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A phase 3, randomized study of ofatumumab combined with bendamustine in rituximab‐refractory iNHL (COMPLEMENT A + B study)
Summary The standard of care for indolent non‐Hodgkin lymphoma (iNHL) is rituximab, an anti‐CD20 antibody, with/without chemotherapy. However, multiple relapses are common in these patients. This phase 3, randomized study compared outcomes of a combination of ofatumumab (a second‐generation anti‐CD2...
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Published in: | British journal of haematology 2021-06, Vol.193 (6), p.1123-1133 |
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container_title | British journal of haematology |
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creator | Rummel, Mathias J. Janssens, Ann MacDonald, David Keating, Mary‐Margaret Zaucha, Jan M. Davis, Jaclyn Lasher, Janet Babanrao Pisal, Chaitali Izquierdo, Miguel Friedberg, Jonathan W. |
description | Summary
The standard of care for indolent non‐Hodgkin lymphoma (iNHL) is rituximab, an anti‐CD20 antibody, with/without chemotherapy. However, multiple relapses are common in these patients. This phase 3, randomized study compared outcomes of a combination of ofatumumab (a second‐generation anti‐CD20 antibody) and bendamustine, with bendamustine alone in patients unresponsive to prior rituximab‐based treatment. Overall, 346 patients were randomized to receive either the combination or bendamustine alone. Bendamustine was given for ≤8 cycles and ofatumumab for ≤12 cycles. The primary end‐point was progression‐free survival (PFS) after 215 protocol‐defined events assessed by independent review committee (IRC). Median IRC‐assessed PFS was 16·7 and 13·8 months in the combination and monotherapy arms respectively [hazard ratio (HR) = 0·82; P = 0·1390]. Median overall survival (OS) was 58·2 and 51·8 months in the combination and monotherapy arms respectively (HR = 0·89, P = 0·4968). The safety profile was consistent with previous reports. Overall, 73% and 80% of patients in the combination and monotherapy arms, respectively, experienced a ≥grade 3 adverse event. The study did not meet its primary end‐point. No significant improvement in PFS and OS was seen with the combination of ofatumumab and bendamustine as compared with bendamustine alone in rituximab‐refractory iNHL (NCT01077518). |
doi_str_mv | 10.1111/bjh.17420 |
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The standard of care for indolent non‐Hodgkin lymphoma (iNHL) is rituximab, an anti‐CD20 antibody, with/without chemotherapy. However, multiple relapses are common in these patients. This phase 3, randomized study compared outcomes of a combination of ofatumumab (a second‐generation anti‐CD20 antibody) and bendamustine, with bendamustine alone in patients unresponsive to prior rituximab‐based treatment. Overall, 346 patients were randomized to receive either the combination or bendamustine alone. Bendamustine was given for ≤8 cycles and ofatumumab for ≤12 cycles. The primary end‐point was progression‐free survival (PFS) after 215 protocol‐defined events assessed by independent review committee (IRC). Median IRC‐assessed PFS was 16·7 and 13·8 months in the combination and monotherapy arms respectively [hazard ratio (HR) = 0·82; P = 0·1390]. Median overall survival (OS) was 58·2 and 51·8 months in the combination and monotherapy arms respectively (HR = 0·89, P = 0·4968). The safety profile was consistent with previous reports. Overall, 73% and 80% of patients in the combination and monotherapy arms, respectively, experienced a ≥grade 3 adverse event. The study did not meet its primary end‐point. No significant improvement in PFS and OS was seen with the combination of ofatumumab and bendamustine as compared with bendamustine alone in rituximab‐refractory iNHL (NCT01077518).</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/bjh.17420</identifier><identifier>PMID: 33973233</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adverse events ; anti‐CD20 ; bendamustine ; CD20 antigen ; Chemotherapy ; Hematology ; Non-Hodgkin's lymphoma ; ofatumumab ; Rituximab ; rituximab‐refractory indolent non‐Hodgkin lymphoma ; Survival</subject><ispartof>British journal of haematology, 2021-06, Vol.193 (6), p.1123-1133</ispartof><rights>2021 The Authors. published by British Society for Haematology and John Wiley & Sons Ltd.