Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
J Thorac Oncol. 2011 Apr;6(4):658-60. doi: 10.1097/JTO.0b013e31820e17cb.
Designs for biomarker validation have been proposed and utilized in the Phase III oncology clinical trial setting. Broadly speaking, these designs follow either an enrichment (i.e., targeted) strategy or an all-comers (i.e., unselected) strategy. An enrichment design screens patients for the presence or absence of a marker or a panel of markers, and then only includes patients who either have or do not have a certain marker characteristic or profile. In contrast, all patients meeting the eligibility criteria (regardless of a particular biomarker status) are entered into an all-comers design. The strength of the preliminary evidence, the prevalence of the marker, the reproducibility and validity of the assay and the feasibility of real time marker assessment play a major role in the choice of the design. In this report, we discuss the parameters under which the enrichment or an all-comers design strategy would be appropriate for Phase II trials.
在肿瘤学 III 期临床试验中,已经提出并应用了生物标志物验证的设计方案。从广义上讲,这些设计方案要么采用富集(即靶向)策略,要么采用全面(即无选择)策略。富集设计方案筛选患者是否存在标志物或标志物组合,并仅纳入具有特定标志物特征或特征的患者。相比之下,所有符合入组标准的患者(无论特定生物标志物状态如何)都纳入全面设计方案。初步证据的强度、标志物的流行程度、检测方法的可重复性和有效性以及实时标志物评估的可行性在设计方案的选择中起着重要作用。在本报告中,我们讨论了富集或全面设计方案策略适用于 II 期试验的参数。