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KRAS野生型转移性结直肠癌患者治疗中原发肿瘤定位及HER2表达的预后和预测意义:来自塞尔维亚的单中心经验

Prognostic and Predictive Significance of Primary Tumor Localization and HER2 Expression in the Treatment of Patients with KRAS Wild-Type Metastatic Colorectal Cancer: Single-Centre Experience from Serbia.

作者信息

Radić Jelena, Nikolić Ivan, Kolarov-Bjelobrk Ivana, Vasiljević Tijana, Djurić Aleksandar, Vidović Vladimir, Kožik Bojana

机构信息

Faculty of Medicine, University of Novi Sad, 21000 Novi Sad, Serbia.

Department of Medical Oncology, Oncology Institute of Vojvodina, 21204 Sremska Kamenica, Serbia.

出版信息

J Pers Med. 2024 Aug 20;14(8):879. doi: 10.3390/jpm14080879.

Abstract

The treatment of patients with metastatic colorectal cancer (mCRC) is complex and is impacted by the location of the primary tumor (LPT). Our study aims to emphasize the importance of LPT as a prognostic and predictive marker as well as to examine the significance of HER2 overexpression in patients with mCRC, particularly in relation to the response to Epidermal Growth Factor Receptor Antibody treatment (anti-EGFR therapy). In this study, 181 patients with Kirsten RAS (KRAS) wild-type mCRC who received anti-EGFR therapy were included. Among them, 101 had left colon cancer (LCC) and 80 had right colon cancer (RCC). Results demonstrated that patients with KRAS wild-type LCC had better median overall survival (OS) (43 vs. 33 months, = 0.005) and progression-free survival (PFS) (6 vs. 3 months, < 0.001) compared to those with RCC. Multivariate analysis identified mucinous adenocarcinoma ( < 0.001), RCC location ( = 0.022), perineural invasion ( = 0.034), and tumors at the resection margin ( = 0.001) as independent predictors of OS, while mucinous adenocarcinoma ( = 0.001) and RCC location ( = 0.004) independently correlated with significantly shorter PFS. In addition, human epidermal growth factor receptor 2 (HER2) positive expression was significantly associated with worse PFS compared to HER2 negative results ( < 0.001). In conclusion, LPT is an important marker for predicting outcomes in the treatment of wild-type mCRC using anti-EGFR therapy, since patients with RCC have a statistically significantly shorter PFS and OS. Further investigation is needed to understand the role of HER2 overexpression in wild-type mCRC, as these patients also exhibit shorter survival.

摘要

转移性结直肠癌(mCRC)患者的治疗较为复杂,且受原发肿瘤位置(LPT)的影响。我们的研究旨在强调LPT作为预后和预测标志物的重要性,并探讨HER2过表达在mCRC患者中的意义,特别是与表皮生长因子受体抗体治疗(抗EGFR治疗)反应的关系。本研究纳入了181例接受抗EGFR治疗的 Kirsten 大鼠肉瘤病毒癌基因同源物(KRAS)野生型mCRC患者。其中,101例为左结肠癌(LCC),80例为右结肠癌(RCC)。结果表明,与RCC患者相比,KRAS野生型LCC患者的中位总生存期(OS)更好(43个月对33个月,P = 0.005),无进展生存期(PFS)更长(6个月对3个月,P < 0.001)。多因素分析确定黏液腺癌(P < 0.001)、RCC位置(P = 0.022)、神经周围浸润(P = 0.034)和切缘肿瘤(P = 0.001)是OS的独立预测因素,而黏液腺癌(P = 0.001)和RCC位置(P = 0.004)与显著更短的PFS独立相关。此外,与HER2阴性结果相比,人表皮生长因子受体2(HER2)阳性表达与更差的PFS显著相关(P < 0.001)。总之,LPT是预测抗EGFR治疗野生型mCRC疗效的重要标志物,因为RCC患者的PFS和OS在统计学上显著更短。需要进一步研究以了解HER2过表达在野生型mCRC中的作用,因为这些患者的生存期也较短。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80b1/11355236/11b89b1cbce0/jpm-14-00879-g001.jpg

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