Long-term fatigue and quality of life among epithelial ovarian cancer survivors: a GINECO case/control VIVROVAIRE I study.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
01 05 2019
Historique:
pubmed: 10 3 2019
medline: 13 6 2020
entrez: 10 3 2019
Statut: ppublish

Résumé

Few data are available on long-term fatigue (LTF) and quality of life (QoL) among epithelial ovarian cancer survivors (EOCS). In this case-control study, we compared LTF, symptoms and several QoL domains in EOCS relapse-free ≥3 years after first-line treatment and age-matched healthy women. EOCS were recruited from 25 cooperative GINECO centers in France. Controls were randomly selected from the electoral rolls. All participants completed validated self-reported questionnaires: fatigue (FACIT-F), QoL (FACT-G/O), neurotoxicity (FACT-Ntx), anxiety/depression (HADS), sleep disturbance (ISI), and physical activity (IPAQ). Severe LTF (SLTF) was defined as a FACIT-F score <37/52. Univariate and multivariate logistic regressions were conducted to analyze SLTF and its influencing factors in EOCS. A total of 318 EOCS and 318 controls were included. EOCS were 63-year-old on average, with FIGO stage I/II (50%), III/IV (48%); 99% had received platinum and taxane chemotherapy, with an average 6-year follow-up. There were no differences between the two groups in socio-demographic characteristics and global QoL. EOCS had poorer FACIT-F scores (40 versus 45, P < 0.0001), lower functional well-being scores (18 versus 20, P = 0.0002), poorer FACT-O scores (31 versus 34 P < 0.0001), and poorer FACT-Ntx scores (35 versus 39, P < 0.0001). They also reported more SLTF (26% versus 13%, P = 0.0004), poorer sleep quality (63% versus 47%, P = 0.0003), and more depression (22% versus 13%, P = 0.01). Fewer than 20% of EOCS and controls exercised regularly. In multivariate analyses, EOCS with high levels of depression, neurotoxicity, and sleep disturbance had an increased risk of developing SLTF (P < 0.01). Compared with controls, EOCS presented similar QoL but persistent LTF, EOC-related symptoms, neurotoxicity, depression, and sleep disturbance. Depression, neuropathy, and sleep disturbance are the main conditions associated with severe LTF.

Sections du résumé

BACKGROUND
Few data are available on long-term fatigue (LTF) and quality of life (QoL) among epithelial ovarian cancer survivors (EOCS). In this case-control study, we compared LTF, symptoms and several QoL domains in EOCS relapse-free ≥3 years after first-line treatment and age-matched healthy women.
PATIENTS AND METHODS
EOCS were recruited from 25 cooperative GINECO centers in France. Controls were randomly selected from the electoral rolls. All participants completed validated self-reported questionnaires: fatigue (FACIT-F), QoL (FACT-G/O), neurotoxicity (FACT-Ntx), anxiety/depression (HADS), sleep disturbance (ISI), and physical activity (IPAQ). Severe LTF (SLTF) was defined as a FACIT-F score <37/52. Univariate and multivariate logistic regressions were conducted to analyze SLTF and its influencing factors in EOCS.
RESULTS
A total of 318 EOCS and 318 controls were included. EOCS were 63-year-old on average, with FIGO stage I/II (50%), III/IV (48%); 99% had received platinum and taxane chemotherapy, with an average 6-year follow-up. There were no differences between the two groups in socio-demographic characteristics and global QoL. EOCS had poorer FACIT-F scores (40 versus 45, P < 0.0001), lower functional well-being scores (18 versus 20, P = 0.0002), poorer FACT-O scores (31 versus 34 P < 0.0001), and poorer FACT-Ntx scores (35 versus 39, P < 0.0001). They also reported more SLTF (26% versus 13%, P = 0.0004), poorer sleep quality (63% versus 47%, P = 0.0003), and more depression (22% versus 13%, P = 0.01). Fewer than 20% of EOCS and controls exercised regularly. In multivariate analyses, EOCS with high levels of depression, neurotoxicity, and sleep disturbance had an increased risk of developing SLTF (P < 0.01).
CONCLUSION
Compared with controls, EOCS presented similar QoL but persistent LTF, EOC-related symptoms, neurotoxicity, depression, and sleep disturbance. Depression, neuropathy, and sleep disturbance are the main conditions associated with severe LTF.

