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肿瘤ERCC1表达对完全切除的非小细胞肺癌患者辅助化疗后治疗结果的预测价值

Predictive Value of Tumor ERCC1 Expression for Treatment Outcomes After Adjuvant Chemotherapy in Patients with Completely Resected Non-Small Cell Lung Cancer.

作者信息

Nakata Masao, Saisho Shinsuke, Soh Junichi, Okumura Norihito, Nakamura Hiroshige, Yamashita Motohiro, Toyooka Shinichi, Date Hiroshi

机构信息

Department of General Thoracic Surgery, Kawasaki Medical School, Kurashiki, Okayama, Japan.

Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

出版信息

Cancer Manag Res. 2025 Jul 19;17:1477-1486. doi: 10.2147/CMAR.S517916. eCollection 2025.

DOI:10.2147/CMAR.S517916
PMID:40704297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12285891/
Abstract

PURPOSE

To evaluate the predictive value of tumor expression of the excision repair cross-complementation group 1 gene (ERCC1) for the treatment outcomes after platinum-based adjuvant chemotherapy in patients with completely resected non-small cell lung cancer (NSCLC).

METHODS

In this study, we conducted immunohistochemical analysis using a mouse monoclonal anti-ERCC1 antibody (clone 8F1) of operative specimens obtained from 238 patients enrolled in the SLCG0401 study which compared paclitaxel plus carboplatin (CBDCA+PTX) with uracil-tegafur (UFT) as adjuvant chemotherapy for stage IB-IIIA NSCLC. The overall survival (OS) of the patients was compared according to the ERCC1 expression status and adjuvant chemotherapy employed.

RESULTS

Of the 238 specimens, 102 (42.9%) showed a positive result for ERCC1 expression. There were no significant differences in the patient characteristics or OS between the tumor ERCC1-positive and -negative patient groups. Among the patients with ERCC1-negative tumors, there was no significant difference in the survival between patient groups treated with CBDCA+PTX and UFT (HR=0.932, 95% CI: 0.52-1.67, p=0.814). However, among the patients with ERCC1-positive tumors, CBDCA+PTX treatment tended to yield an inferior outcome, in terms of the OS, as compared with UFT treatment (HR=1.852, 95% CI: 0.92-3.73, p=0.080). Multivariate analysis showed that ERCC1 expression was not an independent predictor of the OS following CBDCA+PTX treatment in completely resected NSCLC patients.

CONCLUSION

In completely resected NSCLC patients with positive tumor ERCC1 expression, adjuvant CBDCA+PTX treatment tended to yield an inferior outcome as compared with UFT treatment in terms of the OS. However, immunohistochemical analysis with the 8F1 antibody cannot be used for clinical decision making at this point.

摘要

目的

评估完全切除的非小细胞肺癌(NSCLC)患者中,切除修复交叉互补组1基因(ERCC1)的肿瘤表达对铂类辅助化疗后治疗结果的预测价值。

方法

在本研究中,我们使用小鼠单克隆抗ERCC1抗体(克隆8F1)对238例参与SLCG0401研究的患者的手术标本进行免疫组化分析,该研究比较了紫杉醇联合卡铂(CBDCA+PTX)与替加氟尿嘧啶(UFT)作为IB-IIIA期NSCLC辅助化疗的疗效。根据ERCC1表达状态和所采用的辅助化疗方案比较患者的总生存期(OS)。

结果

在238个标本中,102个(42.9%)ERCC1表达呈阳性。肿瘤ERCC1阳性和阴性患者组之间的患者特征或OS无显著差异。在ERCC1阴性肿瘤患者中,接受CBDCA+PTX和UFT治疗的患者组之间的生存期无显著差异(HR=0.932,95%CI:0.52-1.67,p=0.814)。然而,在ERCC1阳性肿瘤患者中,与UFT治疗相比,CBDCA+PTX治疗在OS方面的结果往往较差(HR=1.852,95%CI:0.92-3.73,p=0.080)。多因素分析表明,ERCC1表达不是完全切除的NSCLC患者接受CBDCA+PTX治疗后OS的独立预测因素。

结论

在肿瘤ERCC1表达阳性的完全切除的NSCLC患者中,就OS而言,辅助CBDCA+PTX治疗的结果往往比UFT治疗差。然而,目前使用8F1抗体进行免疫组化分析不能用于临床决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/21a309e5321b/CMAR-17-1477-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/44c96d7372b6/CMAR-17-1477-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/0e81bc6d4f95/CMAR-17-1477-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/34c5e715e69d/CMAR-17-1477-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/16d31b6175df/CMAR-17-1477-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/4371f40770ac/CMAR-17-1477-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/21a309e5321b/CMAR-17-1477-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/44c96d7372b6/CMAR-17-1477-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/0e81bc6d4f95/CMAR-17-1477-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/34c5e715e69d/CMAR-17-1477-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/16d31b6175df/CMAR-17-1477-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/4371f40770ac/CMAR-17-1477-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ca/12285891/21a309e5321b/CMAR-17-1477-g0006.jpg

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