将减量化疗和 blinatumomab 作为新诊断的 Ph 阴性 B 细胞前体急性淋巴细胞白血病的诱导治疗:2 期试验。

IF 29.5 1区 医学 Q1 HEMATOLOGY
Jing Lu, Huiying Qiu, Ying Wang, Xin Zhou, Haiping Dai, Xuzhang Lu, Xiaofei Yang, Bin Gu, Ming Hong, Miao Miao, Ruinan Lu, Jun Wang, Qian Wu, Mengxing Xue, Yun Wang, Ailing Deng, Yaoyao Shen, Yin Liu, Xueqing Dou, Yutian Lei, Depei Wu, Yu Zhu, Suning Chen
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引用次数: 0

摘要

在急性B细胞前体淋巴细胞白血病(BCP-ALL)的一线治疗中,Blinatumomab是一种很有前景的治疗药物,它能提高治疗效果。为减轻CD19选择压力并降低blinatumomab相关毒性反应的发生率,建议在使用blinatumomab前进行治疗前化疗。2022年9月至2023年12月,我们在新诊断的费城染色体阴性BCP-ALL(Ph阴性BCP-ALL)患者中开展了一项单臂、多中心、2期试验(NCT05557110)。参试者先接受为期7天的减量化疗(RDC)诱导治疗,包括伊达比星、文德辛和地塞米松,然后接受为期2周的blinatumomab治疗。未能达到复合完全缓解(CRc)的患者再接受2周的blinatumomab治疗。主要终点是初始诱导治疗后的CRc率。在35名入组患者中,33人(94%)在接受2周的blinatumomab治疗后达到CRc,30人(86%)达到可测量残留疾病(MRD)阴性。两名患者将blinatumomab延长至4周。在接受2周或4周的blinatumomab治疗后,所有患者都达到了CR(35/35),89%的患者(31/35)达到了MRD阴性。达到CR的中位时间为22天。免疫效应细胞相关神经毒性综合征为数不多(14%,均为1级)。3级或以上的非血液学不良事件包括肺炎(17%)、败血症(6%)和细胞因子释放综合征(9%)。中位随访时间为11.5个月,估计1年总生存率和1年无进展生存率分别为97.1%和82.2%。这些研究结果证实,RDC后加用blinatumomab是一种有效且耐受性良好的诱导方案,适用于新诊断的Ph阴性BCP-ALL,支持向强度更低、靶向性更强的治疗方法转变。试验注册:https://www.clinicaltrials.Gov 。标识符 NCT05557110。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced-dose chemotherapy and blinatumomab as induction treatment for newly diagnosed Ph-negative B-cell precursor acute lymphoblastic leukemia: a phase 2 trial.

Blinatumomab has emerged as a promising component of first-line therapy for acute B-cell precursor lymphoblastic leukemia (BCP-ALL), bolstering treatment efficacy. To mitigate CD19 selection pressure and reduce the incidence of blinatumomab-associated toxicities, pre-treatment chemotherapy is recommended before administering blinatumomab. From September 2022 to December 2023, we conducted a single-arm, multicenter, phase 2 trial (NCT05557110) in newly diagnosed Philadelphia chromosome-negative BCP-ALL (Ph-negative BCP-ALL) patients. Participants received induction treatment with reduced-dose chemotherapy (RDC), comprising idarubicin, vindesine, and dexamethasone over 7 days, followed by 2 weeks of blinatumomab. Those failing to achieve composite complete remission (CRc) received an additional 2 weeks of blinatumomab. The primary endpoint was the CRc rate post initial induction treatment. Of the 35 enrolled patients, 33 (94%) achieved CRc after 2 weeks of blinatumomab, with 30 (86%) achieving measurable residual disease (MRD) negativity. Two patients extended blinatumomab to 4 weeks. With either 2 or 4 weeks of blinatumomab treatment, all patients achieved CR (35/35) and 89% (31/35) were MRD negativity. The median time to CR was 22 days. Immune effector cell-associated neurotoxicity syndrome was limited (14%, all grade 1). Non-hematological adverse events of grade 3 or higher included pneumonia (17%), sepsis (6%), and cytokine release syndrome (9%). With a median follow-up of 11.5 months, estimated 1-year overall survival and 1-year progression-free survival rates were 97.1% and 82.2%, respectively. These findings affirm that RDC followed by blinatumomab is an effective and well-tolerated induction regimen for newly diagnosed Ph-negative BCP-ALL, supporting a shift towards less intensive and more targeted therapeutic approaches. Trial registration: https://www.clinicaltrials.Gov . Identifier NCT05557110.

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来源期刊
CiteScore
48.10
自引率
2.10%
发文量
169
审稿时长
6-12 weeks
期刊介绍: The Journal of Hematology & Oncology, an open-access journal, publishes high-quality research covering all aspects of hematology and oncology, including reviews and research highlights on "hot topics" by leading experts. Given the close relationship and rapid evolution of hematology and oncology, the journal aims to meet the demand for a dedicated platform for publishing discoveries from both fields. It serves as an international platform for sharing laboratory and clinical findings among laboratory scientists, physician scientists, hematologists, and oncologists in an open-access format. With a rapid turnaround time from submission to publication, the journal facilitates real-time sharing of knowledge and new successes.
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