Suppr超能文献

阿西替尼在意大利多耐药慢性期慢性髓性白血病(CML-CP)患者群体中同情用药的真实世界疗效概况。

Real-World Efficacy Profile of Compassionate Use of Asciminib in an Italian, Multi-Resistant Chronic-Phase Chronic Myeloid Leukemia (CML-CP) Patient Population.

作者信息

Breccia Massimo, Rossi Antonella Russo, Giai Valentina, Martino Bruno, Fava Carmen, Annunziata Mario, Abruzzese Elisabetta, Binotto Gianni, Baratè Claudia, Nardozza Aurelio Pio, Misto Alessandra, Coco Paola, Calafiore Valeria, Carraro Maria Cristina, Cattina Federica, Cavazzini Francesco, Corsetti Maria Teresa, Crucitti Lara, Crugnola Monica, Di Veroli Ambra, Ditonno Paolo, Ermacora Anna, Ferrara Felicetto, Genua Angelo, Gozzini Antonella, Impera Stefana, Iurlo Alessandra, Levato Luciano, Luciano Luigia, Miggiano Maria Cristina, De Gobbi Marco, Santoro Marco, Scappini Barbara, Scortechini Anna Rita, Patriarca Andrea, Rosati Serena, Russo Sabina, Sancetta Rosaria, Sanpaolo Grazia, Santeramo Teresa Maria, Sibilla Silvia, Sorà Federica, Sportoletti Paolo, Stagno Fabio, Trabacchi Elena, Castagnetti Fausto

机构信息

Division of Hematology, Department of Translational and Precision Medicine, Azienda Policlinico Umberto I, Sapienza University, Rome, Italy.

Hematology and Transplantation Unit, University of Bari, Bari, Italy.

出版信息

Hematol Oncol. 2025 May;43(3):e70101. doi: 10.1002/hon.70101.

Abstract

Chronic myeloid leukemia (CML) patients who have experienced failure and/or intolerance to multiple lines of treatment have limited therapeutic possibilities. Asciminib is a first-in-class tyrosine kinase inhibitor (TKI) that inhibits the ABL Myristoyl Pocket (STAMP or Specifically Targeting the ABL Myristoyl Pocket) within the BCR::ABL1 oncoprotein. This retrospective Italian analysis reports the efficacy and safety outcomes of asciminib in treating 77 CML patients in chronic phase (CML-CP) within a compassionate use setting. Patients were heavily pretreated with a median of 3 TKIs (55.8% had prior ponatinib exposure). Overall, 57.1% and 42.9% patients switched to asciminib because of resistance and intolerance, respectively. Asciminib maintained or improved molecular responses (MRs) in most patients: as best response, 41 patients (53%) achieved a MR3 or better, with 25 patients (32.5%) reaching deep molecular response (DMR). Greater percentages of intolerant patients achieved MR compared with resistant patients, although the probability of reaching at least a MR3 was not significant between the two groups (p = 0.116). Patients with the T315I mutation responded to asciminib, while ponatinib pre-treated patients showed lower MR improvements compared to naïve patients and had a lower probability to reach a MR3 versus naïve patients (p = 0.0262). These results highlight asciminib remarkable tolerability and efficacy in real-world CML-CP patient population, including heavily pretreated patients, those intolerant and resistant to previous TKIs, and presenting several comorbidities. TRAIL REGISTRATION: The identification code for the MAP is CABL001AIT01M.

摘要

经历过多种治疗方案失败和/或不耐受的慢性髓性白血病(CML)患者的治疗选择有限。阿伐替尼是一种一流的酪氨酸激酶抑制剂(TKI),可抑制BCR::ABL1癌蛋白中的ABL肉豆蔻酰口袋(STAMP,即特异性靶向ABL肉豆蔻酰口袋)。这项意大利回顾性分析报告了在同情用药环境下,阿伐替尼治疗77例慢性期CML(CML-CP)患者的疗效和安全性结果。患者接受了大量预处理,中位使用3种TKI(55.8%曾使用过波纳替尼)。总体而言,分别有57.1%和42.9%的患者因耐药和不耐受而改用阿伐替尼。阿伐替尼在大多数患者中维持或改善了分子反应(MR):作为最佳反应,41例患者(53%)达到MR3或更好,25例患者(32.5%)达到深度分子反应(DMR)。不耐受患者达到MR的比例高于耐药患者,尽管两组之间达到至少MR3的概率无显著差异(p = 0.116)。T315I突变患者对阿伐替尼有反应,而与未接受过波纳替尼治疗的患者相比,接受过波纳替尼预处理的患者MR改善较低,且达到MR3的概率低于未接受过波纳替尼治疗的患者(p = 0.0262)。这些结果突出了阿伐替尼在现实世界CML-CP患者群体中的显著耐受性和疗效,包括经过大量预处理的患者、对先前TKI不耐受和耐药的患者以及患有多种合并症的患者。试验注册:MAP的识别码为CABL001AIT01M。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验