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and
-Interferon in Experimental Human Ovarian Cancer
Imperial Cancer Research Fund, Lincoln's Inn Fields, London, WC2A 3PX, United Kingdom [F. R. B., B. G. W., E. M.], and Laboratory of Molecular Biology, University of Ghent, Ledeganckstratte 35, B-9000, Ghent, Belgium [W. F.]
We have studied the activity of recombinant human
-interferon and recombinant human tumor necrosis factor
against four human ovarian cancer i.p. xenografts OS, LA, HN, and DO derived from primary tumor material. In the OS xenograft all control mice died by 42 days and therapy starting 7 days after tumor cell injection with 5 x 104 units recombinant human
-interferon or 1 µg recombinant human tumor necrosis factor
alone had no significant effect on cumulative survival in three separate experiments. However, a combination of the two agents resulted in 85% cumulative survival at 150 days. This combination therapy also significantly increased survival of mice treated as late as 21 days after tumor cell injection. In the LA xenograft (where control mice were all dead by 23 days) therapy with either agent alone, or a combination, more than doubled survival time of mice. In the HN xenograft all control mice were dead at 22 days whereas either therapy alone or in combination gave +85% cumulative survival at 100 days. In a fourth xenograft, DO, survival of mice in the combination therapy group was significantly increased. Thus these two biological therapies, alone or in combination, show significant activity against human ovarian cancer cells.
1 To whom requests for reprints should be addressed.
Received 3/ 3/87. Revised 5/29/87. Accepted 6/16/87.
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