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Enregistrement W4417004592 · doi:10.1182/blood-2025-6990

Time burden of treatment with parenteral hypomethylating agents in combination with venetoclax among patients with newly diagnosed Acute Myeloid Leukemia

2025· article· en· W4417004592 sur OpenAlexaff
Amer M. Zeidan, Ruizhi Zhao, Arthur Voegel, Dina Terloyeva, Maryia Zhdanava, Anabelle Tardif‐Samson, Claire Vanden Eynde, Harold Keer, Dominic Pilon

Notice bibliographique

RevueBlood · 2025
Typearticle
Langueen
DomaineMedicine
ThématiqueAcute Myeloid Leukemia Research
Établissements canadiensGroup for Research in Decision Analysis
Organismes subventionnairesnon disponible
Mots-clésVenetoclaxAzacitidineHypomethylating agentRegimenMyeloid leukemiaOff-label useChemotherapy regimenChemotherapyRetrospective cohort study

Résumé

récupéré en direct d'OpenAlex

Abstract INTRODUCTION: Standard of care for patients with newly diagnosed acute myeloid leukemia (AML) who are not eligible for intensive chemotherapy is a parenteral hypomethylating agent (HMA) - azacitidine or decitabine, also referred to as DNA methyltransferase inhibitors - combined with oral venetoclax. This regimen requires repeated HMA administration in a clinical setting over a cycle of 28 days, placing a substantial time burden on patients affected by the disease. The logistical demands of frequent clinic visits may negatively impact patient quality of life and contribute to early treatment discontinuation. Despite the wide adoption of HMA-venetoclax therapy, its time burden for patients remains poorly characterized. The goal of this study is to address this gap by quantifying the time burden associated with initiation of parenteral HMA combined with venetoclax in routine clinical practice among patients with newly diagnosed AML. METHODS: This is a retrospective study of adults with newly diagnosed AML initiated on parenteral HMA combined with venetoclax using the Humana Healthcare Research Database (01/2019–12/2024), a US claims database of Medicare Advantage beneficiaries. The index date was defined as the date of the first HMA administration up to 60 days after the first AML diagnosis and between October 16, 2020 and June 30, 2024; patients had a prescription fill for venetoclax in the 30-day window before or after the index date. A washout period of ≥12 months of continuous insurance eligibility before the first observed AML diagnosis was required to ensure patients were newly diagnosed. The period of 12 months of continuous insurance eligibility before the index date (i.e., baseline) was used to describe patient characteristics. Outcomes were described during the follow-up period, which spanned from the index date until the end of continuous insurance eligibility or data availability, for a maximum of 6 months. Time burden was defined as the number of distinct days with all-cause healthcare visits, including inpatient days, and days with emergency room (ER), outpatient, and other visits. Days with outpatient visits were further stratified into distinct days with HMA administration, transfusion support, other AML treatment administration-related visits or other outpatient visits. Time at home was defined as days not spent in an inpatient or ER setting for any cause, and without outpatient visits related to cancer care. RESULTS: A total of 737 patients with newly diagnosed AML were initiated on the HMA combined with venetoclax therapy. Mean age at initiation was 76.3 years; 55.4% were male, 83.2% were White, 10.7% were Black, and the rest had other or unknown race. Over a third (38.7%) had myelodysplastic syndrome (MDS) during the baseline period. The index HMA was azacitidine for 70.4% of patients and decitabine for 29.6%. Most patients (93.6%) received the index HMA in the outpatient setting, 4.2% in the inpatient setting, and 2.2% in other settings. During the mean follow-up period of 4.8 months, patients spent a mean of 12.9 days per month on all-cause healthcare visits, including 3.4 days spent in inpatient setting, 0.3 days in ER setting, and 9.2 days in outpatient setting. In terms of outpatient days, patients spent a mean of 3.8 days per month receiving HMA therapy, 1.0 days receiving transfusion support, and the rest of the outpatient time receiving other AML and non-AML care. Patients spent a mean of 18.6 days per month at home or receiving non-cancer-related outpatient care. CONCLUSIONS: Patients with newly diagnosed AML ineligible for intensive chemotherapy spend over a third of their time engaged in medical care, and a substantial portion of this time is dedicated to receiving HMA therapy. These findings highlight a substantial time burden among patients and a need for alternative effective treatment options to optimize the delivery of medical care.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,003
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: Observationnel
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,006
Score d'incertitude au seuil0,012

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0000,003
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0010,001
Études des sciences et des technologies0,0000,000
Communication savante0,0010,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0020,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,011
Tête enseignante GPT0,262
Écart entre enseignants0,252 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2025
Routes d'admission1
Résumé présentoui

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