INSERM, Établissement Français du Sang de Bretagne, Unité Mixte de Recherche (UMR) S1236, Université de Rennes 1, Rennes, France.
Service d'Hématologie Clinique, Centre Hospitalier Universitaire, Rennes, France.
Eur J Haematol. 2024 Sep;113(3):290-297. doi: 10.1111/ejh.14225. Epub 2024 May 7.
IMAGE is a retrospective cohort study of patients enrolled in early access programs (EAPs) in France with relapsed/refractory multiple myeloma (RRMM) receiving isatuximab with pomalidomide and dexamethasone (Isa-Pd).
Patients aged ≥18 years with RRMM who received ≥1 dose of Isa under the EAPs between July 29, 2019 and August 30, 2020 were included. Effectiveness endpoints included progression-free survival (PFS) and response rates. Verbatim terms for adverse events (AEs) were coded using the Medical Dictionary for Regulatory Activities and not graded for severity.
A total of 294 and 299 patients were included in the effectiveness and safety populations, respectively. IMAGE included patients who received one prior line of treatment (10.2%) and were daratumumab-refractory (19.1%). At median follow-up of 14.2 months, median PFS in the effectiveness population was 12.4 months (95% CI 9.0-15.0). Overall response and very good partial response rates were 46.3% and 27.9%, respectively. Subgroup analyses reflected similar results. In the safety population, 26.4% of patients reported at least one AE; the most common any-grade AE was neutropenia (9.4%).
IMAGE demonstrated Isa-Pd had meaningful effectiveness in median PFS and depth of response and no new safety signals in a real-world context, consistent with clinical trial results.
IMAGE 是一项回顾性队列研究,纳入了在法国接受伊沙佐米联合泊马度胺和地塞米松(Isa-Pd)治疗的复发/难治性多发性骨髓瘤(RRMM)接受早期准入计划(EAP)的患者。
该研究纳入了年龄≥18 岁、在 2019 年 7 月 29 日至 2020 年 8 月 30 日期间接受至少 1 剂 EAP 下伊沙佐米治疗的 RRMM 患者。有效性终点包括无进展生存期(PFS)和缓解率。使用监管活动医学词典对不良事件(AE)的术语进行了直译,并未对其严重程度进行分级。
有效性和安全性人群中分别纳入了 294 例和 299 例患者。IMAGE 纳入了既往接受过 1 线治疗(10.2%)和达雷妥尤单抗难治(19.1%)的患者。在中位随访 14.2 个月时,有效性人群的中位 PFS 为 12.4 个月(95%CI 9.0-15.0)。总缓解率和非常好的部分缓解率分别为 46.3%和 27.9%。亚组分析结果相似。在安全性人群中,26.4%的患者报告至少有 1 例 AE;最常见的任何级别 AE 为中性粒细胞减少症(9.4%)。
在真实世界环境中,IMAGE 研究表明 Isa-Pd 方案在中位 PFS 和缓解深度方面具有显著疗效,且无新的安全性信号,与临床试验结果一致。