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首页> 外文期刊>Bone marrow transplantation >Hematopoietic stem cell transplantation in relapsed ALK plus anaplastic large cell lymphoma in children and adolescents: a study on behalf of the SFCE and SFGM-TC
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Hematopoietic stem cell transplantation in relapsed ALK plus anaplastic large cell lymphoma in children and adolescents: a study on behalf of the SFCE and SFGM-TC

机译:儿童和青少年复发性ALK加间变性大细胞淋巴瘤的造血干细胞移植:代表SFCE和SFGM-TC的研究

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摘要

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is a treatment option for relapsed anaplastic large cell lymphoma (ALCL) in children, but reports on its efficacy in this disease are still limited. We analyzed data concerning 34 patients under 18 years of age prospectively registered in the French SFGM-TC database, who had undergone an allo-SCT for the treatment of ALK+ ALCL between 1993 and 2011. At transplant, 28 patients (82.4%) were in CR, whereas 6 exhibited detectable disease. Conditioning regimens were mostly myelo-ablative (n = 31). With a median follow-up of 6 years, 5-year overall and event-free survival rates were 70% (SE = 8%) and 58% (SE = 9%), respectively. The 5-year cumulative incidence of relapse and treatment-related mortality was 18% (SE = 7%) and 24% (SE = 8%), respectively. Six patients had relapsed (median time, 141 days (35-235)). A durable CR had been obtained in 4/6 patients after injection of donor lymphocytes (n = 1) or vinblastine-corticosteroid therapy (n = 3). Ten patients had died, eight due to transplant toxicity and two due to progressive disease. Allo-SCT is an efficient treatment for pediatric patients with high-risk relapsed ALK+ ALCL. However, the overall morbidity of allo-SCT raises questions about its place, given the efficacy of targeted agents currently under development in this disease.
机译:同种异体造血干细胞移植(allo-SCT)是儿童复发性间变性大细胞淋巴瘤(ALCL)的治疗选择,但有关其在这种疾病中的疗效的报道仍然有限。我们分析了法国SFGM-TC数据库中前瞻性登记的34名18岁以下患者的数据,这些患者在1993年至2011年间接受了allo-SCT治疗ALK + ALCL。在移植时,有28例患者(82.4%) CR,而6例可检测到疾病。调理方案大多为清髓疗法(n = 31)。中位随访期为6年,5年总生存率和无事件生存率分别为70%(SE = 8%)和58%(SE = 9%)。复发和治疗相关死亡率的5年累积发生率分别为18%(SE = 7%)和24%(SE = 8%)。 6例患者复发(中位时间141天(35-235))。注射供体淋巴细胞(n = 1)或长春碱-皮质激素治疗(n = 3)后,有4/6名患者获得了持久的CR。 10例患者死亡,8例归因于移植物毒性,2例归因于疾病进展。 Allo-SCT是治疗高危复发性ALK + ALCL的小儿患者的有效方法。然而,考虑到目前正在发展的这种疾病的靶向药物的功效,allo-SCT的总体发病率引发了对其位置的质疑。

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