Medical Oncology Clinic, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Data Centre, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Oncologist. 2021 Dec;26(12):1062-1070. doi: 10.1002/onco.13906. Epub 2021 Aug 4.
Biomarkers in clinical trials have led to massive incorporation of research biopsies, with potentially risks and no direct benefit for patients. In 2018, the American Society of Clinical Oncology (ASCO) released an ethical framework to provide guidance on incorporating research biopsies in cancer clinical trials.
We collected biopsy requirements of cancer clinical trials conducted at Institut Jules Bordet (IJB) between 2015 and 2019 to examine adherence with the ASCO Ethical Framework. We used logistic regression models to test the association between the request for biopsy, the request for tissue, and the adherence to the ASCO framework as well as some trial characteristics.
Between January 2015 and December 2019, 178 oncological studies were conducted at IJB. Of these, 138 (78%) were sponsored by industry, 132 (74%) were phase II and III studies, and 141 (79%) concerned metastatic disease. Tissue was required for inclusion for 119 (67%) studies, among which 59 required at least one new biopsy. Adherence to ASCO's Ethical Framework was 67% for studies requiring tissue and went down to 39% for studies requiring at least one new biopsy. In multivariate analysis, requests for tissue or new biopsies increased in early-phase studies (p < .001, p < .001, respectively) and in studies investigating innovative treatments (immunotherapy or targeted therapies; p < .01, p = .02). Compliance to the ASCO framework significantly decreased with time (p < .001) and in early-phase studies (p < .001).
Numerous studies required tissue or new biopsies for exploratory objectives of unknown clinical utility. Requests for tissue increased over the years, whereas compliance to ASCO's Ethical Framework decreased.
In 2019, the American Society of Clinical Oncology (ASCO) developed an ethical framework to provide guidance on incorporating research biopsies in clinical trials. This study underlines the growing request for tissue in clinical trials with potentially no impact on drug development and no benefit to actual or future patients. Adherence to ASCO's Ethical Framework decreases through time. These results highlight the importance of improving the ethics of research biopsies. ASCO's Ethical Framework offers an opportunity to improve quality of care in clinical research by maximizing scientific utility and allowing for clinically meaningful correlative science and safe access to innovative treatments for a maximum number of patients.
临床试验中的生物标志物导致了大量研究活检的纳入,这可能对患者存在风险,而没有直接获益。2018 年,美国临床肿瘤学会(ASCO)发布了一个伦理框架,为癌症临床试验中纳入研究活检提供指导。
我们收集了 2015 年至 2019 年在 Jules Bordet 研究所(IJB)进行的癌症临床试验的活检要求,以检验对 ASCO 伦理框架的遵守情况。我们使用逻辑回归模型检验了活检、组织要求与 ASCO 框架的符合程度以及一些试验特征之间的关联。
2015 年 1 月至 2019 年 12 月,IJB 开展了 178 项肿瘤学研究。其中,138 项(78%)由工业界赞助,132 项(74%)为 II 期和 III 期研究,141 项(79%)涉及转移性疾病。119 项(67%)研究要求纳入组织,其中 59 项需要至少进行一次新的活检。需要组织的研究中,ASCO 伦理框架的遵守率为 67%,而需要至少一次新活检的研究中,遵守率下降至 39%。多变量分析显示,早期研究(p<0.001,p<0.001)和创新性治疗(免疫治疗或靶向治疗)研究(p<0.01,p=0.02)中,组织或新活检的要求增加。随着时间的推移(p<0.001)和早期研究(p<0.001),对 ASCO 框架的遵守率显著下降。
许多研究需要组织或新的活检来探索未知的临床效用。对组织的需求逐年增加,而对 ASCO 伦理框架的遵守率却下降了。
2019 年,美国临床肿瘤学会(ASCO)制定了一个伦理框架,为临床试验中纳入研究活检提供指导。本研究强调了临床试验中对组织的日益增长的需求,而这对药物开发没有影响,对现有的或未来的患者也没有获益。对 ASCO 伦理框架的遵守率随时间下降。这些结果突显了改进研究活检伦理的重要性。ASCO 的伦理框架为通过最大限度地提高科学实用性,允许进行具有临床意义的相关性科学,并为尽可能多的患者安全获得创新性治疗,来改善临床研究中的护理质量提供了机会。