Consensus in controversy: The modified Delphi method applied to Gynecologic Oncology practice.


Journal Article

OBJECTIVES: To determine the degree of consensus regarding the probabilities of outcomes associated with IP/IV and IV chemotherapy. METHODS: A survey was administered to an expert panel using the Delphi method. Ten ovarian cancer experts were asked to estimate outcomes for patients receiving IP/IV or IV chemotherapy. The clinical estimates were: 1) probability of completing six cycles of chemotherapy, 2) probability of surviving five years, 3) median survival, and 4) probability of ER/hospital visits during treatment. Estimates for two patients, one with a low comorbidity index (patient 1) and the other with a moderate index (patient 2), were included. The survey was administered in three rounds, and panelists could revise their subsequent responses based on review of the anonymous opinions of their peers. RESULTS: The ranges were smaller for IV compared with IP/IV therapy. Ranges decreased with each round. Consensus converged around outcomes related to IP/IV chemotherapy for: 1) completion of 6 cycles of therapy (type 1 patient, 62%, type 2 patient, 43%); 2) percentage of patients surviving 5 years (type 1 patient, 66%, type 2 patient, 47%); and 3) median survival (type 1 patient, 83 months, type 2 patient, 58 months). The group required three rounds to achieve consensus on the probabilities of ER/hospital visits (type 1 patient, 24%, type 2 patient, 35%). CONCLUSIONS: Initial estimates of survival and adverse events associated with IP/IV chemotherapy differ among experts. The Delphi process works to build consensus and may be a pragmatic tool to inform patients of their expected outcomes.

Full Text

Duke Authors

Cited Authors

  • Cohn, DE; Havrilesky, LJ; Osann, K; Lipscomb, J; Hsieh, S; Walker, JL; Wright, AA; Alvarez, RD; Karlan, BY; Bristow, RE; DiSilvestro, PA; Wakabayashi, MT; Morgan, R; Mukamel, DB; Wenzel, L

Published Date

  • September 2015

Published In

Volume / Issue

  • 138 / 3

Start / End Page

  • 712 - 716

PubMed ID

  • 26177553

Pubmed Central ID

  • 26177553

Electronic International Standard Serial Number (EISSN)

  • 1095-6859

Digital Object Identifier (DOI)

  • 10.1016/j.ygyno.2015.07.014


  • eng

Conference Location

  • United States