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复发/难治性多发性骨髓瘤(1-3 线既往治疗)的真实世界治疗模式和结局:Flatiron 数据库。

Real-world treatment patterns and outcomes in relapsed/refractory multiple myeloma (1-3 prior lines): Flatiron database.

机构信息

Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI.

Department of Internal Medicine II, Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.

出版信息

Blood Adv. 2024 Oct 8;8(19):5062-5071. doi: 10.1182/bloodadvances.2024012640.

Abstract

In the context of multiple myeloma (MM), early use of the immunomodulatory drug lenalidomide has led to an increased population of patients with lenalidomide-refractory MM in early-line settings, but their outcomes are not well characterized. Herein, we report treatment patterns, survival outcomes, prognostic variables, and attrition rates for patients with proteasome inhibitor-exposed, lenalidomide-refractory MM, treated with 1 to 3 prior lines of therapy (LOT). From 12 767 patients with MM in the Flatiron Health database between January 2016 and April 2022, 1455 met the inclusion criteria. The most common subsequent treatments were triplet combinations (41.6% of patients); daratumumab/pomalidomide/dexamethasone was the most common treatment regimen (13.2%). Median real-world progression-free survival (RW-PFS) and overall survival (OS) were 6.5 months and 44.4 months, respectively. RW-PFS was similar in patients with 1, 2, or 3 prior LOT. International Staging System stage III, Eastern Cooperative Oncology Group performance status of 1, hemoglobin <12 g/dL, high-risk cytogenetics, and refractoriness to anti-CD38 antibody at baseline were associated with worse RW-PFS and OS. Outcomes remained similar for patients who received National Comprehensive Cancer Network-preferred treatments and those who received treatments after 2020. In 561 patients with 1 prior LOT at inclusion, the cumulative attrition rate from LOT 2 to 5 was 85%, which included 25% patients who died and 60% with no further treatment. Patients with lenalidomide-refractory MM who have received 1 to 3 prior LOT have poor outcomes and progress rapidly through available therapies, highlighting the need for more effective treatments early in the disease course, before patients are lost to attrition.

摘要

在多发性骨髓瘤(MM)的背景下,早期使用免疫调节剂来那度胺导致早期一线治疗中出现了更多的来那度胺耐药 MM 患者,但他们的预后情况尚不清楚。在此,我们报告了接受过蛋白酶体抑制剂治疗且对来那度胺耐药的 MM 患者的治疗模式、生存结局、预后变量和损失率,这些患者接受了 1 至 3 线治疗(LOT)。在 2016 年 1 月至 2022 年 4 月期间,Flatiron Health 数据库中的 12767 例 MM 患者中,有 1455 例符合纳入标准。最常见的后续治疗是三联治疗(41.6%的患者);达雷妥尤单抗/来那度胺/地塞米松是最常见的治疗方案(13.2%)。中位真实世界无进展生存期(RW-PFS)和总生存期(OS)分别为 6.5 个月和 44.4 个月。在接受 1、2 或 3 线 LOT 的患者中,RW-PFS 相似。国际分期系统(ISS)III 期、东部肿瘤协作组(ECOG)体力状态 1、血红蛋白<12g/dL、高危细胞遗传学以及基线时对抗 CD38 抗体耐药与 RW-PFS 和 OS 较差相关。对于接受国家综合癌症网络(NCCN)推荐治疗的患者和接受 2020 年后治疗的患者,结局仍然相似。在纳入的 1455 例患者中,有 1 线 LOT 的患者中,从 LOT2 到 LOT5 的累积损失率为 85%,其中包括 25%的死亡患者和 60%的无进一步治疗患者。接受过 1 至 3 线 LOT 的来那度胺耐药 MM 患者预后较差,并且迅速通过现有治疗方案进展,这凸显了在疾病早期,在患者因损失而无法接受治疗之前,需要更早地使用更有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a2f/11459902/2895fae6de06/BLOODA_ADV-2024-012640-ga1.jpg

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