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Efficacy of lazertinib for symptomatic or asymptomatic brain metastases in treatment‐naive patients with advanced EGFR mutation‐positive non‐small cell lung cancer: Protocol of an open‐label, single‐arm phase II trial
Introduction Non‐small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutation has a higher incidence of brain metastases than wild‐type EGFR mutations. Osimertinib, a third‐generation EGFR tyrosine kinase inhibitor (TKI), targets both EGFR‐TKI sensitizing and T790M‐resistance...
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Published in: | Thoracic cancer 2023-08, Vol.14 (22), p.2233-2237 |
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creator | Lee, Bora Ji, Wonjun Lee, Jae Cheol Song, Si Yeol Shin, Young Seob Cho, Young Hyun Park, Ji Eun Park, Hyungjun Choi, Chang‐Min |
description | Introduction
Non‐small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutation has a higher incidence of brain metastases than wild‐type EGFR mutations. Osimertinib, a third‐generation EGFR tyrosine kinase inhibitor (TKI), targets both EGFR‐TKI sensitizing and T790M‐resistance mutations and has a higher brain penetration rate relative to first‐ and second‐generation EGFR‐TKIs. Therefore, osimertinib has become a preferred first‐line therapy for advanced EGFR mutation‐positive NSCLC. However, lazertinib, an emerging EGFR‐TKI, has shown higher selectivity toward EGFR mutations and improved penetration of the blood–brain barrier compared to osimertinib in preclinical studies. This trial will evaluate the efficacy of lazertinib as a first‐line therapy in patients with EGFR mutation‐positive NSCLC who have brain metastases, with or without additional local therapy.
Methods
This is a single‐center, open‐label, single‐arm phase II trial. A total of 75 patients with advanced EGFR mutation‐positive NSCLC will be recruited. Eligible patients will receive oral lazertinib 240 mg, once daily until disease progression or intolerable toxicity is detected. Patients with moderate to severe symptoms related to brain metastasis will simultaneously receive local therapy for the brain. The primary endpoints are progression‐free survival and intracranial progression‐free survival.
Discussion
Lazertinib, in combination with local therapy for the brain, if necessary, is expected to improve the clinical benefit in advanced EGFR mutation‐positive NSCLC with brain metastases, as a first‐line treatment.
Based on previous studies, the efficacy of lazertinib for brain metastasis is anticipated to be satisfactory in EGFR mutation‐positive NSCLC. This is the protocol for a single‐center, single‐arm phase II trial that will evaluate the efficacy of lazertinib with or without local therapy as a first‐line treatment of patients with EGFR mutation‐positive NSCLC, who also present with brain metastases. |
doi_str_mv | 10.1111/1759-7714.15018 |
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Non‐small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutation has a higher incidence of brain metastases than wild‐type EGFR mutations. Osimertinib, a third‐generation EGFR tyrosine kinase inhibitor (TKI), targets both EGFR‐TKI sensitizing and T790M‐resistance mutations and has a higher brain penetration rate relative to first‐ and second‐generation EGFR‐TKIs. Therefore, osimertinib has become a preferred first‐line therapy for advanced EGFR mutation‐positive NSCLC. However, lazertinib, an emerging EGFR‐TKI, has shown higher selectivity toward EGFR mutations and improved penetration of the blood–brain barrier compared to osimertinib in preclinical studies. This trial will evaluate the efficacy of lazertinib as a first‐line therapy in patients with EGFR mutation‐positive NSCLC who have brain metastases, with or without additional local therapy.
Methods
This is a single‐center, open‐label, single‐arm phase II trial. A total of 75 patients with advanced EGFR mutation‐positive NSCLC will be recruited. Eligible patients will receive oral lazertinib 240 mg, once daily until disease progression or intolerable toxicity is detected. Patients with moderate to severe symptoms related to brain metastasis will simultaneously receive local therapy for the brain. The primary endpoints are progression‐free survival and intracranial progression‐free survival.
Discussion
Lazertinib, in combination with local therapy for the brain, if necessary, is expected to improve the clinical benefit in advanced EGFR mutation‐positive NSCLC with brain metastases, as a first‐line treatment.
