Journal
BRITISH JOURNAL OF HAEMATOLOGY
Volume 190, Issue 3, Pages 371-384Publisher
WILEY
DOI: 10.1111/bjh.16539
Keywords
non-Hodgkin lymphoma; late effects; adolescent and young adult; population-based study
Categories
Funding
- Rich and Weissman Family Lymphoma and Survivorship Fund St. Baldrick's Research Grant
- National Research Service Award (NRSA) for Primary Medical Care, from the Health Resources and Services Administration (HRSA) [T32HP300370401]
- National Center for Advancing Translational Science (NCATS), National Institute of Health [UL1 0000860]
- California Department of Public Health [103885]
- National Cancer Institute's Surveillance, Epidemiology and End Results Program [HHSN261201000140C, HHSN261201000035C, HHSN261201000034C]
- Centers for Disease Control and Prevention's National Program of Cancer Registries [U58DP003862-01]
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Little is known about the incidence of late effects following non-Hodgkin lymphoma (NHL) among adolescent and young adult (AYA, 15-39 years) survivors. Using data from the California Cancer Registry linked to hospital discharge, we estimated the cumulative incidence of late effects at 10 years among AYAs diagnosed with NHL during 1996-2012, who survived >= 2 years. Cox proportional-hazards models were used to investigate the influence of sociodemographic and clinical factors on the occurrence of late effects. Of 4392 HIV-uninfected patients, the highest incident diseases were: endocrine (18 center dot 5%), cardiovascular (11 center dot 7%), and respiratory (5 center dot 0%), followed by secondary primary malignancy (SPM, 2 center dot 6%), renal and neurologic (2 center dot 2%), liver/pancreatic (2 center dot 0%), and avascular necrosis (1 center dot 2%). Among the 425 HIV-infected survivors, incidence was higher for all late effects, especially over threefold increased risk of SPM, compared to HIV-uninfected patients (8 center dot 1% vs. 2 center dot 6%). In multivariable models for HIV-uninfected patients, public or no health insurance (vs. private), residence in lower socioeconomic neighbourhoods (vs. higher), and receipt of a haematopoietic stem cell transplant were associated with a greater risk of most late effects. Our findings of substantial incidence of late effects among NHL AYA survivors emphasise the need for longterm follow-up and appropriate survivorship care to reduce morbidity and mortality in this vulnerable population.
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