High-dose therapy with peripheral blood progenitor cell transplantation in multiple myeloma

被引:39
作者
Goldschmidt, H [1 ]
Hegenbart, U [1 ]
Wallmeier, M [1 ]
Hohaus, S [1 ]
Engenhart, R [1 ]
Wannenmacher, M [1 ]
Haas, R [1 ]
机构
[1] UNIV HEIDELBERG,DEPT RADIOL,D-69115 HEIDELBERG,GERMANY
关键词
high-dose melphalan; multiple myeloma; peripheral blood progenitor cell transplantation; total body irradiation;
D O I
10.1023/A:1008252227512
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The objective of our study was to evaluate the efficacy and toxicity of a high-dose melphalan-based (HD-Mel) therapy with or without total body irradiation (TBI) followed by peripheral blood progenitor (PBPC) transplantation in patients with multiple myeloma (MM). Patients and methods: Between June 1992 and May 1996, 100 patients (67 males/33 females) with a median age of 51 years (range 30-65) were transplanted al our centre. PBPC were collected during G-CSF-enhanced leukocyte recovery following high-dose chemotherapy. Fifty patients were treated with TBI + melphalan 140 mg/m(2), while 50 patients received melphalan 200 mg/m(2). Results: Following PBPC autografting, the median time to reach platelets greater than or equal to 20 x 10(9)/1 and neutrophils greater than or equal to 0.5 x 10(9)/1 was 11 and 14 days with no difference between the treatment groups. In the TBI group significantly longer periods of total parenteral nutrition were required due to severe mucositis. Two patients from the TBI group died due to transplantation-related complications. Following high-dose treatment, remission slate improved in 43 out of 98 patients. No statistically significant advantage in reaching CR or PR was observed with TBI + HD-Mel compared to the treatment with HD-Mel alone. Conclusion: Dose-escalated treatments, with particular regard to the inclusion or omission of TBI, should be prospectively investigated to find the best high-dose regimen.
引用
收藏
页码:243 / 246
页数:4
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