Value of CDR1-AS as a predictive and prognostic biomarker for patients with breast cancer receiving neoadjuvant chemotherapy in a prospective Chinese cohort

IF 2.8 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Chenwei Yuan, Yaqian Xu, Liheng Zhou, Jing Peng, Rui Sha, Yanping Lin, Shuguang Xu, Yumei Ye, Fan Yang, Tingting Yan, Xinrui Dong, Yaohui Wang, Wenjin Yin, Jinsong Lu
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引用次数: 0

Abstract

Neoadjuvant chemotherapy (NAC) is an effective treatment for locally advanced breast cancer (BC). However, there are no effective biomarkers for evaluating its efficacy. CDR1-AS, well known for its important role in tumorigenesis, is a famous circular RNA involved in the chemosensitivity of cancers other than BC. However, the predictive role of CDR1-AS in the efficacy and prognosis of NAC for BC has not been fully elucidated. We herein aimed to clarify this role. The present study included patients treated with paclitaxel-cisplatin-based NAC. The expression of CDR1-AS was detected by real-time quantitative reverse transcription polymerase chain reaction testing. The predictive value of CDR1-AS expression was examined in pathological complete response (pCR) after NAC using logistic regression analysis. The relationship between CDR1-AS expression and survival was demonstrated using the Kaplan–Meier method, and tested by log-rank test and Cox proportional hazards regression model. The present study enrolled 106 patients with BC. Multivariate logistic regression analysis revealed that CDR1-AS expression was an independent predictive factor for pCR (odds ratio [OR] = 0.244; 95% confidence interval [CI] 0.081–0.732; p = 0.012). Furthermore, pCR benefits with low CDR1-AS expression were observed across all subgroups. The Kaplan–Meier curves and log-rank test suggested that the CDR1-AS high-expression group showed significantly better disease-free survival (DFS; log-rank p = 0.022) and relapse-free survival (RFS; log-rank p = 0.012) than the CDR1-AS low-expression group. Multivariate analysis revealed that CDR1-AS expression was an independent prognostic factor for DFS (adjusted HR = 0.177; 95% CI 0.034–0.928, p = 0.041), RFS (adjusted HR = 0.061; 95% CI 0.006–0.643, p = 0.020), and distant disease-free survival (adjusted HR = 0.061; 95% CI 0.006–0.972, p = 0.047). CDR1-AS may be a potential novel predictive biomarker of pCR and survival benefit in patients with locally advanced BC receiving NAC. This may help identify specific chemosensitive individuals and build personalized treatment strategies.
在中国前瞻性队列中,CDR1-AS作为接受新辅助化疗的乳腺癌患者的预测和预后生物标志物的价值
新辅助化疗(NAC)是治疗局部晚期乳腺癌(BC)的有效方法。然而,目前还没有有效的生物标志物来评估其疗效。CDR1-AS 因其在肿瘤发生中的重要作用而众所周知,它是一种著名的环状 RNA,与 BC 以外癌症的化疗敏感性有关。然而,CDR1-AS对NAC治疗BC的疗效和预后的预测作用尚未完全阐明。我们在此旨在阐明这一作用。本研究纳入了接受紫杉醇-顺铂为基础的新农合治疗的患者。通过实时定量反转录聚合酶链反应检测CDR1-AS的表达。采用逻辑回归分析法检验了CDR1-AS表达对NAC治疗后病理完全反应(pCR)的预测价值。CDR1-AS表达与生存之间的关系采用Kaplan-Meier法,并通过log-rank检验和Cox比例危险回归模型进行检验。本研究共纳入106例BC患者。多变量逻辑回归分析显示,CDR1-AS表达是pCR的独立预测因素(几率比[OR] = 0.244; 95%置信区间[CI] 0.081-0.732; p = 0.012)。此外,在所有亚组中都观察到了 CDR1-AS 低表达对 pCR 的益处。卡普兰-梅耶曲线和对数秩检验表明,CDR1-AS高表达组的无病生存期(DFS;对数秩P = 0.022)和无复发生存期(RFS;对数秩P = 0.012)明显优于CDR1-AS低表达组。多变量分析显示,CDR1-AS表达是DFS(调整后HR = 0.177; 95% CI 0.034-0.928, p = 0.041)、RFS(调整后HR = 0.061; 95% CI 0.006-0.643, p = 0.020)和远处无病生存期(调整后HR = 0.061; 95% CI 0.006-0.972, p = 0.047)的独立预后因素。CDR1-AS可能是接受NAC治疗的局部晚期BC患者pCR和生存获益的潜在新型预测生物标志物。这可能有助于识别特定的化疗敏感个体并制定个性化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Medical Research
European Journal of Medical Research 医学-医学:研究与实验
CiteScore
3.20
自引率
0.00%
发文量
247
审稿时长
>12 weeks
期刊介绍: European Journal of Medical Research publishes translational and clinical research of international interest across all medical disciplines, enabling clinicians and other researchers to learn about developments and innovations within these disciplines and across the boundaries between disciplines. The journal publishes high quality research and reviews and aims to ensure that the results of all well-conducted research are published, regardless of their outcome.
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