Bevacizumab (Avastin®) in cancer treatment: A review of 15 years of clinical experience and future outlook
•Bevacizumab (Avastin®), a VEGF-A targeting monoclonal antibody, was the first approved angiogenesis inhibitor.•Approved in a range of solid tumor indications, bevacizumab is an important part of the standard of care in oncology.•The recently identified immune modulatory roles of VEGF provide a powe...
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Veröffentlicht in: | Cancer treatment reviews 2020-06, Vol.86, p.102017-102017, Article 102017 |
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creator | Garcia, Josep Hurwitz, Herbert I. Sandler, Alan B. Miles, David Coleman, Robert L Deurloo, Regula Chinot, Olivier L |
description | •Bevacizumab (Avastin®), a VEGF-A targeting monoclonal antibody, was the first approved angiogenesis inhibitor.•Approved in a range of solid tumor indications, bevacizumab is an important part of the standard of care in oncology.•The recently identified immune modulatory roles of VEGF provide a powerful rationale for combination therapies.•First clinical studies of the combination of bevacizumab with immune checkpoint inhibitors have shown efficacy.
When the VEGF-A-targeting monoclonal antibody bevacizumab (Avastin®) entered clinical practice more than 15 years ago, it was one of the first targeted therapies and the first approved angiogenesis inhibitor. Marking the beginning for a new line of anti-cancer treatments, bevacizumab remains the most extensively characterized anti-angiogenetic treatment. Initially approved for treatment of metastatic colorectal cancer in combination with chemotherapy, its indications now include metastatic breast cancer, non-small-cell lung cancer, glioblastoma, renal cell carcinoma, ovarian cancer and cervical cancer. This review provides an overview of the clinical experience and lessons learned since bevacizumab’s initial approval, and highlights how this knowledge has led to the investigation of novel combination therapies.
In the past 15 years, our understanding of VEGF’s role in the tumor microenvironment has evolved. We now know that VEGF not only plays a major role in controlling blood vessel formation, but also modulates tumor-induced immunosuppression. These immunomodulatory properties of bevacizumab have opened up new perspectives for combination therapy approaches, which are being investigated in clinical trials. Specifically, the combination of bevacizumab with cancer immunotherapy has recently been approved in non-small-cell lung cancer and clinical benefit was also demonstrated for treatment of hepatocellular carcinoma. However, despite intense investigation, reliable and validated biomarkers that would enable a more personalized use of bevacizumab remain elusive.
Overall, bevacizumab is expected to remain a key agent in cancer therapy, both due to its established efficacy in approved indications and its promise as a partner in novel targeted combination treatments. |
doi_str_mv | 10.1016/j.ctrv.2020.102017 |
format | Article |
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When the VEGF-A-targeting monoclonal antibody bevacizumab (Avastin®) entered clinical practice more than 15 years ago, it was one of the first targeted therapies and the first approved angiogenesis inhibitor. Marking the beginning for a new line of anti-cancer treatments, bevacizumab remains the most extensively characterized anti-angiogenetic treatment. Initially approved for treatment of metastatic colorectal cancer in combination with chemotherapy, its indications now include metastatic breast cancer, non-small-cell lung cancer, glioblastoma, renal cell carcinoma, ovarian cancer and cervical cancer. This review provides an overview of the clinical experience and lessons learned since bevacizumab’s initial approval, and highlights how this knowledge has led to the investigation of novel combination therapies.
In the past 15 years, our understanding of VEGF’s role in the tumor microenvironment has evolved. We now know that VEGF not only plays a major role in controlling blood vessel formation, but also modulates tumor-induced immunosuppression. These immunomodulatory properties of bevacizumab have opened up new perspectives for combination therapy approaches, which are being investigated in clinical trials. Specifically, the combination of bevacizumab with cancer immunotherapy has recently been approved in non-small-cell lung cancer and clinical benefit was also demonstrated for treatment of hepatocellular carcinoma. However, despite intense investigation, reliable and validated biomarkers that would enable a more personalized use of bevacizumab remain elusive.
