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Trastuzumab Deruxtecan in HER2-Positive Metastatic Breast Cancer Patients with Brain Metastases: A DESTINY-Breast01 Subgroup Analysis
DESTINY-Breast01 (NCT03248492) evaluated trastuzumab deruxtecan (T-DXd; DS-8201) in patients with heavily pretreated HER2-positive metastatic breast cancer (mBC). We present a subgroup of 24 patients with a history of treated brain metastases (BM), a population with limited treatment options. In pat...
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Published in: | Cancer discovery 2022-12, Vol.12 (12), p.2754-2762 |
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creator | Jerusalem, Guy Park, Yeon Hee Yamashita, Toshinari Hurvitz, Sara A Modi, Shanu Andre, Fabrice Krop, Ian E Gonzàlez Farré, Xavier You, Benoit Saura, Cristina Kim, Sung-Bae Osborne, Cynthia R Murthy, Rashmi K Gianni, Lorenzo Takano, Toshimi Liu, Yali Cathcart, Jillian Lee, Caleb Perrin, Christophe |
description | DESTINY-Breast01 (NCT03248492) evaluated trastuzumab deruxtecan (T-DXd; DS-8201) in patients with heavily pretreated HER2-positive metastatic breast cancer (mBC). We present a subgroup of 24 patients with a history of treated brain metastases (BM), a population with limited treatment options. In patients with BMs, the confirmed objective response rate (cORR) was 58.3% [95% confidence interval (CI), 36.6%-77.9%], and the median progression-free survival (mPFS) was 18.1 months (95% CI, 6.7-18.1 months). In patients without BMs (n = 160), cORR was 61.3% and mPFS was 16.4 months. Eight patients (47.1%) experienced a best overall intracranial response of partial response or complete response. Seven patients (41.2%) had a best percentage change in brain lesion diameter from baseline consistent with stable disease. Two patients (8.3%) with BMs and two (1.3%) without BMs experienced progression in the brain. The safety profile of T-DXd was consistent with previous studies. The durable clinical activity of T-DXd in this population warrants further investigation.
Advances in treating HER2-positive metastatic breast cancer have greatly improved patient outcomes, but intracranial progression remains an important risk for which few therapeutic options are currently available. T-DXd demonstrated durable efficacy in patients with stable, treated BMs. This article is highlighted in the In This Issue feature, p. 2711. |
doi_str_mv | 10.1158/2159-8290.CD-22-0837 |
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Advances in treating HER2-positive metastatic breast cancer have greatly improved patient outcomes, but intracranial progression remains an important risk for which few therapeutic options are currently available. T-DXd demonstrated durable efficacy in patients with stable, treated BMs. This article is highlighted in the In This Issue feature, p. 2711.</description><identifier>ISSN: 2159-8274</identifier><identifier>ISSN: 2159-8290</identifier><identifier>EISSN: 2159-8290</identifier><identifier>DOI: 10.1158/2159-8290.CD-22-0837</identifier><identifier>PMID: 36255231</identifier><language>eng</language><publisher>United States: American Association for Cancer Research Inc</publisher><subject>Brain Neoplasms ; Brain Neoplasms - drug therapy ; Brain Neoplasms - secondary ; Breast Neoplasms ; Breast Neoplasms - pathology ; Camptothecin ; Camptothecin - therapeutic use ; Female ; Human health sciences ; Humans ; Immunoconjugates ; Immunoconjugates - therapeutic use ; Oncologie ; Oncology ; Receptor, ErbB-2 ; Research Briefs ; Sciences de la santé humaine ; Trastuzumab ; Trastuzumab - therapeutic use ; trastuzumab deruxtecan</subject><ispartof>Cancer discovery, 2022-12, Vol.12 (12), p.2754-2762</ispartof><rights>2022 The Authors; Published by the American Association for Cancer Research.