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Quality of Life and Adverse Events: Prognostic Relationships in Long-Term Ovarian Cancer Survival

  • Lari Wenzel*
  • , Kathryn Osann
  • , Chelsea McKinney
  • , David Cella
  • , Giulia Fulci
  • , Mary J. Scroggins
  • , Heather A. Lankes
  • , Victoria Wang
  • , Kenneth P. Nephew
  • , George L. Maxwell
  • , Samuel C. Mok
  • , Thomas P. Conrads
  • , Austin Miller
  • , Robert S. Mannel
  • , Heidi J. Gray
  • , Parviz Hanjani
  • , Warner K. Huh
  • , Nick Spirtos
  • , Mario M. Leitao
  • , Gretchen Glaser
  • Sudarshan K. Sharma, Alessandro D. Santin, Paul Sperduto, Shashikant B. Lele, Robert A. Burger, Bradley J. Monk, Michael Birrer
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Background: There is a critical need to identify patient characteristics associated with long-term ovarian cancer survival. Methods: Quality of life (QOL), measured by the Functional Assessment of Cancer Therapy-Ovarian-Trial Outcome Index (FACT-O-TOI), including physical, functional, and ovarian-specific subscales, was compared between long-term survivors (LTS) (8+ years) and short-term survivors (STS) (<5 years) of GOG 218 at baseline; before cycles 4, 7, 13, 21; and 6 months post-treatment using linear and longitudinal mixed models adjusted for covariates. Adverse events (AEs) were compared between survivor groups at each assessment using generalized linear models. All P values are 2-sided. Results: QOL differed statistically significantly between STS (N = 1115) and LTS (N = 260) (P <. 001). Baseline FACT-O-TOI and FACT-O-TOI change were independently associated with long-term survival (odds ratio = 1.05, 95% confidence interval = 1.03 to 1.06 and odds ratio = 1.06, 95% confidence interval = 1.05 to 1.07, respectively). A 7-point increase in baseline QOL was associated with a 38.0% increase in probability of LTS, and a 9-point increase in QOL change was associated with a 67.0% increase in odds for LTS. QOL decreased statistically significantly with increasing AE quartiles (cycle 4 quartiles: 0-5 vs 6-8 vs 9-11 vs ≥12 AEs, P =. 01; cycle 21 quartiles: 0-2 vs 3 vs 4-5 vs ≥6 AEs, P =. 001). Further, LTS reported statistically significantly better QOL compared with STS (P =. 03 and P =. 01, cycles 4 and 21, respectively), with similar findings across higher AE grades. Conclusions: Baseline and longitudinal QOL change scores distinguished LTS vs STS and are robust prognosticators for long-term survival. Results have trial design and supportive care implications, providing meaningful prognostic value in this understudied population.

Original languageEnglish
Pages (from-to)1369-1378
Number of pages10
JournalJournal of the National Cancer Institute
Volume113
Issue number10
DOIs
StatePublished - 1 Oct 2021

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