Breast Cancer Translational Research Laboratory, Faculty of Medicine, Université Libre de Bruxelles, Institut Jules Bordet, Brussels, Belgium.
Lancet Oncol. 2012 Jun;13(6):e240-8. doi: 10.1016/S1470-2045(11)70378-3.
The neoadjuvant setting provides a unique opportunity to study the effect of systemic treatments on breast cancer biology and to identify clinically useful prognostic and predictive biomarkers. Discrepancies and inconsistencies in the use of definitions and endpoint assessments in this setting confound the analysis and interpretation of results across clinical trials and hinder research progress. This Review represents a joint effort of the Breast International Group and the National Cancer Institute-sponsored North American Breast Cancer Group to provide clinicians and researchers with a series of standardised definitions and endpoints that could be implemented in future neoadjuvant clinical trials. Definitions of the setting of interest and of survival endpoints are recommended, together with proposals for standard assessment of the response to treatment, use of functional and molecular imaging endpoints, and characterisation and selection of the population to treat. We expect that implementation of these recommendations will improve the conduct, reporting, and effectiveness of clinical trials and fully exploit the clinical and scientific potential of the neoadjuvant setting in breast cancer.
新辅助治疗环境为研究全身治疗对乳腺癌生物学的影响以及确定临床上有用的预后和预测生物标志物提供了独特的机会。在这种环境下,定义和终点评估的使用存在差异和不一致,这使得临床试验之间的分析和解释变得复杂,并阻碍了研究进展。这篇综述代表了乳腺国际集团和美国国家癌症研究所赞助的北美乳腺癌集团的共同努力,为临床医生和研究人员提供了一系列标准的定义和终点,可在未来的新辅助临床试验中实施。建议对相关的治疗环境和生存终点进行定义,并提出治疗反应标准评估、功能和分子成像终点的应用,以及人群的特征和选择的建议。我们预计,这些建议的实施将改善临床试验的实施、报告和效果,并充分发挥新辅助治疗在乳腺癌中的临床和科学潜力。