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Targeting complete response with upfront bortezomib consolidation versus observation after the achievement of complete response following autologous transplantation for multiple myeloma (TUBA study)
Complete response (CR) after treatment for multiple myeloma is associated with superior progression‐free survival (PFS). Multiple myeloma patients were prospectively recruited for induction treatment with bortezomib and dexamethasone (BD) followed by autologous hematopoietic cell transplantation (au...
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Published in: | Hematological oncology 2018-02, Vol.36 (1), p.202-209 |
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creator | Nakasone, Hideki Terasako‐Saito, Kiriko Hirano, Teiichi Wake, Atsushi Shimizu, Seiichi Kurita, Naoki Yamazaki, Etsuko Usuki, Kensuke Akazawa, Kohei Kanda, Junya Minauchi, Koichiro Yamamoto, Go Tanimoto, Shiori Kamoshita, Masaharu Yokoyama, Yasuhisa Miyaoka, Etsuo Ota, Shuichi Kako, Shinichi Izutsu, Koji Kanda, Yoshinobu |
description | Complete response (CR) after treatment for multiple myeloma is associated with superior progression‐free survival (PFS). Multiple myeloma patients were prospectively recruited for induction treatment with bortezomib and dexamethasone (BD) followed by autologous hematopoietic cell transplantation (auto‐HCT) between 2010 and 2012. If patients did not achieve CR after auto‐HCT, BD consolidation therapy was added to target CR.
After the BD induction phase (n = 46), greater than or equal to CR was achieved in 4 patients (8%). After auto‐HCT (n = 34), greater than or equal to CR was achieved in 9 patients (20%) and very good partial response (VGPR) was achieved in 11 (24%). Of the 24 patients who received auto‐HCT and whose response was less than CR, 21 received BD consolidation therapy for a median of 4 courses. Finally, the maximum response with or without BD consolidation was greater than or equal to CR in 19 (41%), VGPR in 7 (15%), and PR in 6 (13%). Through BD consolidation, CR was achieved in 8 of 11 patients with post‐HCT VGPR and in 2 of 12 patients with post‐HCT PR.
In total, 4 year PFS and overall survival were 43 and 80%, respectively. After adjusting for clinical factors, there was no difference in PFS between CR patients after auto‐HCT and BD consolidation, while patients with less than or equal to VGPR after consolidation had a significantly lower PFS.
Patients with post‐HCT CR showed good PFS, and targeting CR through BD consolidation could improve the CR rate. It would be worthwhile to prospectively compare the efficacy of consolidation only for patients who failed to achieve CR to a universal consolidation strategy. |
doi_str_mv | 10.1002/hon.2452 |
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After the BD induction phase (n = 46), greater than or equal to CR was achieved in 4 patients (8%). After auto‐HCT (n = 34), greater than or equal to CR was achieved in 9 patients (20%) and very good partial response (VGPR) was achieved in 11 (24%). Of the 24 patients who received auto‐HCT and whose response was less than CR, 21 received BD consolidation therapy for a median of 4 courses. Finally, the maximum response with or without BD consolidation was greater than or equal to CR in 19 (41%), VGPR in 7 (15%), and PR in 6 (13%). Through BD consolidation, CR was achieved in 8 of 11 patients with post‐HCT VGPR and in 2 of 12 patients with post‐HCT PR.
In total, 4 year PFS and overall survival were 43 and 80%, respectively. After adjusting for clinical factors, there was no difference in PFS between CR patients after auto‐HCT and BD consolidation, while patients with less than or equal to VGPR after consolidation had a significantly lower PFS.
