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小儿急性淋巴细胞白血病极晚期复发的结局:东京儿童癌症研究组(TCCSG)的回顾性分析

Outcome of pediatric acute lymphoblastic leukemia with very late relapse: a retrospective analysis by the Tokyo Children's Cancer Study Group (TCCSG).

作者信息

Kato Motohiro, Manabe Atsushi, Saito Akiko M, Koh Katsuyoshi, Inukai Takeshi, Ogawa Chitose, Goto Hiroyuki, Tsuchida Masahiro, Ohara Akira

机构信息

Department of Pediatrics, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan,

出版信息

Int J Hematol. 2015 Jan;101(1):52-7. doi: 10.1007/s12185-014-1710-z. Epub 2014 Nov 29.

Abstract

Relapse period is strongly associated with second relapse risk in relapsed acute lymphoblastic leukemia (ALL) in children. In this context, the treatment outcome of very late relapse should be better; however, data regarding very late relapse is limited. We retrospectively analyzed the outcomes of two consecutive Tokyo Children's Cancer Study Group (TCCSG) ALL trials (1995-2004) with a focus on late relapse, which was divided into two categories: late relapse (6-24 months from the end of therapy, n = 48) and very late relapse (>24 months from the end of therapy, n = 57). Forty-three patients (29 late relapse and 14 very late relapse) received allogeneic hematopoietic stem cell transplantation (HSCT) at second remission. The event-free survival (EFS) probabilities of late relapse and very late relapse were 54.5 ± 7.3 and 64.8 ± 6.8 % at 7 years, respectively (P = 0.36), and were not significantly different. However, the second relapse incidence of late relapse (34.7 ± 7.1 %) was higher than that of very late relapse (15.5 ± 5.1 %, P = 0.03). The second relapse risk was low for very late relapse ALL, which suggests that these patients should be treated without allogeneic HSCT.

摘要

复发期与儿童复发性急性淋巴细胞白血病(ALL)的第二次复发风险密切相关。在这种情况下,极晚期复发的治疗效果应该更好;然而,关于极晚期复发的数据有限。我们回顾性分析了东京儿童癌症研究组(TCCSG)连续进行的两项ALL试验(1995 - 2004年)的结果,重点关注晚期复发,晚期复发分为两类:晚期复发(治疗结束后6 - 24个月,n = 48)和极晚期复发(治疗结束后>24个月,n = 57)。43例患者(29例晚期复发和14例极晚期复发)在第二次缓解期接受了异基因造血干细胞移植(HSCT)。晚期复发和极晚期复发的无事件生存(EFS)概率在7年时分别为54.5±7.3%和64.8±6.8%(P = 0.36),无显著差异。然而,晚期复发的第二次复发发生率(34.7±7.1%)高于极晚期复发(15.5±5.1%,P = 0.03)。极晚期复发ALL的第二次复发风险较低,这表明这些患者在治疗时可不进行异基因HSCT。

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