Journal
CANCER IMMUNOLOGY IMMUNOTHERAPY
Volume 59, Issue 10, Pages 1521-1530Publisher
SPRINGER
DOI: 10.1007/s00262-010-0879-0
Keywords
Bromohydrin pyrophosphate; V gamma 9V delta 2 T lymphocyte; Phase I trial; Solid tumors
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V gamma 9V delta 2 (gamma delta) T lymphocytes, a critical peripheral blood lymphocyte subset, are directly cytotoxic against many solid and hematologic tumor types. V gamma 9V delta 2 T lymphocytes can be selectively expanded in vivo with BrHPP (IPH1101) and IL-2. The present phase I trial was conducted with the aim of determining the maximum-tolerated dose (MTD) and safety of IPH1101 combined with a low dose of IL-2 in patients with solid tumors. A 1-h intravenous infusion of IPH11 was administered alone at cycle 1, combined with a low dose of SC IL-2 (1 MIU/M-2 d1 to d7) in the subsequent cycles (day 1 every 3 weeks). The dose of IPH1101 was escalated from 200 to 1,800 mg/m(2). As much as 28 patients with solid tumors underwent a total of 109 treatment cycles. Pharmacodynamics data demonstrate that gamma delta T lymphocyte amplification in humans requires the co-administration of IL-2 and is dependent on IPH 1101 dose. Dose-limiting toxicity occurred in two patients at a dose of 1,800 mg/m(2): one grade 3 fever (1 patient) and one grade 3 hypotension (1 patient) suggesting cytokine release syndrome immediately following the first infusion. At lower doses the treatment was well tolerated; the most frequent adverse events were mild fever, chills and abdominal pain, without exacerbation in the IL-2 combined cycles. IPH1101 in combination with SC low-dose IL-2 is safe, well tolerated and induces a potent gamma delta T lymphocyte expansion in patients. Its clinical activity will be evaluated in phase II clinical trials.
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