Loading…
Overall Survival of Patients With Unresectable or Metastatic BRAF V600-Mutant Acral/Cutaneous Melanoma Administered Dabrafenib Plus Trametinib: Long-Term Follow-Up of a Multicenter, Single-Arm Phase IIa Trial
To examine the long-term survival outcome of dabrafenib in combination with trametinib in Chinese patients with unresectable or metastatic acral/cutaneous melanoma with BRAF-V600 mutation and to explore potential predictors of effectiveness. This was a long-term follow-up of Chinese patients with un...
Saved in:
Published in: | Frontiers in oncology 2021-08, Vol.11, p.720044-720044 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3 |
---|---|
cites | cdi_FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3 |
container_end_page | 720044 |
container_issue | |
container_start_page | 720044 |
container_title | Frontiers in oncology |
container_volume | 11 |
creator | Mao, Lili Ding, Ya Bai, Xue Sheng, Xinan Dai, Jie Chi, Zhihong Cui, Chuanliang Kong, Yan Fan, Yun Xu, Yanjun Wang, Xuan Tang, Bixia Lian, Bin Yan, Xieqiao Li, Siming Zhou, Li Wei, Xiaoting Li, Caili Guo, Jun Zhang, Xiaoshi Si, Lu |
description | To examine the long-term survival outcome of dabrafenib in combination with trametinib in Chinese patients with unresectable or metastatic acral/cutaneous melanoma with BRAF-V600 mutation and to explore potential predictors of effectiveness.
This was a long-term follow-up of Chinese patients with unresectable or metastatic BRAF V600-mutant acral/cutaneous melanoma administered dabrafenib (150 mg twice daily) plus trametinib (2 mg once daily) in an open-label, multicenter, single-arm, phase IIa study (NCT02083354). Efficacy endpoints included objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS). The impacts of baseline characteristics on PFS and OS were analyzed.
A total of sixty patients were included. The median age was 48 years, and 24 patients (40.0%) were male. Totally 12 individuals (20.0%) had acral melanoma, and 45 (75.0%) had failed previous systemic therapy. Up to July 2020, the median duration of follow-up was 37.0 (95% confidence interval [CI] 29.1-44.9) months. The updated ORR was 71.7% (95%CI 60.3%-83.1%). The 3-year OS rate was 28.8% (95%CI 19.1-43.6%) in the overall population, and 35.7% (95%CI 15.5-82.4%) in acral melanoma patients. The median DOR was 7.5 months (95%CI 4.5 to 10.5). Baseline normal lactic dehydrogenase (LDH), metastatic organ sites |
doi_str_mv | 10.3389/fonc.2021.720044 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_3c16dfb2acaa443b86ee7bdc3445159e</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_3c16dfb2acaa443b86ee7bdc3445159e</doaj_id><sourcerecordid>2571924518</sourcerecordid><originalsourceid>FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3</originalsourceid><addsrcrecordid>eNpVkk1vEzEQhlcIRKvSOyfkIwc29dreLw5IaSAQKVEjmgA3a-ydTbbyroO9G8S_5CfhJaVqffHXO8_M2G8UvU7ohPOivKptpyeMsmSSM0qFeBadM8ZFXAr-4_mj9Vl06f0dDSNLaUL5y-iMi5SKvMzOoz83R3RgDLkd3LE5giG2JmvoG