</rights><rights>2022 The Authors; Published by the American Association for Cancer Research 2022 American Association for Cancer Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-2e1ade0ea87f96662b25925c0f032d7525c2e74bab748a4c169945541f36bef73</citedby><cites>FETCH-LOGICAL-c503t-2e1ade0ea87f96662b25925c0f032d7525c2e74bab748a4c169945541f36bef73</cites><orcidid>0000-0002-6630-4221 ; 0000-0002-5797-7037 ; 0000-0002-6380-5944 ; 0000-0002-2989-5296 ; 0000-0002-3177-8857 ; 0000-0002-2618-0180 ; 0000-0002-8417-5291 ; 0000-0003-4156-9212 ; 0000-0001-5588-8332 ; 0000-0001-8230-2544 ; 0000-0001-8040-4985 ; 0000-0002-8845-0043 ; 0000-0002-0103-4718 ; 0000-0001-7808-7191 ; 0000-0001-5795-8357 ; 0000-0001-6427-7373 ; 0000-0003-2125-3755 ; 0000-0001-8296-5065</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36255231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jerusalem, Guy</creatorcontrib><creatorcontrib>Park, Yeon Hee</creatorcontrib><creatorcontrib>Yamashita, Toshinari</creatorcontrib><creatorcontrib>Hurvitz, Sara A</creatorcontrib><creatorcontrib>Modi, Shanu</creatorcontrib><creatorcontrib>Andre, Fabrice</creatorcontrib><creatorcontrib>Krop, Ian E</creatorcontrib><creatorcontrib>Gonzàlez Farré, Xavier</creatorcontrib><creatorcontrib>You, Benoit</creatorcontrib><creatorcontrib>Saura, Cristina</creatorcontrib><creatorcontrib>Kim, Sung-Bae</creatorcontrib><creatorcontrib>Osborne, Cynthia R</creatorcontrib><creatorcontrib>Murthy, Rashmi K</creatorcontrib><creatorcontrib>Gianni, Lorenzo</creatorcontrib><creatorcontrib>Takano, Toshimi</creatorcontrib><creatorcontrib>Liu, Yali</creatorcontrib><creatorcontrib>Cathcart, Jillian</creatorcontrib><creatorcontrib>Lee, Caleb</creatorcontrib><creatorcontrib>Perrin, Christophe</creatorcontrib><title>Trastuzumab Deruxtecan in HER2-Positive Metastatic Breast Cancer Patients with Brain Metastases: A DESTINY-Breast01 Subgroup Analysis</title><title>Cancer discovery</title><addtitle>Cancer Discov</addtitle><description>DESTINY-Breast01 (NCT03248492) evaluated trastuzumab deruxtecan (T-DXd; DS-8201) in patients with heavily pretreated HER2-positive metastatic breast cancer (mBC). We present a subgroup of 24 patients with a history of treated brain metastases (BM), a population with limited treatment options. In patients with BMs, the confirmed objective response rate (cORR) was 58.3% [95% confidence interval (CI), 36.6%-77.9%], and the median progression-free survival (mPFS) was 18.1 months (95% CI, 6.7-18.1 months). In patients without BMs (n = 160), cORR was 61.3% and mPFS was 16.4 months. Eight patients (47.1%) experienced a best overall intracranial response of partial response or complete response. Seven patients (41.2%) had a best percentage change in brain lesion diameter from baseline consistent with stable disease. Two patients (8.3%) with BMs and two (1.3%) without BMs experienced progression in the brain. The safety profile of T-DXd was consistent with previous studies. The durable clinical activity of T-DXd in this population warrants further investigation.
