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
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
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.
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.
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.
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.
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
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.
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
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.
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.
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.
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.
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
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.
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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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.