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采用DFCI-ALL方案对复发性急性淋巴细胞白血病患儿进行二次诱导治疗。

Second induction in pediatric patients with recurrent acute lymphoid leukemia using DFCI-ALL protocols.

作者信息

Dalle Jean-Hugues, Moghrabi Albert, Rousseau Pierre, Leclerc Jean-Marie, Barrette Stephane, Bernstein Mark L, Champagne Josette, David Michele, Demers Jocelyn, Duval Michel, Hume Heather, Meyer Patrick, Champagne Martin A

机构信息

Division of Hematology-Oncology, Hôpital Sainte Justine, Montréal, Quebec, Canada.

出版信息

J Pediatr Hematol Oncol. 2005 Feb;27(2):73-9. doi: 10.1097/01.mph.0000152860.97998.32.

Abstract

Between 15% and 30% of children with acute lymphoblastic leukemia (ALL) experience disease recurrence. With the possible exception of patients presenting with late isolated extramedullary relapse, induction of second complete remission (CR) is employed as a stepping stone to allogeneic hematopoietic stem cell transplantation (HSCT). The authors report their institutional experience in the management of children with recurrent ALL using the Dana Farber Cancer Institute (DFCI) ALL protocol in patients treated initially with that same protocol. Successful reinduction was followed by allogeneic HSCT when possible. Between April 1986 and May 2003, 34 patients with recurrent ALL, treated at initial diagnosis with DFCI-ALL protocol therapy, were given the same protocol as repeat induction chemotherapy. The median age was 4.6 years at diagnosis and 7.1 years at recurrence. Median duration of CR1 was 30.3 months. Second CR was obtained in 29 (85%) patients. Twenty went on to allogeneic HSCT; 10 of them currently remain in CR. Two additional patients treated with chemotherapy without HSCT are also in continuous CR2. Overall, 13 (38%) of the 34 patients are alive with a median follow-up of 105 months. There were no toxic deaths due to the reinduction therapy. One child died of cardiac failure after autologous HSCT. The treatment of children with recurrent ALL using the DFCI-ALL protocol induction regimen after initial use of the same protocol is associated with a high rate of second CR with no excess toxicity. However, the overall prognosis in these patients remains unsatisfactory and needs to be improved.

摘要

15%至30%的急性淋巴细胞白血病(ALL)患儿会出现疾病复发。除了出现晚期孤立髓外复发的患者外,诱导第二次完全缓解(CR)被用作异基因造血干细胞移植(HSCT)的一个步骤。作者报告了他们在使用达纳-法伯癌症研究所(DFCI)ALL方案治疗初诊采用该方案的复发性ALL患儿方面的机构经验。成功再诱导后,尽可能进行异基因HSCT。在1986年4月至2003年5月期间,34例复发性ALL患儿在初诊时接受DFCI-ALL方案治疗,此次给予相同方案作为重复诱导化疗。诊断时的中位年龄为4.6岁,复发时为7.1岁。CR1的中位持续时间为30.3个月。29例(85%)患者获得第二次CR。20例继续接受异基因HSCT;其中10例目前仍处于CR状态。另外2例接受化疗而非HSCT治疗的患者也处于持续CR2状态。总体而言,34例患者中有13例(38%)存活,中位随访时间为105个月。再诱导治疗未导致毒性死亡。1例患儿在自体HSCT后死于心力衰竭。初诊使用相同方案后,采用DFCI-ALL方案诱导方案治疗复发性ALL患儿,第二次CR率高且无额外毒性。然而,这些患者的总体预后仍不令人满意,需要改善。

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