Pomalidomide Treatment in Relapsed/Refractory Multiple Myeloma Patients-Real-World Data From Hungary.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2022-10-03 eCollection Date: 2022-01-01 DOI:10.3389/pore.2022.1610645
Szilvia Lovas, Nóra Obajed Al-Ali, Gergely Varga, Virág Szita, Hussain Alizadeh, Márk Plander, Péter Rajnics, Árpád Illés, Zsuzsa Szemlaky, Gábor Mikala, László Váróczy
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引用次数: 1

Abstract

Pomalidomide is a third generation immunomodulatory drug in the treatment of refractory and relapsed multiple myeloma patients. Our aim was to investigate the efficacy and safety of pomalidomide therapy in a real world setting. Eighty-six Hungarian patients were included, 45 of whom received pomalidomide ± an alkylating agent, while in 38 of them pomalidomide was combined with a proteasome inhibitor. 56 patients (65%) showed any response to the treatment with 18 complete or very good partial remissions and 38 partial remissions. At a median duration of follow-up of 18.6 months, the median progression-free survival (PFS) was 9.03 months, while the median overall survival (OS) was 16.53 months in the whole cohort. Patients with early stage disease (R-ISS 1 and 2) had better survival results than those with stage 3 myeloma (p = 0.002). Neither the number of prior treatment lines, nor lenalidomide refractoriness had a significant impact on PFS. PFS was found similar between the cohort of patients with impaired renal function and the cohort without kidney involvement. During the study, eight mortal infections and two fatal bleeding complications occurred, however, mild hematologic and gastrointestinal toxicities were identified as the most frequent adverse events. The results of our investigations confirm that pomalidomide is an effective treatment option for relapsed/refractory MM, besides, the safety profile is satisfactory in subjects with both normal and impaired renal function.

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泊马度胺治疗复发/难治性多发性骨髓瘤患者——来自匈牙利的真实世界数据
波马度胺是治疗难治性和复发性多发性骨髓瘤的第三代免疫调节药物。我们的目的是在现实环境中研究泊马度胺治疗的有效性和安全性。86名匈牙利患者纳入研究,其中45名患者使用泊马度胺±一种烷基化剂,38名患者使用泊马度胺联合一种蛋白酶体抑制剂。56例患者(65%)对治疗有任何反应,其中18例完全或非常好的部分缓解,38例部分缓解。在18.6个月的中位随访期间,整个队列的中位无进展生存期(PFS)为9.03个月,而中位总生存期(OS)为16.53个月。早期疾病(R-ISS 1和2)患者的生存结果优于3期骨髓瘤患者(p = 0.002)。先前治疗线的数量和来那度胺的难治性对PFS都没有显著影响。发现PFS在肾功能受损患者队列和无肾脏受累患者队列之间相似。在研究期间,发生了8例致命感染和2例致命出血并发症,然而,轻度血液和胃肠道毒性被确定为最常见的不良事件。我们的研究结果证实,泊马度胺是复发/难治性MM的有效治疗选择,此外,在肾功能正常和受损的受试者中,安全性都令人满意。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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