First-Line Anaplastic Lymphoma Kinase (ALK) Inhibitors for ALK-Positive Lung Cancer in Asian Populations: Systematic Review and Network Meta-Analysis
Various anaplastic lymphoma kinase inhibitors (ALKIs) have been approved for first-line use in treating anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). To date, no head-to-head comparison of these newer generation ALKIs has been made, and different efficacies of ALKIs...
Gespeichert in:
Veröffentlicht in: | Journal of clinical medicine 2021-09, Vol.10 (19), p.4376 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 19 |
container_start_page | 4376 |
container_title | Journal of clinical medicine |
container_volume | 10 |
creator | Wu, Kuan-Li Chen, Hsiao-Ling Tsai, Ying-Ming Lee, Tai-Huang Chang, Hsiu-Mei Tsai, Yu-Chen Chuang, Cheng-Hao Chang, Yong-Chieh Tu, Yu-Kang Yang, Chih-Jen Hung, Jen-Yu Chong, Inn-Wen |
description | Various anaplastic lymphoma kinase inhibitors (ALKIs) have been approved for first-line use in treating anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). To date, no head-to-head comparison of these newer generation ALKIs has been made, and different efficacies of ALKIs may present across ethnicity. This study aims to compare newer generation ALKIs for treatment efficacy in Asian groups using network meta-analysis. Phase II/III trials that enrolled treatment-naïve Asian ALK-rearranged NSCLC patients treated by ALKIs were included. Progression-free survival (PFS) and overall response rate (ORR) of each trial were extracted as indicators of drug efficacy. Surfaces under cumulative ranking curves (SUCRAs) were calculated as a numeric presentation of the overall ranking associated with each agent. After a systematic literature review, six phase III clinical trials were included. Our results showed that newer generation ALKIs, such as alectinib, brigatinib, ensartinib, and lorlatinib, all demonstrated superior efficacy to crizotinib. Among those, ensartinib exhibited the best overall SUCRA value and ranked first among all agents. According to our network meta-analysis, ensartinib may currently be the most effective first-line treatment for Asian patients with ALK-positive NSCLC. However, this conclusion needs further validation by a larger scale of clinical trials or posthoc analysis of Asian populations. Moreover, in our comparison, low-dose alectinib (300 mg twice daily) exhibited an efficacy profile similar to a higher dose regimen in Asian populations. |
doi_str_mv | 10.3390/jcm10194376 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8509704</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2580990858</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-fb5752c35b0f138ba335b96f4c5e88ec190fa44abcd88fcac01436db9edb24ae3</originalsourceid><addsrcrecordid>eNpdkd1u1DAQhS0EolXpFS9giZsilOLETmJzgbRaUagaoOLn2po4k66XxE5tZ6t9EN6X9EeoMDczmvl0dEaHkJc5O-VcsbdbM-YsV4LX1RNyWLC6zhiX_Omj-YAcx7hlS0kpirx-Tg64qATjShyS32c2xJQ11iFdOZgGiMka2uzHaeNHoBfWQUR6smouXtNzt7GtTT5E2vtAl1126aNNdoe0md0VXYMzGKh1dBUtOHrpp3mAZL2L7-j3fUw4wq38N9xZvKHgOvoF040Pv-hnTJAtDoZ9tPEFedbDEPH4oR-Rn2cffqw_Zc3Xj-frVZMZLquU9W1Zl4XhZcv6nMsW-DKqqhemRCnR5Ir1IAS0ppOyN2BYLnjVtQq7thCA_Ii8v9ed5nbEzqBLAQY9BTtC2GsPVv97cXajr_xOy5KpmolF4ORBIPjrGWPSo40GhwEc-jnqopR5rVQp6wV99R-69XNYHr6jmFJMlnKh3txTJvgYA_Z_zeRM3yauHyXO_wBv-57_</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2580990858</pqid></control><display><type>article</type><title>First-Line Anaplastic Lymphoma Kinase (ALK) Inhibitors for ALK-Positive Lung Cancer in Asian Populations: Systematic Review and Network Meta-Analysis</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Wu, Kuan-Li ; Chen, Hsiao-Ling ; Tsai, Ying-Ming ; Lee, Tai-Huang ; Chang, Hsiu-Mei ; Tsai, Yu-Chen ; Chuang, Cheng-Hao ; Chang, Yong-Chieh ; Tu, Yu-Kang ; Yang, Chih-Jen ; Hung, Jen-Yu ; Chong, Inn-Wen</creator><creatorcontrib>Wu, Kuan-Li ; Chen, Hsiao-Ling ; Tsai, Ying-Ming ; Lee, Tai-Huang ; Chang, Hsiu-Mei ; Tsai, Yu-Chen ; Chuang, Cheng-Hao ; Chang, Yong-Chieh ; Tu, Yu-Kang ; Yang, Chih-Jen ; Hung, Jen-Yu ; Chong, Inn-Wen</creatorcontrib><description>Various anaplastic lymphoma kinase inhibitors (ALKIs) have been approved for first-line use in treating anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). To date, no head-to-head comparison of these newer generation ALKIs has been made, and different efficacies of ALKIs may present across ethnicity. This study aims to compare newer generation ALKIs for treatment efficacy in Asian groups using network meta-analysis. Phase II/III trials that enrolled treatment-naïve Asian ALK-rearranged NSCLC patients treated by ALKIs were included. Progression-free survival (PFS) and overall response rate (ORR) of each trial were extracted as indicators of drug efficacy. Surfaces under cumulative ranking curves (SUCRAs) were calculated as a numeric presentation of the overall ranking associated with each agent. After a systematic literature review, six phase III clinical trials were included. Our results showed that newer generation ALKIs, such as alectinib, brigatinib, ensartinib, and lorlatinib, all demonstrated superior efficacy to crizotinib. Among those, ensartinib exhibited the best overall SUCRA value and ranked first among all agents. According to our network meta-analysis, ensartinib may currently be the most effective first-line treatment for Asian patients with ALK-positive NSCLC. However, this conclusion needs further validation by a larger scale of clinical trials or posthoc analysis of Asian populations. Moreover, in our comparison, low-dose alectinib (300 mg twice daily) exhibited an efficacy profile similar to a higher dose regimen in Asian populations.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm10194376</identifier><identifier>PMID: 34640394</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Bias ; Cancer therapies ; Clinical medicine ; Clinical trials ; Drug dosages ; Drug efficacy ; FDA approval ; Intervention ; Kinases ; Lung cancer ; Lymphoma ; Medical prognosis ; Meta-analysis ; Mutation ; Review ; Systematic review</subject><ispartof>Journal of clinical medicine, 2021-09, Vol.10 (19), p.4376</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-fb5752c35b0f138ba335b96f4c5e88ec190fa44abcd88fcac01436db9edb24ae3</citedby><cites>FETCH-LOGICAL-c386t-fb5752c35b0f138ba335b96f4c5e88ec190fa44abcd88fcac01436db9edb24ae3</cites><orcidid>0000-0002-3576-7936 ; 0000-0002-2461-474X ; 0000-0002-0341-7747 ; 0000-0001-6662-6522 ; 0000-0003-4239-4012 ; 0000-0001-8328-8684 ; 0000-0003-3353-7501</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509704/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509704/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Wu, Kuan-Li</creatorcontrib><creatorcontrib>Chen, Hsiao-Ling</creatorcontrib><creatorcontrib>Tsai, Ying-Ming</creatorcontrib><creatorcontrib>Lee, Tai-Huang</creatorcontrib><creatorcontrib>Chang, Hsiu-Mei</creatorcontrib><creatorcontrib>Tsai, Yu-Chen</creatorcontrib><creatorcontrib>Chuang, Cheng-Hao</creatorcontrib><creatorcontrib>Chang, Yong-Chieh</creatorcontrib><creatorcontrib>Tu, Yu-Kang</creatorcontrib><creatorcontrib>Yang, Chih-Jen</creatorcontrib><creatorcontrib>Hung, Jen-Yu</creatorcontrib><creatorcontrib>Chong, Inn-Wen</creatorcontrib><title>First-Line Anaplastic Lymphoma Kinase (ALK) Inhibitors for ALK-Positive Lung Cancer in Asian Populations: Systematic Review and Network Meta-Analysis</title><title>Journal of clinical medicine</title><description>Various anaplastic lymphoma kinase inhibitors (ALKIs) have been approved for first-line use in treating anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). To date, no head-to-head comparison of these newer generation ALKIs has been made, and different efficacies of ALKIs may present across ethnicity. This study aims to compare newer generation ALKIs for treatment efficacy in Asian groups using network meta-analysis. Phase II/III trials that enrolled treatment-naïve Asian ALK-rearranged NSCLC patients treated by ALKIs were included. Progression-free survival (PFS) and overall response rate (ORR) of each trial were extracted as indicators of drug efficacy. Surfaces under cumulative ranking curves (SUCRAs) were calculated as a numeric presentation of the overall ranking associated with each agent. After a systematic literature review, six phase III clinical trials were included. Our results showed that newer generation ALKIs, such