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Axicabtagene Ciloleucel 治疗大 B 细胞淋巴瘤的生存期

英文原题:Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma.

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Survival with Axicabtagene Ciloleucel in Large B-Cell Lymphoma.

PubMed 2023/06/05(内容时间) N Engl J Med Q1 · IF 84.5(JCR 2025)

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研究概要

在中位随访 47.2 个月时,axi-cel 作为早期复发/难治性大 B 细胞淋巴瘤患者的二线治疗,其总生存期显著长于标准治疗。(由 Kite 资助;ZUMA-7 ClinicalTrials.gov 注册号,NCT03391466。)

研究思路结论见上方概要

在这项3期试验的主要结局分析中,接受axicabtagene ciloleucel(axi-cel,一种自体抗CD19CAR-T 细胞疗法)作为二线治疗的早期复发/难治性大B细胞淋巴瘤患者,其无事件生存期显著长于接受标准治疗的患者。需要更长期结局的数据。

在这项试验中,我们将早期复发/难治性大B细胞淋巴瘤患者按1:1的比例随机分配,接受axi-cel或标准治疗(2至3个周期的化学免疫治疗后,对治疗有应答的患者接受高剂量化疗联合自体干细胞移植)。主要结局是无事件生存期,关键次要结局是缓解和总生存期。在此,我们报告首例患者随机分组后5年时预设的总生存期分析结果。

共有359例患者被随机分配接受axi-cel(180例)或标准治疗(179例)。中位随访47.2个月时,axi-cel组报告死亡82例,标准治疗组报告死亡95例。axi-cel组的中位总生存期未达到,标准治疗组为31.1个月;估计4年总生存率分别为54.6%和46.0%(死亡风险比0.73;95% CI,0.54至0.98;分层双侧log-rank检验P = 0.03)。在意向治疗人群中观察到axi-cel带来的生存获益,该人群包括74%的原发性难治性疾病及其他高危特征患者。研究者评估的中位无进展生存期在axi-cel组为14.7个月,在标准治疗组为3.7个月,估计4年百分比分别为41.8%和24.4%(风险比0.51;95% CI,0.38至0.67)。自无事件生存期主要分析以来,未发生新的治疗相关死亡。

展开英文摘要原文

In an analysis of the primary outcome of this phase 3 trial, patients with early relapsed or refractory large B-cell lymphoma who received axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor T-cell therapy, as second-line treatment had significantly longer event-free survival than those who received standard care. Data were needed on longer-term outcomes.

In this trial, we randomly assigned patients with early relapsed or refractory large B-cell lymphoma in a 1:1 ratio to receive either axi-cel or standard care (two to three cycles of chemoimmunotherapy followed by high-dose chemotherapy with autologous stem-cell transplantation in patients who had a response). The primary outcome was event-free survival, and key secondary outcomes were response and overall survival. Here, we report the results of the prespecified overall survival analysis at 5 years after the first patient underwent randomization.

A total of 359 patients underwent randomization to receive axi-cel (180 patients) or standard care (179 patients). At a median follow-up of 47.2 months, death had been reported in 82 patients in the axi-cel group and in 95 patients in the standard-care group. The median overall survival was not reached in the axi-cel group and was 31.1 months in the standard-care group; the estimated 4-year overall survival was 54.6% and 46.0%, respectively (hazard ratio for death, 0.73; 95% confidence interval [CI], 0.54 to 0.98; P = 0.03 by stratified two-sided log-rank test). This increased survival with axi-cel was observed in the intention-to-treat population, which included 74% of patients with primary refractory disease and other high-risk features. The median investigator-assessed progression-free survival was 14.7 months in the axi-cel group and 3.7 months in the standard-care group, with estimated 4-year percentages of 41.8% and 24.4%, respectively (hazard ratio, 0.51; 95% CI, 0.38 to 0.67). No new treatment-related deaths had occurred since the primary analysis of event-free survival.

At a median follow-up of 47.2 months, axi-cel as second-line treatment for patients with early relapsed or refractory large B-cell lymphoma resulted in significantly longer overall survival than standard care. (Funded by Kite; ZUMA-7 ClinicalTrials.gov number, NCT03391466.).

论文信息

作者
Westin JR、Oluwole OO、Kersten MJ、Miklos DB、Perales MA、Ghobadi A、Rapoport AP、Sureda A
单位
From University of Texas M.D. Anderson Cancer Center, Houston (J.R.W.); Vanderbilt-Ingram Cancer Center, Nashville (O.O.O.); Amsterdam University Medical Center (UMC), University of Amsterdam, Cancer Center Amsterdam, Amsterdam (M.J.K.), UMC Groningen, Groningen (T.M.), and UMC Utrecht, Utrecht (M.C.M.) - all in the Netherlands; Stanford University School of Medicine, Stanford (D.B.M.), and Kite, Santa Monica (Y.Y., S.V., S.F., P.C., S.A.S., M.S., C.T.) - both in California; Memorial Sloan Kettering Cancer Center, New York (M.-A.P.), and University of Rochester School of Medicine, Rochester (P.M.R.) - both in New York; Washington University School of Medicine, St. Louis (A.G.); Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore (A.P.R.); Servei d'Hematologia Clínica, Institut Català d'Oncologia-Hospitalet, Institut de Recerca Biomèdica de Bellvitge, Universitat de Barcelona, Barcelona (A.S.B.); Dana-Farber Cancer Institute, Boston (C.A.J.); University of Iowa, Iowa City (U.F.); Banner M.D. Anderson Cancer Center, Gilbert, AZ (M.U.); the Division of Hematology and Hematologic Oncology, Department of Medicine, Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, NS (M.E.), and Vancouver General Hospital, BC Cancer, University of British Columbia, Vancouver (K.W.S.) - both in Canada; John Theurer Cancer Center, Hackensack, NJ (L.A.L.); the Centre for Clinical Haematology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom (S.C.); Peter MacCallum Cancer Centre, Royal Melbourne Hospital, and the University of Melbourne, Melbourne (M.D.); UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh (K.D.); University of Kansas Cancer Center, Kansas City (J.M.); David and Etta Jonas Center for Cellular Therapy, University of Chicago, Chicago (P.A.R.); and Moffitt Cancer Center, Tampa, FL (F.L.L.).United States
文献类型
III 期临床试验 · 随机对照试验
期刊
The New England journal of medicine2023 Jul 13
原文标识
PubMed 37272527 · DOI 10.1056/NEJMoa2301665