CPX-351联合venetoclax治疗新诊断的高危急性髓性白血病的2期研究

IF 14.6 2区 医学 Q1 HEMATOLOGY
HemaSphere Pub Date : 2025-10-22 eCollection Date: 2025-10-01 DOI:10.1002/hem3.70214
Wei-Ying Jen, Jennifer Croden, Emmanuel Almanza-Huante, Courtney DiNardo, Kelly Chien, Danielle Hammond, Wei Qiao, Yesid Alvarado, Lucia Masarova, Andres E Quesada, Sherry Pierce, Alex Bataller, Guillermo Garcia-Manero, Amin Alousi, Nicholas Short, Naval Daver, Farhad Ravandi, Hagop Kantarjian, Tapan M Kadia
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引用次数: 0

摘要

Venetoclax已与强化化疗方案联合用于治疗急性髓性白血病(AML)。本研究旨在探讨venetoclax联合全剂量CPX-351 (CPX + VEN)治疗新诊断AML的安全性和有效性。17例患者接受治疗,中位年龄为59岁(43-69岁);71%有继发性AML, 47%有低甲基化剂(HMA)暴露史,59%有骨髓增生异常综合征(MDS)相关(MR)突变,47%有复杂核型,29%有TP53突变。总缓解率(ORR)为82% (95% CI, 57-96),综合完全缓解率(CRc)为71% (95% CI, 50-93)。MR突变患者的ORR为100% (95% CI, 69-100),其中CRc为90% (95% CI, 55-100)。既往暴露于HMA的患者结直肠癌发生率为63% (95% CI, 24-91)。中位随访时间为11.8个月,中位总生存期(OS)为12.8个月(95% CI, 5-NE), 2年OS为34% (95% CI, 10-61)。MR突变患者的中位OS为17.9个月,而无MR突变患者的中位OS为5.1个月(P = 0.039)。14名应答患者中有12名(86%)进行了干细胞移植(SCT);中位无复发生存期(95% CI, 1-32)和总生存期(OS)分别为14.7个月和14.7个月(95% CI, 4-25)。4周死亡率为0%,8周死亡率为17%。最常见的不良事件与骨髓抑制有关。CPX + VEN导致高缓解率,并使大多数高度不良的ND AML患者进展到同种异体SCT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Phase 2 study of CPX-351 in combination with venetoclax in patients with newly diagnosed high-risk acute myeloid leukemia.

Venetoclax has been combined with intensive chemotherapy regimens in the treatment of acute myeloid leukemia (AML). We aimed to investigate the safety and efficacy of venetoclax combined with full-dose CPX-351 (CPX + VEN) in newly diagnosed (ND) AML. Seventeen patients with a median age of 59 years (range, 43-69) were treated; 71% had secondary AML, 47% had prior hypomethylating agent (HMA) exposure, 59% had myelodysplastic syndrome (MDS)-related (MR) mutations, 47% had complex karyotype, and 29% were TP53 mutated. The overall response rate (ORR) was 82% (95% CI, 57-96) with a composite complete remission rate (CRc) of 71% (95% CI, 50-93). Patients with MR mutations had an ORR of 100% (95% CI, 69-100), including a CRc of 90% (95% CI, 55-100). Patients with prior HMA exposure had a CRc of 63% (95% CI, 24-91). With a median follow-up time of 11.8 months, the median overall survival (OS) was 12.8 months (95% CI, 5-NE) with a 2-year OS of 34% (95% CI, 10-61). Patients with MR mutations had a median OS of 17.9 months versus 5.1 months in patients without MR mutations (P = 0.039). Twelve (86%) of 14 responding patients proceeded to stem cell transplant (SCT); the median recurrence-free survival and OS landmarked from date of SCT were 14.7 months (95% CI, 1-32) and 14.7 months (95% CI, 4-25), respectively. The 4-week mortality was 0% and the 8-week mortality was 17%. The most common adverse events were related to myelosuppression. CPX + VEN resulted in high remission rates and enabled progression to allogenic SCT for the majority of a highly adverse group of ND AML patients.

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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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