Based on previous studies, the efficacy of lazertinib for brain metastasis is anticipated to be satisfactory in EGFR mutation‐positive NSCLC. This is the protocol for a single‐center, single‐arm phase II trial that will evaluate the efficacy of lazertinib with or without local therapy as a first‐line treatment of patients with EGFR mutation‐positive NSCLC, who also present with brain metastases.</description><identifier>ISSN: 1759-7706</identifier><identifier>EISSN: 1759-7714</identifier><identifier>DOI: 10.1111/1759-7714.15018</identifier><identifier>PMID: 37365915</identifier><language>eng</language><publisher>Melbourne: John Wiley & Sons Australia, Ltd</publisher><subject>Asymptomatic ; Brain cancer ; brain metastases ; Brain Neoplasms - drug therapy ; Brain Neoplasms - genetics ; Cancer therapies ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - pathology ; Clinical Trials, Phase II as Topic ; Decision trees ; Effectiveness ; epidermal growth factor receptor ; ErbB Receptors ; Humans ; Informed consent ; Intracranial pressure ; lazertinib ; Lung cancer ; Lung diseases ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; Magnetic resonance imaging ; Medical prognosis ; Metastasis ; Mutation ; Nervous system ; non‐small cell lung cancer ; Protein Kinase Inhibitors - pharmacology ; Radiation therapy ; Response rates ; Study Protocol ; Surgery ; Tumors</subject><ispartof>Thoracic cancer, 2023-08, Vol.14 (22), p.2233-2237</ispartof><rights>2023 The Authors. published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.</rights><rights>2023 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5348-985920a89abf35390e8579c6ae3f6f1191e4825d69f8ca95850e340f619e96333</citedby><cites>FETCH-LOGICAL-c5348-985920a89abf35390e8579c6ae3f6f1191e4825d69f8ca95850e340f619e96333</cites><orcidid>0000-0001-7164-2770 ; 0000-0002-2881-4669 ; 0000-0003-1381-7506 ; 0000-0002-5523-5144</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2844902179/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2844902179?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,11542,25732,27903,27904,36991,36992,44569,46031,46455,53770,53772,74873</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37365915$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Bora</creatorcontrib><creatorcontrib>Ji, Wonjun</creatorcontrib><creatorcontrib>Lee, Jae Cheol</creatorcontrib><creatorcontrib>Song, Si Yeol</creatorcontrib><creatorcontrib>Shin, Young Seob</creatorcontrib><creatorcontrib>Cho, Young Hyun</creatorcontrib><creatorcontrib>Park, Ji Eun</creatorcontrib><creatorcontrib>Park, Hyungjun</creatorcontrib><creatorcontrib>Choi, Chang‐Min</creatorcontrib><title>Efficacy of lazertinib for symptomatic or asymptomatic brain metastases in treatment‐naive patients with advanced EGFR mutation‐positive non‐small cell lung cancer: Protocol of an open‐label, single‐arm phase II trial</title><title>Thoracic cancer</title><addtitle>Thorac Cancer</addtitle><description>Introduction
Non‐small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutation has a higher incidence of brain metastases than wild‐type EGFR mutations. Osimertinib, a third‐generation EGFR tyrosine kinase inhibitor (TKI), targets both EGFR‐TKI sensitizing and T790M‐resistance mutations and has a higher brain penetration rate relative to first‐ and second‐generation EGFR‐TKIs. Therefore, osimertinib has become a preferred first‐line therapy for advanced EGFR mutation‐positive NSCLC. However, lazertinib, an emerging EGFR‐TKI, has shown higher selectivity toward EGFR mutations and improved penetration of the blood–brain barrier compared to osimertinib in preclinical studies. This trial will evaluate the efficacy of lazertinib as a first‐line therapy in patients with EGFR mutation‐positive NSCLC who have brain metastases, with or without additional local therapy.
Methods
This is a single‐center, open‐label, single‐arm phase II trial. A total of 75 patients with advanced EGFR mutation‐positive NSCLC will be recruited. Eligible patients will receive oral lazertinib 240 mg, once daily until disease progression or intolerable toxicity is detected. Patients with moderate to severe symptoms related to brain metastasis will simultaneously receive local therapy for the brain. The primary endpoints are progression‐free survival and intracranial progression‐free survival.
Discussion
Lazertinib, in combination with local therapy for the brain, if necessary, is expected to improve the clinical benefit in advanced EGFR mutation‐positive NSCLC with brain metastases, as a first‐line treatment.
