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T 细胞耗竭的异基因移植而不进行供者白细胞输注可使多次复发的淋巴瘤患者获得极好的长期生存。移植后复发的生存预测因素。

T-cell-depleted allogeneic transplant without donor leukocyte infusions results in excellent long-term survival in patients with multiply relapsed Lymphoma. Predictors for survival after transplant relapse.

机构信息

Section of Hematology/Oncology, Department of Medicine, University of Chicago Medical Center, Chicago, IL 60637, USA.

出版信息

Leuk Lymphoma. 2011 Feb;52(2):214-22. doi: 10.3109/10428194.2010.538777. Epub 2010 Dec 10.

Abstract

We analyzed 67 patients with lymphoma who received alemtuzumab-based conditioning regimens for allogeneic stem cell transplant and no post-transplant DLI. The median age was 54 (24-70), 43% had unrelated donors, 34% had chemotherapy refractory disease, and 25% had an elevated LDH. With a median follow-up for survivors of 35 months, the estimated 3-year progression-free survival (PFS) and overall survival (OS) were 30% and 47%, respectively. Chemosensitivity by CT and pre-transplant LDH were independent prognostic factors for both overall survival and progression-free survival. Patient age, performance status, donor type, lymphoma subtype, disease sensitivity by PET, and conditioning regimen did not correlate with PFS and OS. Patients who relapsed greater than 6 months after allogeneic transplant were frequently able to re-enter a subsequent durable remission. Our experience confirms the curative potential of alemtuzumab-containing RIC regimens for allogeneic HCT in patients with relapsed lymphoma without prophylactic DLI. An elevated pre-transplant LDH and chemorefractory disease prior to transplant confer a worse prognosis, while PET scan findings do not have this same implication. Patients who relapse greater than 6 months after their transplant are likely to achieve a subsequent remission with any of a variety of interventions, suggesting that GVL effects can be operative even after recurrence. Our outcomes challenge the utility of the common practice of prophylactic DLI after T-depleted transplant for lymphoma.

摘要

我们分析了 67 例接受基于阿仑单抗的预处理方案行异基因造血干细胞移植且未接受移植后 DLI 的淋巴瘤患者。中位年龄为 54 岁(24-70 岁),43%的患者为无关供者,34%的患者为化疗耐药疾病,25%的患者乳酸脱氢酶升高。在幸存者的中位随访 35 个月时,估计 3 年无进展生存率(PFS)和总生存率(OS)分别为 30%和 47%。CT 检查的化疗敏感性和移植前乳酸脱氢酶是总生存和无进展生存的独立预后因素。患者年龄、表现状态、供者类型、淋巴瘤亚型、PET 检查的疾病敏感性以及预处理方案与 PFS 和 OS 均无相关性。在异基因移植后 6 个月以上复发的患者经常能够重新进入后续的持久缓解。我们的经验证实了阿仑单抗联合 RIC 方案在无预防性 DLI 的情况下对复发淋巴瘤患者进行异基因造血干细胞移植的潜在疗效。移植前乳酸脱氢酶升高和移植前化疗耐药疾病预示着更差的预后,而 PET 扫描结果并无此相同的意义。在移植后 6 个月以上复发的患者可能会通过各种干预措施获得后续缓解,这表明即使在复发后 GVL 效应也可能起作用。我们的结果对淋巴瘤患者在 T 细胞耗竭移植后进行预防性 DLI 的常见做法的实用性提出了挑战。

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Alemtuzumab in allogeneic hematopoetic stem cell transplantation.阿仑单抗在异基因造血干细胞移植中的应用。
Expert Opin Biol Ther. 2011 Aug;11(8):1099-111. doi: 10.1517/14712598.2011.592824. Epub 2011 Jun 27.

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