-x6T743_Z5sO4cedQ_KILGOrLAH3weJJtdfp3PyLaM0Xg09dD2Z6gC7mo0btIMPWgOdbYFMq7bpGt-jw4p8BOWgxq5RZG2CauOgxT7cq_dkabtdvEHXkrk1xv6Kt4exJCCrwYSUoSx078ht0-0MxtMgW-_BI1ksIGAaMK-iFzUYj5f380W0nX_azL7Ey5vPi9l0GWuRsT7OlYKkrIqCiiJN0kJjlYuy5Hme0yQvEp5zDkWqeAFlnYJimc5UwTUoFeRM8YtoceJWFu7kwTUtuN_SQiP_HVi3k-BCwQYl10lW1YqBBhCCqyJDzFWluRCBVWJgfTixDoNqsRqbDM_4BPr0pmv2cmePshCMhQ4C4O09wNmfA_peto3XaMzpGyRL86RkIVsRpPQk1c5677B-SJNQOfpKjr6So6_kyVch5M3j8h4C_ruI_wUpQMxY</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2571924518</pqid></control><display><type>article</type><title>Overall Survival of Patients With Unresectable or Metastatic BRAF V600-Mutant Acral/Cutaneous Melanoma Administered Dabrafenib Plus Trametinib: Long-Term Follow-Up of a Multicenter, Single-Arm Phase IIa Trial</title><source>PubMed Central Free</source><creator>Mao, Lili ; Ding, Ya ; Bai, Xue ; Sheng, Xinan ; Dai, Jie ; Chi, Zhihong ; Cui, Chuanliang ; Kong, Yan ; Fan, Yun ; Xu, Yanjun ; Wang, Xuan ; Tang, Bixia ; Lian, Bin ; Yan, Xieqiao ; Li, Siming ; Zhou, Li ; Wei, Xiaoting ; Li, Caili ; Guo, Jun ; Zhang, Xiaoshi ; Si, Lu</creator><creatorcontrib>Mao, Lili ; Ding, Ya ; Bai, Xue ; Sheng, Xinan ; Dai, Jie ; Chi, Zhihong ; Cui, Chuanliang ; Kong, Yan ; Fan, Yun ; Xu, Yanjun ; Wang, Xuan ; Tang, Bixia ; Lian, Bin ; Yan, Xieqiao ; Li, Siming ; Zhou, Li ; Wei, Xiaoting ; Li, Caili ; Guo, Jun ; Zhang, Xiaoshi ; Si, Lu</creatorcontrib><description>To examine the long-term survival outcome of dabrafenib in combination with trametinib in Chinese patients with unresectable or metastatic acral/cutaneous melanoma with BRAF-V600 mutation and to explore potential predictors of effectiveness.
This was a long-term follow-up of Chinese patients with unresectable or metastatic BRAF V600-mutant acral/cutaneous melanoma administered dabrafenib (150 mg twice daily) plus trametinib (2 mg once daily) in an open-label, multicenter, single-arm, phase IIa study (NCT02083354). Efficacy endpoints included objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS). The impacts of baseline characteristics on PFS and OS were analyzed.
A total of sixty patients were included. The median age was 48 years, and 24 patients (40.0%) were male. Totally 12 individuals (20.0%) had acral melanoma, and 45 (75.0%) had failed previous systemic therapy. Up to July 2020, the median duration of follow-up was 37.0 (95% confidence interval [CI] 29.1-44.9) months. The updated ORR was 71.7% (95%CI 60.3%-83.1%). The 3-year OS rate was 28.8% (95%CI 19.1-43.6%) in the overall population, and 35.7% (95%CI 15.5-82.4%) in acral melanoma patients. The median DOR was 7.5 months (95%CI 4.5 to 10.5). Baseline normal lactic dehydrogenase (LDH), metastatic organ sites<3 and complete response to combination therapy with dabrafenib plus trametinib were associated with improved PFS and OS.
Dabrafenib combined with trametinib confer long-term survival in Chinese patients with BRAF V600-mutant, unresectable or metastatic acral/cutaneous melanoma.
