Novel Postneoadjuvant Prognostic Breast Cancer Staging System

医学 肿瘤科 内科学 乳腺癌 癌症 阶段(地层学) 三阴性乳腺癌 AJCC分段系统 多元分析 单变量分析 孕酮受体 临床试验 雌激素受体 登台系统 古生物学 生物
作者
David J. Winchester,Lavisha Singh,Stephen B. Edge,Kimberly H. Allison,William E. Barlow,Veerle Bossuyt,Mariana Chávez‐MacGregor,Emily F. Conant,James L. Connolly,Jennifer F. De Los Santos,Daniel F. Hayes,Nola M. Hylton,Elizabeth A. Mittendorf,Jennifer K. Plichta,Elena Provenzano,Kilian Salerno,Priyanka Sharma,W. Fraser Symmans,Donald L. Weaver,Gabriel N. Hortobágyi
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:43 (17): 1948-1960 被引量:6
标识
DOI:10.1200/jco-24-01739
摘要

PURPOSE Prognostic staging after neoadjuvant chemotherapy (NACT) is not included in American Joint Commission on Cancer (AJCC) staging. This study addressed this deficiency by including responses to therapy with standardized staging variables in a validated prognostic staging system for patients treated with NACT. METHODS The National Cancer Database was queried to identify 140,605 patients treated with NACT between 2010 and 2018. Three response categories (no response, partial response, and complete response [pCR]) were created on the basis of comparison of clinical and post-NACT pathologic staging. Univariate and multivariate analyses of clinical stage, estrogen receptor, progesterone receptor, human epidermal growth factor receptor 2 (HER2), and grade were analyzed for each category. Predictive models for each response category were validated using the bootstrap technique. Calibration plots compared predicted and observed 3-year survival probabilities in the training and validation data sets. RESULTS Each validated model demonstrated statistically significant survival differences in the postneoadjuvant prognostic stage assignment. Of all patients with a pCR, 94.2% were assigned to postneoadjuvant ypStage I compared with 35.5% of patients with no response. Advancing clinical stage had a progressive but small impact on overall survival (OS) with pCR (high-grade, triple-negative breast cancer [TNBC]: cStage I, 97% v cStage IIIB/IIIC, 91%; grade 2 luminal A: 97% v 91%) but was associated with a profound decrease in OS with no response for TNBC or HER2+ disease (high-grade TNBC 89% v 50%) and less profound for grade 2 luminal A disease with no response (97% v 81%). CONCLUSION We present a novel, validated prognostic staging system that predicts OS according to the response to NACT. These data will provide AJCC stage assignments for a growing proportion of patients treated with NACT.
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