| Literature DB >> 25381801 |
Anna Kanerva1, Anniina Koski2, Ilkka Liikanen2, Minna Oksanen2, Timo Joensuu3, Otto Hemminki2, Juni Palmgren4, Kari Hemminki5, Akseli Hemminki6.
Abstract
Oncolytic immunotherapy with cytokine armed replication competent viruses is an emerging approach in cancer treatment. In a recent randomized trial, an increase in response rate was seen but the effect on overall survival is not known with any virus. To facilitate randomized trials, we performed a case-control study assessing the survival of 270 patients treated in an Advanced Therapy Access Program (ATAP), in comparison to matched concurrent controls from the same hospital. The overall survival of all virus treated patients was not increased over controls. However, when analysis was restricted to GMCSF-sensitive tumor types treated with GMSCF-coding viruses, a significant improvement in median survival was present (from 170 to 208 days, P = 0.0012, N = 148). An even larger difference was seen when analysis was restricted to good performance score patients (193 versus 292 days, P = 0.034, N = 90). The survival of ovarian cancer patients was especially promising as median survival nearly quadrupled (P = 0.0003, N = 37). These preliminary data lend support to initiation of randomized clinical trials with GMCSF-coding oncolytic adenoviruses.Entities:
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Year: 2014 PMID: 25381801 PMCID: PMC4445619 DOI: 10.1038/mt.2014.218
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454