Advances in treating HER2-positive metastatic breast cancer have greatly improved patient outcomes, but intracranial progression remains an important risk for which few therapeutic options are currently available. T-DXd demonstrated durable efficacy in patients with stable, treated BMs. This article is highlighted in the In This Issue feature, p. 2711.</description><subject>Brain Neoplasms</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - secondary</subject><subject>Breast Neoplasms</subject><subject>Breast Neoplasms - pathology</subject><subject>Camptothecin</subject><subject>Camptothecin - therapeutic use</subject><subject>Female</subject><subject>Human health sciences</subject><subject>Humans</subject><subject>Immunoconjugates</subject><subject>Immunoconjugates - therapeutic use</subject><subject>Oncologie</subject><subject>Oncology</subject><subject>Receptor, ErbB-2</subject><subject>Research Briefs</subject><subject>Sciences de la santé humaine</subject><subject>Trastuzumab</subject><subject>Trastuzumab - therapeutic use</subject><subject>trastuzumab deruxtecan</subject><issn>2159-8274</issn><issn>2159-8290</issn><issn>2159-8290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVUcFuEzEQXSEQrUr_ACEfuWxrj-31LgeksElppVIqGg6cLK8zmxptdoPtDZQ7_43TpBH44qeZ997M6GXZa0bPGJPlOTBZ5SVU9Kye5gA5Lbl6lh0fys8PWImj7DSE7zQ9UQlJ1cvsiBcgJXB2nP2ZexPi-HtcmYZM0Y-_IlrTE9eTy9kXyG-H4KLbIPmEMRFNdJZ88JggqU1v0ZPbVMM-BvLTxfvUM0m6JwcM78iETGd386ubb_lORxm5G5ulH8Y1mfSmewguvMpetKYLeLr_T7KvF7N5fZlff_54VU-ucyspjzkgMwukaErVVkVRQAOyAmlpSzkslEwQUInGNEqURlhWVOliKVjLiwZbxU-y9zvf9discGHT3t50eu3dyvgHPRin_-_07l4vh42uFCtAiGTAdwadwyXqwTdOb-BR-IjHbqmN1Q1qgKLUnFLGq6R6ux_rhx8jhqhXLljsOtPjMAYNCmQhuSxloood1fohBI_tYTlG9TZ6vc1VbzPW9TRN0dvok-zNv4cdRE9B879VoaqC</recordid><startdate>20221202</startdate><enddate>20221202</enddate><creator>Jerusalem, Guy</creator><creator>Park, Yeon Hee</creator><creator>Yamashita, Toshinari</creator><creator>Hurvitz, Sara A</creator><creator>Modi, Shanu</creator><creator>Andre, Fabrice</creator><creator>Krop, Ian E</creator><creator>Gonzàlez Farré, Xavier</creator><creator>You, Benoit</creator><creator>Saura, Cristina</creator><creator>Kim, Sung-Bae</creator><creator>Osborne, Cynthia R</creator><creator>Murthy, Rashmi K</creator><creator>Gianni, Lorenzo</creator><creator>Takano, Toshimi</creator><creator>Liu, Yali</creator><creator>Cathcart, Jillian</creator><creator>Lee, Caleb</creator><creator>Perrin, Christophe</creator><general>American Association for Cancer Research Inc</general><general>American Association for Cancer Research</general><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>7X8</scope><scope>Q33</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6630-4221</orcidid><orcidid>https://orcid.org/0000-0002-5797-7037</orcidid><orcidid>https://orcid.org/0000-0002-6380-5944</orcidid><orcidid>https://orcid.org/0000-0002-2989-5296</orcidid><orcidid>https://orcid.org/0000-0002-3177-8857</orcidid><orcidid>https://orcid.org/0000-0002-2618-0180</orcidid><orcidid>https://orcid.org/0000-0002-8417-5291</orcidid><orcidid>https://orcid.org/0000-0003-4156-9212</orcidid><orcidid>https://orcid.org/0000-0001-5588-8332</orcidid><orcidid>https://orcid.org/0000-0001-8230-2544</orcidid><orcidid>https://orcid.org/0000-0001-8040-4985</orcidid><orcidid>https://orcid.org/0000-0002-8845-0043</orcidid><orcidid>https://orcid.org/0000-0002-0103-4718</orcidid><orcidid>https://orcid.org/0000-0001-7808-7191</orcidid><orcidid>https://orcid.org/0000-0001-5795-8357</orcidid><orcidid>https://orcid.org/0000-0001-6427-7373</orcidid><orcidid>https://orcid.org/0000-0003-2125-3755</orcidid><orcidid>https://orcid.org/0000-0001-8296-5065</orcidid></search><sort><creationdate>20221202</creationdate><title>Trastuzumab