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 |
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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 |
format | Article |
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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.</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 & 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. Dec 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-9e84914dd707dfdd6591a716db0435d9f7514a698ab80f2169290320eee5af063</citedby><cites>FETCH-LOGICAL-c508t-9e84914dd707dfdd6591a716db0435d9f7514a698ab80f2169290320eee5af063</cites><orcidid>0000-0001-6539-6972 ; 0000-0002-5108-5724 ; 0000-0002-0345-8522 ; 0000-0002-5880-5261 ; 0000-0002-0206-2462 ; 0000-0002-9369-0690 ; 0000-0001-5036-1988 ; 0000-0001-5622-567X ; 0000-0002-5528-0658 ; 0000-0003-2550-7249</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/s40259-018-0322-1$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40259-018-0322-1$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30499082$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:139759353$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><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><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</title><title>BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy</title><addtitle>BioDrugs</addtitle><addtitle>BioDrugs</addtitle><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.</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 & jurisprudence</subject><subject>Response Evaluation Criteria in Solid Tumors</subject><subject>Safety</subject><subject>Solid tumors</subject><subject>Statistical analysis</subject><subject>Studies</subject><subject>Survival</subject><subject>Systematic Review</subject><subject>Targeted cancer therapy</subject><issn>1173-8804</issn><issn>1179-190X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>D8T</sourceid><recordid>eNp1Uk1v1DAQjRCIlsIP4IIscQGJgO18mgPSEpUPqRWIgsTNcpJx12VjL7azS_iV_CQmu0uhB04e-b03b8Z-SfKQ0eeM0upFyCkvREpZndKM85TdSo4Zq0TKBP16e1dnaV3T_Ci5F8IVpbTMRHU3OcpoLgSt-XHyq3HDWnkVzQbIqdbQzZWFEIiyPblQGuJEnCbnzrpu5axakYWNpnW9gUCevIaN6szPcVDtM9JAHH-YXTmLPypr4jjM2FNiLEGr1li0cpZsTVySZgmDi0vwaj0R7Tw5h6hCREaH5JXzOA36Ncp24F-SBbmYQoRhh3-CjYHtzmdWpQucbAom3E_uaLUK8OBwniRf3px-bt6lZx_evm8WZ2lX0DqmAupcsLzvK1r1uu_LQjBVsbJvaZ4VvdBVwXJVilq1NdWclYILfGMKAIXS-I4nSbrvG7awHlu59ri4n6RTRh6uvmEFMq-zigvkv9rzERmg78BGr1Y3ZDcRa5by0m1kicYV59jg8aGBd99HCFFeudHj1kFyJvBf8zxjyGJ7VuddCB70tQOjcg6N3IdGYmjkHBo5ax79O9q14k9KkMAPuyJkL8H_tf5_199bkNJF</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>da Silva, Wânia Cristina</creator><creator>de Araujo, Vânia Eloisa</creator><creator>Lima, Ellias Magalhães e Abreu</creator><creator>dos Santos, Jessica Barreto Ribeiro</creator><creator>Silva, Michael Ruberson Ribeiro da</creator><creator>Almeida, Paulo Henrique Ribeiro Fernandes</creator><creator>de Assis Acurcio, Francisco</creator><creator>Godman, Brian</creator><creator>Kurdi, Amanj</creator><creator>Cherchiglia, Mariângela Leal</creator><creator>Andrade, Eli Iola Gurgel</creator><general>Springer International Publishing</general><general>Springer Nature 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Effectiveness and Safety of Monoclonal Antibodies (Bevacizumab, Cetuximab, and Panitumumab) in Combination with Chemotherapy for Metastatic Colorectal Cancer: A Systematic Review and Meta-Analysis</title><author>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</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 & jurisprudence</topic><topic>Response Evaluation Criteria in Solid Tumors</topic><topic>Safety</topic><topic>Solid tumors</topic><topic>Statistical 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Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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> |
fulltext | fulltext |
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 |
recordid | cdi_swepub_primary_oai_swepub_ki_se_483729 |
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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