</rights><rights>2021 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc/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-c3530-a647fddabe536ab2c5e483eda66e6f541b9bf0df2c0405d38ed4eeccc1f0997f3</citedby><cites>FETCH-LOGICAL-c3530-a647fddabe536ab2c5e483eda66e6f541b9bf0df2c0405d38ed4eeccc1f0997f3</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/33973233$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rummel, Mathias J.</creatorcontrib><creatorcontrib>Janssens, Ann</creatorcontrib><creatorcontrib>MacDonald, David</creatorcontrib><creatorcontrib>Keating, Mary‐Margaret</creatorcontrib><creatorcontrib>Zaucha, Jan M.</creatorcontrib><creatorcontrib>Davis, Jaclyn</creatorcontrib><creatorcontrib>Lasher, Janet</creatorcontrib><creatorcontrib>Babanrao Pisal, Chaitali</creatorcontrib><creatorcontrib>Izquierdo, Miguel</creatorcontrib><creatorcontrib>Friedberg, Jonathan W.</creatorcontrib><title>A phase 3, randomized study of ofatumumab combined with bendamustine in rituximab‐refractory iNHL (COMPLEMENT A + B study)</title><title>British journal of haematology</title><addtitle>Br J Haematol</addtitle><description>Summary
The standard of care for indolent non‐Hodgkin lymphoma (iNHL) is rituximab, an anti‐CD20 antibody, with/without chemotherapy. However, multiple relapses are common in these patients. This phase 3, randomized study compared outcomes of a combination of ofatumumab (a second‐generation anti‐CD20 antibody) and bendamustine, with bendamustine alone in patients unresponsive to prior rituximab‐based treatment. Overall, 346 patients were randomized to receive either the combination or bendamustine alone. Bendamustine was given for ≤8 cycles and ofatumumab for ≤12 cycles. The primary end‐point was progression‐free survival (PFS) after 215 protocol‐defined events assessed by independent review committee (IRC). Median IRC‐assessed PFS was 16·7 and 13·8 months in the combination and monotherapy arms respectively [hazard ratio (HR) = 0·82; P = 0·1390]. Median overall survival (OS) was 58·2 and 51·8 months in the combination and monotherapy arms respectively (HR = 0·89, P = 0·4968). The safety profile was consistent with previous reports. Overall, 73% and 80% of patients in the combination and monotherapy arms, respectively, experienced a ≥grade 3 adverse event. The study did not meet its primary end‐point. No significant improvement in PFS and OS was seen with the combination of ofatumumab and bendamustine as compared with bendamustine alone in rituximab‐refractory iNHL (NCT01077518).</description><subject>Adverse events</subject><subject>anti‐CD20</subject><subject>bendamustine</subject><subject>CD20 antigen</subject><subject>Chemotherapy</subject><subject>Hematology</subject><subject>Non-Hodgkin's lymphoma</subject><subject>ofatumumab</subject><subject>Rituximab</subject><subject>rituximab‐refractory indolent non‐Hodgkin lymphoma</subject><subject>Survival</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp1kc9OGzEQxq2KqgTooS9QWeICahfstb2bPYYobYoC9EDPK_8ZK46yu6m9Fg0HxCP0EXgWHqVPUpelPSB1NNJIMz99M6MPoXeUnNAUp2q1PKElz8krNKKsEFlOOd1BI0JImVHCx7toL4QVIZQRQd-gXcaqkuWMjdDdBG-WMgBmH7GXrekadwsGhz6aLe5sStnHJjZSYd01yrVpeOP6JVbQGtnE0KcWdi32ro8_XOJ-3f_0YL3Ufee32F3OF_hoenXxdTG7mF1e48njw4fHh7Nhw_EBem3lOsDb57qPvn2aXU_n2eLq85fpZJFpJhjJZMFLa4xUIFghVa4F8DEDI4sCCis4VZWyxNhcE06EYWMwHEBrTS2pqtKyfXQ06G589z1C6OvGBQ3rtWyhi6HORS4KwceUJ_TwBbrqom_TdYniNN3DqypRxwOlfRdCerje-PS939aU1H9MqZMp9ZMpiX3_rBhVA-Yf-deFBJwOwI1bw_b_SvXZ-XyQ_A3Em5f4</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Rummel, Mathias J.</creator><creator>Janssens, Ann</creator><creator>MacDonald, David</creator><creator>Keating, Mary‐Margaret</creator><creator>Zaucha, Jan M.</creator><creator>Davis, Jaclyn</creator><creator>Lasher, Janet</creator><creator>Babanrao Pisal, Chaitali</creator><creator>Izquierdo, Miguel</creator><creator>Friedberg, Jonathan W.