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
Service d'Hématologie Centre Hospitalier Universitaire de Nice, Hôpital de l'Archet, Clinique, Nice, France.
Université de Nice-Sophia Antipolis, Nice, France.
Bone Marrow Transplant. 2017 May;52(5):678-682. doi: 10.1038/bmt.2016.360. Epub 2017 Jan 23.
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.
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。