Identifying immunohistochemical biomarkers panel for non-small cell lung cancer in optimizing treatment and forecasting efficacy.

IF 3.4 2区 医学 Q2 ONCOLOGY
Xiaoya Zhang, Junhong Meng, Mingyue Gao, Cheng Gong, Cong Peng, Duxian Liu
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Abstract

Background: Chemotherapy and immunotherapy for non-small-cell lung cancer (NSCLC) are gaining momentum. However, its long-term efficacy remains limited to only a small fraction of patients. Hence, it is crucial to identify reliable immunohistochemical biomarkers to facilitate the formulation of optimal treatment strategies and to predict therapeutic outcomes.

Methods: We retrospectively analyzed a cohort of 140 patients diagnosed with NSCLC who received chemotherapy or immunotherapy. Using bioinformatics analysis and machine learning techniques, we assessed the role of immunohistochemical biomarkers and clinical characteristics in developing a predictive model for treatment options and outcomes in this population.

Results: Our research has found that immunohistochemical biomarkers can accurately predict treatment regimens and progression-free survival in NSCLC patients with an accuracy rate of 82.1%. We identified an exclusive detection panel for the six vital biomarkers. Of particular note is the role of programmed cell death protein 1 ligand 1 (PD-L1) expression in guiding treatment selection, with high expression predicting better outcomes in the immunotherapy group at a cut-off value of 50%. Non-squamous patients who tested positive for thyroid transcription factor 1 had a longer median progression-free survival, while squamous patients who tested positive for p63 protein or cytokeratin 5/6 expression had a longer median progression-free survival.

Conclusions: The results of our study are highly encouraging, as they revealed a significant correlation between immunohistochemical biomarkers, therapeutic regimens, and prognosis. These findings indicate that our immunohistochemical detection panel has great potential for facilitating customization of therapeutic regimens to improve patient care. The insights gained from this study could help clinicians optimize treatment protocols and ultimately enhance clinical outcomes.

确定非小细胞肺癌免疫组化生物标志物面板,以优化治疗和预测疗效。
背景:针对非小细胞肺癌(NSCLC)的化疗和免疫疗法的发展势头日益强劲。然而,其长期疗效仍仅限于一小部分患者。因此,确定可靠的免疫组化生物标志物对制定最佳治疗策略和预测疗效至关重要:我们回顾性分析了140例接受化疗或免疫治疗的NSCLC患者。利用生物信息学分析和机器学习技术,我们评估了免疫组化生物标志物和临床特征在建立该人群治疗方案和疗效预测模型中的作用:我们的研究发现,免疫组化生物标志物可以准确预测NSCLC患者的治疗方案和无进展生存期,准确率高达82.1%。我们确定了六种重要生物标志物的专属检测面板。特别值得注意的是程序性细胞死亡蛋白1配体1(PD-L1)的表达在指导治疗选择中的作用,高表达可预测免疫治疗组的较好疗效,临界值为50%。甲状腺转录因子1阳性的非鳞癌患者中位无进展生存期更长,而p63蛋白或细胞角蛋白5/6表达阳性的鳞癌患者中位无进展生存期更长:我们的研究结果非常鼓舞人心,因为它们揭示了免疫组化生物标志物、治疗方案和预后之间的显著相关性。这些发现表明,我们的免疫组化检测面板在促进定制化治疗方案以改善患者护理方面具有巨大潜力。从这项研究中获得的见解可以帮助临床医生优化治疗方案,最终提高临床疗效。
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
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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