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异基因造血干细胞移植治疗成人 T 细胞白血病/淋巴瘤,特别强调预处理方案:一项全国性回顾性研究。

Allogeneic hematopoietic stem cell transplantation for adult T-cell leukemia-lymphoma with special emphasis on preconditioning regimen: a nationwide retrospective study.

机构信息

Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

出版信息

Blood. 2012 Aug 23;120(8):1734-41. doi: 10.1182/blood-2012-03-414490. Epub 2012 Jun 11.

DOI:10.1182/blood-2012-03-414490
PMID:22689862
Abstract

Adult T-cell leukemia-lymphoma (ATL) is an intractable mature T-cell neoplasm. We performed a nationwide retrospective study of allogeneic hematopoietic stem cell transplantation (HSCT) for ATL in Japan, with special emphasis on the effects of the preconditioning regimen. This is the largest study of ATL patients receiving HSCT. Median overall survival (OS) and 3-year OS of bone marrow or peripheral blood transplantation recipients (n = 586) was 9.9 months (95% confidence interval, 7.4-13.2 months) and 36% (32%-41%), respectively. These values for recipients of myeloablative conditioning (MAC; n = 280) and reduced intensity conditioning (RIC; n = 306) were 9.5 months (6.7-18.0 months) and 39% (33%-45%) and 10.0 months (7.2-14.0 months) and 34% (29%-40%), respectively. Multivariate analysis demonstrated 5 significant variables contributing to poorer OS, namely, older age, male sex, not in complete remission, poor performance status, and transplantation from unrelated donors. Although no significant difference in OS between MAC and RIC was observed, there was a trend indicating that RIC contributed to better OS in older patients. Regarding mortality, RIC was significantly associated with ATL-related mortality compared with MAC. In conclusion, allogeneic HSCT not only with MAC but also with RIC is an effective treatment resulting in long-term survival in selected patients with ATL.

摘要

成人 T 细胞白血病/淋巴瘤(ATL)是一种难治性成熟 T 细胞肿瘤。我们对日本所有接受异基因造血干细胞移植(HSCT)治疗 ATL 的患者进行了一项全国性回顾性研究,特别强调了预处理方案的效果。这是迄今为止最大规模的接受 HSCT 的 ATL 患者研究。骨髓或外周血移植受者(n=586)的中位总生存期(OS)和 3 年 OS 分别为 9.9 个月(95%置信区间,7.4-13.2 个月)和 36%(32%-41%)。接受清髓性预处理(MAC;n=280)和强度降低预处理(RIC;n=306)的受者的这些值分别为 9.5 个月(6.7-18.0 个月)和 39%(33%-45%)和 10.0 个月(7.2-14.0 个月)和 34%(29%-40%)。多变量分析显示,5 个显著变量与较差的 OS 相关,即年龄较大、男性、未完全缓解、表现状态差和来自无关供者的移植。尽管 MAC 和 RIC 之间的 OS 无显著差异,但存在 RIC 有助于年龄较大患者 OS 更好的趋势。关于死亡率,与 MAC 相比,RIC 与 ATL 相关死亡率显著相关。总之,异基因 HSCT 不仅用 MAC,而且用 RIC 也是一种有效的治疗方法,可使选定的 ATL 患者获得长期生存。

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