Time spent at home among older adults with acute myeloid leukemia receiving azacitidine- or venetoclax-based regimens.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 04 2023
Historique:
received: 21 01 2022
medline: 4 4 2023
pubmed: 22 7 2022
entrez: 21 7 2022
Statut: epublish

Résumé

Time at home is a critically important outcome to adults with acute myeloid leukemia (AML) when selecting treatment; however, no study to date has adequately described the amount of time older adults spend at home following initiation of chemotherapy. We queried records from a multi-institution health system to identify adults aged ≥60 years newly diagnosed with AML who were treated with azacitidine or venetoclax and evaluated the proportion of days at home (PDH) following diagnosis. Days were considered "at home" if patients were not admitted or seen in the emergency department or oncology/infusion clinic. Assessed covariates included demographics and disease risk. Associations between PDH and baseline characteristics were evaluated via linear regression, adjusted for log length of follow-up. From 2015-2020, 113 older adults were identified. Most received azacitidine plus venetoclax (51.3%) followed by azacitidine monotherapy (38.9%). The mean PDH for all patients was 0.58 (95% confidence interval: 0.54-0.63, median 0.63). PDH increased among survivors over time. PDH did not differ between therapy groups (adjusted mean, azacitidine plus venetoclax: 0.68; azacitidine monotherapy: 0.66; P=0.64) or between disease risk categories (P=0.34). Compared to patients receiving azacitidine monotherapy, patients receiving azacitidine plus venetoclax had longer clinic visits (median minutes: 127.9 vs. 112.9, P<0.001) and infusion visits (median minutes: 194.3 vs. 132.5, P<0.001). The burden of care for older adults with AML treated with "less intense" chemotherapy is high. The addition of venetoclax to azacitidine did not translate into increased time at home. Future prospective studies should evaluate patient-centered outcomes, including time at home, to inform shared decision-making and drug development.

Identifiants

pubmed: 35861016
doi: 10.3324/haematol.2022.280728
pmc: PMC10071106
doi:

Substances chimiques

Azacitidine M801H13NRU
venetoclax N54AIC43PW
Bridged Bicyclo Compounds, Heterocyclic 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1006-1014

Subventions

Organisme : NCI NIH HHS
ID : L30 CA264755
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002489
Pays : United States
Organisme : AHRQ HHS
ID : T32 HS000032
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Christopher E Jensen (CE)

University of North Carolina School of Medicine, Chapel Hill, NC, USA; University of North Carolina Gillings School of Global Public Health, Chapel Hill, NC.

Hilary M Heiling (HM)

University of North Carolina Gillings School of Global Public Health, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC.

Konan E Beke (KE)

University of North Carolina School of Medicine, Chapel Hill, NC.

Allison M Deal (AM)

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC.

Ashley L Bryant (AL)

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA; University of North Carolina School of Nursing, Chapel Hill, NC.

Lorinda A Coombs (LA)

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA; University of North Carolina School of Nursing, Chapel Hill, NC.

Matthew C Foster (MC)

University of North Carolina School of Medicine, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC.

Daniel R Richardson (DR)

University of North Carolina School of Medicine, Chapel Hill, NC, USA; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC. daniel_richardson@med.unc.edu.

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Classifications MeSH