Overall, bevacizumab is expected to remain a key agent in cancer therapy, both due to its established efficacy in approved indications and its promise as a partner in novel targeted combination treatments.</description><identifier>ISSN: 0305-7372</identifier><identifier>EISSN: 1532-1967</identifier><identifier>DOI: 10.1016/j.ctrv.2020.102017</identifier><identifier>PMID: 32335505</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Angiogenesis Inhibitors ; Antineoplastic Agents, Immunological ; Avastin ; Bevacizumab ; Clinical Trials, Phase II as Topic ; Clinical Trials, Phase III as Topic ; Humans ; Life Sciences ; Molecular Targeted Therapy ; Neoplasms ; Neovascularization, Pathologic ; Randomized Controlled Trials as Topic ; Solid tumors ; VEGF</subject><ispartof>Cancer treatment reviews, 2020-06, Vol.86, p.102017-102017, Article 102017</ispartof><rights>2020 The Authors</rights><rights>Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-f8d7cd521dfd9606d31dbd5149cb23fa0167195bf019254932de4b1239e574603</citedby><cites>FETCH-LOGICAL-c500t-f8d7cd521dfd9606d31dbd5149cb23fa0167195bf019254932de4b1239e574603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0305737220300554$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32335505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03009898$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Garcia, Josep</creatorcontrib><creatorcontrib>Hurwitz, Herbert I.</creatorcontrib><creatorcontrib>Sandler, Alan B.</creatorcontrib><creatorcontrib>Miles, David</creatorcontrib><creatorcontrib>Coleman, Robert L</creatorcontrib><creatorcontrib>Deurloo, Regula</creatorcontrib><creatorcontrib>Chinot, Olivier L</creatorcontrib><title>Bevacizumab (Avastin®) in cancer treatment: A review of 15 years of clinical experience and future outlook</title><title>Cancer treatment reviews</title><addtitle>Cancer Treat Rev</addtitle><description>•Bevacizumab (Avastin®), a VEGF-A targeting monoclonal antibody, was the first approved angiogenesis inhibitor.•Approved in a range of solid tumor indications, bevacizumab is an important part of the standard of care in oncology.•The recently identified immune modulatory roles of VEGF provide a powerful rationale for combination therapies.•First clinical studies of the combination of bevacizumab with immune checkpoint inhibitors have shown efficacy.
When the VEGF-A-targeting monoclonal antibody bevacizumab (Avastin®) entered clinical practice more than 15 years ago, it was one of the first targeted therapies and the first approved angiogenesis inhibitor. Marking the beginning for a new line of anti-cancer treatments, bevacizumab remains the most extensively characterized anti-angiogenetic treatment. Initially approved for treatment of metastatic colorectal cancer in combination with chemotherapy, its indications now include metastatic breast cancer, non-small-cell lung cancer, glioblastoma, renal cell carcinoma, ovarian cancer and cervical cancer. This review provides an overview of the clinical experience and lessons learned since bevacizumab’s initial approval, and highlights how this knowledge has led to the investigation of novel combination therapies.
In the past 15 years, our understanding of VEGF’s role in the tumor microenvironment has evolved. We now know that VEGF not only plays a major role in controlling blood vessel formation, but also modulates tumor-induced immunosuppression. These immunomodulatory properties of bevacizumab have opened up new perspectives for combination therapy approaches, which are being investigated in clinical trials. Specifically, the combination of bevacizumab with cancer immunotherapy has recently been approved in non-small-cell lung cancer and clinical benefit was also demonstrated for treatment of hepatocellular carcinoma. However, despite intense investigation, reliable and validated biomarkers that would enable a more personalized use of bevacizumab remain elusive.
Overall, bevacizumab is expected to remain a key agent in cancer therapy, both due to its established efficacy in approved indications and its promise as a partner in novel targeted combination treatments.</description><subject>Angiogenesis Inhibitors</subject><subject>Antineoplastic Agents, Immunological</subject><subject>Avastin</subject><subject>Bevacizumab</subject><subject>Clinical Trials, Phase II as Topic</subject><subject>Clinical Trials, Phase III as Topic</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Molecular Targeted Therapy</subject><subject>Neoplasms</subject><subject>Neovascularization, Pathologic</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Solid tumors</subject><subject>VEGF</subject><issn>0305-7372</issn><issn>1532-1967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kc1O3DAUha2qqExpX6AL5CUsMvhnnIxRN1PUFqSR2LRry7FvVA9JPNhOWvo0fYI-BE-GQ4Alq6t79Z0j3XMQ-kTJkhJanu2WJoVxyQibDozQ6g1aUMFZQWVZvUULwokoKl6xQ_Q-xh0hRPJSvkOHnHEuBBEL1H6BURv3d-h0jU82o47J9ff_T7HrsdG9gYBTAJ066NM53uAAo4Pf2DeYivt_d6BDnBbTut4Z3WL4s4fgIAux7i1uhjQEwH5Irfc3H9BBo9sIH5_mEfr57euPi8tie_396mKzLYwgJBXN2lbGCkZtY2VJSsupra2gK2lqxhudf6-oFHVDqGRiJTmzsKop4xJEtSoJP0Kns-8v3ap9cJ0Od8prpy43WzXdcjBEruV6pJk9mdl98LcDxKQ6Fw20re7BD1FlV8HEWtAyo2xGTfAxBmhevClRUyNqp6ZG1NSImhvJouMn_6HuwL5InivIwOcZgJxIDjeoaB4DtC6AScp695r_A-sSnGI</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Garcia, Josep</creator><creator>Hurwitz, Herbert I.