https://clinicaltrials.gov/ct2/show/NCT02083354, identifier NCT02083354.</description><identifier>ISSN: 2234-943X</identifier><identifier>EISSN: 2234-943X</identifier><identifier>DOI: 10.3389/fonc.2021.720044</identifier><identifier>PMID: 34504796</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>acral melanoma ; BRAF ; dabrafenib ; melanoma ; Oncology ; trametinib</subject><ispartof>Frontiers in oncology, 2021-08, Vol.11, p.720044-720044</ispartof><rights>Copyright © 2021 Mao, Ding, Bai, Sheng, Dai, Chi, Cui, Kong, Fan, Xu, Wang, Tang, Lian, Yan, Li, Zhou, Wei, Li, Guo, Zhang and Si.</rights><rights>Copyright © 2021 Mao, Ding, Bai, Sheng, Dai, Chi, Cui, Kong, Fan, Xu, Wang, Tang, Lian, Yan, Li, Zhou, Wei, Li, Guo, Zhang and Si 2021 Mao, Ding, Bai, Sheng, Dai, Chi, Cui, Kong, Fan, Xu, Wang, Tang, Lian, Yan, Li, Zhou, Wei, Li, Guo, Zhang and Si</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3</citedby><cites>FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3</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/PMC8422804/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422804/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34504796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mao, Lili</creatorcontrib><creatorcontrib>Ding, Ya</creatorcontrib><creatorcontrib>Bai, Xue</creatorcontrib><creatorcontrib>Sheng, Xinan</creatorcontrib><creatorcontrib>Dai, Jie</creatorcontrib><creatorcontrib>Chi, Zhihong</creatorcontrib><creatorcontrib>Cui, Chuanliang</creatorcontrib><creatorcontrib>Kong, Yan</creatorcontrib><creatorcontrib>Fan, Yun</creatorcontrib><creatorcontrib>Xu, Yanjun</creatorcontrib><creatorcontrib>Wang, Xuan</creatorcontrib><creatorcontrib>Tang, Bixia</creatorcontrib><creatorcontrib>Lian, Bin</creatorcontrib><creatorcontrib>Yan, Xieqiao</creatorcontrib><creatorcontrib>Li, Siming</creatorcontrib><creatorcontrib>Zhou, Li</creatorcontrib><creatorcontrib>Wei, Xiaoting</creatorcontrib><creatorcontrib>Li, Caili</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>Zhang, Xiaoshi</creatorcontrib><creatorcontrib>Si, Lu</creatorcontrib><title>Overall Survival of Patients With Unresectable or Metastatic BRAF V600-Mutant Acral/Cutaneous Melanoma Administered Dabrafenib Plus Trametinib: Long-Term Follow-Up of a Multicenter, Single-Arm Phase IIa Trial</title><title>Frontiers in oncology</title><addtitle>Front Oncol</addtitle><description>To examine the long-term survival outcome of dabrafenib in combination with trametinib in Chinese patients with unresectable or metastatic acral/cutaneous melanoma with BRAF-V600 mutation and to explore potential predictors of effectiveness.
This was a long-term follow-up of Chinese patients with unresectable or metastatic BRAF V600-mutant acral/cutaneous melanoma administered dabrafenib (150 mg twice daily) plus trametinib (2 mg once daily) in an open-label, multicenter, single-arm, phase IIa study (NCT02083354). Efficacy endpoints included objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS). The impacts of baseline characteristics on PFS and OS were analyzed.
A total of sixty patients were included. The median age was 48 years, and 24 patients (40.0%) were male. Totally 12 individuals (20.0%) had acral melanoma, and 45 (75.0%) had failed previous systemic therapy. Up to July 2020, the median duration of follow-up was 37.0 (95% confidence interval [CI] 29.1-44.9) months. The updated ORR was 71.7% (95%CI 60.3%-83.1%). The 3-year OS rate was 28.8% (95%CI 19.1-43.6%) in the overall population, and 35.7% (95%CI 15.5-82.4%) in acral melanoma patients. The median DOR was 7.5 months (95%CI 4.5 to 10.5). Baseline normal lactic dehydrogenase (LDH), metastatic organ sites<3 and complete response to combination therapy with dabrafenib plus trametinib were associated with improved PFS and OS.
Dabrafenib combined with trametinib confer long-term survival in Chinese patients with BRAF V600-mutant, unresectable or metastatic acral/cutaneous melanoma.