Based on previous studies, the efficacy of lazertinib for brain metastasis is anticipated to be satisfactory in EGFR mutation‐positive NSCLC. This is the protocol for a single‐center, single‐arm phase II trial that will evaluate the efficacy of lazertinib with or without local therapy as a first‐line treatment of patients with EGFR mutation‐positive NSCLC, who also present with brain metastases.</description><subject>Asymptomatic</subject><subject>Brain cancer</subject><subject>brain metastases</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - genetics</subject><subject>Cancer therapies</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Clinical Trials, Phase II as Topic</subject><subject>Decision trees</subject><subject>Effectiveness</subject><subject>epidermal growth factor receptor</subject><subject>ErbB Receptors</subject><subject>Humans</subject><subject>Informed consent</subject><subject>Intracranial pressure</subject><subject>lazertinib</subject><subject>Lung cancer</subject><subject>Lung diseases</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Magnetic resonance imaging</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Mutation</subject><subject>Nervous system</subject><subject>non‐small cell lung cancer</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Radiation therapy</subject><subject>Response rates</subject><subject>Study Protocol</subject><subject>Surgery</subject><subject>Tumors</subject><issn>1759-7706</issn><issn>1759-7714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFksFu1DAURSMEolXpmh2yxIZFp7XjOInZoGo0LSNVAqGytl4ce8aVYwc7mWpY8Ql8I_wIzkwZtWx4iuJc-_jq5elm2WuCz0mqC1IxPqsqUpwThkn9LDs-7Dw_fOPyKDuN8Q6nojXHOXuZHdGKlowTdpz9XmhtJMgt8hpZ-K7CYJxpkPYBxW3XD76DwUiUJDzWTQDjUKcGiOlRESU1BAVDp9zw68dPB2ajUJ_YpCO6N8MaQbsBJ1WLFtdXX1A3DunUuwT3Ppph4t1Oxg6sRVKllx3dCsnpVniPPgc_eOnt1Co45Hs10RYaZc9QNG5lVdIQOtSvU09ouUwtGbCvshcabFSnD-tJ9vVqcTv_OLv5dL2cX97MJKNFPeM14zmGmkOjKaMcq5pVXJagqC41IZyoos5ZW3JdS-CsZljRAuuScMVLSulJttz7th7uRB9MB2ErPBix2_BhJSCNV1olAFNapKKKtEXbFA2nuoKcQEl0rnOVvD7svfqx6VQr0xQD2CemT0-cWYuV3wiCKS-riieHdw8OwX8bVRxEZ-I0VHDKj1HkNcU5YRUhCX37D3rnx-DSrBJVFCk0ZGd4sadk8DEGpQ_dECymQIopcmKKn9gFMt148_gnDvzf-CWA7YF7Y9X2f37idn65N_4DH6zzng</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Lee, Bora</creator><creator>Ji, Wonjun</creator><creator>Lee, Jae Cheol</creator><creator>Song, Si Yeol</creator><creator>Shin, Young Seob</creator><creator>Cho, Young Hyun</creator><creator>Park, Ji Eun</creator><creator>Park, Hyungjun</creator><creator>Choi, Chang‐Min</creator><general>John Wiley & Sons Australia, Ltd</general><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><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><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7164-2770</orcidid><orcidid>https://orcid.org/0000-0002-2881-4669</orcidid><orcidid>https://orcid.org/0000-0003-1381-7506</orcidid><orcidid>https://orcid.org/0000-0002-5523-5144</orcidid></search><sort><creationdate>202308</creationdate><title>Efficacy of lazertinib for symptomatic or asymptomatic brain metastases in treatment‐naive patients with advanced EGFR mutation‐positive non‐small cell lung cancer: Protocol of an open‐label, single‐arm phase II trial</title><author>Lee, Bora ; Ji, Wonjun ; Lee, Jae Cheol ; Song, Si Yeol ; Shin, Young Seob ; Cho, Young Hyun ; Park, Ji Eun ; Park, Hyungjun ; Choi, Chang‐Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5348-985920a89abf35390e8579c6ae3f6f1191e4825d69f8ca95850e340f619e96333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Asymptomatic</topic><topic>Brain cancer</topic><topic>brain metastases</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - genetics</topic><topic>Cancer therapies</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Clinical Trials, Phase II as Topic</topic><topic>Decision trees</topic><topic>Effectiveness</topic><topic>epidermal growth factor receptor</topic><topic>ErbB Receptors</topic><topic>Humans</topic><topic>Informed consent</topic><topic>Intracranial pressure</topic><topic>lazertinib</topic><topic>Lung cancer</topic><topic>Lung diseases</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Magnetic resonance imaging</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Mutation</topic><topic>Nervous system</topic><topic>non‐small cell lung cancer</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Radiation therapy</topic><topic>Response rates</topic><topic>Study Protocol</topic><topic>Surgery</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Bora</creatorcontrib><creatorcontrib>Ji, Wonjun</creatorcontrib><creatorcontrib>Lee, Jae