Volume 36, Issue 1 pp. 202-209
ORIGINAL RESEARCH ARTICLE

Targeting complete response with upfront bortezomib consolidation versus observation after the achievement of complete response following autologous transplantation for multiple myeloma (TUBA study)

Hideki Nakasone

Hideki Nakasone

Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan

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Kiriko Terasako-Saito

Kiriko Terasako-Saito

Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan

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Teiichi Hirano

Teiichi Hirano

Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan

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Atsushi Wake

Atsushi Wake

Department of Hematology, Toranomon Hospital Kajigaya, Kawasaki, Japan

Okinaka Memorial Institute of Medical Research, Tokyo, Japan

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Seiichi Shimizu

Seiichi Shimizu

Department of Hematology, Tsuchiura Kyodo General Hospital, Tsuchiura, Japan

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Naoki Kurita

Naoki Kurita

Department of Hematology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Etsuko Yamazaki

Etsuko Yamazaki

Department of Hematology and Clinical Immunology, Yokohama City University Hospital, Yokohama, Japan

Clinical Laboratory Department, Yokohama City University Hospital, Yokohama, Japan

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Kensuke Usuki

Kensuke Usuki

Department of Hematology, NTT Medical Center Tokyo, Tokyo, Japan

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Kohei Akazawa

Kohei Akazawa

Department of Medical Informatics, Niigata University Medical and Dental Hospital, Niigata, Japan

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Junya Kanda

Junya Kanda

Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan

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Koichiro Minauchi

Koichiro Minauchi

Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan

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Go Yamamoto

Go Yamamoto

Department of Hematology, Toranomon Hospital, Tokyo, Japan

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Shiori Tanimoto

Shiori Tanimoto

Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan

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Masaharu Kamoshita

Masaharu Kamoshita

Department of Hematology, Tsuchiura Kyodo General Hospital, Tsuchiura, Japan

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Yasuhisa Yokoyama

Yasuhisa Yokoyama

Department of Hematology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Etsuo Miyaoka

Etsuo Miyaoka

Department of Mathematics, Faculty of Science Division II, Tokyo University of Science, Tokyo, Japan

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Shuichi Ota

Shuichi Ota

Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan

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Shinichi Kako

Shinichi Kako

Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan

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Koji Izutsu

Koji Izutsu

Department of Hematology, Toranomon Hospital, Tokyo, Japan

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Yoshinobu Kanda

Corresponding Author

Yoshinobu Kanda

Division of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan

Correspondence

Yoshinobu Kanda MD/PhD, Division of Hematology, Saitama Medical University, Jichi Medical University, 1-847 Amanuma-cho Omiya-ku, Saitama 330-8503, Japan.

Email: [email protected]

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First published: 06 July 2017
Citations: 2
HN and KT-S contributed equally to this study.

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.

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