University of Rochester Medical Center, Rochester, New York.
American Society of Clinical Oncology, Alexandria, Virginia.
Clin Cancer Res. 2021 May 1;27(9):2424-2429. doi: 10.1158/1078-0432.CCR-20-3868. Epub 2021 Feb 9.
Performance status (PS) is one of the most common eligibility criteria. Many trials are limited to patients with high-functioning PS, resulting in important differences between trial participants and patient populations with the disease. In addition, existing PS measures are subjective and susceptible to investigator bias.
A multidisciplinary working group of the American Society of Clinical Oncology and Friends of Cancer Research evaluated how PS eligibility criteria could be more inclusive. The working group recommendations are based on a literature search, review of trials, simulation study, and multistakeholder consensus. The working group prioritized inclusiveness and access to investigational therapies, while balancing patient safety and study integrity.
Broadening PS eligibility criteria may increase the number of potentially eligible patients for a given clinical trial, thus shortening accrual time. It may also result in greater participant diversity, potentially reduce trial participant and patient disparities, and enable clinicians to more readily translate trial results to patients with low-functioning PS. Potential impact on outcomes was explored through a simulation trial demonstrating that when the number of Eastern Cooperative Oncology Group PS2 participants was relatively small, the effect on the estimated HR and power was modest, even when PS2 patients did not derive a treatment benefit.
Expanding PS eligibility criteria to be more inclusive may be justified in many cases and could result in faster accrual rates and more representative trial populations..
体能状态(PS)是最常见的入选标准之一。许多试验仅限于功能状态良好的患者,导致试验参与者与患有该疾病的患者群体之间存在重要差异。此外,现有的 PS 测量方法是主观的,容易受到研究者的偏见影响。
美国临床肿瘤学会和癌症研究之友的一个多学科工作组评估了如何使 PS 入选标准更具包容性。工作组的建议基于文献检索、试验评估、模拟研究和多方利益相关者共识。工作组优先考虑包容性和获得研究性治疗的机会,同时平衡患者安全性和研究完整性。
放宽 PS 入选标准可能会增加给定临床试验中潜在合格患者的数量,从而缩短入组时间。它还可能导致更多样化的参与者,潜在地减少试验参与者和患者之间的差异,并使临床医生更易于将试验结果转化为功能状态较差的患者。通过模拟试验探索了对结果的潜在影响,该试验表明,当东部肿瘤协作组 PS2 参与者的数量相对较少时,对估计 HR 和功效的影响是适度的,即使 PS2 患者没有从治疗中获益。
在许多情况下,扩大 PS 入选标准以提高包容性是合理的,并且可能导致更快的入组率和更具代表性的试验人群。