Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
The Alfred Hospital, Melbourne, VIC, Australia.
Blood Cancer J. 2024 Mar 26;14(1):54. doi: 10.1038/s41408-024-00996-x.
Despite an increasing desire to use historical cohorts as "synthetic" controls for new drug evaluation, limited data exist regarding the comparability of real-world outcomes to those in clinical trials. Governmental cancer data often lacks details on treatment, response, and molecular characterization of disease sub-groups. The Australasian Leukaemia and Lymphoma Group National Blood Cancer Registry (ALLG NBCR) includes source information on morphology, cytogenetics, flow cytometry, and molecular features linked to treatment received (including transplantation), response to treatment, relapse, and survival outcome. Using data from 942 AML patients enrolled between 2012-2018, we assessed age and disease-matched control and interventional populations from published randomized trials that led to the registration of midostaurin, gemtuzumab ozogamicin, CPX-351, oral azacitidine, and venetoclax. Our analyses highlight important differences in real-world outcomes compared to clinical trial populations, including variations in anthracycline type, cytarabine intensity and scheduling during consolidation, and the frequency of allogeneic hematopoietic cell transplantation in first remission. Although real-world outcomes were comparable to some published studies, notable differences were apparent in others. If historical datasets were used to assess the impact of novel therapies, this work underscores the need to assess diverse datasets to enable geographic differences in treatment outcomes to be accounted for.
尽管越来越希望使用历史队列作为新药评估的“合成”对照,但关于真实世界结果与临床试验结果的可比性的数据有限。政府癌症数据通常缺乏关于治疗、反应和疾病亚组分子特征的详细信息。澳大利亚白血病和淋巴瘤组国家血液癌症登记处(ALLG NBCR)包括与所接受治疗(包括移植)、治疗反应、复发和生存结果相关的形态学、细胞遗传学、流式细胞术和分子特征的来源信息。使用 2012-2018 年间登记的 942 名 AML 患者的数据,我们评估了年龄和疾病匹配的对照和干预人群,这些人群来自发表的随机试验,这些试验导致了 midostaurin、gemtuzumab ozogamicin、CPX-351、口服阿扎胞苷和 venetoclax 的注册。我们的分析强调了与临床试验人群相比,真实世界结果的重要差异,包括巩固治疗期间蒽环类药物类型、阿糖胞苷强度和方案以及首次缓解时异基因造血细胞移植的频率的变化。尽管真实世界的结果与一些已发表的研究相当,但在其他研究中也明显存在差异。如果使用历史数据集来评估新疗法的影响,这项工作强调需要评估不同的数据集,以说明治疗结果的地理差异。