[阿扎胞苷和 Venetoclax 7 天联合疗法(7+7疗法)的安全性和有效性]。

Yuki Osada, Hikari Kanai-Sudo, Taro Mizuki, Sakae Tanosaki, Ken Suzuki
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引用次数: 0

摘要

急性髓性白血病(AML)患者不适合接受强化化疗,预后较差。阿扎胞苷和 Venetoclax 的联合治疗已被证明具有很高的总有效率和缓解率,即使是不符合积极化疗条件的患者也不例外。然而,治疗后骨髓抑制往往会延长,还可能发生感染。严重的骨髓抑制通常通过剂量滴定来解决,但具体的剂量滴定方法尚未明确。我们采用了阿扎胞苷加文替曲塞的标准诱导疗法,如果囊泡下降到20%或更低,则从下一周期开始改用7+7疗法,将文替曲塞缩短至7天。在我们治疗的19例患者(中位年龄80岁)中,MLFS以上的反应率为100%,CR为57.9%,CRc(CR+CRi)为78.8%,中位OS为693天,中位PFS为458天,之前未治疗的患者未达到中位OS。这表明,7+7 是一种高效且耐受性良好的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Safety and efficacy of 7-day administration of azacitidine and venetoclax combination therapy (7+7 therapy)].

Acute myelogenous leukemia (AML) has a poor prognosis in patients who are ineligible for intensive chemotherapy. The combination of azacitidine and venetoclax has been shown to have high overall efficiency and remission rates, even in patients ineligible for aggressive chemotherapy. However, myelosuppression is often prolonged after treatment, and infection can also occur. Severe myelosuppression is often addressed by dose titration, but specific dose titration methods have not been clarified. We used the standard induction therapy with azacitidine plus venetoclax, and if blasts decreased to 20% or less, switched to 7+7 therapy to shorten venetoclax to 7 days starting from the next cycle. In the 19 patients we treated (median age 80 years), response rate above MLFS was 100%, CR 57.9%, CRc (CR+CRi) 78.8%, median OS 693 days, median PFS 458 days, and median OS was not reached in previously untreated patients. This indicates that 7+7 is a highly effective and well-tolerated treatment.

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