Cheol</creatorcontrib><creatorcontrib>Song, Si Yeol</creatorcontrib><creatorcontrib>Shin, Young Seob</creatorcontrib><creatorcontrib>Cho, Young Hyun</creatorcontrib><creatorcontrib>Park, Ji Eun</creatorcontrib><creatorcontrib>Park, Hyungjun</creatorcontrib><creatorcontrib>Choi, Chang‐Min</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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 (ProQuest)</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><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Thoracic cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Bora</au><au>Ji, Wonjun</au><au>Lee, Jae Cheol</au><au>Song, Si Yeol</au><au>Shin, Young Seob</au><au>Cho, Young Hyun</au><au>Park, Ji Eun</au><au>Park, Hyungjun</au><au>Choi, Chang‐Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of lazertinib for symptomatic or asymptomatic brain metastases in treatment‐naive patients with advanced EGFR mutation‐positive non‐small cell lung cancer: Protocol of an open‐label, single‐arm phase II trial</atitle><jtitle>Thoracic cancer</jtitle><addtitle>Thorac Cancer</addtitle><date>2023-08</date><risdate>2023</risdate><volume>14</volume><issue>22</issue><spage>2233</spage><epage>2237</epage><pages>2233-2237</pages><issn>1759-7706</issn><eissn>1759-7714</eissn><abstract>Introduction
Non‐small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutation has a higher incidence of brain metastases than wild‐type EGFR mutations. Osimertinib, a third‐generation EGFR tyrosine kinase inhibitor (TKI), targets both EGFR‐TKI sensitizing and T790M‐resistance mutations and has a higher brain penetration rate relative to first‐ and second‐generation EGFR‐TKIs. Therefore, osimertinib has become a preferred first‐line therapy for advanced EGFR mutation‐positive NSCLC. However, lazertinib, an emerging EGFR‐TKI, has shown higher selectivity toward EGFR mutations and improved penetration of the blood–brain barrier compared to osimertinib in preclinical studies. This trial will evaluate the efficacy of lazertinib as a first‐line therapy in patients with EGFR mutation‐positive NSCLC who have brain metastases, with or without additional local therapy.
Methods
This is a single‐center, open‐label, single‐arm phase II trial. A total of 75 patients with advanced EGFR mutation‐positive NSCLC will be recruited. Eligible patients will receive oral lazertinib 240 mg, once daily until disease progression or intolerable toxicity is detected. Patients with moderate to severe symptoms related to brain metastasis will simultaneously receive local therapy for the brain. The primary endpoints are progression‐free survival and intracranial progression‐free survival.
Discussion
Lazertinib, in combination with local therapy for the brain, if necessary, is expected to improve the clinical benefit in advanced EGFR mutation‐positive NSCLC with brain metastases, as a first‐line treatment.
Based on previous studies, the efficacy of lazertinib for brain metastasis is anticipated to be satisfactory in EGFR mutation‐positive NSCLC. This is the protocol for a single‐center, single‐arm phase II trial that will evaluate the efficacy of lazertinib with or without local therapy as a first‐line treatment of patients with EGFR mutation‐positive NSCLC, who also present with brain metastases.</abstract><cop>Melbourne</cop><pub>John Wiley & Sons Australia, Ltd</pub><pmid>37365915</pmid><doi>10.1111/1759-7714.15018</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-7164-2770</orcidid><orcidid>https://orcid.org/0000-0002-2881-4669</orcidid><orcidid>https://orcid.org/0000-0003-1381-7506</orcidid><orcidid>https://orcid.org/0000-0002-5523-5144</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Asymptomatic Brain cancer brain metastases Brain Neoplasms - drug therapy Brain Neoplasms - genetics Cancer therapies Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - pathology Clinical Trials, Phase II as Topic Decision trees Effectiveness epidermal growth factor receptor ErbB Receptors Humans Informed consent Intracranial pressure lazertinib Lung cancer Lung diseases Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - pathology Magnetic resonance imaging Medical prognosis Metastasis Mutation Nervous system non‐small cell lung cancer Protein Kinase Inhibitors - pharmacology Radiation therapy Response rates Study Protocol Surgery Tumors |
title | Efficacy of lazertinib for symptomatic or asymptomatic brain metastases in treatment‐naive patients with advanced EGFR mutation‐positive non‐small cell lung cancer: Protocol of an open‐label, single‐arm phase II trial |
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