A randomized phase II study of ipilimumab at 3 (ipi3) or 10 mg/kg (ipi10) alone or in combination with high dose interferon-alfa (HDI) in advanced melanoma (E3611)
Autor: | Sandra J. Lee, Mark A. Taylor, Robert M. Conry, Mark R. Albertini, Phu Van Truong, Stuart J. Wong, John M. Kirkwood, Uma N. M. Rao, Jerry W. Mitchell, Ahmad A. Tarhini, Noel Laudi, Arun Nagarajan |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Cancer Research business.industry Phases of clinical research Ipilimumab Pharmacology Blockade 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Oncology Immunity Interferon 030220 oncology & carcinogenesis medicine business Tremelimumab Interferon alfa medicine.drug Advanced melanoma |
Zdroj: | Journal of Clinical Oncology. 35:9542-9542 |
ISSN: | 1527-7755 0732-183X |
DOI: | 10.1200/jco.2017.35.15_suppl.9542 |
Popis: | 9542 Background: Interferon-α (IFN) favors a Th1 shift in immunity. Combining CTLA4 blockade with IFN may downregulate CTLA4 suppressive elements. Prior data from a phase II of tremelimumab and HDI showed promising efficacy supporting the current study. Methods: E3611 had a 2x2 factorial design (A: ipi10 + HDI; B: ipi10; C: ipi3 + HDI; D: ipi3) to evaluate (i) no HDI vs. HDI (across ipi doses) and (ii) ipi3 vs. ipi10 (across HDI status). We hypothesized that median progression free survival (PFS) would improve from 3 to 6 months (mos) with HDI vs. no HDI and with ipi10 vs. ipi3. Based on the log-rank test for 80 patients (pts) these comparisons would have 82% power at 2-sided type I error of 0.10. Results: Median follow up 26.4 mos. PFS and overall survival (OS) (eligible and treated pts; N = 80: 18 III/M1a, 24 M1b, 38 M1c) are shown in Table 1. There were no significant differences in PFS or OS when evaluating HDI vs. no HDI or ipi10 vs. ipi3 (Table 1). Response (RECIST) among response evaluable pts (and 4 pts with early death) (N = 76) is shown in Table 1. Stable disease (SD) in 7 (A), 6 (B), 8 (C) and 6 (D). Adverse events (AEs) were consistent with the toxicity profiles of ipi and HDI and included 3 grade 5 AEs considered at least possibly related: 1 in A (suicide), 1 in B (lung infection and hemorrhage) and 1 in C (adult respiratory distress syndrome). One patient in B died of gastrointestinal bleed and cardiac arrest while on corticosteroids to treat temporal arteritis and vision loss. Conclusions: Within the limitations of the sample size, there were no significant differences in PFS with HDI vs. no HDI or ipi10 vs. ipi3. Response and PFS with ipi10 were superior to historical controls and similar to the combination. Correlative studies are ongoing. Clinical trial information: NCT01708941. [Table: see text] |
Databáze: | OpenAIRE |
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