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复发或难治性外周T细胞淋巴瘤患者按治疗方案对罗米地辛的反应。

Responses to romidepsin by line of therapy in patients with relapsed or refractory peripheral T-cell lymphoma.

作者信息

Foss Francine, Pro Barbara, Miles Prince H, Sokol Lubomir, Caballero Dolores, Horwitz Steven, Coiffier Bertrand

机构信息

Yale Cancer Center, New Haven, Connecticut.

Thomas Jefferson University, Philadelphia, Pennsylvania.

出版信息

Cancer Med. 2017 Jan;6(1):36-44. doi: 10.1002/cam4.939. Epub 2016 Dec 16.

Abstract

Peripheral T-cell lymphoma (PTCL) is a heterogeneous group of aggressive non-Hodgkin lymphomas typically associated with poor prognosis. Most patients with PTCL receive chemotherapy as first-line treatment, but many experience rapid relapse. For patients with relapsed/refractory PTCL, responses to treatment and long-term outcomes tend to worsen with increasing lines of therapy. Romidepsin is a potent class I histone deacetylase inhibitor approved by the US Food and Drug Administration for the treatment of PTCL in patients who have received ≥1 prior therapy. A pivotal phase 2 trial of romidepsin in patients with relapsed/refractory PTCL demonstrated an objective response rate of 25% (33/130), including 15% with confirmed/unconfirmed complete response, and a median duration of response of 28 months. In the analysis presented herein, romidepsin was shown to have similar responses and long-term outcomes in patients with 1, 2, and ≥3 prior lines of treatment, including in patients with disease refractory to the last prior therapy. Although adverse events increased with increasing lines of treatment, the rate of dose modifications and discontinuations due to adverse events was not significantly different. These data support the use of romidepsin as salvage treatment for PTCL irrespective of the number of prior therapies.

摘要

外周T细胞淋巴瘤(PTCL)是一组异质性侵袭性非霍奇金淋巴瘤,通常预后较差。大多数PTCL患者接受化疗作为一线治疗,但许多患者会迅速复发。对于复发/难治性PTCL患者,随着治疗线数的增加,治疗反应和长期预后往往会恶化。罗米地辛是一种强效的I类组蛋白去乙酰化酶抑制剂,已被美国食品药品监督管理局批准用于治疗接受过≥1次先前治疗的PTCL患者。一项针对复发/难治性PTCL患者的罗米地辛关键2期试验显示,客观缓解率为25%(33/130),包括15%的确诊/未确诊完全缓解,中位缓解持续时间为28个月。在本文所呈现的分析中,罗米地辛在接受过1、2和≥3线先前治疗的患者中显示出相似的反应和长期预后,包括对最后一次先前治疗难治的疾病患者。尽管不良事件随着治疗线数的增加而增加,但因不良事件导致的剂量调整和停药率并无显著差异。这些数据支持将罗米地辛用作PTCL的挽救治疗,而不论先前治疗的次数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aff/5269566/d728740ffb8b/CAM4-6-36-g001.jpg

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