</creator><general>Blackwell Publishing Ltd</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>202106</creationdate><title>A phase 3, randomized study of ofatumumab combined with bendamustine in rituximab‐refractory iNHL (COMPLEMENT A + B study)</title><author>Rummel, Mathias J. ; Janssens, Ann ; MacDonald, David ; Keating, Mary‐Margaret ; Zaucha, Jan M. ; Davis, Jaclyn ; Lasher, Janet ; Babanrao Pisal, Chaitali ; Izquierdo, Miguel ; Friedberg, Jonathan W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3530-a647fddabe536ab2c5e483eda66e6f541b9bf0df2c0405d38ed4eeccc1f0997f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adverse events</topic><topic>anti‐CD20</topic><topic>bendamustine</topic><topic>CD20 antigen</topic><topic>Chemotherapy</topic><topic>Hematology</topic><topic>Non-Hodgkin's lymphoma</topic><topic>ofatumumab</topic><topic>Rituximab</topic><topic>rituximab‐refractory indolent non‐Hodgkin lymphoma</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rummel, Mathias J.</creatorcontrib><creatorcontrib>Janssens, Ann</creatorcontrib><creatorcontrib>MacDonald, David</creatorcontrib><creatorcontrib>Keating, Mary‐Margaret</creatorcontrib><creatorcontrib>Zaucha, Jan M.</creatorcontrib><creatorcontrib>Davis, Jaclyn</creatorcontrib><creatorcontrib>Lasher, Janet</creatorcontrib><creatorcontrib>Babanrao Pisal, Chaitali</creatorcontrib><creatorcontrib>Izquierdo, Miguel</creatorcontrib><creatorcontrib>Friedberg, Jonathan W.</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rummel, Mathias J.</au><au>Janssens, Ann</au><au>MacDonald, David</au><au>Keating, Mary‐Margaret</au><au>Zaucha, Jan M.</au><au>Davis, Jaclyn</au><au>Lasher, Janet</au><au>Babanrao Pisal, Chaitali</au><au>Izquierdo, Miguel</au><au>Friedberg, Jonathan W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A phase 3, randomized study of ofatumumab combined with bendamustine in rituximab‐refractory iNHL (COMPLEMENT A + B study)</atitle><jtitle>British journal of haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2021-06</date><risdate>2021</risdate><volume>193</volume><issue>6</issue><spage>1123</spage><epage>1133</epage><pages>1123-1133</pages><issn>0007-1048</issn><eissn>1365-2141</eissn><abstract>Summary
The standard of care for indolent non‐Hodgkin lymphoma (iNHL) is rituximab, an anti‐CD20 antibody, with/without chemotherapy. However, multiple relapses are common in these patients. This phase 3, randomized study compared outcomes of a combination of ofatumumab (a second‐generation anti‐CD20 antibody) and bendamustine, with bendamustine alone in patients unresponsive to prior rituximab‐based treatment. Overall, 346 patients were randomized to receive either the combination or bendamustine alone. Bendamustine was given for ≤8 cycles and ofatumumab for ≤12 cycles. The primary end‐point was progression‐free survival (PFS) after 215 protocol‐defined events assessed by independent review committee (IRC). Median IRC‐assessed PFS was 16·7 and 13·8 months in the combination and monotherapy arms respectively [hazard ratio (HR) = 0·82; P = 0·1390]. Median overall survival (OS) was 58·2 and 51·8 months in the combination and monotherapy arms respectively (HR = 0·89, P = 0·4968). The safety profile was consistent with previous reports. Overall, 73% and 80% of patients in the combination and monotherapy arms, respectively, experienced a ≥grade 3 adverse event. The study did not meet its primary end‐point. No significant improvement in PFS and OS was seen with the combination of ofatumumab and bendamustine as compared with bendamustine alone in rituximab‐refractory iNHL (NCT01077518).</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>33973233</pmid><doi>10.1111/bjh.17420</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adverse events anti‐CD20 bendamustine CD20 antigen Chemotherapy Hematology Non-Hodgkin's lymphoma ofatumumab Rituximab rituximab‐refractory indolent non‐Hodgkin lymphoma Survival |
title | A phase 3, randomized study of ofatumumab combined with bendamustine in rituximab‐refractory iNHL (COMPLEMENT A + B study) |
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