Patients with post‐HCT CR showed good PFS, and targeting CR through BD consolidation could improve the CR rate. It would be worthwhile to prospectively compare the efficacy of consolidation only for patients who failed to achieve CR to a universal consolidation strategy.</description><identifier>ISSN: 0278-0232</identifier><identifier>EISSN: 1099-1069</identifier><identifier>DOI: 10.1002/hon.2452</identifier><identifier>PMID: 28681529</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Autografts ; autologous hematopoietic cell transplantation ; Bortezomib ; Bortezomib - therapeutic use ; Consolidation ; Consolidation Chemotherapy ; Dexamethasone ; Female ; Humans ; Male ; Middle Aged ; Multiple myeloma ; Multiple Myeloma - surgery ; Multiple Myeloma - therapy ; Patients ; Stem cell transplantation ; Survival ; Targeted cancer therapy ; targeting complete response ; Therapy ; Transplantation ; Transplantation, Autologous ; Treatment Outcome</subject><ispartof>Hematological oncology, 2018-02, Vol.36 (1), p.202-209</ispartof><rights>Copyright © 2017 John Wiley & Sons, Ltd.</rights><rights>Copyright © 2018 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3492-a1287f6f9735f11902fc2a4302cd5e90f1852a59703b429aac9f81876ef0ea693</citedby><cites>FETCH-LOGICAL-c3492-a1287f6f9735f11902fc2a4302cd5e90f1852a59703b429aac9f81876ef0ea693</cites><orcidid>0000-0001-5812-9315</orcidid></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/28681529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakasone, Hideki</creatorcontrib><creatorcontrib>Terasako‐Saito, Kiriko</creatorcontrib><creatorcontrib>Hirano, Teiichi</creatorcontrib><creatorcontrib>Wake, Atsushi</creatorcontrib><creatorcontrib>Shimizu, Seiichi</creatorcontrib><creatorcontrib>Kurita, Naoki</creatorcontrib><creatorcontrib>Yamazaki, Etsuko</creatorcontrib><creatorcontrib>Usuki, Kensuke</creatorcontrib><creatorcontrib>Akazawa, Kohei</creatorcontrib><creatorcontrib>Kanda, Junya</creatorcontrib><creatorcontrib>Minauchi, Koichiro</creatorcontrib><creatorcontrib>Yamamoto, Go</creatorcontrib><creatorcontrib>Tanimoto, Shiori</creatorcontrib><creatorcontrib>Kamoshita, Masaharu</creatorcontrib><creatorcontrib>Yokoyama, Yasuhisa</creatorcontrib><creatorcontrib>Miyaoka, Etsuo</creatorcontrib><creatorcontrib>Ota, Shuichi</creatorcontrib><creatorcontrib>Kako, Shinichi</creatorcontrib><creatorcontrib>Izutsu, Koji</creatorcontrib><creatorcontrib>Kanda, Yoshinobu</creatorcontrib><title>Targeting complete response with upfront bortezomib consolidation versus observation after the achievement of complete response following autologous transplantation for multiple myeloma (TUBA study)</title><title>Hematological oncology</title><addtitle>Hematol Oncol</addtitle><description>Complete response (CR) after treatment for multiple myeloma is associated with superior progression‐free survival (PFS). Multiple myeloma patients were prospectively recruited for induction treatment with bortezomib and dexamethasone (BD) followed by autologous hematopoietic cell transplantation (auto‐HCT) between 2010 and 2012. If patients did not achieve CR after auto‐HCT, BD consolidation therapy was added to target CR.
After the BD induction phase (n = 46), greater than or equal to CR was achieved in 4 patients (8%). After auto‐HCT (n = 34), greater than or equal to CR was achieved in 9 patients (20%) and very good partial response (VGPR) was achieved in 11 (24%). Of the 24 patients who received auto‐HCT and whose response was less than CR, 21 received BD consolidation therapy for a median of 4 courses. Finally, the maximum response with or without BD consolidation was greater than or equal to CR in 19 (41%), VGPR in 7 (15%), and PR in 6 (13%). Through BD consolidation, CR was achieved in 8 of 11 patients with post‐HCT VGPR and in 2 of 12 patients with post‐HCT PR.
In total, 4 year PFS and overall survival were 43 and 80%, respectively. After adjusting for clinical factors, there was no difference in PFS between CR patients after auto‐HCT and BD consolidation, while patients with less than or equal to VGPR after consolidation had a significantly lower PFS.
