Interferon-gamma in the first-line therapy of ovarian cancer: a randomized phase III trial
2000

Interferon-gamma for Ovarian Cancer Treatment

Sample size: 148 publication Evidence: moderate

Author Information

Author(s): Windbichler G H, Hausmaninger H, Stummvoll W, Graf A H, Kainz C, Lahodny J, Denison U, Müller-Holzner E, Marth C

Primary Institution: Department of Obstetrics and Gynaecology, University Hospital, Innsbruck, Austria

Hypothesis

Does adding interferon-gamma to standard chemotherapy improve outcomes for ovarian cancer patients?

Conclusion

Adding interferon-gamma to chemotherapy for ovarian cancer improves progression-free survival without increasing toxicity.

Supporting Evidence

  • Progression-free survival improved from 38% in controls to 51% in the treatment group.
  • Median times to progression were 17 months for controls and 48 months for the treatment group.
  • Three-year overall survival was 58% for controls and 74% for the treatment group.
  • Complete clinical responses were observed in 68% of patients receiving interferon-gamma.

Takeaway

This study tested a new medicine called interferon-gamma to see if it helps women with ovarian cancer live longer without their cancer getting worse. It worked better than the usual treatment.

Methodology

A randomized controlled trial comparing standard chemotherapy with and without interferon-gamma in ovarian cancer patients.

Limitations

The study did not reach median overall survival, and some results were not statistically significant.

Participant Demographics

Patients with FIGO stage Ic–IIIc ovarian cancer who had undergone primary surgery.

Statistical Information

P-Value

0.031

Confidence Interval

0.28–0.82

Statistical Significance

p=0.031

Digital Object Identifier (DOI)

10.1054/bjoc.1999.1053

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication