Phase I rapid dose-escalation study of AGS-1C4D4, a human anti-PSCA (prostate stem cell antigen) monoclonal antibody, in patients with castration-resistant prostate cancer: a PCCTC trial

被引:21
作者
Antonarakis, Emmanuel S. [1 ]
Carducci, Michael A. [1 ]
Eisenberger, Mario A. [1 ]
Denmeade, Samuel R. [1 ]
Slovin, Susan F. [2 ]
Jelaca-Maxwell, Kathy [3 ]
Vincent, Martha E. [3 ]
Scher, Howard I. [2 ]
Morris, Michael J. [2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Prostate Canc Res Program, Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD 21231 USA
[2] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[3] Agensys Inc, Santa Monica, CA 90404 USA
关键词
AGS-1C4D4; Castration-resistant prostate cancer; Monoclonal antibody; Phase I; PSCA; RADICAL PROSTATECTOMY; GLEASON SCORE; TUMOR-GROWTH; EXPRESSION; METASTASIS; DEATH;
D O I
10.1007/s00280-011-1759-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose AGS-1C4D4 is a human monoclonal antibody against prostate stem cell antigen (PSCA), a cell-surface protein expressed by most prostate cancers. AGS-1C4D4 is produced in Chinese hamster ovary (CHO) cells and has an identical sequence to AGS-PSCA, an anti-PSCA antibody produced in mouse hybridoma cells that has completed Phase I testing. Preclinical studies demonstrated comparability of AGS-1C4D4 to AGS-PSCA with respect to pharmacokinetics (PK) and tumor inhibition. However, because of differences in antibody-dependent cellular cytotoxicity between AGS-PSCA and AGS-1C4D4, a limited Phase I trial using AGS-1C4D4 was performed evaluating safety and PK. Patients and methods Thirteen patients with metastatic castration-resistant prostate cancer were enrolled. AGS-1C4D4 was administered intravenously every 3 weeks for four planned doses at 6, 12, 24, or 48 mg/kg. Primary endpoints were safety and PK. Secondary endpoints were immunogenicity and clinical activity. Disease assessments were conducted every 12 weeks and included radiographic and PSA evaluations. Patients with stable disease could receive extended treatment beyond four infusions. Results Adverse events were primarily grade 1-2, without any grade 3-4 drug-related toxicities or infusion reactions. Anti-AGS-1C4D4 antibodies were not detected. Similar to AGS-PSCA, serum AGS-1C4D4 concentrations declined biphasically and elimination was characterized by slow clearance (CL) and a long terminal half-life (t(1/2)). Median CL for the four dose levels ranged from 0.10 to 0.14 ml/h kg, and t(1/2) ranged from 2.2 to 2.9 weeks. No PSA reductions >= 50% were observed. Six patients (46%) had radiographically stable disease, lasting a median of 24 weeks. Conclusion AGS-1C4D4 was well-tolerated and demonstrated linear PK. Despite preclinical differences in antibody-dependent cellular cytotoxicity, AGS-1C4D4 and AGS-PSCA have similar safety and PK profiles. The recommended Phase II dose is 48 mg/kg.
引用
收藏
页码:763 / 771
页数:9
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