Identifiants

pubmed: 30851097
pii: S0923-7534(19)31163-9
doi: 10.1093/annonc/mdz074
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

845-852

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

F Joly (F)

Department of Oncology, Centre François Baclesse, Caen; INSERM, U1086, Caen; UMR-S1077, University of Caen Basse-Normandie, Caen; Department of Oncology, CHU de Caen, Caen. Electronic address: f.joly@baclesse.unicancer.fr.

D Ahmed-Lecheheb (D)

Department of Oncology, Centre François Baclesse, Caen; INSERM, U1086, Caen.

E Kalbacher (E)

Department of Oncology, CHU Jean Minjoz, Besançon.

N Heutte (N)

Department of Clinical Research, Centre François Baclesse, Caen.

B Clarisse (B)

Department of Clinical Research, Centre François Baclesse, Caen.

J M Grellard (JM)

Department of Clinical Research, Centre François Baclesse, Caen.

F Gernier (F)

INSERM, U1086, Caen; Department of Clinical Research, Centre François Baclesse, Caen.

D Berton-Rigaud (D)

Department of Oncology, Institut de Cancérologie de l'Ouest, Site René Gauducheau, Saint Herblain.

O Tredan (O)

Department of Oncology, Centre Léon Bérard, Lyon.

M Fabbro (M)

Department of Oncology, Institut Régional du Cancer, Montpellier.

A M Savoye (AM)

Department of Oncology, Institut Jean Godinot, Reims.

J E Kurtz (JE)

Department of Oncology, Hôpitaux Universitaires de Strasbourg, Strasbourg.

J Alexandre (J)

Department of Oncology, Hôpital Cochin, Paris.

P Follana (P)

Department of Oncology, Centre Antoine Lacassagne, Nice.

V Delecroix (V)

Department of Oncology, Clinique Mutualiste de l'Estuaire, Saint-Nazaire.

N Dohollou (N)

Department of Oncology, Polyclinique Bordeaux Nord Aquitaine, Bordeaux.

C Roemer-Becuwe (C)

Department of Oncology, Centre d'Oncologie de Gentilly, Nancy.

G De Rauglaudre (G)

Department of Oncology, Institut Sainte Catherine, Avignon.

A Lortholary (A)

Department of Oncology, Centre Catherine de Sienne, Nantes.

K Prulhiere (K)

Department of Oncology, Institut du Cancer Courlancy, Reims.

A Lesoin (A)

Department of Oncology, Centre Oscar Lambret, Lille.

A Zannetti (A)

Department of Oncology, Centre Hospitalier de Cholet, Cholet.

S N'Guyen (S)

Department of Oncology, CH Pau, Pau.

S Trager-Maury (S)

Department of Oncology, GHPSO Senlis, Senlis.

L Chauvenet (L)

Department of Oncology, Centre Hospitalier de Sens, Sens.

S Abadie Lacourtoisie (S)

Department of Oncology, Institut de Cancérologie de l'Ouest, Site Paul Papin, Angers.

A Gompel (A)

Department of Oncology, Hôpitaux Universitaires Cochin Hôtel-Dieu Broca, Paris.

C Lhommé (C)

Department of Oncology, Gustave Roussy, Villejuif.

A Floquet (A)

Department of Oncology, Institut Bergonié, Bordeaux, France.

P Pautier (P)

Department of Oncology, Gustave Roussy, Villejuif.

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Classifications MeSH