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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.
- Source :
-
Cancer chemotherapy and pharmacology [Cancer Chemother Pharmacol] 2012 Mar; Vol. 69 (3), pp. 763-71. Date of Electronic Publication: 2011 Oct 22. - Publication Year :
- 2012
-
Abstract
- 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.<br />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.<br />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.<br />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.
- Subjects :
- Aged
Aged, 80 and over
Androgen Antagonists administration & dosage
Androgen Antagonists therapeutic use
Antibodies, Monoclonal adverse effects
Antibodies, Monoclonal immunology
Antibodies, Monoclonal pharmacokinetics
Antibodies, Monoclonal therapeutic use
Antigens, Neoplasm
Antineoplastic Agents adverse effects
Antineoplastic Agents immunology
Antineoplastic Agents pharmacokinetics
Antineoplastic Agents therapeutic use
Cohort Studies
Dose-Response Relationship, Drug
Drug Resistance, Neoplasm
GPI-Linked Proteins antagonists & inhibitors
Humans
Infusions, Intravenous
Male
Middle Aged
Prostate-Specific Antigen blood
Prostatic Neoplasms immunology
Prostatic Neoplasms metabolism
Prostatic Neoplasms pathology
Treatment Outcome
Antibodies, Monoclonal administration & dosage
Antineoplastic Agents administration & dosage
Neoplasm Proteins antagonists & inhibitors
Prostatic Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1432-0843
- Volume :
- 69
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Cancer chemotherapy and pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 22020316
- Full Text :
- https://doi.org/10.1007/s00280-011-1759-9