Patient-reported outcomes predict overall survival in older patients with acute myeloid leukemia.


Journal

Journal of geriatric oncology
ISSN: 1879-4076
Titre abrégé: J Geriatr Oncol
Pays: Netherlands
ID NLM: 101534770

Informations de publication

Date de publication:
09 2022
Historique:
received: 23 02 2021
revised: 15 07 2021
accepted: 07 09 2021
pubmed: 16 9 2021
medline: 21 9 2022
entrez: 15 9 2021
Statut: ppublish

Résumé

Patient-reported outcomes (PROs) predict overall survival (OS) in many cancer types, but there is little evidence of their prognostic value in older patients with acute myeloid leukemia (AML). We examined whether the Functional Assessment of Cancer Therapy - Leukemia (FACT-Leu) predicted OS beyond established prognostic factors among these patients. Data were from AML2002 (n = 309), a randomized phase 2/3 study comparing decitabine plus talacotuzumab versus decitabine alone in older AML patients ineligible for intensive chemotherapy. We used ridge-penalized Cox proportional hazards models to estimate the association between baseline FACT-Leu scales and OS. We then conducted a bootstrap analysis to determine how often FACT-Leu scales appeared in forward- and backward- selected "final models" predicting OS relative to prognosticators from the AML Composite Model (AML-CM; e.g., chronic comorbidities, previous cancer, cytogenetic/molecular risk). In ridge-penalized models, the FACT-Leu Physical Well-Being (PWB), Trial Outcomes Index (TOI), and Total scales predicted OS. Adjusting for AML-CM factors, an important increase (3 points) in PWB score was associated with a 14% reduction in the hazard of death. In the bootstrap analysis, the PWB scale appeared in 93% of backward- and 98% of forward selected models, while the TOI [57% (backward), 79% (forward)] and FACT-Leu Total [51% (backward), 78% (forward)] appeared less often in final models. These results indicate PROs' value for predicting outcomes among older AML patients and underscore the need to more systematically collect PRO data in routine care with these patients. gov Registration: NCT02472145.

Identifiants

pubmed: 34521609
pii: S1879-4068(21)00208-3
doi: 10.1016/j.jgo.2021.09.007
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Decitabine 776B62CQ27

Banques de données

ClinicalTrials.gov
['NCT02472145']

Types de publication

Clinical Trial, Phase II Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

935-939

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest We report the following potential conflicts or perceived conflicts. Jianming He, Renee Pierson, Christina Loefgren are employees of Janssen Global Services. David Cella and John Devin Peipert are employees of Northwestern University and David Cella is the President of FACIT.org. Dr. Efficace reports consultancy for Abbvie, Amgen, Janssen, Orsenix, Takeda, and grants from Amgen (to his Institution), outside the submitted work.

Auteurs

John Devin Peipert (JD)

Department of Medical Social Sciences, Northwestern University, Chicago, IL, USA. Electronic address: john.peipert@northwestern.edu.

Fabio Efficace (F)

Department of Medical Social Sciences, Northwestern University, Chicago, IL, USA; Italian Group for Adult Hematologic Disease (GIMEMA), Health Outcomes Research Unit, Rome, Italy.

Renee Pierson (R)

Janssen Global Services, LLC, Raritan, NJ, USA.

Christina Loefgren (C)

Janssen Global Services, LLC, Raritan, NJ, USA.

David Cella (D)

Department of Medical Social Sciences, Northwestern University, Chicago, IL, USA.

Jianming He (J)

Janssen Global Services, LLC, Raritan, NJ, USA.

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Classifications MeSH