Real-World Treatment Patterns and Outcomes in Patients With Lenalidomide-Refractory Multiple Myeloma With 1 to 3 Prior Lines: SEER-Medicare Database

IF 2.7 4区 医学 Q2 HEMATOLOGY Clinical Lymphoma, Myeloma & Leukemia Pub Date : 2025-01-23 DOI:10.1016/j.clml.2025.01.009
Binod Dhakal , Jinghua He , Jordan M. Schecter , William Deraedt , Ana Slaughter , Carolina Lonardi , Sandhya Nair , Jianming He , Seina Lee , Patricia Cost , Nitin Patel , Mythili Koneru , Hermann Einsele
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Abstract

Background

Early continuous lenalidomide use for multiple myeloma (MM) treatment has led to more patients with lenalidomide-refractory disease at earlier lines of therapy (LOTs). Real-world treatment practices and outcomes in elderly patients with comorbidities are not well characterized.

Materials and Methods

Using the Surveillance, Epidemiology, and End Results-Medicare database, we analyzed data from patients who were diagnosed with MM between 2014 and 2019, had 1 to 3 prior LOTs, including a proteasome inhibitor and an immunomodulatory drug, and were lenalidomide refractory. Patients were followed from index (initiation of first subsequent LOT after meeting eligibility criteria and after January 1, 2016) until death, end of continuous Medicare enrollment, or December 31, 2020.

Results

This analysis included 1297 patients (median age, 75 years). The mean National Cancer Institute Comorbidity Index score was 0.87 and 81% had at least 1 comorbidity. Singlet, doublet, and triplet therapies each accounted for ∼30% of index regimens. The most common regimens, ± corticosteroid, were daratumumab-pomalidomide (15%), pomalidomide (13%), and daratumumab (12%). Median overall survival and time to next treatment (TTNT) were 29.3 and 8.5 months, respectively. TTNT decreased with successive LOTs (1 prior LOT, 11.0 months; 3 prior LOTs, 6.1 months).

Conclusion

Elderly patients with comorbidities and lenalidomide-refractory disease after 1 to 3 LOTs receive suboptimal regimens, have poor outcomes, and move rapidly through treatments, highlighting the need for new effective treatments for this difficult-to-treat population.
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来那度胺难治性多发性骨髓瘤患者的现实世界治疗模式和结果:SEER-Medicare数据库。
背景:早期连续使用来那度胺治疗多发性骨髓瘤(MM)导致更多患者在早期治疗线(LOTs)中出现来那度胺难治性疾病。现实世界的治疗实践和结果,老年患者的合并症并没有很好地表征。材料和方法:使用监测、流行病学和最终结果医疗保险数据库,我们分析了2014年至2019年期间被诊断为MM的患者的数据,这些患者先前有1至3次LOTs,包括蛋白酶体抑制剂和免疫调节药物,并且是来那度胺难解的。患者从指标(在符合资格标准后和2016年1月1日之后开始第一次后续LOT)开始随访,直到死亡、连续医疗保险登记结束或2020年12月31日。结果:本分析纳入1297例患者(中位年龄75岁)。国家癌症研究所共病指数的平均得分为0.87,81%的患者至少有一种共病。单线、双线和三线治疗各占指标方案的30%。最常见的治疗方案(±皮质类固醇)是达拉单抗-波马度胺(15%)、波马度胺(13%)和达拉单抗(12%)。中位总生存期和到下一次治疗的时间(TTNT)分别为29.3个月和8.5个月。TTNT随连续批次而下降(前批次1次,11.0个月;前3批,6.1个月)。结论:伴有合并症和来那度胺难治性疾病的老年患者在1 - 3批次后接受的方案不理想,预后较差,并且通过治疗的速度很快,突出了对这一难以治疗人群的新的有效治疗方法的需求。
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来源期刊
CiteScore
2.70
自引率
3.70%
发文量
1606
审稿时长
26 days
期刊介绍: Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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