Deruxtecan in HER2-Positive Metastatic Breast Cancer Patients with Brain Metastases: A DESTINY-Breast01 Subgroup Analysis</title><author>Jerusalem, Guy ; Park, Yeon Hee ; Yamashita, Toshinari ; Hurvitz, Sara A ; Modi, Shanu ; Andre, Fabrice ; Krop, Ian E ; Gonzàlez Farré, Xavier ; You, Benoit ; Saura, Cristina ; Kim, Sung-Bae ; Osborne, Cynthia R ; Murthy, Rashmi K ; Gianni, Lorenzo ; Takano, Toshimi ; Liu, Yali ; Cathcart, Jillian ; Lee, Caleb ; Perrin, Christophe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-2e1ade0ea87f96662b25925c0f032d7525c2e74bab748a4c169945541f36bef73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Brain Neoplasms</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - secondary</topic><topic>Breast Neoplasms</topic><topic>Breast Neoplasms - pathology</topic><topic>Camptothecin</topic><topic>Camptothecin - therapeutic use</topic><topic>Female</topic><topic>Human health sciences</topic><topic>Humans</topic><topic>Immunoconjugates</topic><topic>Immunoconjugates - therapeutic use</topic><topic>Oncologie</topic><topic>Oncology</topic><topic>Receptor, ErbB-2</topic><topic>Research Briefs</topic><topic>Sciences de la santé humaine</topic><topic>Trastuzumab</topic><topic>Trastuzumab - therapeutic use</topic><topic>trastuzumab deruxtecan</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jerusalem, Guy</creatorcontrib><creatorcontrib>Park, Yeon Hee</creatorcontrib><creatorcontrib>Yamashita, Toshinari</creatorcontrib><creatorcontrib>Hurvitz, Sara A</creatorcontrib><creatorcontrib>Modi, Shanu</creatorcontrib><creatorcontrib>Andre, Fabrice</creatorcontrib><creatorcontrib>Krop, Ian E</creatorcontrib><creatorcontrib>Gonzàlez Farré, Xavier</creatorcontrib><creatorcontrib>You, Benoit</creatorcontrib><creatorcontrib>Saura, Cristina</creatorcontrib><creatorcontrib>Kim, Sung-Bae</creatorcontrib><creatorcontrib>Osborne, Cynthia R</creatorcontrib><creatorcontrib>Murthy, Rashmi K</creatorcontrib><creatorcontrib>Gianni, Lorenzo</creatorcontrib><creatorcontrib>Takano, Toshimi</creatorcontrib><creatorcontrib>Liu, Yali</creatorcontrib><creatorcontrib>Cathcart, Jillian</creatorcontrib><creatorcontrib>Lee, Caleb</creatorcontrib><creatorcontrib>Perrin, Christophe</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Université de Liège - Open Repository and Bibliography (ORBI)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer discovery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jerusalem, Guy</au><au>Park, Yeon Hee</au><au>Yamashita, Toshinari</au><au>Hurvitz, Sara A</au><au>Modi, Shanu</au><au>Andre, Fabrice</au><au>Krop, Ian E</au><au>Gonzàlez Farré, Xavier</au><au>You, Benoit</au><au>Saura, Cristina</au><au>Kim, Sung-Bae</au><au>Osborne, Cynthia R</au><au>Murthy, Rashmi K</au><au>Gianni, Lorenzo</au><au>Takano, Toshimi</au><au>Liu, Yali</au><au>Cathcart, Jillian</au><au>Lee, Caleb</au><au>Perrin, Christophe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trastuzumab Deruxtecan in HER2-Positive Metastatic Breast Cancer Patients with Brain Metastases: A DESTINY-Breast01 Subgroup Analysis</atitle><jtitle>Cancer discovery</jtitle><addtitle>Cancer