Long-term fatigue in survivors of non-Hodgkin lymphoma: The Lymphoma Study Association SIMONAL cross-sectional study.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 03 09 2018
revised: 06 02 2019
accepted: 06 02 2019
pubmed: 23 3 2019
medline: 25 3 2020
entrez: 23 3 2019
Statut: ppublish

Résumé

Long-term survivors of non-Hodgkin lymphoma (NHL) must cope with treatment complications and late toxicities that affect their health-related quality of life. Little is known about the risk-to-benefit ratio of new agents like rituximab. The impact of treatment regimens and health disorders on long-term fatigue levels was investigated in a cross-sectional study. Two self-administered questionnaires, the 20-item Multidimensional Fatigue Inventory (MFI-20) and a Life Situation Questionnaire, were mailed in 2015 to NHL survivors enrolled onto 12 successive clinical studies (1993-2010) conducted by the Lymphoma Study Association. Private addresses were obtained for 3317 survivors, of whom 1671 (50%) returned the questionnaires. Severe fatigue was defined as MFI-20 scores ≥60 on dimension scales scored from 0 to 100. Linear regression models were used to assess factors that were linked to increased fatigue levels. The study population included 906 men and 765 women, and the median age was 64 years (age range, 24-95 years). Overall, 811 survivors had received cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP)-like chemotherapy, 518 had received high-dose CHOP, and 342 had undergone upfront autologous stem cell transplantation; 829 survivors also had received rituximab. In total, 1100 survivors (66%) reported 1 or more late health disorders. Severe fatigue was reported by 602 survivors (37%). Increased fatigue levels were associated (P < .001) with increased age, obesity, and the presence of health disorders, but not with initial treatment or rituximab. The survey confirms that high proportions long-term NHL survivors have severe fatigue. The results suggest that initial treatment and the receipt of rituximab have no influence on the development of long-term fatigue.

Sections du résumé

BACKGROUND
Long-term survivors of non-Hodgkin lymphoma (NHL) must cope with treatment complications and late toxicities that affect their health-related quality of life. Little is known about the risk-to-benefit ratio of new agents like rituximab. The impact of treatment regimens and health disorders on long-term fatigue levels was investigated in a cross-sectional study.
METHODS
Two self-administered questionnaires, the 20-item Multidimensional Fatigue Inventory (MFI-20) and a Life Situation Questionnaire, were mailed in 2015 to NHL survivors enrolled onto 12 successive clinical studies (1993-2010) conducted by the Lymphoma Study Association. Private addresses were obtained for 3317 survivors, of whom 1671 (50%) returned the questionnaires. Severe fatigue was defined as MFI-20 scores ≥60 on dimension scales scored from 0 to 100. Linear regression models were used to assess factors that were linked to increased fatigue levels.
RESULTS
The study population included 906 men and 765 women, and the median age was 64 years (age range, 24-95 years). Overall, 811 survivors had received cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP)-like chemotherapy, 518 had received high-dose CHOP, and 342 had undergone upfront autologous stem cell transplantation; 829 survivors also had received rituximab. In total, 1100 survivors (66%) reported 1 or more late health disorders. Severe fatigue was reported by 602 survivors (37%). Increased fatigue levels were associated (P < .001) with increased age, obesity, and the presence of health disorders, but not with initial treatment or rituximab.
CONCLUSIONS
The survey confirms that high proportions long-term NHL survivors have severe fatigue. The results suggest that initial treatment and the receipt of rituximab have no influence on the development of long-term fatigue.

Identifiants

pubmed: 30901086
doi: 10.1002/cncr.32040
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2291-2299

Informations de copyright

© 2019 American Cancer Society.

Références

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Auteurs

Nicolas Mounier (N)

Onco-Hematology Unit, l'Archet Hospital, Nice University Hospital Center, University of Côte d'Azur, Nice, France.

Sabine Anthony (S)

Clinical Research and Innovation Office, Cimiez Hospital, Nice University Hospital Center, University of Côte d'Azur, Nice, France.

Raphaël Busson (R)

Mathematics, Information, and Engineering Systems (MIIS) Doctoral School, Caen-Normandy University, Caen, France.
French Center on eHealth, North-West Region Data Processing Center and French National League Against Cancer Clinical Research Platform, Caen, France.

Catherine Thieblemont (C)

Hemato-Oncology Unit, Saint-Louis University Hospital Center, Public Hospital Network of Paris, Paris, France.

Vincent Ribrag (V)

Hematology Unit, Gustave Roussy Cancer Campus, Villejuif, France.

Hervé Tilly (H)

Hematology Department and French Institute of Health and Medical Research (INSERM) Unit 1243, Henri Becquerel Center, Rouen, France.

Corinne Haioun (C)

Lymphoid Malignancies Unit, Henri Mondor University Hospital Center, Public Hospital Network of Paris, Créteil, France.

René-Olivier Casasnovas (RO)

Hematology Unit and French Institute of Health and Medical Research (INSERM) Unit 1231, Bocage Hospital, Dijon Bourgogne Regional University Hospital Center, Dijon, France.

Franck Morschhauser (F)

Hematology Transfusion Institute, Claude Huriez Hospital, Lille Regional University Hospital Center, Lille, France.

Pierre Feugier (P)

Hematology Unit, Brabois Hospital, Nancy University Hospital Center, Vandœuvre-lès-Nancy, France.

Richard Delarue (R)

Hematology Unit, Necker University Hospital for Sick Children, Public Hospital Network of Paris, Paris, France.

Loic Ysebaert (L)

Oncopole, Toulouse University Cancer Institute, Toulouse, France.

Catherine Sebban (C)

Hematology Unit, Léon Bérard Center, Lyon, France.

Florence Broussais-Guillaumot (F)

Clinical Research Department-Lymphoma Study Association, Lyon South Hospital Center, Pierre-Bénite, France.

Gandhi Damaj (G)

Basse-Normandy Hematology Institute, Côte de Nacre Regional University Hospital Center, Caen, France.

Virginie Nerich (V)

Regional Federative Institute of Cancerology, Besancon, France.

Jean-Philippe Jais (JP)

Laboratory of Biostatistics, Paris V University-Descartes, Paris, France.

Lilian Laborde (L)

Paoli-Calmettes Institute-Provence-Alpes-Côte d'Azur (IPC-PACA) Data Processing Center, Marseille, France.

Gilles Salles (G)

Faculty of Medicine, Claude Bernard University, Lyon, France.
Hematology Department, Lyon South Hospital Center, Pierre-Bénite, France.

Michel Henry-Amar (M)

French Center on eHealth, North-West Region Data Processing Center and French National League Against Cancer Clinical Research Platform, Caen, France.

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