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髓系肿瘤移植后复发的治疗:阿扎胞苷和供者淋巴细胞输注作为挽救性治疗。

Managing post allograft relapse of myeloid neoplasms: azacitidine and donor lymphocyte infusions as salvage therapy.

机构信息

Bone Marrow Transplant Program, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA, USA.

出版信息

Leuk Lymphoma. 2019 Nov;60(11):2733-2743. doi: 10.1080/10428194.2019.1605066. Epub 2019 May 3.

Abstract

Azacitidine (Aza) may promote cytotoxic effects against hematologic tumor cells when combined with donor lymphocyte infusions (DLIs). This study sought to verify Aza-DLI's efficacy and tolerability in patients with relapsed acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) following allogeneic stem cell transplantation (SCT) and identify cohorts benefitting most from therapy. Twenty-eight patients with recurrent AML or MDS following SCT received Aza-DLI. One-year overall survival (OS) after therapy initiation was 44%; two-year OS was 35%. Molecular/cytogenetic-only relapse, the development of cGVHD after therapy initiation, and a greater number of Aza and DLI were associated with remission. There was a trend toward higher absolute CD4+ cell count in those achieving remission. This study demonstrates Aza-DLI to be effective and highlights the importance of minimal residual disease testing and alloreactivity in managing post allograft relapsed hematological malignancy.

摘要

阿扎胞苷(Aza)与供者淋巴细胞输注(DLI)联合使用时可能对血液系统肿瘤细胞具有细胞毒性作用。本研究旨在验证阿扎胞苷-DLI 对异基因造血干细胞移植(SCT)后复发的急性髓系白血病(AML)或骨髓增生异常综合征(MDS)患者的疗效和耐受性,并确定最受益于该治疗的患者群体。28 例 SCT 后复发的 AML 或 MDS 患者接受了阿扎胞苷-DLI 治疗。治疗开始后 1 年的总生存率(OS)为 44%;2 年 OS 为 35%。仅分子/细胞遗传学复发、治疗开始后发生 cGVHD 以及更多的阿扎胞苷和 DLI 与缓解相关。达到缓解的患者的绝对 CD4+细胞计数呈上升趋势。本研究表明阿扎胞苷-DLI 是有效的,并强调了微小残留病检测和同种异体反应性在管理移植后复发血液系统恶性肿瘤中的重要性。

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