Discov</addtitle><date>2022-12-02</date><risdate>2022</risdate><volume>12</volume><issue>12</issue><spage>2754</spage><epage>2762</epage><pages>2754-2762</pages><issn>2159-8274</issn><issn>2159-8290</issn><eissn>2159-8290</eissn><abstract>DESTINY-Breast01 (NCT03248492) evaluated trastuzumab deruxtecan (T-DXd; DS-8201) in patients with heavily pretreated HER2-positive metastatic breast cancer (mBC). We present a subgroup of 24 patients with a history of treated brain metastases (BM), a population with limited treatment options. In patients with BMs, the confirmed objective response rate (cORR) was 58.3% [95% confidence interval (CI), 36.6%-77.9%], and the median progression-free survival (mPFS) was 18.1 months (95% CI, 6.7-18.1 months). In patients without BMs (n = 160), cORR was 61.3% and mPFS was 16.4 months. Eight patients (47.1%) experienced a best overall intracranial response of partial response or complete response. Seven patients (41.2%) had a best percentage change in brain lesion diameter from baseline consistent with stable disease. Two patients (8.3%) with BMs and two (1.3%) without BMs experienced progression in the brain. The safety profile of T-DXd was consistent with previous studies. The durable clinical activity of T-DXd in this population warrants further investigation.
Advances in treating HER2-positive metastatic breast cancer have greatly improved patient outcomes, but intracranial progression remains an important risk for which few therapeutic options are currently available. T-DXd demonstrated durable efficacy in patients with stable, treated BMs. This article is highlighted in the In This Issue feature, p. 2711.</abstract><cop>United States</cop><pub>American Association for Cancer Research Inc</pub><pmid>36255231</pmid><doi>10.1158/2159-8290.CD-22-0837</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6630-4221</orcidid><orcidid>https://orcid.org/0000-0002-5797-7037</orcidid><orcidid>https://orcid.org/0000-0002-6380-5944</orcidid><orcidid>https://orcid.org/0000-0002-2989-5296</orcidid><orcidid>https://orcid.org/0000-0002-3177-8857</orcidid><orcidid>https://orcid.org/0000-0002-2618-0180</orcidid><orcidid>https://orcid.org/0000-0002-8417-5291</orcidid><orcidid>https://orcid.org/0000-0003-4156-9212</orcidid><orcidid>https://orcid.org/0000-0001-5588-8332</orcidid><orcidid>https://orcid.org/0000-0001-8230-2544</orcidid><orcidid>https://orcid.org/0000-0001-8040-4985</orcidid><orcidid>https://orcid.org/0000-0002-8845-0043</orcidid><orcidid>https://orcid.org/0000-0002-0103-4718</orcidid><orcidid>https://orcid.org/0000-0001-7808-7191</orcidid><orcidid>https://orcid.org/0000-0001-5795-8357</orcidid><orcidid>https://orcid.org/0000-0001-6427-7373</orcidid><orcidid>https://orcid.org/0000-0003-2125-3755</orcidid><orcidid>https://orcid.org/0000-0001-8296-5065</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Brain Neoplasms Brain Neoplasms - drug therapy Brain Neoplasms - secondary Breast Neoplasms Breast Neoplasms - pathology Camptothecin Camptothecin - therapeutic use Female Human health sciences Humans Immunoconjugates Immunoconjugates - therapeutic use Oncologie Oncology Receptor, ErbB-2 Research Briefs Sciences de la santé humaine Trastuzumab Trastuzumab - therapeutic use trastuzumab deruxtecan |
title | Trastuzumab Deruxtecan in HER2-Positive Metastatic Breast Cancer Patients with Brain Metastases: A DESTINY-Breast01 Subgroup Analysis |
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