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


Journal

Journal of the National Cancer Institute
ISSN: 1460-2105
Titre abrégé: J Natl Cancer Inst
Pays: United States
ID NLM: 7503089

Informations de publication

Date de publication:
01 10 2021
Historique:
received: 29 09 2020
revised: 15 01 2021
accepted: 05 03 2021
pubmed: 18 3 2021
medline: 25 2 2022
entrez: 17 3 2021
Statut: ppublish

Résumé

There is a critical need to identify patient characteristics associated with long-term ovarian cancer survival. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 33729494
pii: 6174697
doi: 10.1093/jnci/djab034
pmc: PMC8486331
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1369-1378

Subventions

Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233193
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180822
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233290
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189867
Pays : United States

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Lari Wenzel (L)

Department of Medicine and Program in Public Health, University of California, Irvine, CA, USA.

Kathryn Osann (K)

Department of Medicine and Program in Public Health, University of California, Irvine, CA, USA.

Chelsea McKinney (C)

Department of Medicine and Program in Public Health, University of California, Irvine, CA, USA.

David Cella (D)

Department of Medical Social Sciences, Northwestern University Health System, Chicago, IL, USA.

Giulia Fulci (G)

GlaxoSmithKline; Waltham, MA, USA.

Mary J Scroggins (MJ)

International Gynecology Cancer Society, Austin, TX, USA.

Heather A Lankes (HA)

NRG Oncology, Philadelphia, PA, USA.

Victoria Wang (V)

Department of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.

Kenneth P Nephew (KP)

Medical Sciences Program, Indiana University School of Medicine-Bloomington, Bloomington, IN, USA.

George L Maxwell (GL)

Women's Health Integrated Research Center at Inova Health System, Women's Service Line, Inova Health System, Falls Church, VA, USA.

Samuel C Mok (SC)

Department of Gynecological Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Thomas P Conrads (TP)

Women's Health Integrated Research Center at Inova Health System, Women's Service Line, Inova Health System, Falls Church, VA, USA.

Austin Miller (A)

Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.

Robert S Mannel (RS)

Stephenson Cancer Center, Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Oklahoma, Oklahoma City, OK, USA.

Heidi J Gray (HJ)

Gynecologic Oncology, University of Washington Medical Center, Seattle, WA, USA.

Parviz Hanjani (P)

Gynecologic Oncology, Abington-Jefferson Health, Abington, PA, USA.

Warner K Huh (WK)

University of Alabama Highlands, Birmingham, AL, USA.

Nick Spirtos (N)

Women's Cancer Center of Nevada, Las Vegas, NV, USA.

Mario M Leitao (MM)

Memorial Sloan Kettering Cancer and Weill Cornell Medical Center, New York, NY, USA.

Gretchen Glaser (G)

Gynecologic Oncology, Mayo Clinic, Owatonna, MN, USA.

Sudarshan K Sharma (SK)

AMITA Health Physicians, Hinsdale, IL, USA.

Alessandro D Santin (AD)

Department of Obstetrics, Gynecology and Reproductive Services, Yale University School of Medicine, New Haven, CT, USA.

Paul Sperduto (P)

Minneapolis Radiation Oncology and Metro-Minnesota Community Oncology Research Consortium, St. Louis Park, MN, USA.

Shashikant B Lele (SB)

Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.

Robert A Burger (RA)

Genentech, Oceanside, CA, USA.

Bradley J Monk (BJ)

Division of Gynecologic Oncology, Arizona Oncology (US Oncology Network), University of Arizona College of Medicine, Phoenix, AZ, USA.

Michael Birrer (M)

Winthrop P. Rockefeller Cancer Institute University of Arkansas for Medical Sciences, Little Rock, AR, USA.

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