Six months of maintenance chemotherapy after intensified treatment for acute lymphoblastic leukemia of childhood

被引:74
|
作者
Toyoda, Y
Manabe, A
Tsuchida, M
Hanada, R
Ikuta, K
Okimoto, Y
Ohara, A
Ohkawa, Y
Mori, T
Ishimoto, K
Sato, T
Kaneko, T
Maeda, M
Koike, K
Shitara, T
Hoshi, Y
Hosoya, R
Tsunematsu, Y
Bessho, F
Nakazawa, S
Saito, T
机构
[1] Kanagawa Childrens Med Ctr, Dept Oncol, Minami Ku, Yokohama, Kanagawa 2328555, Japan
[2] Yokohama City Univ, Sch Med, Dept Pediat, Yokohama, Kanagawa 232, Japan
[3] Univ Tokyo, Dept Pediat Hematol Oncol, Inst Med Sci, Tokyo, Japan
[4] Tokyo Med & Dent Univ, Sch Med, Dept Pediat, Tokyo 113, Japan
[5] Keio Univ, Sch Med, Tokyo 108, Japan
[6] Juntendo Univ, Sch Med, Tokyo 113, Japan
[7] St Lukes Int Hosp, Nippon Med Sch, Tokyo, Japan
[8] Teikyo Univ, Sch Med, Tokyo 173, Japan
[9] Tokyo Metropolitan Kiyose Childrens Hosp, Dept Hematol Oncol, Tokyo, Japan
[10] Natl Childrens Hosp, Dept Hematol, Tokyo, Japan
[11] Natl Childrens Med Res Ctr, Tokyo 154, Japan
[12] Ibaraki Childrens Hosp, Dept Pediat, Mito, Ibaraki, Japan
[13] Saitama Childrens Med Ctr, Dept Hematol Oncol, Iwatsuki, Saitama, Japan
[14] Chiba Childrens Hosp, Dept Hematol Oncol, Chiba, Japan
[15] Chiba Univ, Sch Med, Dept Pediat, Chiba, Japan
[16] Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano 390, Japan
[17] Gunma Childrens Med Ctr, Dept Hematol Oncol, Maebashi, Gumma, Japan
[18] Yamanashi Med Univ, Dept Pediat, Kofu, Japan
关键词
D O I
10.1200/JCO.2000.18.7.1508
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We postulated that intensification of chemotherapy immediately after remission induction might reduce the leukemic cell burden sufficiently to allow an abbreviated period of antimetabolite therapy. Patients and Methods: Three hundred forty-seven children (ages 1 to 15 years) with previously untreated acute lymphoblastic leukemia (ALL) were enrolled onto the Tokyo L92-13 study, which excluded patients with mature B-cell ALL and patients less than 1 year old. One hundred twenty-four patients were classified as standard risk, 122 as high risk, and 101 as extremely high risk, according to age, peripheral-blood leukocyte count selected genetic abnormalities, and immunophenotype. All subjects received four drugs for remission induction, followed by a risk-directed multidrug intensification phase and therapy for presymptomatic leukemia in the CNS. Maintenance chemotherapy with oral mercaptopurine and methotrexate was administered for 6 months, with all treatment stopped by 1 year after diagnosis. Results: The mean (+/- SD) event-free survival (EFS) and overall survival rates far all patients were 59.5% +/- 3.4% and 81.5% +/- 2.2%, respectively, at 5.5 years after diagnosis. EFS rates by risk category were similar (60.2% +/- 6.0% for standard risk, 57.7% +/- 5.6% for high risk, and 62.5% +/- 5.7% for extremely high risk), whereas overall survival rates differed significantly (91.2% +/- 2.7%, 80.0% +/- 4.1%, and 72.1% +/- 4.5%, respectively, P < .0001 by the lag-rank test). There were 107 relapses. Eighty-five (79.4%) of these 107 patients achieved second complete remissions, with subsequent EFS rates of 61.5% +/- 7.9% (standard risk), 42.6% +/- 8.1% (high risk), and 9.6% +/- 6.4% (extremely high risk). Of the five risk factors analyzed, only the response to prednisolone monotherapy among extremely high-risk patients proved important. Conclusion: Early treatment intensification did nat compensate for a truncated phase of maintenance chemotherapy in children with standard or high-risk ALL, However, 6 months of antimetabolite treatment seemed adequate for extremely high-risk patients who were good responders to prednisolone and received intensified chemotherapy that included high-dose cytarabine early in the clinical course. (C) 2000 by American Society of Clinical Oncology.
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收藏
页码:1508 / 1516
页数:9
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