A randomized study of interferon-α versus interferon-α and low-dose arabinosyl cytosine in chronic myeloid leukemia

被引:123
作者
Baccarani, M
Rosti, G
de Vivo, A
Bonifazi, F
Russo, D
Martinelli, G
Testoni, N
Amabile, M
Fiacchini, M
Montefusco, E
Saglio, G
Tura, S
机构
[1] Univ Bologna, S Orsola Hosp, Inst Hematol & Med Oncol, I-40138 Bologna, Italy
[2] Udine Univ Hosp, Div Hematol, Udine, Italy
[3] Univ Roma La Sapienza, Div Hematol, Rome, Italy
[4] Univ Turin, Div Internal Med, Orbassano, Italy
关键词
D O I
10.1182/blood.V99.5.1527
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Interferon-alpha (IFN-alpha) has significantly prolonged survival in chronic myeloid leukemia (CIVIL), but some patients do not respond and many responses are not durable. To improve the results, IFN-alpha has been combined with other treatments, but so far only the association with low-dose arabinosyl cytosine (LDAC) has been shown to increase the response rate and to prolong survival. Here are reported the results of a study of 538 Philadelphia chromosome-positive CML patients who were assigned at random to treatment with IFN-alpha2a alone or in combination with LDAC. The scheduled dose of IFN-alpha2a was 5(6) IU/m(2)/d. The scheduled dose of AC was 40 mg/d for the first 10 days of each month of treatment. The efficacy endpoints were a complete hematologic response rate at 6 months (62% in the IFN-alpha-plus-LDAC arm versus 55% in the IFN-alpha arm; P =.11), major cytogenetic response (MCgR) rate at 24 months (28% versus 18%; P =.003), and overall survival (5-year survival, 68% versus 65%; P =.77). Treatment did not affect overall survival within different prognostic risk groups: low, intermediate, or high. Also the duration of MCgR was identical. The results of this study confirm the results of a similar French study only for the response rate, not for survival, suggesting that the relationship between cytogenetic response and survival may be extremely variable and that a meta-analysis of these and other studies of IFN-alpha versus IFN-alpha plus LDAC is required to settle the issue of the role of LDAC in the treatment of CML. (C) 2002 by The American Society of Hematology.
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页码:1527 / 1535
页数:9
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