An effective chemotherapeutic regimen for acute myeloid leukemia and myelodysplastic syndrome in children with Down's syndrome

被引:51
作者
Kojima, S
Sako, M
Kato, K
Hosoi, G
Sato, T
Ohara, A
Koike, K
Okimoto, Y
Nishimura, S
Akiyama, Y
Yoshikawa, T
Ishii, E
Okamura, J
Yazaki, M
Hayashi, Y
Eguchi, M
Tsukimoto, I
Ueda, K
机构
[1] Nagoya Univ, Sch Med, Dept Dev Pediat, Nagoya, Aichi 466, Japan
[2] Osaka City Gen Hosp, Dept Pediat, Osaka, Japan
[3] Japanese Red Cross Nagoya First Hosp, Childrens Med Ctr, Div Hematol, Nagoya, Aichi, Japan
[4] Chiba Univ, Sch Med, Dept Pediat, Chiba, Japan
[5] Toho Univ, Sch Med, Dept Pediat 1, Tokyo, Japan
[6] Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano 390, Japan
[7] Chiba Childrens Hosp, Div Hematol Oncol, Chiba, Japan
[8] Hiroshima Univ, Sch Med, Dept Pediat, Hiroshima, Japan
[9] Kyoto Univ, Sch Med, Dept Pediat, Kyoto 606, Japan
[10] Fujita Hlth Univ, Sch Med, Dept Pediat, Toyoake, Aichi 47011, Japan
[11] Hamanoumachi Hosp, Dept Pediat, Fukuoka 810, Japan
[12] Kyushu Natl Canc Ctr, Sect Pediat, Fukuoka, Japan
[13] Nagoya City Univ, Sch Med, Dept Pediat, Nagoya, Aichi 467, Japan
[14] Univ Tokyo, Dept Pediat, Tokyo 113, Japan
[15] Dokkyo Univ, Sch Med, Dept Pediat, Tochigi, Japan
关键词
acute myeloid leukemia; myelodysplastic syndrome; Down's syndrome;
D O I
10.1038/sj.leu.2401754
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent pediatric collaborative studies of acute myeloid leukemia (AML), patients with Down's syndrome (DS) have better outcome than other patients when they were treated according to their intensive AML protocols. This may be attributed to enhanced sensitivity of DS AML cells to selected chemotherapeutic agents. We evaluated a less intensive chemotherapeutic regimen which was specifically designed for children with AML-DS. Remission induction chemotherapy consisted of daunorubicin (25 mg/m(2)/day for 2 days), cytosine arabinoside (100 mg/m(2)/day for 7 days), and etoposide (150 mg/m(2)/day for 3 days). Patients received one to seven courses of consolidation therapy of the same regimen. Thirty-three patients were enrolled on the study and their clinical, hematologic and immunophenotypic features were analyzed. Of the 33 patients, all were younger than 4 years and diagnosed as having acute megakaryoblastic leukemia or myelodysplastic syndrome. All patients achieved a complete remission and estimated 8 year event-free survival rate was 80 +/- 7%. Three patients relapsed and two died due to cardiac toxicity and one due to septic shock. The results of our study showed that patients with AML-DS constitute a unique biologic subgroup and should be treated according to a less intensive protocol designed for AML-DS.
引用
收藏
页码:786 / 791
页数:6
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