When are second allogeneic bone marrow transplants indicated in pediatric patients?

被引:0
|
作者
Calderwood, S
Doyle, JJ
Rolland-Grinton, M
Zafar, M
Roifman, C
Freedman, MH
Saunders, EF
机构
[1] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Div Hematol Oncol, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Div Immunol, Toronto, ON M5G 1X8, Canada
关键词
allogeneic bone marrow transplantation; pediatrics; outcome;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to describe the outcomes of 22 consecutive second allogeneic bone-marrow transplantations (BMTs) in pediatric patients, in hopes of contributing to the development of guidelines for performing second BMTs. We reviewed the charts of all patients receiving a second allogeneic BMT at our center during 1974 to 1996. Patients were grouped according to reason for the second transplant: primary or secondary graft failure or disease relapse. Outcomes were compared with those of a similar group undergoing a first allogeneic BMT. Several factors identified in the Literature as contributing to a poor prognosis after second BMT, including time between transplants and reason for retransplant, were evaluated for effect on survival. Twenty-two patients undergoing second allogeneic BMT had an overall survival (OS) of 36%, and 100-day mortality of 40%, significantly worse than for first BMT patients. OS for 14 patients who received a second transplant for graft failure was 57%, and in this group, time between transplants significantly influenced OS (100% if >6 months, 33% if <6 months). Eight patients who received a second transplant for relapse had a very poor outcome, with 4 of 8 dying from regimen-related toxicity and one dying from relapse. Only 3 of these patients remain alive between 43 and 399 days after the second transplant. We conclude that second BMT has extremely high risks, especially if carried out within 6 months of the first BMT. We suggest that a second BMT is indicated in management of graft failure, but has Limited value in the management of relapse of malignant disease.
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页码:337 / 343
页数:7
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