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真实世界分析 ASCIMINIB 在接受过波那替尼预处理的慢性髓性白血病患者中的安全性和疗效。

Real-life analysis on safety and efficacy of asciminib for ponatinib pretreated patients with chronic myeloid leukemia.

机构信息

Hematology Department, Hospital Universitario Ramón y Cajal, IRYCIS, Universidad de Alcala, Km 9,1. 28034, Madrid, Spain.

Institut Catala d'Oncologia, Hospital Duran Y Reynals, L'Hospitalet de Llobregat, Barcelona, Spain.

出版信息

Ann Hematol. 2022 Oct;101(10):2263-2270. doi: 10.1007/s00277-022-04932-6. Epub 2022 Aug 23.

Abstract

Failure of second-generation tyrosine kinase inhibitors (2GTKI) is a challenging situation in patients with chronic myeloid leukemia (CML). Asciminib, recently approved by the US Federal Drug Administration, has demonstrated in clinical trials a good efficacy and safety profile after failure of 2GTKI. However, no study has specifically addressed response rates to asciminib in ponatinib pretreated patients (PPT). Here, we present data on responses to asciminib from 52 patients in clinical practice, 20 of them (38%) with prior ponatinib exposure. We analyzed retrospectively responses and toxicities under asciminib and compared results between PPT and non-PPT patients.After a median follow-up of 30 months, 34 patients (65%) switched to asciminib due to intolerance and 18 (35%) due to resistance to prior TKIs. Forty-six patients (88%) had received at least 3 prior TKIs. Regarding responses, complete cytogenetic response was achieved or maintained in 74% and 53% for non-PPT and PPT patients, respectively. Deeper responses such as major molecular response and molecular response 4.5 were achieved in 65% and 19% in non-PPT versus 32% and 11% in PPT, respectively. Two patients (4%) harbored the T315I mutation, both PPT.In terms of toxicities, non-PPT displayed 22% grade 3-4 TEAE versus 20% in PPT. Four patients (20% of PPT) suffered from cross-intolerance with asciminib as they did under ponatinib.Our data supports asciminib as a promising alternative in resistant and intolerant non-PPT patients, as well as in intolerant PPT patients; the resistant PPT subset remains as a challenging group in need of further therapeutic options.

摘要

第二代酪氨酸激酶抑制剂(2GTKI)失败是慢性髓性白血病(CML)患者面临的一个挑战。阿西替尼(asciminib)最近获得美国联邦药物管理局批准,临床试验表明,在 2GTKI 治疗失败后,它具有良好的疗效和安全性。然而,尚无研究专门针对 ponatinib 预处理患者(PPT)对阿西替尼的反应率进行研究。在此,我们报告了 52 例临床实践中接受阿西替尼治疗患者的反应数据,其中 20 例(38%)曾接受 ponatinib 治疗。我们回顾性分析了阿西替尼的反应和毒性,并比较了 PPT 和非 PPT 患者的结果。中位随访 30 个月后,由于不耐受,34 例患者(65%)转为阿西替尼治疗,18 例(35%)因先前 TKI 耐药而转为阿西替尼治疗。46 例患者(88%)至少接受过 3 种 TKI 治疗。在反应方面,非 PPT 和 PPT 患者的完全细胞遗传学缓解率分别为 74%和 53%,更深层次的反应(主要分子学缓解和分子学反应 4.5)的缓解率分别为 65%和 19%(非 PPT 与 PPT)和 32%和 11%(非 PPT 与 PPT)。两名患者(4%)携带 T315I 突变,均为 PPT。在毒性方面,非 PPT 患者有 22%的 3-4 级治疗相关不良事件(TEAE),而 PPT 患者为 20%。4 例(20%的 PPT)患者因对 ponatinib 不耐受而对阿西替尼也不耐受。我们的数据支持阿西替尼作为非 PPT 耐药和不耐受患者以及不耐受 PPT 患者的一种有前途的替代方案;而耐药 PPT 亚组仍然是一个具有挑战性的群体,需要进一步的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d83b/9463214/7d23383a0648/277_2022_4932_Fig1_HTML.jpg

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