https://clinicaltrials.gov/ct2/show/NCT02083354, identifier NCT02083354.</description><subject>acral melanoma</subject><subject>BRAF</subject><subject>dabrafenib</subject><subject>melanoma</subject><subject>Oncology</subject><subject>trametinib</subject><issn>2234-943X</issn><issn>2234-943X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkk1vEzEQhlcIRKvSOyfkIwc29dreLw5IaSAQKVEjmgA3a-ydTbbyroO9G8S_5CfhJaVqffHXO8_M2G8UvU7ohPOivKptpyeMsmSSM0qFeBadM8ZFXAr-4_mj9Vl06f0dDSNLaUL5y-iMi5SKvMzOoz83R3RgDLkd3LE5giG2JmvoG-x6T743_Z5sO4cedQ_KILGOrLAH3weJJtdfp3PyLaM0Xg09dD2Z6gC7mo0btIMPWgOdbYFMq7bpGt-jw4p8BOWgxq5RZG2CauOgxT7cq_dkabtdvEHXkrk1xv6Kt4exJCCrwYSUoSx078ht0-0MxtMgW-_BI1ksIGAaMK-iFzUYj5f380W0nX_azL7Ey5vPi9l0GWuRsT7OlYKkrIqCiiJN0kJjlYuy5Hme0yQvEp5zDkWqeAFlnYJimc5UwTUoFeRM8YtoceJWFu7kwTUtuN_SQiP_HVi3k-BCwQYl10lW1YqBBhCCqyJDzFWluRCBVWJgfTixDoNqsRqbDM_4BPr0pmv2cmePshCMhQ4C4O09wNmfA_peto3XaMzpGyRL86RkIVsRpPQk1c5677B-SJNQOfpKjr6So6_kyVch5M3j8h4C_ruI_wUpQMxY</recordid><startdate>20210824</startdate><enddate>20210824</enddate><creator>Mao, Lili</creator><creator>Ding, Ya</creator><creator>Bai, Xue</creator><creator>Sheng, Xinan</creator><creator>Dai, Jie</creator><creator>Chi, Zhihong</creator><creator>Cui, Chuanliang</creator><creator>Kong, Yan</creator><creator>Fan, Yun</creator><creator>Xu, Yanjun</creator><creator>Wang, Xuan</creator><creator>Tang, Bixia</creator><creator>Lian, Bin</creator><creator>Yan, Xieqiao</creator><creator>Li, Siming</creator><creator>Zhou, Li</creator><creator>Wei, Xiaoting</creator><creator>Li, Caili</creator><creator>Guo, Jun</creator><creator>Zhang, Xiaoshi</creator><creator>Si, Lu</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20210824</creationdate><title>Overall Survival of Patients With Unresectable or Metastatic BRAF V600-Mutant Acral/Cutaneous Melanoma Administered Dabrafenib Plus Trametinib: Long-Term Follow-Up of a Multicenter, Single-Arm Phase IIa Trial</title><author>Mao, Lili ; Ding, Ya ; Bai, Xue ; Sheng, Xinan ; Dai, Jie ; Chi, Zhihong ; Cui, Chuanliang ; Kong, Yan ; Fan, Yun ; Xu, Yanjun ; Wang, Xuan ; Tang, Bixia ; Lian, Bin ; Yan, Xieqiao ; Li, Siming ; Zhou, Li ; Wei, Xiaoting ; Li, Caili ; Guo, Jun ; Zhang, Xiaoshi ; Si, Lu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>acral melanoma</topic><topic>BRAF</topic><topic>dabrafenib</topic><topic>melanoma</topic><topic>Oncology</topic><topic>trametinib</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mao, Lili</creatorcontrib><creatorcontrib>Ding, Ya</creatorcontrib><creatorcontrib>Bai, Xue</creatorcontrib><creatorcontrib>Sheng, Xinan</creatorcontrib><creatorcontrib>Dai, Jie</creatorcontrib><creatorcontrib>Chi, Zhihong</creatorcontrib><creatorcontrib>Cui, Chuanliang</creatorcontrib><creatorcontrib>Kong, Yan</creatorcontrib><creatorcontrib>Fan, Yun</creatorcontrib><creatorcontrib>Xu, Yanjun</creatorcontrib><creatorcontrib>Wang, Xuan</creatorcontrib><creatorcontrib>Tang, Bixia</creatorcontrib><creatorcontrib>Lian, Bin</creatorcontrib><creatorcontrib>Yan, Xieqiao</creatorcontrib><creatorcontrib>Li, Siming</creatorcontrib><creatorcontrib>Zhou, Li</creatorcontrib><creatorcontrib>Wei, Xiaoting</creatorcontrib><creatorcontrib>Li, Caili</creatorcontrib><creatorcontrib>Guo, Jun</creatorcontrib><creatorcontrib>Zhang, Xiaoshi</creatorcontrib><creatorcontrib>Si, Lu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Frontiers in oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mao, Lili</au><au>Ding, Ya</au><au>Bai, Xue</au><au>Sheng, Xinan</au><au>Dai, Jie</au><au>Chi, Zhihong</au><au>Cui, Chuanliang</au><au>Kong, Yan</au><au>Fan, Yun</au><au>Xu, Yanjun</au><au>Wang, Xuan</au><au>Tang, Bixia</au><au>Lian, Bin</au><au>Yan, Xieqiao</au><au>Li, Siming</au><au>Zhou, Li</au><au>Wei, Xiaoting</au><au>Li, Caili</au><au>Guo, Jun</au><au>Zhang, Xiaoshi</au><au>Si, Lu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overall Survival of Patients With Unresectable or Metastatic BRAF V600-Mutant Acral/Cutaneous Melanoma Administered Dabrafenib Plus Trametinib: Long-Term Follow-Up of a Multicenter, Single-Arm Phase IIa Trial</atitle><jtitle>Frontiers in oncology</jtitle><addtitle>Front Oncol</addtitle><date>2021-08-24</date><risdate>2021</risdate><volume>11</volume><spage>720044</spage><epage>720044</epage><pages>720044-720044</pages><issn>2234-943X</issn><eissn>2234-943X</eissn><abstract>To examine the long-term survival outcome of dabrafenib in combination with trametinib in Chinese patients with unresectable or metastatic acral/cutaneous melanoma with BRAF-V600 mutation and to explore potential predictors of effectiveness.
