Noninvasive Interrogation of DLL3 Expression in Metastatic Small Cell Lung Cancer

被引:88
|
作者
Sharma, Sai Kiran [1 ,2 ]
Pourat, Jacob [1 ,2 ]
Abdel-Atti, Dalya [1 ,2 ]
Carlin, Sean D. [3 ,4 ]
Piersigilli, Alessandra [3 ,4 ]
Bankovich, Alexander J. [5 ]
Gardner, Eric E. [2 ]
Hamdy, Omar [5 ]
Isse, Kumiko [5 ]
Bheddah, Sheila [5 ]
Sandoval, Joseph [5 ]
Cunanan, Kristen M. [6 ]
Johansen, Eric B. [5 ]
Allaj, Viola [2 ,7 ]
Sisodiya, Vikram [5 ]
Liu, David [5 ]
Zeglis, Brian M. [1 ,8 ,9 ,10 ,11 ]
Rudin, Charles M. [2 ,7 ,8 ]
Dylla, Scott J. [5 ]
Poirier, John T. [2 ,7 ]
Lewis, Jason S. [1 ,2 ,8 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Program Mol Pharmacol, 1275 York Ave, New York, NY 10021 USA
[3] Weill Cornell Med Coll, Mem Sloan Kettering Canc Ctr, Triinst Lab Comparat Pathol, New York, NY USA
[4] Rockefeller Univ, 1230 York Ave, New York, NY 10021 USA
[5] Stemcentrx Inc, San Francisco, CA USA
[6] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[7] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[8] Weill Cornell Med Coll, New York, NY USA
[9] CUNY Hunter Coll, Dept Chem, New York, NY 10021 USA
[10] CUNY, Grad Ctr, New York, NY USA
[11] CUNY, Grad Ctr, PhD Program Chem, New York, NY USA
关键词
POSITRON EMISSION TOMOGRAPHY; ANTIBODY; STATISTICS; ANTIGEN; TUMORS; PET;
D O I
10.1158/0008-5472.CAN-17-0299
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 89Zr-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 in vivo status ofDLL3 expression using PET imaging. Despite low cell-surface abundance ofDLL3, immunoPET imaging with 89Zr-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. (C) 2017 AACR.
引用
收藏
页码:3931 / 3941
页数:11
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