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Prolonged complete hematologic response in relapsed/refractory T-large granular lymphocyte leukemia after bendamustine treatment

机译:苯达莫司汀治疗后复发/难治性T-大颗粒淋巴细胞白血病的完全血液学反应延长

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摘要

T-large granular lymphocyte leukemia (T-LGLL) is a chronic clonal proliferation of effector memory cytotoxic CD3+CD57+CD56 T cells and the current guidelines suggest immunosuppressive therapy as first-line therapy, but the treatment of refractory/relapsed patients is still challenging due to the lack of prospective studies.We describe a series of two refractory/relapsed T-LGLL patients successfully treated with bendamustine, a chemotherapeutic agent largely used for B-cell neoplasms, but poorly investigated for the treatment of T-cell diseases. Complete remission (CR) was achieved in 3 and 6 months, respectively, and maintained for at least 20 months. One patient relapsed after a 20-month CR, but she was responsive to bendamustine therapy again, obtaining a further prolonged CR.Bendamustine as single agent or in combination could be a feasible therapeutic option in refractory/relapsed T-LGLL, especially for elderly patients because of its safety profile.
机译:T-粒状淋巴细胞白血病(T-LGLL)是效应记忆细胞毒性CD3 + CD57 + CD56 - T细胞和细胞的慢性克隆增殖目前的指南建议将免疫抑制疗法作为一线疗法,但是由于缺乏前瞻性研究,难治性/复发性患者的治疗仍然具有挑战性。我们描述了一系列成功地使用苯达莫司汀治疗的两名难治性/复发性T-LGLL患者。化疗剂主要用于B细胞肿瘤,但对T细胞疾病的治疗研究较少。完全缓解(CR)分别在3个月和6个月内达到,并维持至少20个月。一名患者在20个月的CR后复发,但她再次对苯达莫司汀治疗有反应,进一步延长了CR。苯达莫司汀单药或联合治疗可能是难治性/复发性T-LGLL的可行治疗选择,特别是对于老年患者由于其安全性。

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