Phase I/II Study of Ipilimumab for Patients With Metastatic Melanoma.
J Clin Oncol. 2008 Nov 17. [Epub ahead of print]
Weber JS, O'Day S, Urba W, Powderly J, Nichol G, Yellin M, Snively J, Hersh E.
University of Southern California/Norris Comprehensive Cancer Center; The Angeles Clinic and Research Institute, Los Angeles, CA; Robert Franz Cancer Center, Earle A. Chiles Research Institute, Portland, OR; the University of Arizona Cancer Center, Tucson, AZ; Carolina Bio-Oncology Institute, Huntersville, NC; and Medarex, Inc, Annadale, NJ.
PURPOSE:
The primary objective of this phase I/II study was to determine the safety and pharmacokinetic profile of either transfectoma- or a hybridoma-derived ipilimumab. Secondary objectives included determination of a maximum-tolerated dose and assessment of clinical activity.
PATIENTS AND METHODS:
Eighty-eight patients with unresectable stage III or IV melanoma with at least one measurable lesion were treated. Mean age was 59 years, with 65% male and 35% female patients, and 79% of patients had received prior systemic therapy. Single doses of ipilimumab up to 20 mg/kg (group A, single dose), multiple doses up to 5 mg/kg (group A, multiple dose), and multiple doses up to 10 mg/kg (group B) were administered.
RESULTS:
Single dosing up to 20 mg/kg of transfectoma antibody was well tolerated, as were multiple doses up to 10 mg/kg without a maximum-tolerated dose. In group B, dose-limiting toxicity was seen in six of 23 melanoma patients. Grade 3 or 4 immune-related adverse events (irAEs) were observed in 14% of patients (12 of 88 patients), and grade 1 or 2 irAEs were seen in an additional 58%. The half-life of ipilimumab was 359 hours. In group B, there was one partial response (23+ months), one complete response (21+ months), and seven patients with stable disease (SD), for a disease control rate of 39%. Two patients in group B with SD had slow, steady decline in tumor burden that was ongoing at 1 year of observation.
CONCLUSION:
Ipilimumab has activity in patients with metastatic melanoma. Late responses were observed in patients with prolonged SD. |
