Benefit with glofitamab plus chemotherapy in transplant-ineligible R/R DLBCL

IF 81.1 1区 医学 Q1 ONCOLOGY
Diana Romero
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引用次数: 0

Abstract

Chimeric antigen receptor (CAR) T cells have emerged as an effective treatment option for patients with relapsed and/or refractory (R/R) diffuse large B cell lymphoma (DLBCL) who are ineligible for autologous stem-cell transplantation (ASCT), although owing to manufacturing and access-related limitations many patients receive rituximab plus gemcitabine–oxaliplatin. Now, data from the phase III STARGLO trial show that addition of the CD20 × CD3 bispecific T cell engager glofitamab to chemotherapy provides an overall survival (OS) benefit over the rituximab regimen in this setting.

Patients were randomly allocated to receive gemcitabine–oxaliplatin plus either glofitamab (n = 183) or rituximab (n = 91). Most patients (63%) had received only one prior line of therapy. OS was the primary end point.

符合移植条件的R/R DLBCL患者使用格列菲坦单抗加化疗可获益
嵌合抗原受体(CAR)T细胞已成为不符合自体干细胞移植(ASCT)条件的复发和/或难治性弥漫大B细胞淋巴瘤(DLBCL)患者的一种有效治疗选择,但由于生产和获取方面的限制,许多患者接受利妥昔单抗加吉西他滨-奥沙利铂治疗。现在,来自III期STARGLO试验的数据显示,在化疗中加入CD20 × CD3双特异性T细胞吞噬因子格洛菲他单抗,比利妥昔单抗方案更能提高总生存期(OS)。患者被随机分配接受吉西他滨-奥沙利铂+格洛菲他单抗(n = 183)或利妥昔单抗(n = 91)。大多数患者(63%)之前只接受过一种疗法。OS是主要终点。
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来源期刊
CiteScore
99.40
自引率
0.40%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Nature Reviews publishes clinical content authored by internationally renowned clinical academics and researchers, catering to readers in the medical sciences at postgraduate levels and beyond. Although targeted at practicing doctors, researchers, and academics within specific specialties, the aim is to ensure accessibility for readers across various medical disciplines. The journal features in-depth Reviews offering authoritative and current information, contextualizing topics within the history and development of a field. Perspectives, News & Views articles, and the Research Highlights section provide topical discussions, opinions, and filtered primary research from diverse medical journals.
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