Pancreatic cancer can seldom be resected, and chemotherapy has only a limit
ed effect on survival or tumour load. We did a phase I/II trial in 14 patie
nts with pancreatic cancer to assess the safety of local activation of low-
dose ifosfamide. We encapsulated genetically modified allogeneic cells, whi
ch expressed a cytochrome P450 enzyme, in cellulose sulphate and delivered
them by supraselective angiography to the tumour vasculature. These cells l
ocally activated systemically administered ifosfamide. The tumours of four
patients regressed after treatment, and those of the other ten individuals
who completed the study remained stable. Median survival was doubled in the
treatment group by comparison with historic controls, and 1-year survival
rate was three times better. Further studies of this cell-therapy-based tre
atment combined with chemotherapy for inoperable pancreatic cancer are warr
anted.