Department of Medical Sciences, Hematology Section, University of Ferrara, Cona - Ferrara, Italy.
GIMEMA Foundation, Rome, Italy.
Hematol Oncol. 2021 Aug;39(3):326-335. doi: 10.1002/hon.2861. Epub 2021 Mar 26.
Because the efficacy of new drugs reported in trials may not translate into similar results when used in the real-life, we analyzed the efficacy of idelalisib and rituximab (IR) in 149 patients with relapsed/refractory chronic lymphocytic leukemia treated at 34 GIMEMA centers. Median progression-free survival (PFS) and overall survival were 22.9 and 44.5 months, respectively; performance status (PS) ≥2 and ≥3 previous lines of therapy were associated with shorter PFS and overall survival (OS). 48% of patients were on treatment at 12 months; the experience of the centers (≥5 treated patients) and PS 0-1 were associated with a significantly longer treatment duration (p = 0.015 and p = 0.002, respectively). TP53 disruption had no prognostic significance. The overall response rate to subsequent treatment was 49.2%, with median OS of 15.5 months and not reached in patients who discontinued, respectively, for progression and for toxicity (p < 0.01). Treatment breaks ≥14 days were recorded in 96% of patients and adverse events mirrored those reported in trials. In conclusion, this real-life analysis showed that IR treatment duration was longer at experienced centers, that the ECOG PS and ≥3 lines of previous therapy are strong prognostic factor and that the overall outcome with this regimen was superimposable to that reported in a randomized trial.
由于临床试验中报告的新药疗效在实际应用中可能无法转化为类似结果,我们分析了在 34 个 GIMEMA 中心治疗的 149 例复发/难治性慢性淋巴细胞白血病患者中伊德拉利昔布和利妥昔单抗(IR)的疗效。中位无进展生存期(PFS)和总生存期(OS)分别为 22.9 和 44.5 个月;表现状态(PS)≥2 和≥3 线既往治疗与较短的 PFS 和 OS 相关。48%的患者在 12 个月时仍在接受治疗;中心经验(≥5 例治疗患者)和 PS 0-1 与治疗持续时间显著延长相关(p=0.015 和 p=0.002)。TP53 缺失无预后意义。随后治疗的总缓解率为 49.2%,中位 OS 分别为 15.5 个月,因进展和毒性而停药的患者未达到,分别为 15.5 个月(p<0.01)。96%的患者记录了≥14 天的治疗中断,不良事件与试验报告的一致。总之,这项真实世界的分析表明,经验丰富的中心的 IR 治疗持续时间更长,ECOG PS 和≥3 线既往治疗是强烈的预后因素,并且该方案的总体结果与随机试验报告的结果相似。