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Brentuximab vedotin consolidation post-autologous stem cell transplant in Hodgkin lymphoma patients at risk of residual disease: number needed to treat
The number needed to treat (NNT) with brentuximab vedotin consolidation therapy post-autologous stem cell transplant (ASCT) versus placebo in the phase 3 AETHERA trial to avoid one additional event of disease progression/death was evaluated. AETHERA included 329 Hodgkin lymphoma patients at increase...
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Published in: | Leukemia & lymphoma 2018-01, Vol.59 (1), p.69-76 |
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creator | Gautam, Ashish Zhu, Yanyan Ma, Esprit Lee, Shih-Yuan Zagadailov, Erin Teasell, Jeremy Richhariya, Akshara Bonthapally, Vijayveer Huebner, Dirk |
description | The number needed to treat (NNT) with brentuximab vedotin consolidation therapy post-autologous stem cell transplant (ASCT) versus placebo in the phase 3 AETHERA trial to avoid one additional event of disease progression/death was evaluated. AETHERA included 329 Hodgkin lymphoma patients at increased risk of progression post-ASCT who received brentuximab vedotin 1.8 mg/kg (n = 165) or placebo (n = 164) on day 1 of each 21-d cycle (up to 16 cycles). Over 60 months, the NNT with brentuximab vedotin ranged from 4.08 to 7.79 for the intent-to-treat population, 3.18-6.07 for patients with ≥2 risk factors, and 2.98-5.65 for patients with ≥3 risk factors. At various time points, and dependent on the risk group, 3-8 patients would need to be treated with brentuximab vedotin consolidation therapy to prevent a disease progression/death, compared with placebo. Patients with increased risk of relapse may benefit most from brentuximab vedotin. |
doi_str_mv | 10.1080/10428194.2017.1324160 |
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AETHERA included 329 Hodgkin lymphoma patients at increased risk of progression post-ASCT who received brentuximab vedotin 1.8 mg/kg (n = 165) or placebo (n = 164) on day 1 of each 21-d cycle (up to 16 cycles). Over 60 months, the NNT with brentuximab vedotin ranged from 4.08 to 7.79 for the intent-to-treat population, 3.18-6.07 for patients with ≥2 risk factors, and 2.98-5.65 for patients with ≥3 risk factors. At various time points, and dependent on the risk group, 3-8 patients would need to be treated with brentuximab vedotin consolidation therapy to prevent a disease progression/death, compared with placebo. Patients with increased risk of relapse may benefit most from brentuximab vedotin.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/10428194.2017.1324160</identifier><identifier>PMID: 28583027</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Adolescent ; Adult ; Aged ; Antineoplastic Agents, Immunological - therapeutic use ; Brentuximab vedotin ; CD30 ; Combined Modality Therapy ; Consolidation Chemotherapy ; Disease Progression ; Female ; Hematopoietic Stem Cell Transplantation ; Hodgkin Disease - drug therapy ; Hodgkin Disease - mortality ; Hodgkin Disease - pathology ; Hodgkin lymphoma ; Humans ; Immunoconjugates - therapeutic use ; Intention to Treat Analysis ; Male ; Middle Aged ; Neoplasm, Residual - pathology ; numbers needed to treat ; Proportional Hazards Models ; Risk Factors ; Transplantation, Autologous ; Treatment Outcome ; Young Adult</subject><ispartof>Leukemia & lymphoma, 2018-01, Vol.59 (1), p.69-76</ispartof><rights>2017 Informa UK Limited, trading as Taylor & Francis Group 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c366t-d1c2db7739cbefa48d246412ae4f22341a7e256a2f19adfc5b37e24ecc68599d3</citedby><cites>FETCH-LOGICAL-c366t-d1c2db7739cbefa48d246412ae4f22341a7e256a2f19adfc5b37e24ecc68599d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28583027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gautam, Ashish</creatorcontrib><creatorcontrib>Zhu, Yanyan</creatorcontrib><creatorcontrib>Ma, Esprit</creatorcontrib><creatorcontrib>Lee, Shih-Yuan</creatorcontrib><creatorcontrib>Zagadailov, Erin</creatorcontrib><creatorcontrib>Teasell, Jeremy</creatorcontrib><creatorcontrib>Richhariya, Akshara</creatorcontrib><creatorcontrib>Bonthapally, Vijayveer</creatorcontrib><creatorcontrib>Huebner, Dirk</creatorcontrib><title>Brentuximab vedotin consolidation post-autologous stem cell transplant in Hodgkin lymphoma patients at risk of residual disease: number needed to treat</title><title>Leukemia & lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>The number needed to treat (NNT) with brentuximab vedotin consolidation therapy post-autologous stem cell transplant (ASCT) versus placebo in the phase 3 AETHERA trial to avoid one additional event of disease progression/death was evaluated. AETHERA included 329 Hodgkin lymphoma patients at increased risk of progression post-ASCT who received brentuximab vedotin 1.8 mg/kg (n = 165) or placebo (n = 164) on day 1 of each 21-d cycle (up to 16 cycles). Over 60 months, the NNT with brentuximab vedotin ranged from 4.08 to 7.79 for the intent-to-treat population, 3.18-6.07 for patients with ≥2 risk factors, and 2.98-5.65 for patients with ≥3 risk factors. At various time points, and dependent on the risk group, 3-8 patients would need to be treated with brentuximab vedotin consolidation therapy to prevent a disease progression/death, compared with placebo. Patients with increased risk of relapse may benefit most from brentuximab vedotin.