This was a long-term follow-up of Chinese patients with unresectable or metastatic BRAF V600-mutant acral/cutaneous melanoma administered dabrafenib (150 mg twice daily) plus trametinib (2 mg once daily) in an open-label, multicenter, single-arm, phase IIa study (NCT02083354). Efficacy endpoints included objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS). The impacts of baseline characteristics on PFS and OS were analyzed.
A total of sixty patients were included. The median age was 48 years, and 24 patients (40.0%) were male. Totally 12 individuals (20.0%) had acral melanoma, and 45 (75.0%) had failed previous systemic therapy. Up to July 2020, the median duration of follow-up was 37.0 (95% confidence interval [CI] 29.1-44.9) months. The updated ORR was 71.7% (95%CI 60.3%-83.1%). The 3-year OS rate was 28.8% (95%CI 19.1-43.6%) in the overall population, and 35.7% (95%CI 15.5-82.4%) in acral melanoma patients. The median DOR was 7.5 months (95%CI 4.5 to 10.5). Baseline normal lactic dehydrogenase (LDH), metastatic organ sites<3 and complete response to combination therapy with dabrafenib plus trametinib were associated with improved PFS and OS.
Dabrafenib combined with trametinib confer long-term survival in Chinese patients with BRAF V600-mutant, unresectable or metastatic acral/cutaneous melanoma.
https://clinicaltrials.gov/ct2/show/NCT02083354, identifier NCT02083354.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>34504796</pmid><doi>10.3389/fonc.2021.720044</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2234-943X |
ispartof | Frontiers in oncology, 2021-08, Vol.11, p.720044-720044 |
issn | 2234-943X 2234-943X |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_3c16dfb2acaa443b86ee7bdc3445159e |
source | PubMed Central Free |
subjects | acral melanoma BRAF dabrafenib melanoma Oncology trametinib |
title | Overall Survival of Patients With Unresectable or Metastatic BRAF V600-Mutant Acral/Cutaneous Melanoma Administered Dabrafenib Plus Trametinib: Long-Term Follow-Up of a Multicenter, Single-Arm Phase IIa Trial |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T04%3A31%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Overall%20Survival%20of%20Patients%20With%20Unresectable%20or%20Metastatic%20BRAF%20V600-Mutant%20Acral/Cutaneous%20Melanoma%20Administered%20Dabrafenib%20Plus%20Trametinib:%20Long-Term%20Follow-Up%20of%20a%20Multicenter,%20Single-Arm%20Phase%20IIa%20Trial&rft.jtitle=Frontiers%20in%20oncology&rft.au=Mao,%20Lili&rft.date=2021-08-24&rft.volume=11&rft.spage=720044&rft.epage=720044&rft.pages=720044-720044&rft.issn=2234-943X&rft.eissn=2234-943X&rft_id=info:doi/10.3389/fonc.2021.720044&rft_dat=%3Cproquest_doaj_%3E2571924518%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c462t-7bba19d880485158ced74993777017813733a85b38a9f5ab26c6b83cabb5152b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2571924518&rft_id=info:pmid/34504796&rfr_iscdi=true |