TY - JOUR
T1 - Quality of Life and Adverse Events
T2 - Prognostic Relationships in Long-Term Ovarian Cancer Survival
AU - Wenzel, Lari
AU - Osann, Kathryn
AU - McKinney, Chelsea
AU - Cella, David
AU - Fulci, Giulia
AU - Scroggins, Mary J.
AU - Lankes, Heather A.
AU - Wang, Victoria
AU - Nephew, Kenneth P.
AU - Maxwell, George L.
AU - Mok, Samuel C.
AU - Conrads, Thomas P.
AU - Miller, Austin
AU - Mannel, Robert S.
AU - Gray, Heidi J.
AU - Hanjani, Parviz
AU - Huh, Warner K.
AU - Spirtos, Nick
AU - Leitao, Mario M.
AU - Glaser, Gretchen
AU - Sharma, Sudarshan K.
AU - Santin, Alessandro D.
AU - Sperduto, Paul
AU - Lele, Shashikant B.
AU - Burger, Robert A.
AU - Monk, Bradley J.
AU - Birrer, Michael
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press. All rights reserved.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85117391116&partnerID=8YFLogxK
U2 - 10.1093/jnci/djab034
DO - 10.1093/jnci/djab034
M3 - Article
C2 - 33729494
AN - SCOPUS:85117391116
SN - 0027-8874
VL - 113
SP - 1369
EP - 1378
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 10
ER -