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Brentuximab vedotin</subject><subject>CD30</subject><subject>Combined Modality Therapy</subject><subject>Consolidation Chemotherapy</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hodgkin Disease - drug therapy</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - pathology</subject><subject>Hodgkin lymphoma</subject><subject>Humans</subject><subject>Immunoconjugates - therapeutic use</subject><subject>Intention to Treat Analysis</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm, Residual - pathology</subject><subject>numbers needed to treat</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Transplantation, Autologous</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1TAQhiMEohd4BJCXbHLwLTdWQAUUqVI37dqa2JNi6tjBdgrnSfq6ODqnLFnNaPT__2jmq6o3jO4Y7el7RiXv2SB3nLJuxwSXrKXPqlNG-VBzScXzrZe83kQn1VlKPymlzdDyl9UJ75teUN6dVo-fI_q8_rEzjOQBTcjWEx18Cs4ayDZ4soSUa1hzcOEurImkjDPR6BzJEXxaHPhMiusymLv7Ut1-Xn6EGchS_CU8Ecgk2nRPwkQiJmtWcMTYhJDwA_HrPGIkHtGgITmUVIT8qnoxgUv4-ljPq9uvX24uLuur62_fLz5d1Vq0ba4N09yMXScGPeIEsjdctpJxQDlxLiSDDnnTAp_YAGbSzSjKQKLWbd8MgxHn1btD7hLDrxVTVrNN23HgsRyr2EBb2dGm74q0OUh1DClFnNQSy9viXjGqNibqiYnamKgjk-J7e1yxjjOaf64nCEXw8SCwfgpxht8hOqMy7F2IU3mxtkmJ_-_4C55jn24</recordid><startdate>20180102</startdate><enddate>20180102</enddate><creator>Gautam, Ashish</creator><creator>Zhu, Yanyan</creator><creator>Ma, Esprit</creator><creator>Lee, Shih-Yuan</creator><creator>Zagadailov, Erin</creator><creator>Teasell, Jeremy</creator><creator>Richhariya, Akshara</creator><creator>Bonthapally, Vijayveer</creator><creator>Huebner, Dirk</creator><general>Taylor & Francis</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></search><sort><creationdate>20180102</creationdate><title>Brentuximab vedotin consolidation post-autologous stem cell transplant in Hodgkin lymphoma patients at risk of residual disease: number needed to treat</title><author>Gautam, Ashish ; Zhu, Yanyan ; Ma, Esprit ; Lee, Shih-Yuan ; Zagadailov, Erin ; Teasell, Jeremy ; Richhariya, Akshara ; Bonthapally, Vijayveer ; Huebner, Dirk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-d1c2db7739cbefa48d246412ae4f22341a7e256a2f19adfc5b37e24ecc68599d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents, Immunological - therapeutic use</topic><topic>Brentuximab vedotin</topic><topic>CD30</topic><topic>Combined Modality Therapy</topic><topic>Consolidation Chemotherapy</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hodgkin Disease - drug therapy</topic><topic>Hodgkin Disease - mortality</topic><topic>Hodgkin Disease - pathology</topic><topic>Hodgkin lymphoma</topic><topic>Humans</topic><topic>Immunoconjugates - therapeutic use</topic><topic>Intention to Treat Analysis</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm, Residual - pathology</topic><topic>numbers needed to treat</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Transplantation, Autologous</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gautam, Ashish</creatorcontrib><creatorcontrib>Zhu, Yanyan</creatorcontrib><creatorcontrib>Ma, Esprit</creatorcontrib><creatorcontrib>Lee, Shih-Yuan</creatorcontrib><creatorcontrib>Zagadailov, Erin</creatorcontrib><creatorcontrib>Teasell, Jeremy</creatorcontrib><creatorcontrib>Richhariya, Akshara</creatorcontrib><creatorcontrib>Bonthapally, Vijayveer</creatorcontrib><creatorcontrib>Huebner, Dirk</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><jtitle>Leukemia & lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gautam, Ashish</au><au>Zhu, Yanyan</au><au>Ma, Esprit</au><au>Lee, Shih-Yuan</au><au>Zagadailov, Erin</au><au>Teasell, Jeremy</au><au>Richhariya, Akshara</au><au>Bonthapally, Vijayveer</au><au>Huebner, Dirk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brentuximab vedotin consolidation post-autologous stem cell transplant in Hodgkin lymphoma patients at risk of residual disease: number needed to treat</atitle><jtitle>Leukemia & lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2018-01-02</date><risdate>2018</risdate><volume>59</volume><issue>1</issue><spage>69</spage><epage>76</epage><pages>69-76</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>The number needed to treat (NNT) with brentuximab vedotin consolidation therapy post-autologous stem cell transplant (ASCT) versus placebo in the phase 3 AETHERA trial to avoid one additional event of disease progression/death was evaluated. 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subjects | Adolescent Adult Aged Antineoplastic Agents, Immunological - therapeutic use Brentuximab vedotin CD30 Combined Modality Therapy Consolidation Chemotherapy Disease Progression Female Hematopoietic Stem Cell Transplantation Hodgkin Disease - drug therapy Hodgkin Disease - mortality Hodgkin Disease - pathology Hodgkin lymphoma Humans Immunoconjugates - therapeutic use Intention to Treat Analysis Male Middle Aged Neoplasm, Residual - pathology numbers needed to treat Proportional Hazards Models Risk Factors Transplantation, Autologous Treatment Outcome Young Adult |
title | Brentuximab vedotin consolidation post-autologous stem cell transplant in Hodgkin lymphoma patients at risk of residual disease: number needed to treat |
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