate the comparative effectiveness and safety of three MoAbs (bevacizumab, cetuximab and panitumumab) associated with fluoropyrimidine-based chemotherapy regimens and compared to fluoropyrimidine-based chemotherapy alone in patients with mCRC, through an updated systematic review and meta-analysis of concurrent or non-concurrent observational cohort studies, to guide authorities and the judiciary. Method A systematic review and meta-analysis was performed based on cohort studies published in databases up to November 2017. Effectiveness measures included OS, PFS, post-progression survival (PPS), Response Evaluation Criteria In Solid Tumors (RECIST), response rate, metastasectomy and safety. The methodological quality of the studies was also evaluated. Results A total of 21 observational cohort studies were included. There were statistically significant and clinically relevant benefits in patients treated with bevacizumab versus no bevacizumab mainly around OS, PFS, PPS and the metastasectomy rate, but not for the disease control rates. However, there was an increase in treatment-related toxicities and concerns with the heterogeneity of the studies. Conclusion The results pointed to an advantage in favor of bevacizumab for OS, PFS, PPS, and metastasectomy. Although this advantage may be considered clinically modest, bevacizumab represents a hope for increased survival and a chance of metastasectomy for patients with mCRC. However, there are serious adverse events associated with its use, especially severe hypertension and gastrointestinal perforation, that need to be considered.</description><subject>5-Fluorouracil</subject><subject>Acids</subject><subject>Antibodies</subject><subject>Antineoplastic Combined Chemotherapy Protocols - economics</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bevacizumab</subject><subject>Bevacizumab - economics</subject><subject>Bevacizumab - therapeutic use</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brazil</subject><subject>Cancer Research</subject><subject>Cancer therapies</subject><subject>Cetuximab - economics</subject><subject>Cetuximab - therapeutic use</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - mortality</subject><subject>Cost-Benefit Analysis</subject><subject>Disease control</subject><subject>Disease-Free Survival</subject><subject>Drug resistance</subject><subject>Fees, Pharmaceutical</subject><subject>Fluorouracil - economics</subject><subject>Fluorouracil - therapeutic use</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Hypertension - chemically induced</subject><subject>Hypertension - epidemiology</subject><subject>Immunoglobulins</subject><subject>Immunotherapy</subject><subject>Incidence</subject><subject>Internet</subject><subject>Intestinal Perforation - chemically induced</subject><subject>Intestinal Perforation - epidemiology</subject><subject>Irinotecan</subject><subject>Irinotecan - economics</subject><subject>Irinotecan - therapeutic use</subject><subject>Meta-analysis</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Molecular Medicine</subject><subject>Monoclonal antibodies</subject><subject>Oxaliplatin</subject><subject>Oxaliplatin - economics</subject><subject>Oxaliplatin - therapeutic use</subject><subject>Panitumumab - economics</subject><subject>Panitumumab - therapeutic use</subject><subject>Patients</subject><subject>Pharmaceutical industry</subject><subject>Pharmacotherapy</subject><subject>Reimbursement Mechanisms - legislation &amp; 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de Araujo, Vânia Eloisa ; Lima, Ellias Magalhães e Abreu ; dos Santos, Jessica Barreto Ribeiro ; Silva, Michael Ruberson Ribeiro da ; Almeida, Paulo Henrique Ribeiro Fernandes ; de Assis Acurcio, Francisco ; Godman, Brian ; Kurdi, Amanj ; Cherchiglia, Mariângela Leal ; Andrade, Eli Iola Gurgel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-9e84914dd707dfdd6591a716db0435d9f7514a698ab80f2169290320eee5af063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>5-Fluorouracil</topic><topic>Acids</topic><topic>Antibodies</topic><topic>Antineoplastic Combined Chemotherapy Protocols - economics</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Bevacizumab</topic><topic>Bevacizumab - economics</topic><topic>Bevacizumab - therapeutic use</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brazil</topic><topic>Cancer Research</topic><topic>Cancer therapies</topic><topic>Cetuximab - economics</topic><topic>Cetuximab - therapeutic use</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - mortality</topic><topic>Cost-Benefit Analysis</topic><topic>Disease control</topic><topic>Disease-Free Survival</topic><topic>Drug resistance</topic><topic>Fees, Pharmaceutical</topic><topic>Fluorouracil - economics</topic><topic>Fluorouracil - therapeutic use</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Hypertension - chemically induced</topic><topic>Hypertension - epidemiology</topic><topic>Immunoglobulins</topic><topic>Immunotherapy</topic><topic>Incidence</topic><topic>Internet</topic><topic>Intestinal Perforation - chemically induced</topic><topic>Intestinal Perforation - epidemiology</topic><topic>Irinotecan</topic><topic>Irinotecan - economics</topic><topic>Irinotecan - therapeutic use</topic><topic>Meta-analysis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Molecular Medicine</topic><topic>Monoclonal antibodies</topic><topic>Oxaliplatin</topic><topic>Oxaliplatin - economics</topic><topic>Oxaliplatin - therapeutic use</topic><topic>Panitumumab - economics</topic><topic>Panitumumab - therapeutic use</topic><topic>Patients</topic><topic>Pharmaceutical industry</topic><topic>Pharmacotherapy</topic><topic>Reimbursement Mechanisms - legislation &amp; jurisprudence</topic><topic>Response Evaluation Criteria in Solid Tumors</topic><topic>Safety</topic><topic>Solid tumors</topic><topic>Statistical analysis</topic><topic>Studies</topic><topic>Survival</topic><topic>Systematic Review</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>da Silva, Wânia Cristina</creatorcontrib><creatorcontrib>de Araujo, Vânia Eloisa</creatorcontrib><creatorcontrib>Lima, Ellias Magalhães e Abreu</creatorcontrib><creatorcontrib>dos Santos, Jessica Barreto Ribeiro</creatorcontrib><creatorcontrib>Silva, Michael Ruberson Ribeiro da</creatorcontrib><creatorcontrib>Almeida, Paulo Henrique Ribeiro Fernandes</creatorcontrib><creatorcontrib>de Assis Acurcio, Francisco</creatorcontrib><creatorcontrib>Godman, Brian</creatorcontrib><creatorcontrib>Kurdi, Amanj</creatorcontrib><creatorcontrib>Cherchiglia, Mariângela Leal</creatorcontrib><creatorcontrib>Andrade, Eli Iola Gurgel</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Docstoc</collection><collection>Immunology Abstracts</collection><collection>Health &amp; 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Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>da Silva, Wânia Cristina</au><au>de Araujo, Vânia Eloisa</au><au>Lima, Ellias Magalhães e Abreu</au><au>dos Santos, Jessica Barreto Ribeiro</au><au>Silva, Michael Ruberson Ribeiro da</au><au>Almeida, Paulo Henrique Ribeiro Fernandes</au><au>de Assis Acurcio, Francisco</au><au>Godman, Brian</au><au>Kurdi, Amanj</au><au>Cherchiglia, Mariângela Leal</au><au>Andrade, Eli Iola Gurgel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Effectiveness and Safety of Monoclonal Antibodies (Bevacizumab, Cetuximab, and Panitumumab) in Combination with Chemotherapy for Metastatic Colorectal Cancer: A Systematic Review and Meta-Analysis</atitle><jtitle>BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy</jtitle><stitle>BioDrugs</stitle><addtitle>BioDrugs</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>32</volume><issue>6</issue><spage>585</spage><epage>606</epage><pages>585-606</pages><issn>1173-8804</issn><eissn>1179-190X</eissn><abstract>Background The last decade has seen the increasing use of biological medicines in combination with chemotherapy containing 5-fluorouracil/oxaliplatin or irinotecan for the treatment of metastatic colorectal cancer (mCRC). These combinations have resulted in increased progression-free survival (PFS) in patients with mCRC; however, there are remaining concerns over the extent of their effect on overall survival (OS). Published studies to date suggest no major differences between the three currently available monoclonal antibodies (MoAbs); however, there are differences in costs. In addition, there is rising litigation in Brazil in order to access these medicines as they are currently not