Predicting Therapeutic Antibody Delivery into Human Head and Neck Cancers

医学 抗体 头颈部癌 药物输送 病理 癌症 癌症研究 肿瘤科 免疫学 内科学 化学 有机化学
作者
Guolan Lu,Shayan Fakurnejad,Brock A. Martin,Nynke S. van den Berg,Stan van Keulen,Naoki Nishio,Ashley Zhu,Stefania U. Chirita,Quan Zhou,Rebecca W. Gao,Christina S. Kong,Nancy J. Fischbein,Mrudula Penta,A. Dimitrios Colevas,Eben L. Rosenthal
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:26 (11): 2582-2594 被引量:32
标识
DOI:10.1158/1078-0432.ccr-19-3717
摘要

The efficacy of antibody-based therapeutics depends on successful drug delivery into solid tumors; therefore, there is a clinical need to measure intratumoral antibody distribution. This study aims to develop and validate an imaging and computation platform to directly quantify and predict antibody delivery into human head and neck cancers in a clinical study.Twenty-four patients received systemic infusion of a near-infrared fluorescence-labeled therapeutic antibody followed by surgical tumor resection. A computational platform was developed to quantify the extent of heterogeneity of intratumoral antibody distribution. Both univariate and multivariate regression analyses were used to select the most predictive tumor biological factors for antibody delivery. Quantitative image features from the pretreatment MRI were extracted and correlated with fluorescence imaging of antibody delivery.This study not only confirmed heterogeneous intratumoral antibody distribution in-line with many preclinical reports, but also quantified the extent of interpatient, intertumor, and intratumor heterogeneity of antibody delivery. This study demonstrated the strong predictive value of tumor size for intratumoral antibody accumulation and its significant impact on antibody distribution in both primary tumor and lymph node metastasis. Furthermore, this study established the feasibility of using contrast-enhanced MRI to predict antibody delivery.This study provides a clinically translatable platform to measure antibody delivery into solid tumors and yields valuable insight into clinically relevant antibody tumor penetration, with implications in the selection of patients amenable to antibody therapy and the design of more effective dosing strategies.

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