First-line treatment in older patients with Hodgkin lymphoma: a Surveillance, Epidemiology, and End Results (SEER)-Medicare population-based study.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
07 2020
Historique:
received: 27 09 2019
accepted: 14 01 2020
pubmed: 25 2 2020
medline: 3 3 2021
entrez: 25 2 2020
Statut: ppublish

Résumé

While Hodgkin lymphoma (HL) is highly curable in younger patients, older patients have higher relapse and death rates, which may reflect age-related factors, distinct disease biology and/or treatment decisions. We described the association between patient, disease and geographic factors and first-line treatment in older patients (≥65 years) with incident HL using Surveillance, Epidemiology, and End Results (SEER)-Medicare data from 1999 to 2014 (n = 2825). First-line treatment initiated at ≤4 months after diagnosis was categorised as: full chemotherapy regimen (n = 699, 24·7%); partial chemotherapy regimen (n = 1016, 36·0%); single chemotherapy agent or radiotherapy (n = 382, 13·5%); and no treatment (n = 728, 25·8%). Among the fully treated, ABVD [doxorubicin (Adriamycin), bleomycin, vinblastine, dacarbazine]/AVD was most common (n = 635, 90·8%). Adjusted multinomial logistic regression identified factors associated with treatment. Older age, Medicaid dual eligibility, not married, frailty, cardiac comorbidity, prior cancer, earlier diagnosis date, histology, advanced disease Stage, B symptoms and South region were independently associated with increased odds of not receiving full chemotherapy regimens. In conclusion, we found variability in first-line HL treatment for older patients. Treatment differences by Medicaid and region may indicate disparities. Even after adjusting for frailty and cardiac comorbidity, age was associated with treatment, suggesting factors such as end-of-life care or shared decision-making may influence treatment in older patients.

Identifiants

pubmed: 32090325
doi: 10.1111/bjh.16525
pmc: PMC7368808
mid: NIHMS1579219
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

222-235

Subventions

Organisme : NHLBI NIH HHS
ID : K24 HL132008
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002545
Pays : United States

Informations de copyright

© 2020 British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Angie Mae Rodday (AM)

Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.
Department of Medicine, Tufts University School of Medicine, Boston, MA, USA.

Theresa Hahn (T)

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

Anita J Kumar (AJ)

Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.
Department of Medicine, Tufts University School of Medicine, Boston, MA, USA.

Peter K Lindenauer (PK)

Institute for Healthcare Delivery and Population Science, University of Massachusetts Medical School - Baystate, Springfield, MA, USA.

Jonathan W Friedberg (JW)

Wilmot Cancer Institute, Rochester, NY, USA.

Andrew M Evens (AM)

Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.

Susan K Parsons (SK)

Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.
Department of Medicine, Tufts University School of Medicine, Boston, MA, USA.

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