Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Clin Lymphoma Myeloma Leuk. 2021 Jun;21(6):379-385. doi: 10.1016/j.clml.2021.01.018. Epub 2021 Jan 30.
The continuous advances in the treatment landscape of multiple myeloma has led to the approval of several novel agents and their combinations that significantly improved patient outcomes. Despite their undoubtful effectiveness in the context of clinical trials, their impact on real-world (RW) clinical practice remains debatable. RW data on the role of novel agents and their combinations among patients with relapsed/refractory multiple myeloma have confirmed the efficacy of proteasome inhibitors, immunomodulatory drugs, and monoclonal antibodies. However, the magnitude of the benefit and the safety profile may differ among RW studies and between RW and pivotal clinical trials. Several variables may pertain to these observations and include patient selection, ethnicity, age, comorbidities, disease stage at diagnosis and at relapse, number of prior lines of therapy, disease subtype, presence of renal impairment, extramedullary disease, and cytogenetic abnormalities. All these contribute to a varying degree of disease and patient heterogeneity among the studies that may result in a differential treatment effect. The expertise of each medical center and the treatment setting in terms of availability and drug access are particularly important as well. Interestingly, RW observations may serve as proof of concept for designing novel clinical trials, as is the case with retreatment studies. In conclusion, clinical trial and RW data are complementary, and they should be considered to improve both clinical trial design and clinical practice.
多发性骨髓瘤治疗领域的不断进步导致了几种新型药物及其联合方案的批准,这些药物显著改善了患者的预后。尽管这些药物在临床试验中无疑是有效的,但它们在真实世界(RW)临床实践中的影响仍存在争议。RW 数据证实了新型药物及其联合方案在复发性/难治性多发性骨髓瘤患者中的疗效,包括蛋白酶体抑制剂、免疫调节剂和单克隆抗体。然而,在 RW 研究和 RW 与关键临床试验之间,获益的程度和安全性特征可能存在差异。有几个变量可能与这些观察结果有关,包括患者选择、种族、年龄、合并症、诊断时和复发时的疾病阶段、先前治疗线的数量、疾病亚型、肾功能损害、髓外疾病和细胞遗传学异常。所有这些都导致了研究中疾病和患者异质性的不同程度,这可能导致治疗效果的差异。每个医疗中心的专业知识以及治疗环境在药物的可获得性和获取方面也非常重要。有趣的是,RW 观察结果可能为设计新型临床试验提供概念验证,正如再治疗研究的情况一样。总之,临床试验和 RW 数据是互补的,应考虑将它们用于改进临床试验设计和临床实践。