PO.CL01.12 · 临床研究
用于全面表征肿瘤及相关微环境的抗体药物偶联物免疫肿瘤学面板
Antibody-drug conjugate immuno-oncology panel for comprehensive characterization of the tumor and associated microenvironment
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
抗体药物偶联物(ADC)代表着一类快速发展的靶向治疗药物,整合了单克隆抗体的特异性与小分子药物的强效细胞毒性。通过接头将抗体与高活性载荷偶联,ADC能够将细胞毒性药物选择性递送至肿瘤细胞,同时最大限度地减少全身毒性。关键性研究已展示了令人信服的证据,表明这种抗癌治疗策略可显著改善患者结局。尽管取得了显著成功,但肿瘤异质性和预测临床疗效等挑战一直难以克服。由于ADC依赖靶抗原的精确空间定位来优化治疗疗效,因此需要蛋白表达的亚细胞分辨率。为深入了解肿瘤内的空间模式和异质性,我们使用了Paletrra™(NeoGenomics Laboratories, Inc)平台。Paletrra™是一个专有的多重免疫荧光(mIF)平台,用于在单张FFPE切片中可视化和表征多达60种蛋白生物标志物,并对组织样本中的蛋白表达提供高分辨率的空间和定量分析。在此,我们报告了一个新颖的市售抗体面板的设计和使用,以支持肺癌和乳腺癌样本中的ADC开发。该面板可测量常见的ADC靶点,如B7-H3、B7-H4、c-MET、EGFR、HER2、HER3和TROP2,并结合膜标志物以实现膜表达与胞质表达之间的亚细胞区分。定量图像分析能够对蛋白表达进行归一化并计算膜与胞质表达比值,提供增强的生物学背景。此外,由于ADC已被证明可调节肿瘤免疫微环境,面板中的额外标志物可深入了解肿瘤样本内的免疫原性、细胞关系和整体结构生物学。该检测方法的应用支持ADC的转化研究和临床开发,有助于识别具有最佳靶点表达和定位的患者。
查看英文原文 English abstract
Antibody-drug conjugates (ADCs) represent a rapidly advancing class of targeted therapeutics that integrate the specificity of monoclonal antibodies with the potent cytotoxicity of small-molecule drugs. By coupling antibodies to highly active payloads through linkers, ADCs enable selective delivery of cytotoxic agents to tumor cells while minimizing systemic toxicity. Pivotal studies have shown compelling evidence that this strategy of anti-cancer therapeutics can dramatically improve outcomes for patients. Despite notable success, challenges such as tumor heterogeneity and predicting clinical efficacy have been difficult to overcome. Because ADCs rely on precise spatial localization of target antigens to optimize treatment efficacy, subcellular resolution of protein expression is required. To provide insight into spatial patterns and heterogeneity within a tumor, we used the Paletrra™ (NeoGenomics Laboratories, Inc) platform. Paletrra™ is a proprietary multiplex immunofluorescence (mIF) platform for the visualization and characterization of up to 60 protein biomarkers in a single FFPE section and offers high-resolution spatial and quantitative analysis of protein expression in tissue samples. Herein we report the design and use of a novel panel of commercially available antibodies to support ADC development in lung and breast cancer samples. The panel can measure common ADC targets such as B7-H3, B7-H4, c-MET, EGFR, HER2, HER3, and TROP2 combined with a membrane marker to enable subcellular differentiation between membrane and cytoplasmic expression. Quantitative image analysis enables normalization of protein expression and computation of membrane-to-cytoplasmic expression ratio, providing enhanced biological context. Moreover, because ADCs have been shown to modulate the tumor immune microenvironment, additional markers in the panel provide insight into immunogenicity, cellular relationships, and overall structural biology within the tumor samples. Application of this assay supports translational research and clinical development of ADCs, facilitating identification of patients with optimal target expression and localization.
利益披露 Disclosure
S. F. Lam,
NeoGenomics Laboratories Employment.
K. Gallagher,
NeoGemonics Laboratories Employment.
M. Rohafza,
NeoGenomics Employment.
C. Todorov,
NeoGenomics Laboratories Employment.
H. Nunns,
NeoGenomics Laboratories Employment.
M. Thio,
NeoGenomics Laboratories Employment.
F. Sahafi,
NeoGenomics Laboratories Employment.
K. Pham,
NeoGenomics Laboratories Employment.
V. Gomez,
NeoGenomics Laboratories Employment.
E. A. Parnell,
NeoGenomics Laboratories Employment.
Q. Au,
NeoGenomics Laboratories Employment.