Antitumor Activity in Melanoma and Anti-Self Responses in a Phase I Trial With the Anti-Cytotoxic T Lymphocyte–Associated Antigen 4 Monoclonal Antibody CP-675,206

医学 黑色素瘤 细胞毒性T细胞 抗原 免疫学 免疫系统 癌症 抗体 内科学 单克隆抗体 淋巴细胞 胃肠病学 癌症研究 体外 生物化学 化学
作者
Antoni Ribas,Luis H. Camacho,Gabriel Lopez‐Berestein,Dmitri Pavlov,C. A. Bulanhagui,Robert Millham,Begoña Comı́n-Anduix,James M. Reuben,Elisabeth Seja,Charla A. Parker,Amarnath Sharma,John A. Glaspy,Jesús Gómez-Navarro
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:23 (35): 8968-8977 被引量:583
标识
DOI:10.1200/jco.2005.01.109
摘要

Purpose Cytotoxic T lymphocyte–associated antigen 4 (CTLA4) blockade with CP-675,206, a fully human anti-CTLA4 monoclonal antibody, may break peripheral immunologic tolerance leading to effective immune responses to cancer in humans. A phase I trial was conducted to test the safety of CP-675,206. Patients and Methods Thirty-nine patients with solid malignancies (melanoma, n = 34; renal cell, n = 4; colon, n = 1) received an intravenous (IV) infusion of CP-675,206 at seven dose levels. The primary objective was to determine the maximum-tolerated dose and the recommended phase II dose. Results Dose-limiting toxicities and autoimmune phenomena included diarrhea, dermatitis, vitiligo, panhypopituitarism and hyperthyroidism. Two patients experienced complete responses (maintained for 34+ and 25+ months), and there were two partial responses (26+ and 25+ months) among 29 patients with measurable melanoma. There have been no relapses thus far after objective response to therapy. Four other patients had stable disease at end of study evaluation (16, 7, 7, and 4 months). Additionally, five patients had extended periods without disease progression (36+, 35+, 26+, 24+, and 23+ months) after local treatment of progressive metastases. Longer systemic exposure to CP-675,206 achieved in higher dose cohorts predicted for a higher probability of response. Conclusion CP-675,206 can be administered safely to humans as a single IV dose up to 15 mg/kg, resulting in breaking of peripheral immune tolerance to self-tissues and antitumor activity in melanoma.
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