非清髓性异基因造血细胞移植治疗复发、难治及转化型惰性非霍奇金淋巴瘤

Nonmyeloablative allogeneic hematopoietic cell transplantation in relapsed, refractory, and transformed indolent non-Hodgkin's lymphoma.

作者信息

Rezvani Andrew R, Storer Barry, Maris Michael, Sorror Mohamed L, Agura Edward, Maziarz Richard T, Wade James C, Chauncey Thomas, Forman Stephen J, Lange Thoralf, Shizuru Judith, Langston Amelia, Pulsipher Michael A, Sandmaier Brenda M, Storb Rainer, Maloney David G

机构信息

Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, MS D1-100, Seattle, WA 98109, USA.

出版信息

J Clin Oncol. 2008 Jan 10;26(2):211-7. doi: 10.1200/JCO.2007.11.5477. Epub 2007 Dec 3.

Abstract

PURPOSE

Few effective treatment options exist for chemotherapy-refractory indolent or transformed non-Hodgkin's lymphoma (NHL). We examined the outcome of nonmyeloablative allogeneic hematopoietic cell transplantation (HCT) in this setting.

PATIENTS AND METHODS

Sixty-two patients with indolent or transformed NHL were treated with allogeneic HCT from related (n = 34) or unrelated (n = 28) donors after conditioning with 2 Gy of total-body irradiation with or without fludarabine. Nine unrelated donors were mismatched for >/= one HLA antigen. Sixteen patients had histologic transformation before HCT. Twenty patients (32%) had progressive disease after previous high-dose therapy with autologous HCT. Median age was 54 years, and patients had received a median of six lines of treatment before HCT. Median follow-up time after HCT was 36.6 months.

RESULTS

At 3 years, the estimated overall survival (OS) and progression-free survival (PFS) rates were 52% and 43%, respectively, for patients with indolent disease, and 18% and 21%, respectively, for patients with transformed disease. Patients with indolent disease and related donors (n = 26) had 3-year estimated OS and PFS rates of 67% and 54%, respectively. The incidences of grade 2 to 4 acute graft-versus-host disease (GVHD), grade 3 and 4 acute GVHD, and extensive chronic GVHD were 63%, 18%, and 47%, respectively. Among survivors, the median Karnofsky performance status at last follow-up was 85%.

CONCLUSION

Nonmyeloablative allogeneic HCT can produce durable disease-free survival in patients with relapsed or refractory indolent NHL, even in this relatively elderly and heavily pretreated cohort. Outcomes were particularly good in patients with untransformed disease and related donors, whereas patients with transformed disease did poorly. Long-term survivors reported good overall functional status.

摘要

目的

对于化疗难治性惰性或转化型非霍奇金淋巴瘤(NHL),几乎没有有效的治疗选择。我们在此背景下研究了非清髓性异基因造血细胞移植(HCT)的疗效。

患者与方法

62例惰性或转化型NHL患者在接受2 Gy全身照射(有或无氟达拉滨)预处理后,接受来自相关供者(n = 34)或无关供者(n = 28)的异基因HCT。9例无关供者与≥1个HLA抗原不匹配。16例患者在HCT前发生组织学转化。20例患者(32%)在先前接受自体HCT的高剂量治疗后出现疾病进展。中位年龄为54岁,患者在HCT前接受的治疗中位数为6线。HCT后的中位随访时间为36.6个月。

结果

3年时,惰性疾病患者的估计总生存率(OS)和无进展生存率(PFS)分别为52%和43%,转化型疾病患者分别为18%和21%。惰性疾病且供者为相关供者的患者(n = 26)3年估计OS和PFS率分别为67%和54%。2至4级急性移植物抗宿主病(GVHD)、3级和4级急性GVHD以及广泛慢性GVHD的发生率分别为63%、18%和47%。在幸存者中,最后一次随访时的中位卡诺夫斯基功能状态为85%。

结论

非清髓性异基因HCT可为复发或难治性惰性NHL患者带来持久的无病生存,即使是在这个相对年长且预处理充分的队列中。未转化疾病且供者为相关供者的患者预后特别好,而转化型疾病患者预后较差。长期幸存者报告总体功能状态良好。

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