Original Article

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Korean J Hematol 2010; 45(3):

Published online September 30, 2010

https://doi.org/10.5045/kjh.2010.45.3.183

© The Korean Society of Hematology

Bortezomib and melphalan as a conditioning regimen for autologous stem cell transplantation in multiple myeloma

Se Ryeon Lee1, Seok Jin Kim2*, Yong Park1, Hwa Jung Sung1, Chul Won Choi1, and Byung Soo Kim1

1Department of Internal Medicine, Korea University Medical Center, Seoul, Korea.

2Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Correspondence to : Correspondence to Seok Jin Kim, M.D., Ph.D. Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50, Irwon-dong, Gangnam-gu, Seoul 135-710, Korea. Tel: +82-2-3410-1766, Fax: +82-2-3410-1754, kstwoh@skku.edu

Received: April 30, 2010; Revised: July 23, 2010; Accepted: September 2, 2010

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

High-dose melphalan (200 mg/m2) with autologous stem cell transplantation (ASCT) is the standard treatment for young patients with multiple myeloma (MM). However, the response rates after ASCT are often unsatisfactory. We performed a pilot study by using bortezomib-melphalan as conditioning regimen for ASCT in Korean patients with MM.

Methods

The conditioning regimen consisted of administration of intravenous infusion of bortezomib 1.0 mg/m2 on days -4 and -1 and melphalan 50 mg/m2 (day -4) and 150 mg/m2 (day -1). In this study, we enrolled 6 newly diagnosed patients and 2 patients with relapse.

Results

The disease status of the 6 newly diagnosed patients at ASCT was as follows: 1 complete remission (CR), 1 very good partial remission (VGPR), and 4 partial remissions (PRs). The disease status of the 2 relapsed patients at ASCT was PR. All patients except 1 showed adequate hematologic recovery after ASCT. The median time for the absolute neutrophil counts to increase over 500/mm3 was 13 days (range, 10-19 days). Six patients with VGPR or PR at the time of transplantation showed an improvement in response to CR after ASCT. The patients were followed up without any maintenance treatment after ASCT except 1 patient who died during ASCT. During the follow-up period, CR was maintained in 3 newly diagnosed patients, but the other 4 patients, including 2 newly diagnosed patients, relapsed.

Conclusion

Conditioning regimen consisting of bortezomib and melphalan may be effective for ASCT in MM; however, the feasibility of this regimen should be further evaluated in large study populations.

Keywords Multiple myeloma, Bortezomib, Melphalan

Article

Original Article

Korean J Hematol 2010; 45(3): 183-187

Published online September 30, 2010 https://doi.org/10.5045/kjh.2010.45.3.183

Copyright © The Korean Society of Hematology.

Bortezomib and melphalan as a conditioning regimen for autologous stem cell transplantation in multiple myeloma

Se Ryeon Lee1, Seok Jin Kim2*, Yong Park1, Hwa Jung Sung1, Chul Won Choi1, and Byung Soo Kim1

1Department of Internal Medicine, Korea University Medical Center, Seoul, Korea.

2Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Correspondence to: Correspondence to Seok Jin Kim, M.D., Ph.D. Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50, Irwon-dong, Gangnam-gu, Seoul 135-710, Korea. Tel: +82-2-3410-1766, Fax: +82-2-3410-1754, kstwoh@skku.edu

Received: April 30, 2010; Revised: July 23, 2010; Accepted: September 2, 2010

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

High-dose melphalan (200 mg/m2) with autologous stem cell transplantation (ASCT) is the standard treatment for young patients with multiple myeloma (MM). However, the response rates after ASCT are often unsatisfactory. We performed a pilot study by using bortezomib-melphalan as conditioning regimen for ASCT in Korean patients with MM.

Methods

The conditioning regimen consisted of administration of intravenous infusion of bortezomib 1.0 mg/m2 on days -4 and -1 and melphalan 50 mg/m2 (day -4) and 150 mg/m2 (day -1). In this study, we enrolled 6 newly diagnosed patients and 2 patients with relapse.

Results

The disease status of the 6 newly diagnosed patients at ASCT was as follows: 1 complete remission (CR), 1 very good partial remission (VGPR), and 4 partial remissions (PRs). The disease status of the 2 relapsed patients at ASCT was PR. All patients except 1 showed adequate hematologic recovery after ASCT. The median time for the absolute neutrophil counts to increase over 500/mm3 was 13 days (range, 10-19 days). Six patients with VGPR or PR at the time of transplantation showed an improvement in response to CR after ASCT. The patients were followed up without any maintenance treatment after ASCT except 1 patient who died during ASCT. During the follow-up period, CR was maintained in 3 newly diagnosed patients, but the other 4 patients, including 2 newly diagnosed patients, relapsed.

Conclusion

Conditioning regimen consisting of bortezomib and melphalan may be effective for ASCT in MM; however, the feasibility of this regimen should be further evaluated in large study populations.

Keywords: Multiple myeloma, Bortezomib, Melphalan

Fig 1.

Figure 1.

Schematic diagram of the bortezomib and melphalan conditioning regimen. B, bortezomib 1 mg/m2; M50, melphalan 50 mg/m2; M150, melphalan 150 mg/m2; PBSC, peripheral blood stem cell.

Blood Research 2010; 45: 183-187https://doi.org/10.5045/kjh.2010.45.3.183

Table 1 . Summary of patients..

a)Age and performance status at diagnosis, b)Durie-salmon stage, c)International staging system stage..

Abbreviations: No, number; ECOG, eastern cooperative oncology group; DS stage, Durie-salmon stage; ISS stage, International staging system stage; ANC, absolute neutrophil count; ASCT, autologous stem cell transplantation; NA, not applicable; CR, complete remission; VGPR, very good partial remission; PR, partial remission..


Table 2 . Non-hematologic toxicities..


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