Advanced Squamous Cell Carcinoma of the Lung: Current Treatment Approaches and the Role of Afatinib

Options for the treatment of squamous cell lung carcinoma expanded in recent years with the introduction of the immune checkpoint inhibitors into routine clinical practice in both the first- and second-line settings but are still limited. As a result, pembrolizumab, given either alone or in combinat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:OncoTargets and therapy 2020-01, Vol.13, p.9305-9321
Hauptverfasser: Santos, Edgardo S, Hart, Lowell
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 9321
container_issue
container_start_page 9305
container_title OncoTargets and therapy
container_volume 13
creator Santos, Edgardo S
Hart, Lowell
description Options for the treatment of squamous cell lung carcinoma expanded in recent years with the introduction of the immune checkpoint inhibitors into routine clinical practice in both the first- and second-line settings but are still limited. As a result, pembrolizumab, given either alone or in combination with platinum-based chemotherapy, is now a standard first-line treatment for squamous cell lung cancer. However, few options exist once patients have progressed on immune checkpoint inhibitors and chemotherapy. In this setting, the irreversible ErbB family blocker, afatinib, has a potential role as second or subsequent therapy for some patients. The Phase III LUX-Lung 8 study demonstrated that afatinib significantly prolonged progression-free and overall survival compared with erlotinib in patients with squamous cell lung carcinoma. Notably, retrospective, ad-hoc biomarker analyses of a subset of patients from LUX-Lung 8 suggested that patients with ErbB family mutations derived particular benefit from afatinib, especially those with ErbB2 (HER2) mutations. Afatinib has a manageable and predictable safety profile, and adverse events can be managed with the use of a tolerability-guided dose modification protocol. Until more data are available, afatinib could be considered as a potential second-line treatment option for patients who have progressed on combined pembrolizumab and platinum-based chemotherapy and are ineligible for more established second-line options, or as a third-line option in patients who have received first-line immunotherapy, and second-line chemotherapy or chemotherapy and antiangiogenesis therapy. However, further data are required to support the use of afatinib following immunotherapy. Given that treatment options are limited in both of these settings, investigating an agent with an entirely new mechanism of action is warranted. If available, molecular analysis to identify ErbB family mutations or the use of proteomic profiling could help to further isolate patients who are likely to derive the most benefit from afatinib.
doi_str_mv 10.2147/OTT.S250446
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7519820</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2451552792</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-4a4069d33d253dfe4d956905a2434be6b35f3fbaac41b81d996df34ccc5aff3e3</originalsourceid><addsrcrecordid>eNpdkVtLJDEQhYO4qOv65B8I-CLIuLlPxwdhaNwLDAjr-Byqc3FaupMx6R7w32-PDrLuUxXUV4eqcxA6p-SaUTH_fr9aXT8wSYRQB-iE0nk1U5qTw3_6Y_S1lGdClKqYOELHnBNFBdUnyC7cFqL1Dj-8jNCnseDadx2uIds2ph5wCnhYe7wc49MNrsecfRzwKnsY-l232GxyArv2BUN0b-if1Pnd2iLA0Ma2-Ya-BOiKP9vXU_T4425V_5ot73_-rhfLmeWVGmYCBFHace6Y5C544bRUmkhggovGq4bLwEMDYAVtKuq0Vi5wYa2VEAL3_BTdvutuxqb3zk7nZejMJrc95FeToDWfJ7Fdm6e0NXNJdcXIJHC5F8jpZfRlMH1b7GQHRD85Y5iQtBKSUzqhF_-hz2nMcXrvjZKSzTWbqKt3yuZUSvbh4xhKzC48M4Vn9uHxv5Tai8I</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2451552792</pqid></control><display><type>article</type><title>Advanced Squamous Cell Carcinoma of the Lung: Current Treatment Approaches and the Role of Afatinib</title><source>Taylor &amp; Francis Open Access</source><source>DOVE Medical Press Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Santos, Edgardo S ; Hart, Lowell</creator><creatorcontrib>Santos, Edgardo S ; Hart, Lowell</creatorcontrib><description>Options for the treatment of squamous cell lung carcinoma expanded in recent years with the introduction of the immune checkpoint inhibitors into routine clinical practice in both the first- and second-line settings but are still limited. As a result, pembrolizumab, given either alone or in combination with platinum-based chemotherapy, is now a standard first-line treatment for squamous cell lung cancer. However, few options exist once patients have progressed on immune checkpoint inhibitors and chemotherapy. In this setting, the irreversible ErbB family blocker, afatinib, has a potential role as second or subsequent therapy for some patients. The Phase III LUX-Lung 8 study demonstrated that afatinib significantly prolonged progression-free and overall survival compared with erlotinib in patients with squamous cell lung carcinoma. Notably, retrospective, ad-hoc biomarker analyses of a subset of patients from LUX-Lung 8 suggested that patients with ErbB family mutations derived particular benefit from afatinib, especially those with ErbB2 (HER2) mutations. Afatinib has a manageable and predictable safety profile, and adverse events can be managed with the use of a tolerability-guided dose modification protocol. Until more data are available, afatinib could be considered as a potential second-line treatment option for patients who have progressed on combined pembrolizumab and platinum-based chemotherapy and are ineligible for more established second-line options, or as a third-line option in patients who have received first-line immunotherapy, and second-line chemotherapy or chemotherapy and antiangiogenesis therapy. However, further data are required to support the use of afatinib following immunotherapy. Given that treatment options are limited in both of these settings, investigating an agent with an entirely new mechanism of action is warranted. If available, molecular analysis to identify ErbB family mutations or the use of proteomic profiling could help to further isolate patients who are likely to derive the most benefit from afatinib.