EFFECT OF PRIOR INTERFERON-ALFA THERAPY ON THE OUTCOME OF ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR CHRONIC MYELOGENOUS LEUKEMIA

被引:64
作者
GIRALT, SA
KANTARJIAN, HM
TALPAZ, M
RIOS, MB
DELGIGLIO, A
ANDERSSON, BS
PRZEPIORKA, D
DEISSEROTH, AB
CHAMPLIN, RE
机构
[1] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT HEMATOL,1515 HOLCOMBE BLVD,BOX 65,HOUSTON,TX 77030
[2] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT CLIN IMMUNOL,HOUSTON,TX 77030
[3] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT BIOL THERAPEUT,HOUSTON,TX 77030
关键词
D O I
10.1200/JCO.1993.11.6.1055
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine whether prior interferon alfa (IFN-A) treatment affects the outcome of allogeneic bone marrow transplantation. Patients and Methods: We analyzed the outcome of 77 patients with chronic myelogenous leukemia (CML) who received transplants from an HLA-identical donor using a total-body irradiation-containing preparative regimen. Engraftment, acute and chronic graft-versus-host disease (GVHD), survival, and disease-free survival were compared between patients who had previously received interferon (IFN+) to those who had not (IFN-). Forty-one patients were transplanted in chronic phase and 36 had more advanced CML. The IFN+ group had received IFN-A in doses of 3 to 5 × 106 U/m2 three times a week or more for at least 4 weeks anytime before transplantation. Results: For patients in chronic phase, there were no significant differences between the IFN+ group and the IFN- group in regard to neutrophils recovery more than 1.0 × 109/L (29 v 24), platelet recovery more than 50 × 109/L (33 v 36), incidence of grade II to IV GVHD (23% v 28%), incidence of chronic GVHD (39% v 47%), disease-free survival (46% ± 11% v 59% ± 13%), relapse (9% v 11%), or 100-day transplant-related mortality (22% v 16%). In patients with more advanced stage disease, there was also no significant differences between the IFN+ group and the IFN- group in regard to these outcomes. Conclusion: Prior treatment with IFN-A did not adversely affect transplant outcome. Further studies are required to better understand the complementary roles of IFN-A and allogeneic bone marrow transplantation for the treatment of CML.
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页码:1055 / 1061
页数:7
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