reimbursed. Objective The aim was to investigate the comparative effectiveness and safety of three MoAbs (bevacizumab, cetuximab and panitumumab) associated with fluoropyrimidine-based chemotherapy regimens and compared to fluoropyrimidine-based chemotherapy alone in patients with mCRC, through an updated systematic review and meta-analysis of concurrent or non-concurrent observational cohort studies, to guide authorities and the judiciary. Method A systematic review and meta-analysis was performed based on cohort studies published in databases up to November 2017. Effectiveness measures included OS, PFS, post-progression survival (PPS), Response Evaluation Criteria In Solid Tumors (RECIST), response rate, metastasectomy and safety. The methodological quality of the studies was also evaluated. Results A total of 21 observational cohort studies were included. There were statistically significant and clinically relevant benefits in patients treated with bevacizumab versus no bevacizumab mainly around OS, PFS, PPS and the metastasectomy rate, but not for the disease control rates. However, there was an increase in treatment-related toxicities and concerns with the heterogeneity of the studies. Conclusion The results pointed to an advantage in favor of bevacizumab for OS, PFS, PPS, and metastasectomy. Although this advantage may be considered clinically modest, bevacizumab represents a hope for increased survival and a chance of metastasectomy for patients with mCRC. However, there are serious adverse events associated with its use, especially severe hypertension and gastrointestinal perforation, that need to be considered.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>30499082</pmid><doi>10.1007/s40259-018-0322-1</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0001-6539-6972</orcidid><orcidid>https://orcid.org/0000-0002-5108-5724</orcidid><orcidid>https://orcid.org/0000-0002-0345-8522</orcidid><orcidid>https://orcid.org/0000-0002-5880-5261</orcidid><orcidid>https://orcid.org/0000-0002-0206-2462</orcidid><orcidid>https://orcid.org/0000-0002-9369-0690</orcidid><orcidid>https://orcid.org/0000-0001-5036-1988</orcidid><orcidid>https://orcid.org/0000-0001-5622-567X</orcidid><orcidid>https://orcid.org/0000-0002-5528-0658</orcidid><orcidid>https://orcid.org/0000-0003-2550-7249</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1173-8804
ispartof BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy, 2018-12, Vol.32 (6), p.585-606
issn 1173-8804
1179-190X
language eng
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source MEDLINE; SWEPUB Freely available online; SpringerLink Journals - AutoHoldings
subjects 5-Fluorouracil
Acids
Antibodies
Antineoplastic Combined Chemotherapy Protocols - economics
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Bevacizumab
Bevacizumab - economics
Bevacizumab - therapeutic use
Biomedical and Life Sciences
Biomedicine
Brazil
Cancer Research
Cancer therapies
Cetuximab - economics
Cetuximab - therapeutic use
Chemotherapy
Colorectal cancer
Colorectal carcinoma
Colorectal Neoplasms - drug therapy
Colorectal Neoplasms - mortality
Cost-Benefit Analysis
Disease control
Disease-Free Survival
Drug resistance
Fees, Pharmaceutical
Fluorouracil - economics
Fluorouracil - therapeutic use
Growth factors
Humans
Hypertension - chemically induced
Hypertension - epidemiology
Immunoglobulins
Immunotherapy
Incidence
Internet
Intestinal Perforation - chemically induced
Intestinal Perforation - epidemiology
Irinotecan
Irinotecan - economics
Irinotecan - therapeutic use
Meta-analysis
Metastases
Metastasis
Molecular Medicine
Monoclonal antibodies
Oxaliplatin
Oxaliplatin - economics
Oxaliplatin - therapeutic use
Panitumumab - economics
Panitumumab - therapeutic use
Patients
Pharmaceutical industry
Pharmacotherapy
Reimbursement Mechanisms - legislation & jurisprudence
Response Evaluation Criteria in Solid Tumors
Safety
Solid tumors
Statistical analysis
Studies
Survival
Systematic Review
Targeted cancer therapy
title Comparative Effectiveness and Safety of Monoclonal Antibodies (Bevacizumab, Cetuximab, and Panitumumab) in Combination with Chemotherapy for Metastatic Colorectal Cancer: A Systematic Review and Meta-Analysis
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