Mosunetuzumab and Polatuzumab Vedotin as First-line Treatment for Large B Cell Lymphoma in Older Unfit or Frail Patients

IF 23.9 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2026-10-05 DOI:10.1182/blood.2026035116
Adam J. Olszewski,Herbert A. Eradat,Abraham Avigdor,Netanel A. Horowitz,Matthew S. McKinney,Seung Tae Lee,Juan Miguel Bergua Burgues,Antonia Rodriguez Izquierdo,Mariana Bastos-Oreiro,Chezi Ganzel,Tae Min Kim,Youngwoo Jeon,Michał Taszner,Mayur S. Narkhede,Won Seog Kim,Ho-Jin Shin,Dariusz Woszczyk,Neta Goldschmidt,Avrita Singh,Michael C. Wei,Jue Wang,Connie Lee Batlevi,Wahib Ead,Martin Janousek,Gila Sellam,Wojciech Jurczak
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引用次数: 0

Abstract

Older or medically unfit patients with diffuse large B-cell lymphoma (DLBCL) frequently cannot tolerate standard anthracycline-based immunochemotherapy, creating a persistent unmet clinical need. We conducted a multicenter, international, open-label phase I/II trial evaluating an immunotherapy-based first-line approach using subcutaneous mosunetuzumab in combination with polatuzumab vedotin in previously untreated patients classified as unfit or frail by simplified geriatric assessment (sGA). Participants received six cycles of polatuzumab vedotin with step-up-dosing of subcutaneous mosunetuzumab, followed by mosunetuzumab monotherapy for a planned total of eight cycles. The primary endpoint was objective response rate (ORR) at end of treatment, assessed by independent review using PET-CT Lugano 2014 criteria. Among participants treated at full dose (n=101), the median age was 81 years with 58% classified as unfit and 41% as frail by sGA. The ORR at the end of treatment was 61.4% (95% CI, 51.1-70.9), with a complete response (CR) rate of 56.4%. The best observed ORR and CR rates on therapy were 80.2% and 66.3%, respectively. With a median follow-up of 36.5 months, median investigator-assessed duration of response and overall survival were not reached; estimated 2-year progression-free and overall survival were 52.2% and 62.4%, respectively. Cytokine release syndrome occurred in 30.6% of participants and was predominantly grade 1. Infection-related mortality was observed, largely during the COVID-19 pandemic and among participants classified as frail. This geriatric assessment-guided treatment demonstrated durable efficacy and may represent a potential first-line treatment option for carefully selected unfit or frail patients with newly diagnosed DLBCL. Trial registration: #NCT03677154.
Mosunetuzumab和Polatuzumab Vedotin作为老年不适应或体弱患者大B细胞淋巴瘤的一线治疗
老年或医学上不适合的弥漫性大b细胞淋巴瘤(DLBCL)患者经常不能耐受标准的基于蒽环类药物的免疫化疗,造成持续未满足的临床需求。我们进行了一项多中心、国际、开放标签的I/II期试验,评估了一种基于免疫治疗的一线方法,该方法使用皮下mosunetuzumab联合polatuzumab vedotin治疗先前未经治疗的经简化老年评估(sGA)分类为不适合或虚弱的患者。参与者接受6个周期的polatuzumab vedotin和逐步增加皮下mosunetuzumab剂量,然后是mosunetuzumab单药治疗,计划总共8个周期。主要终点是治疗结束时的客观缓解率(ORR),采用PET-CT Lugano 2014标准进行独立评估。在全剂量治疗的参与者中(n=101),中位年龄为81岁,58%被sGA分类为不健康,41%被sGA分类为虚弱。治疗结束时ORR为61.4% (95% CI, 51.1-70.9),完全缓解(CR)率为56.4%。治疗后观察到的最佳ORR和CR分别为80.2%和66.3%。中位随访36.5个月,研究者评估的中位缓解持续时间和总生存期未达到;估计2年无进展生存率和总生存率分别为52.2%和62.4%。细胞因子释放综合征发生在30.6%的参与者中,主要是1级。观察到与感染相关的死亡率,主要是在COVID-19大流行期间以及被归类为虚弱的参与者中。这种以老年评估为指导的治疗显示出持久的疗效,对于精心挑选的不适合或体弱的新诊断的DLBCL患者来说,可能是一种潜在的一线治疗选择。试验注册:#NCT03677154。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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