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免疫治疗纳入成人 B 细胞急性淋巴细胞白血病治疗

英文原题:Incorporation of Immunotherapy Into Adult B-Cell Acute Lymphoblastic Leukemia Therapy.

查看英文原题

Incorporation of Immunotherapy Into Adult B-Cell Acute Lymphoblastic Leukemia Therapy.

PubMed 2025/07/14(内容时间) J Natl Compr Canc Netw Q1 · IF 17.5(JCR 2025)

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中文摘要

Blinatumomab和inotuzumab ozogamicin在治疗复发/难治性B细胞急性淋巴细胞白血病(B-ALL)方面已显示出疗效,与传统化疗相比可改善结局。在多项临床试验中,接受这些免疫治疗药物治疗的费城染色体(Ph)阳性和Ph阴性B-ALL年轻及年长患者均观察到令人鼓舞的结果。与仅化疗方案相比,inotuzumab ozogamicin和/或blinatumomab治疗可实现高比例的深度可测量残留病阴性,并可能提高生存率,减少对强化化疗的需求,并可能减少对异基因干细胞移植的需求。本文中,我们综述了将blinatumomab和/或inotuzumab ozogamicin纳入一线B-ALL方案的情况,包括在特定患者亚组中潜在使用无化疗方案。我们还探讨了CAR-T 细胞疗法在高危患者一线治疗中的潜在作用,以及进一步改善B-ALL患者结局的新策略。

展开英文摘要原文

Blinatumomab and inotuzumab ozogamicin have demonstrated efficacy in treating relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL) and improving outcomes compared with conventional chemotherapy. Encouraging results have been observed in both younger and older patients with Philadelphia chromosome (Ph)-positive and Ph-negative B-ALL treated with these immunotherapy agents across several clinical trials.

Treatment with inotuzumab ozogamicin and/or blinatumomab leads to high rates of deep measurable residual disease negativity and may enhance survival compared with chemotherapy-only approaches, reducing the need for intensive chemotherapy, and potentially the need for allogeneic stem cell transplantation.

Herein, we review the incorporation of blinatumomab and/or inotuzumab ozogamicin into frontline B-ALL regimens, including the potential use of chemotherapy-free approaches in select patient subgroups.

We also explore the potential role of CAR T-cell therapies in the frontline setting for high-risk patients, as well as novel strategies to further improve outcomes in patients with B-ALL.

论文信息

作者
Haddad FG、Kantarjian H、Short NJ、Jain N、Senapati J、Ravandi F、Jabbour E
单位
1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.United States
文献类型
综述
期刊
Journal of the National Comprehensive Cancer Network : JNCCN2025 Jul 14
原文标识
PubMed 40659041 · DOI 10.6004/jnccn.2025.7050