Department of Hematology, Centre Henri Becquerel, Rouen, France.
Institut national de la santé et de la recherche médicale U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.
Blood Adv. 2022 Dec 27;6(24):6169-6179. doi: 10.1182/bloodadvances.2022007609.
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.
LNH03-6B 试验是一项 3 期随机试验,评估了一线利妥昔单抗、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)给药在年龄 60 至 80 岁且 aaIPI(年龄调整国际预后指数)评分≥1(作为 NCT00144755 注册)的弥漫性大 B 细胞淋巴瘤(DLBCL)患者中的疗效。我们在试验结束时实施了一项前瞻性长期随访计划。主要终点是无进展生存期(PFS)和总生存期(OS)。复发模式、首次进展后的 PFS(PFS2)和 OS(OS2)是次要终点。LNH03-6B 在 ClinicalTrials.gov 上注册,编号为#NCT00144755。在 LNH03-6B 试验中,304 名和 296 名患者分别被分配接受 8 个周期的 R-CHOP14 或 R-CHOP21。对 384 名仍存活的患者中的 256 名进行了长期随访数据调查。在主要分析时,中位随访时间为 10.1 年,213 名患者进展,140 名患者无进展死亡。10 年 PFS 为 40.4%(95%置信区间,35.9-44.9)。10 年 OS 基于 302 例死亡,估计为 50%(43-56)。在 213 名患者中,105 名(49%)在二线治疗后进展,77 名患者无第二次进展而死亡(36%)。1 年 PFS2 和 1 年 OS2 分别估计为 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,根据 PFS 和 OS,R-CHOP-14 和 R-CHOP21 组的 DLBCL 患者的结局相似。在 CAR-T 细胞治疗前的二线化疗中,进展或复发导致预后不良。在这一人群中,需要新的一线治疗方法和二线替代治疗方法。