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[两种治疗方案用于低危儿童急性淋巴细胞白血病的长期结果。11月20日国家医疗中心的经验]

[Long-term results of 2 therapeutic protocols in children with acute lymphoblastic leukemia of usual risk. Experience at the 20th of November National Medical Center].

作者信息

López-Hernández M A, de Diego Flores-Chapa J, Borbolla-Escoboza J R, Trueba-Christy E, Carrillo-Rosales T, González-Avante M

机构信息

Servicio de Hematología, Centro Médico Nacional 20 de noviembre, ISSSTE, México, D.F.

出版信息

Gac Med Mex. 1998 Mar-Apr;134(2):145-51.

PMID:9618993
Abstract

The purpose of this study is to know the disease-free survival in children with acute lymphoblastic leukemia (ALL), submitted to two therapeutic programs. Habitual risk was defined as age older than 2 and younger than 10 years, without neurological, mediastinal or testicular infiltrations, leukocytes < 25 x 10(9)/l and morphologic cell type distinct of L-3. The first group (LAL81) included 30 patients, from 1981 to 1986, and they received: induction with vincristine (VCR) and prednisone (PDN); consolidation with mercaptopurine (MP), cytosine arabinoside (ARA) and doxorubicin (DOX); prophylaxis to the central nervous system (CNS) with radiotherapy and methotrexate (MTX)-ARA-hydrocortisone (HDR) intrathecal, and maintenance with MP and MTX. In the second group (LAL87), 28 patients were included from 1987 to 1993. They received: induction with VCR, PDN and lasparaginase (ASP); consolidation with MP, ARA, DOX, carmustine (BCNU) and cyclophosphamide (CFA); prophylaxis to the (CNS) with intrathecal MTX-ARA-HDR, and maintenance with MP and MTX. There was just one therapeutic failure. In the LAL81, protocol 11 relapses and 9 in LAL87 (p = 0.71) were observed. Of these, two in each group went to the CNS. The disease-free survival in LAL81 was 0.39 at 14 years; in LAL87, was 0.53 at 8 years (p = 0.62).

摘要

本研究的目的是了解接受两种治疗方案的急性淋巴细胞白血病(ALL)患儿的无病生存率。将年龄大于2岁且小于10岁、无神经、纵隔或睾丸浸润、白细胞<25×10⁹/L且形态学细胞类型不同于L-3的情况定义为低危。第一组(LAL81)包括1981年至1986年的30例患者,他们接受了:长春新碱(VCR)和泼尼松(PDN)诱导;巯嘌呤(MP)、阿糖胞苷(ARA)和阿霉素(DOX)巩固;中枢神经系统(CNS)放疗及鞘内注射甲氨蝶呤(MTX)-阿糖胞苷-氢化可的松(HDR)预防,以及MP和MTX维持治疗。第二组(LAL87)包括1987年至1993年的28例患者。他们接受了:VCR、PDN和天冬酰胺酶(ASP)诱导;MP、ARA、DOX、卡莫司汀(BCNU)和环磷酰胺(CFA)巩固;鞘内注射MTX-ARA-HDR预防(CNS),以及MP和MTX维持治疗。仅有1例治疗失败。在LAL81中观察到11例复发,在LAL87中观察到9例复发(p = 0.71)。其中,每组各有2例复发至CNS。LAL81组14年时的无病生存率为0.39;LAL87组8年时的无病生存率为0.53(p = 0.62)。

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