Prognostic impact of valemetostat in relapsed/refractory adult T-cell leukaemia-lymphoma.

IF 3.8 2区 医学 Q1 HEMATOLOGY
Takafumi Shichijo, Hiro Tatetsu, Yusuke Higuchi, Toshikazu Miyakawa, Kisato Nosaka, Takahisa Nakamura, Shinya Endo, Asami Yamada, Atsushi Wada, Yuki Okamoto, Toshiro Kawakita, Hitoshi Suzushima, Masao Matsuoka, Jun-Ichirou Yasunaga
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引用次数: 0

Abstract

The prognosis for patients with relapsed/refractory (R/R) adult T-cell leukaemia-lymphoma (ATL) remains dismal. Recently, valemetostat, a dual inhibitor for enhancer of zeste homologue (EZH) 1 and 2, was approved in Japan for R/R aggressive ATL. However, there is no real-world data on the efficacy and prognosis of valemetostat. We therefore analysed clinical outcomes in 28 patients with R/R aggressive ATL who received valemetostat at three hospitals in Kumamoto Prefecture between February 2023 and January 2025. The overall response rate (ORR) and complete response (CR) rate were 54.2% and 33.3% respectively. With a median follow-up of 19.2 months (7.3-21.7) for surviving patients, the median survival time was 15.8 months and median progression-free survival (PFS) was 8.3 months. The probabilities of 1-year overall survival (OS) and PFS were 55.8% and 44.1% respectively. Furthermore, the probabilities of 1-year duration of response and duration of CR were 56.2% and 71.4% respectively. Notably, the probability of 1-year OS was 90.9% in patients who achieved CR/partial response (PR) ('responders') compared to 17.0% in patients who did not achieve CR/PR (p < 0.001). Thus, valemetostat has the potential to be a reliable therapy for patients with R/R aggressive ATL, especially for responders.

缬美他汀对复发/难治性成人t细胞白血病淋巴瘤预后的影响。
复发/难治性(R/R)成人t细胞白血病淋巴瘤(ATL)患者的预后仍然令人沮丧。最近,zeste同源物(EZH) 1和2增强剂的双重抑制剂valemetostat在日本被批准用于R/R侵袭性ATL。然而,没有关于valemetostat的疗效和预后的真实数据。因此,我们分析了2023年2月至2025年1月期间熊本县三家医院接受valemetostat治疗的28例R/R侵袭性ATL患者的临床结果。总缓解率(ORR)为54.2%,完全缓解率(CR)为33.3%。存活患者的中位随访时间为19.2个月(7.3-21.7),中位生存时间为15.8个月,中位无进展生存期(PFS)为8.3个月。1年总生存率(OS)和PFS分别为55.8%和44.1%。1年缓解持续时间和CR持续时间的概率分别为56.2%和71.4%。值得注意的是,在达到CR/部分缓解(PR)(“应答者”)的患者中,1年OS的概率为90.9%,而未达到CR/PR的患者为17.0%
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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