Patients with post‐HCT CR showed good PFS, and targeting CR through BD consolidation could improve the CR rate. 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pharmacology</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Autografts</topic><topic>autologous hematopoietic cell transplantation</topic><topic>Bortezomib</topic><topic>Bortezomib - therapeutic use</topic><topic>Consolidation</topic><topic>Consolidation Chemotherapy</topic><topic>Dexamethasone</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multiple myeloma</topic><topic>Multiple Myeloma - surgery</topic><topic>Multiple Myeloma - therapy</topic><topic>Patients</topic><topic>Stem cell transplantation</topic><topic>Survival</topic><topic>Targeted cancer therapy</topic><topic>targeting complete response</topic><topic>Therapy</topic><topic>Transplantation</topic><topic>Transplantation, Autologous</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakasone, Hideki</creatorcontrib><creatorcontrib>Terasako‐Saito, Kiriko</creatorcontrib><creatorcontrib>Hirano, Teiichi</creatorcontrib><creatorcontrib>Wake, Atsushi</creatorcontrib><creatorcontrib>Shimizu, Seiichi</creatorcontrib><creatorcontrib>Kurita, Naoki</creatorcontrib><creatorcontrib>Yamazaki, Etsuko</creatorcontrib><creatorcontrib>Usuki, Kensuke</creatorcontrib><creatorcontrib>Akazawa, Kohei</creatorcontrib><creatorcontrib>Kanda, Junya</creatorcontrib><creatorcontrib>Minauchi, Koichiro</creatorcontrib><creatorcontrib>Yamamoto, Go</creatorcontrib><creatorcontrib>Tanimoto, Shiori</creatorcontrib><creatorcontrib>Kamoshita, Masaharu</creatorcontrib><creatorcontrib>Yokoyama, Yasuhisa</creatorcontrib><creatorcontrib>Miyaoka, Etsuo</creatorcontrib><creatorcontrib>Ota, Shuichi</creatorcontrib><creatorcontrib>Kako, Shinichi</creatorcontrib><creatorcontrib>Izutsu, Koji</creatorcontrib><creatorcontrib>Kanda, Yoshinobu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Hematological oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakasone, Hideki</au><au>Terasako‐Saito, Kiriko</au><au>Hirano, Teiichi</au><au>Wake, Atsushi</au><au>Shimizu, Seiichi</au><au>Kurita, Naoki</au><au>Yamazaki, Etsuko</au><au>Usuki, Kensuke</au><au>Akazawa, Kohei</au><au>Kanda, Junya</au><au>Minauchi, Koichiro</au><au>Yamamoto, Go</au><au>Tanimoto, Shiori</au><au>Kamoshita, Masaharu</au><au>Yokoyama, Yasuhisa</au><au>Miyaoka, Etsuo</au><au>Ota, Shuichi</au><au>Kako, Shinichi</au><au>Izutsu, Koji</au><au>Kanda, Yoshinobu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting complete response with upfront bortezomib consolidation versus observation after the achievement of complete response following autologous transplantation for multiple myeloma (TUBA study)</atitle><jtitle>Hematological oncology</jtitle><addtitle>Hematol Oncol</addtitle><date>2018-02</date><risdate>2018</risdate><volume>36</volume><issue>1</issue><spage>202</spage><epage>209</epage><pages>202-209</pages><issn>0278-0232</issn><eissn>1099-1069</eissn><abstract>Complete response (CR) after treatment for multiple myeloma is associated with superior progression‐free survival (PFS). Multiple myeloma patients were prospectively recruited for induction treatment with bortezomib and dexamethasone (BD) followed by autologous hematopoietic cell transplantation (auto‐HCT) between 2010 and 2012. If patients did not achieve CR after auto‐HCT, BD consolidation therapy was added to target CR.
After the BD induction phase (n = 46), greater than or equal to CR was achieved in 4 patients (8%). After auto‐HCT (n = 34), greater than or equal to CR was achieved in 9 patients (20%) and very good partial response (VGPR) was achieved in 11 (24%). Of the 24 patients who received auto‐HCT and whose response was less than CR, 21 received BD consolidation therapy for a median of 4 courses. Finally, the maximum response with or without BD consolidation was greater than or equal to CR in 19 (41%), VGPR in 7 (15%), and PR in 6 (13%). Through BD consolidation, CR was achieved in 8 of 11 patients with post‐HCT VGPR and in 2 of 12 patients with post‐HCT PR.
In total, 4 year PFS and overall survival were 43 and 80%, respectively. After adjusting for clinical factors, there was no difference in PFS between CR patients after auto‐HCT and BD consolidation, while patients with less than or equal to VGPR after consolidation had a significantly lower PFS.
Patients with post‐HCT CR showed good PFS, and targeting CR through BD consolidation could improve the CR rate. It would be worthwhile to prospectively compare the efficacy of consolidation only for patients who failed to achieve CR to a universal consolidation strategy.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28681529</pmid><doi>10.1002/hon.2452</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5812-9315</orcidid></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - pharmacology Antineoplastic Combined Chemotherapy Protocols - therapeutic use Autografts autologous hematopoietic cell transplantation Bortezomib Bortezomib - therapeutic use Consolidation Consolidation Chemotherapy Dexamethasone Female Humans Male Middle Aged Multiple myeloma Multiple Myeloma - surgery Multiple Myeloma - therapy Patients Stem cell transplantation Survival Targeted cancer therapy targeting complete response Therapy Transplantation Transplantation, Autologous Treatment Outcome |
title | Targeting complete response with upfront bortezomib consolidation versus observation after the achievement of complete response following autologous transplantation for multiple myeloma (TUBA study) |
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