A long term follow-up of a randomized trial comparing interferon-α with busulfan for chronic myelogenous leukemia

被引:22
作者
Ohnishi, K
Tomonaga, M
Kamada, N
Onozawa, K
Kuramoto, A
Dohy, H
Mizoguchi, H
Miyawaki, S
Tsubaki, K
Miura, Y
Omine, M
Kobayashi, T
Naoe, T
Ohshima, T
Hirashima, K
Ohtake, S
Takahashi, I
Morishima, Y
Naito, K
Asou, N
Tanimoto, M
Sakuma, A
Ohno, R
机构
[1] Hamamatsu Univ Sch Med, Dept Med 3, Hamamatsu, Shizuoka 43131, Japan
[2] Nagasaki Univ, Sch Med, Dept Med, Nagasaki 852, Japan
[3] Hiroshima Univ, Res Inst Radiat Biol & Med, Dept Canc Cytogenet, Hiroshima, Japan
[4] Hiroshima Univ, Res Inst Nucl Med & Biol, Dept Med, Hiroshima, Japan
[5] Komagome Municipal Hosp, Dept Chemotherapy, Tokyo, Japan
[6] Hiroshima Red Cross Hosp, Dept Med, Hiroshima, Japan
[7] Atom Bomb Survivors Hosp, Hiroshima, Japan
[8] Tokyo Womens Med Coll, Dept Med, Tokyo 162, Japan
[9] Saiseikai Maebashi Hosp, Maebashi, Gumma, Japan
[10] Kinki Univ, Dept Med, Osaka, Japan
[11] Jichi Med Sch, Dept Med, Div Hematol, Minami Kawachi, Tochigi, Japan
[12] Gunma Univ, Sch Med, Dept Med, Gunma, Japan
[13] Mie Univ, Sch Med, Dept Med, Tsu, Mie 514, Japan
[14] Nagoya Univ, Branch Hosp, Dept Med, Nagoya, Aichi, Japan
[15] Nihon Univ, Sch Med, Dept Med, Tokyo, Japan
[16] Saitama Med Sch, Dept Med, Moroyama, Saitama, Japan
[17] Kanazawa Univ, Sch Med, Dept Med, Kanazawa, Ishikawa 920, Japan
[18] Okayama Univ, Sch Med, Dept Med, Okayama 700, Japan
[19] Meitetsu Hosp, Dept Med, Nagoya, Aichi, Japan
[20] Kumamoto Univ, Sch Med, Dept Med, Kumamoto 860, Japan
[21] Nagoya Univ, Sch Med, Dept Med, Nagoya, Aichi 466, Japan
[22] Tokyo Med & Dent Univ, MRI, Div Med Informat, Tokyo 113, Japan
关键词
interferon-alpha; chronic myelogenous leukemia; busulfan; randomized clinical trial; prognostic factor;
D O I
10.1016/S0145-2126(98)00082-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To evaluate the long-term effectiveness of interferon-alpha (IFN-alpha) therapy in patients with chronic myelogenous leukemia (CML) in chronic phase, we examined the updated outcomes of 159 patients who had been enrolled between 1988 and 1991 into a randomized trial comparing IFN-alpha with busulfan. At a median follow-up of 73 months, the median survival was 71 months in the IFN-alpha group and 55 months in the busulfan group (P = 0.0563), and the median time of remaining in chronic phase was 58 months in the IFN-alpha group and 39 months in the busulfan group (P = 0.4676). Landmark analysis showed a significant advantage in survival (P = 0.009) and duration of chronic phase (P = 0.0001) in patients with any cytogenetic response among the IFN-alpha group. About half patients were discontinued IFN-alpha administration in spite of cytogenetic response in this study. It appears that continuation of IFN-alpha might possibly confer a survival advantage. Pretreatment factors associated with cytogenetic response included high hemoglobin level, low percentage of peripheral basophils and low leukocyte counts. Multivariate analysis identified lower percentage of bone marrow basophilia (P = 0.007) for survival advantage. If a group with a very good prognosis is predicted by a new prognostic model, it might be an option to wait for bone marrow transplantation. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:779 / 786
页数:8
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