Puntambekar Mehak, Shery Neville, Parokkaran Ishaan, Al-Hamas Mohammed
Medicine and Surgery, Pilgrim Hospital, United Lincolnshire Hospitals National Health Service (NHS) Trust, Boston, GBR.
General Medicine, Pilgrim Hospital, United Lincolnshire Hospitals National Health Service (NHS) Trust, Boston, GBR.
Cureus. 2025 Jul 24;17(7):e88647. doi: 10.7759/cureus.88647. eCollection 2025 Jul.
Cancer immunotherapy has transformed the therapeutic landscape for several malignancies, offering durable responses in select patient populations. However, response rates remain variable, underscoring the need for robust predictive and prognostic biomarkers. This narrative review synthesizes current evidence on biomarkers guiding immunotherapy in non-small cell lung cancer (NSCLC), melanoma, breast cancer, and colorectal cancer. Literature was identified through manual screening of PubMed and Scopus using key terms related to immunotherapy biomarkers, with no date restrictions applied; studies published up to May 2025 were included. Clinically validated markers such as programmed death-ligand 1 (PD-L1) and microsatellite instability-high (MSI-H) demonstrate utility but face limitations including assay variability and tumor heterogeneity. Emerging candidates, such as tumor-infiltrating lymphocytes (TILs), relative eosinophil count (REC), lactate dehydrogenase (LDH), and S100 calcium-binding protein B (S100B), offer additional prognostic or predictive value but require further validation. This review adds value by integrating and comparing both validated and emerging biomarkers across tumor types and by emphasizing practical considerations for real-world application. Given the narrative format and focus on selected cancers, the scope is inherently limited, and not all emerging biomarkers or real-world implementation data are fully addressed. Methodological limitations and current gaps in biomarker validation are also discussed.
癌症免疫疗法已经改变了多种恶性肿瘤的治疗格局,在部分患者群体中产生了持久疗效。然而,缓解率仍然存在差异,这凸显了对强大的预测和预后生物标志物的需求。这篇叙述性综述综合了目前关于非小细胞肺癌(NSCLC)、黑色素瘤、乳腺癌和结直肠癌中指导免疫疗法的生物标志物的证据。通过使用与免疫疗法生物标志物相关的关键词手动筛选PubMed和Scopus来确定文献,不设日期限制;纳入截至2025年5月发表的研究。经过临床验证的标志物,如程序性死亡配体1(PD-L1)和微卫星高度不稳定(MSI-H),显示出一定作用,但面临包括检测变异性和肿瘤异质性在内的局限性。新兴的候选标志物,如肿瘤浸润淋巴细胞(TILs)、相对嗜酸性粒细胞计数(REC)、乳酸脱氢酶(LDH)和S100钙结合蛋白B(S100B),具有额外的预后或预测价值,但需要进一步验证。本综述通过整合和比较不同肿瘤类型中已验证和新兴的生物标志物,并强调实际应用中的实际考虑因素,增加了价值。鉴于叙述形式和对特定癌症的关注,范围本质上是有限的,并非所有新兴生物标志物或实际应用数据都得到了充分探讨。还讨论了方法学局限性和生物标志物验证方面当前存在的差距。