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

被引:0
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作者
S Kojima
M Sako
K Kato
G Hosoi
T Sato
A Ohara
K Koike
Y Okimoto
S Nishimura
Y Akiyama
T Yoshikawa
E Ishii
J Okamura
M Yazaki
Y Hayashi
M Eguchi
I Tsukimoto
K Ueda
机构
[1] Nagoya University School of Medicine,Department of Developmental Pediatrics
[2] Osaka City General Hospital,Department of Pediatrics
[3] Children's Medical Center,Division of Hematology/Oncology
[4] Japanese Red Cross Nagoya First Hospital,Department of Pediatrics
[5] School of Medicine,First Department of Pediatrics
[6] Chiba University,Department of Pediatrics
[7] Toho University School of Medicine,Division of Hematology/Oncology
[8] Shinshu University School of Medicine,Department of Pediatrics
[9] Chiba Children's Hospital,Department of Pediatrics
[10] Hiroshima University School of Medicine,Department of Pediatrics
[11] School of Medicine,Department of Pediatrics
[12] Kyoto University,Department of Pediatrics
[13] Fujita Health University School of Medicine,Department of Pediatrics
[14] Hamanomachi Hospital,Department of Pediatrics
[15] Section of Pediatrics,undefined
[16] National Kyushu Cancer Center,undefined
[17] Nagoya City University Medical School,undefined
[18] University of Tokyo,undefined
[19] Dokkyo University School of Medicine,undefined
来源
Leukemia | 2000年 / 14卷
关键词
acute myeloid leukemia; myelodysplastic syndrome; Down's syndrome;
D O I
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学科分类号
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/m2/day for 2 days), cytosine arabinoside (100 mg/m2/day for 7 days), and etoposide (150 mg/m2/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.
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页码:786 / 791
页数:5
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