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急性白血病患儿异基因造血干细胞移植失败后的结局:法国骨髓移植与细胞治疗协会(SFGM-TC)的一项研究

Outcome after failure of allogeneic hematopoietic stem cell transplantation in children with acute leukemia: a study by the société Francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC).

作者信息

Roux C, Tifratene K, Socié G, Galambrun C, Bertrand Y, Rialland F, Jubert C, Pochon C, Paillard C, Sirvent A, Nelken B, Vannier J P, Freycon C, Beguin Y, Raus N, Yakoub-Agha I, Mohty M, Dalle J-H, Michel G, Pradier C, Peffault de Latour R, Rohrlich P-S

机构信息

Service d'Hématologie Centre Hospitalier Universitaire de Nice, Hôpital de l'Archet, Clinique, Nice, France.

Université de Nice-Sophia Antipolis, Nice, France.

出版信息

Bone Marrow Transplant. 2017 May;52(5):678-682. doi: 10.1038/bmt.2016.360. Epub 2017 Jan 23.

Abstract

Allogeneic hematopoietic stem cell transplantation (SCT) contributes to improved outcome in childhood acute leukemia (AL). However, therapeutic options are poorly defined in the case of post-transplantation relapse. We aimed to compare treatment strategies in 334 consecutive children with acute leukemia relapse or progression after SCT in a recent 10-year period. Data could be analyzed in 288 patients (157 ALL, 123 AML and 8 biphenotypic AL) with a median age of 8.16 years at transplantation. The median delay from first SCT to relapse or progression was 182 days. The treatment consisted of chemotherapy alone (n=108), chemotherapy followed by second SCT (n=70), supportive/palliative care (n=67), combination of chemotherapy and donor lymphocyte infusion (DLI; n=30), or isolated reinfusion of donor lymphocytes (DLI; n=13). The median OS duration after relapse was 164 days and differed according to therapy: DLI after chemotherapy=385 days, second allograft=391 days, chemotherapy=174 days, DLI alone=140 days, palliative care=43 days. A second SCT or a combination of chemotherapy and DLI yielded similar outcome (hazard ratio (HR)=0.85, P=0.53) unlike chemotherapy alone (HR=1.43 P=0.04), palliative care (HR=4.24, P<0.0001) or isolated DLI (HR=1,94, P<0.04). Despite limitations in this retrospective setting, strategies including immunointervention appear superior to other approaches, mostly in AML.

摘要

异基因造血干细胞移植(SCT)有助于改善儿童急性白血病(AL)的治疗结果。然而,移植后复发情况下的治疗选择尚不明确。我们旨在比较最近10年中334例SCT后急性白血病复发或进展的连续儿童的治疗策略。对288例患者(157例急性淋巴细胞白血病、123例急性髓系白血病和8例双表型急性白血病)的数据进行了分析,这些患者移植时的中位年龄为8.16岁。从首次SCT到复发或进展的中位间隔时间为182天。治疗包括单纯化疗(n = 108)、化疗后进行第二次SCT(n = 70)、支持性/姑息性治疗(n = 67)、化疗与供体淋巴细胞输注(DLI)联合(n = 30)或单纯供体淋巴细胞输注(DLI;n = 13)。复发后的中位总生存期为164天,且因治疗方法而异:化疗后DLI为385天,第二次同种异体移植为391天,化疗为174天,单纯DLI为140天,姑息性治疗为43天。与单纯化疗(风险比(HR)= 1.43,P = 0.04)、姑息性治疗(HR = 4.24,P < 0.0001)或单纯DLI(HR = 1.94,P < 0.04)不同,第二次SCT或化疗与DLI联合产生了相似的结果(HR = 0.85,P = 0.53)。尽管在这种回顾性研究中有局限性,但包括免疫干预的策略似乎优于其他方法,在急性髓系白血病中尤为如此。

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