as alectinib, brigatinib, ensartinib, and lorlatinib, all demonstrated superior efficacy to crizotinib. Among those, ensartinib exhibited the best overall SUCRA value and ranked first among all agents. According to our network meta-analysis, ensartinib may currently be the most effective first-line treatment for Asian patients with ALK-positive NSCLC. However, this conclusion needs further validation by a larger scale of clinical trials or posthoc analysis of Asian populations. Moreover, in our comparison, low-dose alectinib (300 mg twice daily) exhibited an efficacy profile similar to a higher dose regimen in Asian populations.</description><subject>Bias</subject><subject>Cancer therapies</subject><subject>Clinical medicine</subject><subject>Clinical trials</subject><subject>Drug dosages</subject><subject>Drug efficacy</subject><subject>FDA approval</subject><subject>Intervention</subject><subject>Kinases</subject><subject>Lung cancer</subject><subject>Lymphoma</subject><subject>Medical prognosis</subject><subject>Meta-analysis</subject><subject>Mutation</subject><subject>Review</subject><subject>Systematic review</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkd1u1DAQhS0EolXpFS9giZsilOLETmJzgbRaUagaoOLn2po4k66XxE5tZ6t9EN6X9EeoMDczmvl0dEaHkJc5O-VcsbdbM-YsV4LX1RNyWLC6zhiX_Omj-YAcx7hlS0kpirx-Tg64qATjShyS32c2xJQ11iFdOZgGiMka2uzHaeNHoBfWQUR6smouXtNzt7GtTT5E2vtAl1126aNNdoe0md0VXYMzGKh1dBUtOHrpp3mAZL2L7-j3fUw4wq38N9xZvKHgOvoF040Pv-hnTJAtDoZ9tPEFedbDEPH4oR-Rn2cffqw_Zc3Xj-frVZMZLquU9W1Zl4XhZcv6nMsW-DKqqhemRCnR5Ir1IAS0ppOyN2BYLnjVtQq7thCA_Ii8v9ed5nbEzqBLAQY9BTtC2GsPVv97cXajr_xOy5KpmolF4ORBIPjrGWPSo40GhwEc-jnqopR5rVQp6wV99R-69XNYHr6jmFJMlnKh3txTJvgYA_Z_zeRM3yauHyXO_wBv-57_</recordid><startdate>20210925</startdate><enddate>20210925</enddate><creator>Wu, Kuan-Li</creator><creator>Chen, Hsiao-Ling</creator><creator>Tsai, Ying-Ming</creator><creator>Lee, Tai-Huang</creator><creator>Chang, Hsiu-Mei</creator><creator>Tsai, Yu-Chen</creator><creator>Chuang, Cheng-Hao</creator><creator>Chang, Yong-Chieh</creator><creator>Tu, Yu-Kang</creator><creator>Yang, Chih-Jen</creator><creator>Hung, Jen-Yu</creator><creator>Chong, Inn-Wen</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3576-7936</orcidid><orcidid>https://orcid.org/0000-0002-2461-474X</orcidid><orcidid>https://orcid.org/0000-0002-0341-7747</orcidid><orcidid>https://orcid.org/0000-0001-6662-6522</orcidid><orcidid>https://orcid.org/0000-0003-4239-4012</orcidid><orcidid>https://orcid.org/0000-0001-8328-8684</orcidid><orcidid>https://orcid.org/0000-0003-3353-7501</orcidid></search><sort><creationdate>20210925</creationdate><title>First-Line Anaplastic Lymphoma Kinase (ALK) Inhibitors for ALK-Positive Lung Cancer in Asian Populations: Systematic Review and Network Meta-Analysis</title><author>Wu, Kuan-Li ; Chen, Hsiao-Ling ; Tsai, Ying-Ming ; Lee, Tai-Huang ; Chang, Hsiu-Mei ; Tsai, Yu-Chen ; Chuang, Cheng-Hao ; Chang, Yong-Chieh ; Tu, Yu-Kang ; Yang, Chih-Jen ; Hung, Jen-Yu ; Chong, Inn-Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-fb5752c35b0f138ba335b96f4c5e88ec190fa44abcd88fcac01436db9edb24ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Bias</topic><topic>Cancer therapies</topic><topic>Clinical medicine</topic><topic>Clinical trials</topic><topic>Drug dosages</topic><topic>Drug efficacy</topic><topic>FDA approval</topic><topic>Intervention</topic><topic>Kinases</topic><topic>Lung cancer</topic><topic>Lymphoma</topic><topic>Medical prognosis</topic><topic>Meta-analysis</topic><topic>Mutation</topic><topic>Review</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Kuan-Li</creatorcontrib><creatorcontrib>Chen, Hsiao-Ling</creatorcontrib><creatorcontrib>Tsai, Ying-Ming</creatorcontrib><creatorcontrib>Lee, Tai-Huang</creatorcontrib><creatorcontrib>Chang, Hsiu-Mei</creatorcontrib><creatorcontrib>Tsai, Yu-Chen</creatorcontrib><creatorcontrib>Chuang, Cheng-Hao</creatorcontrib><creatorcontrib>Chang, Yong-Chieh</creatorcontrib><creatorcontrib>Tu, Yu-Kang</creatorcontrib><creatorcontrib>Yang, Chih-Jen</creatorcontrib><creatorcontrib>Hung, Jen-Yu</creatorcontrib><creatorcontrib>Chong, Inn-Wen</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</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 Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Kuan-Li</au><au>Chen, Hsiao-Ling</au><au>Tsai, Ying-Ming</au><au>Lee, Tai-Huang</au><au>Chang, Hsiu-Mei</au><au>Tsai, Yu-Chen</au><au>Chuang, Cheng-Hao</au><au>Chang, Yong-Chieh</au><au>Tu, Yu-Kang</au><au>Yang, Chih-Jen</au><au>Hung, Jen-Yu</au><au>Chong, Inn-Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First-Line Anaplastic Lymphoma Kinase (ALK) Inhibitors for ALK-Positive Lung Cancer in Asian Populations: Systematic Review and Network Meta-Analysis</atitle><jtitle>Journal of clinical medicine</jtitle><date>2021-09-25</date><risdate>2021</risdate><volume>10</volume><issue>19</issue><spage>4376</spage><pages>4376-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>Various anaplastic lymphoma kinase inhibitors (ALKIs) have been approved for first-line use in treating anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC). To date, no head-to-head comparison of these newer generation ALKIs has been made, and different efficacies of ALKIs may present across ethnicity. This study aims to compare newer generation ALKIs for treatment efficacy in Asian groups using network meta-analysis. Phase II/III trials that enrolled treatment-naïve Asian ALK-rearranged NSCLC patients treated by ALKIs were included. Progression-free survival (PFS) and overall response rate (ORR) of each trial were extracted as indicators of drug efficacy. Surfaces under cumulative ranking curves (SUCRAs) were calculated as a numeric presentation of the overall ranking associated with each agent. After a systematic literature review, six phase III clinical trials were included. Our results showed that newer generation ALKIs, such as alectinib, brigatinib, ensartinib, and lorlatinib, all demonstrated superior efficacy to crizotinib. Among those, ensartinib exhibited the best overall SUCRA value and ranked first among all agents. According to our network meta-analysis, ensartinib may currently be the most effective first-line treatment for Asian patients with ALK-positive NSCLC. However, this conclusion needs further validation by a larger scale of clinical trials or posthoc analysis of Asian populations. Moreover, in our comparison, low-dose alectinib (300 mg twice daily) exhibited an efficacy profile similar to a higher dose regimen in Asian populations.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34640394</pmid><doi>10.3390/jcm10194376</doi><orcidid>https://orcid.org/0000-0002-3576-7936</orcidid><orcidid>https://orcid.org/0000-0002-2461-474X</orcidid><orcidid>https://orcid.org/0000-0002-0341-7747</orcidid><orcidid>https://orcid.org/0000-0001-6662-6522</orcidid><orcidid>https://orcid.org/0000-0003-4239-4012</orcidid><orcidid>https://orcid.org/0000-0001-8328-8684</orcidid><orcidid>https://orcid.org/0000-0003-3353-7501</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2077-0383 |
ispartof | Journal of clinical medicine, 2021-09, Vol.10 (19), p.4376 |
issn | 2077-0383 2077-0383 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8509704 |
source | MDPI - Multidisciplinary Digital Publishing Institute; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
subjects | Bias Cancer therapies Clinical medicine Clinical trials Drug dosages Drug efficacy FDA approval Intervention Kinases Lung cancer Lymphoma Medical prognosis Meta-analysis Mutation Review Systematic review |
title | First-Line Anaplastic Lymphoma Kinase (ALK) Inhibitors for ALK-Positive Lung Cancer in Asian Populations: Systematic Review and Network Meta-Analysis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T17%3A34%3A08IST&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=First-Line%20Anaplastic%20Lymphoma%20Kinase%20(ALK)%20Inhibitors%20for%20ALK-Positive%20Lung%20Cancer%20in%20Asian%20Populations:%20Systematic%20Review%20and%20Network%20Meta-Analysis&rft.jtitle=Journal%20of%20clinical%20medicine&rft.au=Wu,%20Kuan-Li&rft.date=2021-09-25&rft.volume=10&rft.issue=19&rft.spage=4376&rft.pages=4376-&rft.issn=2077-0383&rft.eissn=2077-0383&rft_id=info:doi/10.3390/jcm10194376&rft_dat=%3Cproquest_pubme%3E2580990858%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=2580990858&rft_id=info:pmid/34640394&rfr_iscdi=true |