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大剂量甲氨蝶呤晚期强化治疗儿童标危急性淋巴细胞白血病的回顾性分析(CCLSG-S811研究)。儿童癌症与白血病研究组。

Retrospective analysis of late intensification therapy with high-dose methotrexate for standard-risk acute lymphoblastic leukemia in childhood (CCLSG-S811 study). The Children's Cancer and Leukemia Study Group.

作者信息

Koizumi S, Fujimoto T, Sasaki K, Takeda T, Utsumi J, Mimaya J, Ohta S, Ninomiya T, Takaue Y

机构信息

Department of Pediatrics, Aichi Medical University, Japan.

出版信息

Int J Hematol. 1991 Aug;54(4):307-13.

PMID:1777605
Abstract

Using the CCLSG-S811 protocol for children with standard-risk acute lymphoblastic leukemia (ALL), late intensification therapy (LIT) with high-dose methotrexate (HD-MTX) was conducted without randomization. Of 118 eligible patients, 114 attained complete remission and 82 maintained continuous complete remission (CCR) for at least 3 years, completing the entire S811 regimen. Among the latter, 74 patients received LIT with HD-MTX between 2-3 years after CCR onset. MTX (2,000 mg/m2 per dose per week) was administered by 24 h infusion and three doses were given every 12 weeks. Leucovorin rescue (15 mg/m2 i.v.) every 6 h was initiated 12 h after the end of MTX infusion for seven doses. As regular maintenance chemotherapy, intermittent (Regimen A) or continuous (Regimen B) MTX plus 6-mercaptopurine (6MP) combined with pulses of prednisolone and vincristine was administered (Koizumi S, Fujimoto T, Takeda T, et al. Cancer 1988; 61: 1292-1300). Retrospective analysis revealed that patients on Regimen A who started LIT earlier (within 2 years of CCR onset (n = 23)) showed a higher rate of event-free survival (EFS) at 8 years (95.5% +/- 4.4%, mean +/- S.E.) than patients who started LIT later (2.5 years after CCR onset (n = 18, 66.2% +/- 11.3%, p less than 0.01)). In addition, the superiority of four or five courses of the LIT (n = 39) as compared to 2 or 3 courses (n = 35) was noted for both regimens. The data suggest that early and aggressive LIT with HD-MTX may improve the long-term survival of childhood ALL patients.

摘要

采用CCLSG - S811方案对标准风险急性淋巴细胞白血病(ALL)患儿进行治疗,未进行随机分组,采用大剂量甲氨蝶呤(HD - MTX)进行晚期强化治疗(LIT)。在118例符合条件的患者中,114例达到完全缓解,82例维持持续完全缓解(CCR)至少3年,完成了整个S811方案。在后者中,74例患者在CCR开始后2至3年接受了HD - MTX的LIT治疗。MTX(每剂量2000 mg/m²,每周一次)通过24小时输注给药,每12周给药三剂。在MTX输注结束12小时后开始每6小时一次的亚叶酸钙解救(15 mg/m²静脉注射),共七剂。作为常规维持化疗,给予间歇(方案A)或持续(方案B)的MTX加6 - 巯基嘌呤(6MP),联合泼尼松龙和长春新碱脉冲给药(小泉S,藤本T, 武田T等。《癌症》1988年;61: 1292 - 1300)。回顾性分析显示,方案A中较早开始LIT(CCR开始后2年内(n = 23))的患者8年无事件生存率(EFS)(95.5% +/- 4.4%,均值 +/- 标准误)高于较晚开始LIT(CCR开始后2.5年(n = 18, 66.2% +/- 11.3%,p小于0.01))的患者。此外,两种方案中,四或五个疗程的LIT(n = 39)与两或三个疗程(n = 35)相比均具有优势。数据表明,采用HD - MTX进行早期且积极的LIT可能会提高儿童ALL患者的长期生存率。

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