Autologous peripheral blood stem cell transplantation for Japanese multiple myeloma patients: results of a feasibility study
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- NAKAMURA Yuichi
- Department of Hematology, Dokkyo University School of Medicine
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- SAKAMAKI Hisashi
- Hematology Division, Metropolitan Komagome Hospital
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- MUKAI Harumi
- Division of Hematology, Institute of Clinical Medicine, University of Tsukuba
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- KOJIMA Hiroshi
- Division of Hematology, Institute of Clinical Medicine, University of Tsukuba
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- TOMIYAMA Junji
- Department of Internal Medicine, Metropolitan Bokuto Hospital
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- MORI Shin-ichirou
- Hematology Division, Metropolitan Komagome Hospital
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- HIRUMA Kiyoshi
- Blood Transfusion Service, Metropolitan Komagome Hospital
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- NAKAMURA Norihiko
- Department of Internal Medicine, Yokosuka Kyosai Hospital
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- TOYOTA Shigeo
- Department of Internal Medicine, Yokosuka Kyosai Hospital
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- HAMAGUCHI Hiroyuki
- Department of Internal Medicine, Musashino Red Cross Hospital
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- DAN Kazuo
- Third Department of Internal Medicine, Nippon Medical School
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- MITANI Kinuko
- Department of Hematology, Dokkyo University School of Medicine
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- SAITO Kenji
- Department of Hematology, Dokkyo University School of Medicine
Bibliographic Information
- Other Title
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- 多発性骨髄腫に対する自家末梢血幹細胞移植療法
- 臨床研究 多発性骨髄腫に対する自家末梢血幹細胞移植療法--本邦でのプロトコールの実行性についての検討
- リンショウ ケンキュウ タハツセイ コツズイシュ ニ タイスル ジカ マッショウケツ カンサイボウ イショク リョウホウ ホンポウ デ ノ プロトコール ノ ジッコウセイ ニ ツイテ ノ ケントウ
- —本邦でのプロトコールの実行性についての検討—
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Abstract
A feasibility study on high-dose therapy with autologous peripheral blood stem cell transplantation (HDT/PBSCT) was performed in Japanese patients with multiple myeloma (MM). Twenty evaluable patients younger than 65 years old with stage II/III MM were enrolled in this study. Three courses of VAD were used as initial chemotherapy. High-dose etoposide or cyclophosphamide followed by G-CSF was used for PBSCH, and 1.2-89.3 (median 23.4)×106/kg of CD34+ cells were collected. Single (11 patients) or tandem (9 patients) HDT with melphalan (MEL) 200 mg/m2 or MEL 140 mg/m2 plus TBI 10 Gy were performed. The incidence of grade 4 toxicity (JCOG) was 10% and treatment-related mortality was 5%. Complete response and tumor reduction of more than 75% were obtained in 4 (21%) and 16 (84%) out of 19 patients, respectively. The actuarial 3-year overall survival (OS) and event-free survival (EFS) after PBSCT/HDT were 65.6% and 22.0%, respectively. The median EFS duration was 18 months. These preliminary results indicated that HDT/PBSCT is feasible for Japanese MM patients. A prospective randomized clinical trial will be required to assess the efficacy.
Journal
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- Rinsho Ketsueki
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Rinsho Ketsueki 45 (7), 524-529, 2004
The Japanese Society of Hematology
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Details 詳細情報について
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- CRID
- 1390001205033003776
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- NII Article ID
- 10013335569
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- NII Book ID
- AN00252940
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- COI
- 1:STN:280:DC%2BD2cvltFyjsg%3D%3D
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- ISSN
- 18820824
- 04851439
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- NDL BIB ID
- 7039985
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- PubMed
- 15359911
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed