新辅助化疗后非病理完全反应的 T2-3 期乳腺癌患者不良预后风险升高:再生伊斯利特衍生家族成员 4 的意义

IF 3.3 4区 医学 Q2 ONCOLOGY Breast Cancer : Targets and Therapy Pub Date : 2024-09-12 eCollection Date: 2024-01-01 DOI:10.2147/BCTT.S473920
Fan Li, Chuan-Guo Chen, Jiao-Fei Wei, Jia-Wen Lin, Zi-Ang Dou, Jun Shen, Shu-Qin Li
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引用次数: 0

摘要

研究目的在这项研究中,我们旨在确定再生胰岛衍生家族成员 4(Reg IV)在新辅助化疗(NACT)后出现非病理完全反应(non-CR)的 T2-3 期乳腺癌患者中作为独立风险因素和预后预测因子的作用。此外,我们还研究了Reg IV与表皮生长因子受体(EGFR)之间的潜在相关性和相互作用:本研究共纳入了 67 名 T2-3 期乳腺癌患者,他们在 2019 年 9 月至 2021 年 12 月期间接受 NACT 后表现为非CR。分析包括卡普兰-梅耶生存率比较、用于风险量化的集合危险比、用于分离 Reg IV 对预后影响的 Cox 回归分析、用于可视化风险概况的 Riskplots 以及用于评估变量在预测结果中重要性的 SHAP 分析:研究结果表明,Reg IV 阳性的患者预后明显较差(HR:2.62,95% CI:1.06-6.47)。与两种标记物均阴性的患者相比,Reg IV和表皮生长因子受体同时表达的患者预后最差。Cox回归分析证实了Reg IV对预后的独立影响(HR:2.63,95% CI:1.66-3.59)。风险图分析显示,Reg IV 和表皮生长因子受体(EGFR)均呈阳性的患者主要会出现疾病进展。SHAP分析进一步证实了Reg IV对疾病进程的显著影响,但与表皮生长因子受体无实质性交互作用:RegⅣ可能是T2-3期乳腺癌患者在接受NACT治疗后未达到非克罗恩状态的一个独立风险因素和不良预后的预测标志物。
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Elevated Risk of Adverse Prognosis in Patients with T2-3 Stage Breast Cancer Exhibiting Non-Pathological Complete Response Following Neoadjuvant Chemotherapy: Significance of Regenerating Islet-Derived Family Member 4.

Objective: In this study, we aimed to establish the role of regenerating islet-derived family member 4 (Reg IV) as an independent risk factor and prognostic predictor in patients with T2-3 stage breast cancer who exhibit a non-pathological complete response (non-pCR) following neoadjuvant chemotherapy (NACT). Additionally, we examined the potential correlation and interaction between Reg IV and epidermal growth factor receptor (EGFR).

Methods: A total of 67 patients with T2-3 stage breast cancer exhibiting non-pCR after NACT between September 2019 and December 2021 were included in this study. The analysis involved Kaplan-Meier survival comparisons, pooled hazard ratios for risk quantification, Cox regression analysis to isolate the impact of Reg IV on prognosis, Riskplots for visualizing risk profiles, and SHAP analysis to assess the importance of variables in predicting outcomes.

Results: The findings indicate that patients positive for Reg IV had a significantly poorer prognosis (HR: 2.62, 95% CI: 1.06-6.47). Co-expression of Reg IV and EGFR was associated with the worst outcomes compared to patients negative for both markers. Cox regression analysis confirmed the independent prognostic impact of Reg IV (HR: 2.63, 95% CI: 1.66-3.59). Riskplot analysis showed that patients positive for both Reg IV and EGFR predominantly experienced disease progression. SHAP analysis further reinforced the significant effect of Reg IV on the disease course, without substantial interaction with EGFR.

Conclusion: Reg IV may serve as an independent risk factor and predictive marker for adverse outcomes in patients with T2-3 stage breast cancer who do not achieve non-pCR following NACT.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
40
审稿时长
16 weeks
期刊最新文献
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