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转移性小细胞肺癌中DLL3表达的无创检测

Noninvasive Interrogation of DLL3 Expression in Metastatic Small Cell Lung Cancer.

作者信息

Sharma Sai Kiran, Pourat Jacob, Abdel-Atti Dalya, Carlin Sean D, Piersigilli Alessandra, Bankovich Alexander J, Gardner Eric E, Hamdy Omar, Isse Kumiko, Bheddah Sheila, Sandoval Joseph, Cunanan Kristen M, Johansen Eric B, Allaj Viola, Sisodiya Vikram, Liu David, Zeglis Brian M, Rudin Charles M, Dylla Scott J, Poirier John T, Lewis Jason S

机构信息

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.

Program in Molecular Pharmacology, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Cancer Res. 2017 Jul 15;77(14):3931-3941. doi: 10.1158/0008-5472.CAN-17-0299. Epub 2017 May 9.

Abstract

The Notch ligand DLL3 has emerged as a novel therapeutic target expressed in small cell lung cancer (SCLC) and high-grade neuroendocrine carcinomas. Rovalpituzumab teserine (Rova-T; SC16LD6.5) is a first-in-class DLL3-targeted antibody-drug conjugate with encouraging initial safety and efficacy profiles in SCLC in the clinic. Here we demonstrate that tumor expression of DLL3, although orders of magnitude lower in surface protein expression than typical oncology targets of immunoPET, can serve as an imaging biomarker for SCLC. We developed Zr-labeled SC16 antibody as a companion diagnostic agent to facilitate selection of patients for treatment with Rova-T based on a noninvasive interrogation of the status of DLL3 expression using PET imaging. Despite low cell-surface abundance of DLL3, immunoPET imaging with Zr-labeled SC16 antibody enabled delineation of subcutaneous and orthotopic SCLC tumor xenografts as well as distant organ metastases with high sensitivity. Uptake of the radiotracer in tumors was concordant with levels of DLL3 expression and, most notably, DLL3 immunoPET yielded rank-order correlation for response to SC16LD6.5 therapy in SCLC patient-derived xenograft models. .

摘要

Notch配体DLL3已成为一种在小细胞肺癌(SCLC)和高级别神经内分泌癌中表达的新型治疗靶点。罗伐匹妥珠单抗替塞林(Rova-T;SC16LD6.5)是首个靶向DLL3的抗体药物偶联物,在临床上对SCLC显示出令人鼓舞的初步安全性和疗效。在此,我们证明,尽管DLL3在肿瘤中的表达水平在表面蛋白表达上比免疫PET的典型肿瘤学靶点低几个数量级,但它可作为SCLC的成像生物标志物。我们开发了锆标记的SC16抗体作为伴随诊断剂,通过PET成像对DLL3表达状态进行无创检测,以促进选择接受Rova-T治疗的患者。尽管DLL3在细胞表面的丰度较低,但用锆标记的SC16抗体进行免疫PET成像能够以高灵敏度描绘皮下和原位SCLC肿瘤异种移植以及远处器官转移。放射性示踪剂在肿瘤中的摄取与DLL3表达水平一致,最值得注意的是,在SCLC患者来源的异种移植模型中,DLL3免疫PET对SC16LD6.5治疗反应产生了等级相关性。

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