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.
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