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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.
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.  This paper was cited by:Monoclonal antibodies in diagnostics of high-grade gliomas V. P. Baklaushev, K. A. Pavlov, V. P. Chekhonin Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry. Jul 2009, Vol. 3, No. 2: 105-115 CrossRef Immunogenicity of Iodine 131 chimeric tumor necrosis therapy monoclonal antibody in advanced lung cancer patients Hui Wang, Chuanping Cao, Beilei Li, Shaoliang Chen, Jun Yin, Jing Shi, Dan Ye, Qun Tao, Peisheng Hu, Alan Epstein, Dianwen Ju Cancer Immunology, Immunotherapy. Jun 2008, Vol. 57, No. 5: 677-684 CrossRef Trends in therapeutic monoclonal antibodies of cancer Wenfang Shi, Cunye Qu, Qijun Qian Expert Opinion on Therapeutic Patents. Oct 2007, Vol. 17, No. 9: 1047-1059 CrossRef Phase I Study of 131I-Chimeric(ch) TNT-1/B Monoclonal Antibody for the Treatment of Advanced Colon Cancer Hilary Hardy Street, Michael L. Goris, George Albert Fisher, Barry W. Wessels, Cheryl Cho, Carmen Hernandez, Hongyun June Zhu, Yuxia Zhang, Jasvinder Singh Nangiana, Joseph S. Shan, Karen Roberts, Susan J. Knox Cancer Biotherapy & Radiopharmaceuticals. Jun 2006, Vol. 21, No. 3: 243-256 Abstract | Full Text PDF | Reprints & Permissions
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