</description><identifier>ISSN: 1178-6930</identifier><identifier>EISSN: 1178-6930</identifier><identifier>DOI: 10.2147/OTT.S250446</identifier><identifier>PMID: 33061419</identifier><language>eng</language><publisher>Macclesfield: Taylor &amp; Francis Ltd</publisher><subject>Biomarkers ; Cancer therapies ; Chemotherapy ; Epidermal growth factor ; ErbB protein ; ErbB-2 protein ; Genes ; Immune checkpoint inhibitors ; Immunotherapy ; Lung cancer ; Lung carcinoma ; Metastasis ; Monoclonal antibodies ; Mutation ; Patients ; Pembrolizumab ; Platinum ; Review ; Squamous cell carcinoma ; Targeted cancer therapy</subject><ispartof>OncoTargets and therapy, 2020-01, Vol.13, p.9305-9321</ispartof><rights>2020. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Santos and Hart. 2020 Santos and Hart.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-4a4069d33d253dfe4d956905a2434be6b35f3fbaac41b81d996df34ccc5aff3e3</citedby><cites>FETCH-LOGICAL-c386t-4a4069d33d253dfe4d956905a2434be6b35f3fbaac41b81d996df34ccc5aff3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519820/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519820/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3849,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Santos, Edgardo S</creatorcontrib><creatorcontrib>Hart, Lowell</creatorcontrib><title>Advanced Squamous Cell Carcinoma of the Lung: Current Treatment Approaches and the Role of Afatinib</title><title>OncoTargets and therapy</title><description>Options for the treatment of squamous cell lung carcinoma expanded in recent years with the introduction of the immune checkpoint inhibitors into routine clinical practice in both the first- and second-line settings but are still limited. As a result, pembrolizumab, given either alone or in combination with platinum-based chemotherapy, is now a standard first-line treatment for squamous cell lung cancer. However, few options exist once patients have progressed on immune checkpoint inhibitors and chemotherapy. In this setting, the irreversible ErbB family blocker, afatinib, has a potential role as second or subsequent therapy for some patients. The Phase III LUX-Lung 8 study demonstrated that afatinib significantly prolonged progression-free and overall survival compared with erlotinib in patients with squamous cell lung carcinoma. Notably, retrospective, ad-hoc biomarker analyses of a subset of patients from LUX-Lung 8 suggested that patients with ErbB family mutations derived particular benefit from afatinib, especially those with ErbB2 (HER2) mutations. Afatinib has a manageable and predictable safety profile, and adverse events can be managed with the use of a tolerability-guided dose modification protocol. Until more data are available, afatinib could be considered as a potential second-line treatment option for patients who have progressed on combined pembrolizumab and platinum-based chemotherapy and are ineligible for more established second-line options, or as a third-line option in patients who have received first-line immunotherapy, and second-line chemotherapy or chemotherapy and antiangiogenesis therapy. However, further data are required to support the use of afatinib following immunotherapy. Given that treatment options are limited in both of these settings, investigating an agent with an entirely new mechanism of action is warranted. If available, molecular analysis to identify ErbB family mutations or the use of proteomic profiling could help to further isolate patients who are likely to derive the most benefit from afatinib.</description><subject>Biomarkers</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Epidermal growth factor</subject><subject>ErbB protein</subject><subject>ErbB-2 protein</subject><subject>Genes</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Lung cancer</subject><subject>Lung carcinoma</subject><subject>Metastasis</subject><subject>Monoclonal antibodies</subject><subject>Mutation</subject><subject>Patients</subject><subject>Pembrolizumab</subject><subject>Platinum</subject><subject>Review</subject><subject>Squamous cell carcinoma</subject><subject>Targeted cancer therapy</subject><issn>1178-6930</issn><issn>1178-6930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkVtLJDEQhYO4qOv65B8I-CLIuLlPxwdhaNwLDAjr-Byqc3FaupMx6R7w32-PDrLuUxXUV4eqcxA6p-SaUTH_fr9aXT8wSYRQB-iE0nk1U5qTw3_6Y_S1lGdClKqYOELHnBNFBdUnyC7cFqL1Dj-8jNCnseDadx2uIds2ph5wCnhYe7wc49MNrsecfRzwKnsY-l232GxyArv2BUN0b-if1Pnd2iLA0Ma2-Ya-BOiKP9vXU_T4425V_5ot73_-rhfLmeWVGmYCBFHace6Y5C544bRUmkhggovGq4bLwEMDYAVtKuq0Vi5wYa2VEAL3_BTdvutuxqb3zk7nZejMJrc95FeToDWfJ7Fdm6e0NXNJdcXIJHC5F8jpZfRlMH1b7GQHRD85Y5iQtBKSUzqhF_-hz2nMcXrvjZKSzTWbqKt3yuZUSvbh4xhKzC48M4Vn9uHxv5Tai8I</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Santos, Edgardo