蒽环类
乳腺癌
医学
肿瘤科
内科学
紫杉烷
前瞻性队列研究
诺丁汉预后指数
队列
尤登J统计
新辅助治疗
癌症
接收机工作特性
作者
Karolina Edlund,Katrin Madjar,Antje Lebrecht,Bahriye Aktas,Henryk Pilch,G. M. Hoffmann,Manfred Hofmann,Hans‐Christian Kolberg,Daniel Boehm,Marco Johannes Battista,Martina Seehase,Kathrin Stewen,Susanne Gebhard,Cristina Cadenas,Rosemarie Marchan,Walburgis Brenner,Annette Hasenburg,Heinz Koelbl,Christine Solbach,Mathias Gehrmann
标识
DOI:10.1158/1078-0432.ccr-20-2662
摘要
Abstract Purpose: Expression-based classifiers to predict pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) are not routinely used in the clinic. We aimed to build and validate a classifier for pCR after NACT. Patients and Methods: We performed a prospective multicenter study (EXPRESSION) including 114 patients treated with anthracycline/taxane-based NACT. Pretreatment core needle biopsies from 91 patients were used for gene expression analysis and classifier construction, followed by validation in five external cohorts (n = 619). Results: A 20-gene classifier established in the EXPRESSION cohort using a Youden index–based cut-off point predicted pCR in the validation cohorts with an accuracy, AUC, negative predictive value (NPV), positive predictive value, sensitivity, and specificity of 0.811, 0.768, 0.829, 0.587, 0.216, and 0.962, respectively. Alternatively, aiming for a high NPV by defining the cut-off point for classification based on the complete responder with the lowest predicted probability of pCR in the EXPRESSION cohort led to an NPV of 0.960 upon external validation. With this extreme-low cut-off point, a recommendation to not treat with anthracycline/taxane-based NACT would be possible for 121 of 619 unselected patients (19.5%) and 112 of 322 patients with luminal breast cancer (34.8%). The analysis of the molecular subtypes showed that the identification of patients who do not achieve a pCR by the 20-gene classifier was particularly relevant in luminal breast cancer. Conclusions: The novel 20-gene classifier reliably identifies patients who do not achieve a pCR in about one third of luminal breast cancers in both the EXPRESSION and combined validation cohorts.
科研通智能强力驱动
Strongly Powered by AbleSci AI