</creator><creator>Sandler, Alan B.</creator><creator>Miles, David</creator><creator>Coleman, Robert L</creator><creator>Deurloo, Regula</creator><creator>Chinot, Olivier L</creator><general>Elsevier Ltd</general><general>WB Saunders</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>20200601</creationdate><title>Bevacizumab (Avastin®) in cancer treatment: A review of 15 years of clinical experience and future outlook</title><author>Garcia, Josep ; Hurwitz, Herbert I. ; Sandler, Alan B. ; Miles, David ; Coleman, Robert L ; Deurloo, Regula ; Chinot, Olivier L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-f8d7cd521dfd9606d31dbd5149cb23fa0167195bf019254932de4b1239e574603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Angiogenesis Inhibitors</topic><topic>Antineoplastic Agents, Immunological</topic><topic>Avastin</topic><topic>Bevacizumab</topic><topic>Clinical Trials, Phase II as Topic</topic><topic>Clinical Trials, Phase III as Topic</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Molecular Targeted Therapy</topic><topic>Neoplasms</topic><topic>Neovascularization, Pathologic</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Solid tumors</topic><topic>VEGF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garcia, Josep</creatorcontrib><creatorcontrib>Hurwitz, Herbert I.</creatorcontrib><creatorcontrib>Sandler, Alan B.</creatorcontrib><creatorcontrib>Miles, David</creatorcontrib><creatorcontrib>Coleman, Robert L</creatorcontrib><creatorcontrib>Deurloo, Regula</creatorcontrib><creatorcontrib>Chinot, Olivier L</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Cancer treatment reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garcia, Josep</au><au>Hurwitz, Herbert I.</au><au>Sandler, Alan B.</au><au>Miles, David</au><au>Coleman, Robert L</au><au>Deurloo, Regula</au><au>Chinot, Olivier L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bevacizumab (Avastin®) in cancer treatment: A review of 15 years of clinical experience and future outlook</atitle><jtitle>Cancer treatment reviews</jtitle><addtitle>Cancer Treat Rev</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>86</volume><spage>102017</spage><epage>102017</epage><pages>102017-102017</pages><artnum>102017</artnum><issn>0305-7372</issn><eissn>1532-1967</eissn><abstract>•Bevacizumab (Avastin®), a VEGF-A targeting monoclonal antibody, was the first approved angiogenesis inhibitor.•Approved in a range of solid tumor indications, bevacizumab is an important part of the standard of care in oncology.•The recently identified immune modulatory roles of VEGF provide a powerful rationale for combination therapies.•First clinical studies of the combination of bevacizumab with immune checkpoint inhibitors have shown efficacy.
When the VEGF-A-targeting monoclonal antibody bevacizumab (Avastin®) entered clinical practice more than 15 years ago, it was one of the first targeted therapies and the first approved angiogenesis inhibitor. Marking the beginning for a new line of anti-cancer treatments, bevacizumab remains the most extensively characterized anti-angiogenetic treatment. Initially approved for treatment of metastatic colorectal cancer in combination with chemotherapy, its indications now include metastatic breast cancer, non-small-cell lung cancer, glioblastoma, renal cell carcinoma, ovarian cancer and cervical cancer. This review provides an overview of the clinical experience and lessons learned since bevacizumab’s initial approval, and highlights how this knowledge has led to the investigation of novel combination therapies.
In the past 15 years, our understanding of VEGF’s role in the tumor microenvironment has evolved. We now know that VEGF not only plays a major role in controlling blood vessel formation, but also modulates tumor-induced immunosuppression. These immunomodulatory properties of bevacizumab have opened up new perspectives for combination therapy approaches, which are being investigated in clinical trials. Specifically, the combination of bevacizumab with cancer immunotherapy has recently been approved in non-small-cell lung cancer and clinical benefit was also demonstrated for treatment of hepatocellular carcinoma. However, despite intense investigation, reliable and validated biomarkers that would enable a more personalized use of bevacizumab remain elusive.
Overall, bevacizumab is expected to remain a key agent in cancer therapy, both due to its established efficacy in approved indications and its promise as a partner in novel targeted combination treatments.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>32335505</pmid><doi>10.1016/j.ctrv.2020.102017</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Inhibitors Antineoplastic Agents, Immunological Avastin Bevacizumab Clinical Trials, Phase II as Topic Clinical Trials, Phase III as Topic Humans Life Sciences Molecular Targeted Therapy Neoplasms Neovascularization, Pathologic Randomized Controlled Trials as Topic Solid tumors VEGF |
title | Bevacizumab (Avastin®) in cancer treatment: A review of 15 years of clinical experience and future outlook |
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