| Literature DB >> 19936876 |
Kazutaka Sunami1, Katsuji Shinagawa2, Morio Sawamura3, Akira Sakai4, Yoshio Saburi5, Yutaka Imamura6, Ishikazu Mizuno7, Shigehisa Tamaki8, Tomohiko Kamimura9, Hiroyuki Tsuda10, Hisashi Gondo11, Norihiko Hino12, Chihiro Shimazaki13, Akira Miyata14, Fumihito Tajima15, Yoshinobu Takemoto16, Akiyoshi Miwa17, Takaaki Chou18, Mine Harada19.
Abstract
The efficacy and safety of high-dose chemotherapy with tandem autologous peripheral blood stem cell transplantation (auto-PBSCT) were evaluated in a multicenter clinical study of patients with advanced multiple myeloma. Eligible patients (n = 40) were consecutively enrolled in the phase I/II study and received 2-4 cycles of vincristine-adriamycin-dexamethasone regimen. The responding patients underwent PBSC harvesting following high-dose cyclophosphamide and filgrastim administration. The first auto-PBSCT (n = 32) following high-dose melphalan (200 mg/m(2)) was performed within 2 months of PBSC harvesting; the second auto-PBSCT (n = 28) was scheduled 3-6 months later. Treatment-related mortality was 2.5% (n = 1) throughout the protocol. Grade 4 nonhematologic toxicity occurred in 12.5 and 14.3% of the first and second auto-PBSCT patients, respectively. All but one patient (who died) achieved hematopoietic recovery. For the 28 patients completing the second auto-PBSCT, the results were favorable with a response rate of 65% (complete response rate = 27.5%, n = 11); the five-year progression-free survival and overall survival were 20.3 and 66.5%, respectively. In conclusion, high-dose chemotherapy with tandem auto-PBSCT is feasible and safe with a favorable response rate in treating advanced multiple myeloma in Japan.Entities:
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Year: 2009 PMID: 19936876 DOI: 10.1007/s12185-009-0445-8
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490