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Cancer Biotherapy & Radiopharmaceuticals
131I-chTNT Radioimmunotherapy of 43 Patients with Advanced Lung Cancer

To cite this article:
Like Yu, Dian Wen Ju, Wenping Chen, Tian Li, Zhaoqiang Xu, Changying Jiang, Shaoliang Chen, Qun Tao, Dan Ye, Peisheng Hu, Leslie A. Khawli, Clive R. Taylor, Alan L. Epstein. Cancer Biotherapy & Radiopharmaceuticals. 2006, 21(1): 5-14. doi:10.1089/cbr.2006.21.5.

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Like Yu
Nanjing Pulmonary Hospital, Nanjing, China.
Dian Wen Ju
Shanghai MediPharm Biotech Co., Ltd., Shanghai, China.
Wenping Chen
Nanjing Pulmonary Hospital, Nanjing, China.
Tian Li
Nanjing Pulmonary Hospital, Nanjing, China.
Zhaoqiang Xu
Jiangsu People's Hospital, Nanjing, China.
Changying Jiang
Tumor Hospital, Shanghai, China.
Shaoliang Chen
Shanghai Zhongshan Hospital, Fudan University, Shanghai, China.
Qun Tao
Shanghai MediPharm Biotech Co., Ltd., Shanghai, China.
Dan Ye
Shanghai MediPharm Biotech Co., Ltd., Shanghai, China.
Peisheng Hu
Keck School of Medicine at the University of Southern California, Los Angeles, CA.
Leslie A. Khawli
Keck School of Medicine at the University of Southern California, Los Angeles, CA.
Clive R. Taylor
Keck School of Medicine at the University of Southern California, Los Angeles, CA.
Alan L. Epstein
Keck School of Medicine at the University of Southern California, Los Angeles, CA.

The treatment of advanced lung cancer remains a major challenge in clinical medicine, justifying an urgent need for new therapeutic approaches. In a rather unique international collaboration, 43 patients with advanced lung cancer were treated using iodine-131-labeled tumor necrosis therapy chimeric antibody (131I-chTNT). Methods: Patients were treated either with intravenous (i.v.) infusion (n = 22), intratumoral injection using a computer tomography (CT)-guided catheter (n = 16), or combination i.v. and intratumoral infusion (n = 5). All patients, regardless of route of administration, received 2 doses of 131I-chTNT on days 1 and 14. Results: The results showed that of those patients receiving i.v. injection alone, 2 achieved partial response (PR) (9%), 16 had stable disease (73%), and 4 progressed (18%). Of those patients receiving intratumoral injection only, 1 had a complete response (CR) (6%), 8 achieved PR (50%), 7 had stable disease (44%), and none (0%) progressed. Finally, of those patients receiving both i.v. and intratumoral administration, 1 had a CR (20%), 1 achieved PR (20%), 2 had stable disease (40%), and 1 (20%) showed progression. Conclusions: These promising results demonstrate that sufficient doses of radiolabeled antibody can be safely delivered to tumors to cause significant therapeutic effects in advanced lung cancer.

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