S</creator><creator>Hart, Lowell</creator><general>Taylor &amp; Francis Ltd</general><general>Dove</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200101</creationdate><title>Advanced Squamous Cell Carcinoma of the Lung: Current Treatment Approaches and the Role of Afatinib</title><author>Santos, Edgardo S ; Hart, Lowell</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-4a4069d33d253dfe4d956905a2434be6b35f3fbaac41b81d996df34ccc5aff3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Biomarkers</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Epidermal growth factor</topic><topic>ErbB protein</topic><topic>ErbB-2 protein</topic><topic>Genes</topic><topic>Immune checkpoint inhibitors</topic><topic>Immunotherapy</topic><topic>Lung cancer</topic><topic>Lung carcinoma</topic><topic>Metastasis</topic><topic>Monoclonal antibodies</topic><topic>Mutation</topic><topic>Patients</topic><topic>Pembrolizumab</topic><topic>Platinum</topic><topic>Review</topic><topic>Squamous cell carcinoma</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santos, Edgardo S</creatorcontrib><creatorcontrib>Hart, Lowell</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological 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>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>OncoTargets and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santos, Edgardo S</au><au>Hart, Lowell</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Advanced Squamous Cell Carcinoma of the Lung: Current Treatment Approaches and the Role of Afatinib</atitle><jtitle>OncoTargets and therapy</jtitle><date>2020-01-01</date><risdate>2020</risdate><volume>13</volume><spage>9305</spage><epage>9321</epage><pages>9305-9321</pages><issn>1178-6930</issn><eissn>1178-6930</eissn><abstract>Options for the treatment of squamous cell lung carcinoma expanded in recent years with the introduction of the immune checkpoint inhibitors into routine clinical practice in both the first- and second-line settings but are still limited. As a result, pembrolizumab, given either alone or in combination with platinum-based chemotherapy, is now a standard first-line treatment for squamous cell lung cancer. However, few options exist once patients have progressed on immune checkpoint inhibitors and chemotherapy. In this setting, the irreversible ErbB family blocker, afatinib, has a potential role as second or subsequent therapy for some patients. The Phase III LUX-Lung 8 study demonstrated that afatinib significantly prolonged progression-free and overall survival compared with erlotinib in patients with squamous cell lung carcinoma. Notably, retrospective, ad-hoc biomarker analyses of a subset of patients from LUX-Lung 8 suggested that patients with ErbB family mutations derived particular benefit from afatinib, especially those with ErbB2 (HER2) mutations. Afatinib has a manageable and predictable safety profile, and adverse events can be managed with the use of a tolerability-guided dose modification protocol. Until more data are available, afatinib could be considered as a potential second-line treatment option for patients who have progressed on combined pembrolizumab and platinum-based chemotherapy and are ineligible for more established second-line options, or as a third-line option in patients who have received first-line immunotherapy, and second-line chemotherapy or chemotherapy and antiangiogenesis therapy. However, further data are required to support the use of afatinib following immunotherapy. Given that treatment options are limited in both of these settings, investigating an agent with an entirely new mechanism of action is warranted. If available, molecular analysis to identify ErbB family mutations or the use of proteomic profiling could help to further isolate patients who are likely to derive the most benefit from afatinib.</abstract><cop>Macclesfield</cop><pub>Taylor &amp; Francis Ltd</pub><pmid>33061419</pmid><doi>10.2147/OTT.S250446</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1178-6930
ispartof OncoTargets and therapy, 2020-01, Vol.13, p.9305-9321
issn 1178-6930
1178-6930
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7519820
source Taylor & Francis Open Access; DOVE Medical Press Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
subjects Biomarkers
Cancer therapies
Chemotherapy
Epidermal growth factor
ErbB protein
ErbB-2 protein
Genes
Immune checkpoint inhibitors
Immunotherapy
Lung cancer
Lung carcinoma
Metastasis
Monoclonal antibodies
Mutation
Patients
Pembrolizumab
Platinum
Review
Squamous cell carcinoma
Targeted cancer therapy
title Advanced Squamous Cell Carcinoma of the Lung: Current Treatment Approaches and the Role of Afatinib
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T00%3A47%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Advanced%20Squamous%20Cell%20Carcinoma%20of%20the%20Lung:%20Current%20Treatment%20Approaches%20and%20the%20Role%20of%20Afatinib&rft.jtitle=OncoTargets%20and%20therapy&rft.au=Santos,%20Edgardo%20S&rft.date=2020-01-01&rft.volume=13&rft.spage=9305&rft.epage=9321&rft.pages=9305-9321&rft.issn=1178-6930&rft.eissn=1178-6930&rft_id=info:doi/10.2147/OTT.S250446&rft_dat=%3Cproquest_pubme%3E2451552792%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2451552792&rft_id=info:pmid/33061419&rfr_iscdi=true