CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Outcomes of older patients with diffuse large B-cell lymphoma treated with R-CHOP: 10-year follow-up of the LNH03-6B trial.
Outcomes of older patients with diffuse large B-cell lymphoma treated with R-CHOP: 10-year follow-up of the LNH03-6B trial.
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LNH03-6B是一项III期随机试验,评估利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)每2周(R-CHOP14)或每3周(R-CHOP21)给药作为一线治疗,对60至80岁、年龄校正国际预后指数(aaIPI)评分1的弥漫性大B细胞淋巴瘤(DLBCL)患者的疗效(注册号NCT00144755)。试验结束时,研究团队实施了前瞻性长期随访计划。主要终点为无进展生存期(PFS)和总生存期(OS);复发模式及首次进展后的PFS和OS(PFS2、OS2)为次要终点。LNH03-6B在ClinicalTrials.gov注册号为NCT00144755。试验中,304名和296名患者分别接受8个周期R-CHOP14或R-CHOP21。
在主要分析时仍存活的384名患者中,有256名(67%)纳入长期随访分析。中位随访10.1年期间,213名患者出现进展,140名患者在未进展情况下死亡。10年PFS为40.4%(95%置信区间35.9–44.9);依据302例死亡估算的10年OS为50%(43–56)。213名进展患者中,105名(49%)在二线治疗后再次进展,77名(36%)在未发生第二次进展前死亡。1年PFS2和OS2估计分别为37.9%(95%置信区间31.4–44.5)和55.8%(95%置信区间48.8–62.2)。随机分组10年后,R-CHOP14和R-CHOP21组DLBCL患者的PFS和OS结局相近。在CAR-T 时代之前,患者进展或复发后接受二线化疗仍预后较差。该人群有必要探索新的初治方法和替代性二线治疗。
The LNH03-6B trial was a phase 3 randomized trial evaluating the efficacy of first-line rituximab, cyclophosphamide, doxorubicine, vincristine and prednisone (R-CHOP) delivered every 2 weeks (R-CHOP14) or 3 weeks (R-CHOP21) in patients with diffuse large B-cell lymphoma (DLBCL) aged 60 to 80 years with an aaIPI (age-adjusted International Prognostic Index) score 1 (registered as NCT00144755).
We implemented a prospective long-term follow-up program at the end of this trial. The primary endpoints were progression-free survival (PFS) and overall survival (OS). Relapse patterns, PFS and OS after the first progression (PFS2 and OS2) were secondary endpoints. LNH03-6B was registered with ClinicalTrials. gov #NCT00144755. In the LNH03-6B trial, 304 and 296 patients were assigned to receive 8 cycles of R-CHOP14 or R-CHOP21, respectively. Long-term follow-up data were investigated for 256 of 384 (67%) patients still alive at the primary analysis. With a median follow-up of 10. 1 years, 213 patients progressed, and 140 patients died without progression. The 10-year PFS was 40. 4% (95% confidence interval, 35. 9-44.
9). Ten-year OS was based on 302 deaths and estimated at 50% (43-56). Of the 213 patients, 105 (49%) progressed after second-line therapy, and 77 patients died without a second progression (36%). The 1-year PFS2 and 1-year OS2 were estimated at 37. 9% (95% confidence interval, 31. 4-44. 5) and 55. 8% (95% confidence interval, 48. 8-62. 2), respectively.
Ten years after randomization, the outcomes of patients treated for DLBCL were similar according to PFS and OS between the RCHOP-14 and R-CHOP21 groups. Progression or relapse led to poor prognosis after second-line chemotherapy in the pre CAR-T-cell era. Novel approaches in first-line and alternative treatments in second-line treatments are warranted in this population.
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