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Enregistrement W4417011144 · doi:10.1182/blood-2025-1997

Asciminib (ASC) demonstrates continued improvement in patient-reported outcomes (PROs) vs investigator-selected tyrosine kinase inhibitors (IS-TKIs) in newly diagnosed chronic myeloid leukemia (CML): ASC4FIRST week 96 analysis

2025· article· en· W4417011144 sur OpenAlexaff
Jörge E. Cortes, Andreas Hochhaus, Kathryn E. Flynn, Felice Bombaci, Ghayas C. Issa, Richard A. Larson, Jianxiang Wang, Dong‐Wook Kim, Dennis Kim, Jiří Mayer, Yeow Tee Goh, Philipp le Coutre, In Ho Kim, Gabriel Étienne, S. S. Kapoor, Rajendra Jinwal, Kamel Malek, Lillian Yau, Timothy P. Hughes, Naoto Takahashi

Notice bibliographique

RevueBlood · 2025
Typearticle
Langueen
DomaineMedicine
ThématiqueChronic Myeloid Leukemia Treatments
Établissements canadiensPrincess Margaret Cancer Centre
Organismes subventionnairesnon disponible
Mots-clésAdverse effectQuality of life (healthcare)Clinical trialRandomized controlled trialNilotinibMyeloid leukemiaClinical endpointTyrosine-kinase inhibitor

Résumé

récupéré en direct d'OpenAlex

Abstract Introduction Long-term TKI therapy for patients (pts) with CML is efficacious but is associated with adverse events (AEs) affecting quality of life (QOL). Even low-grade AEs can inhibit QOL, resulting in treatment nonadherence and subsequently poor clinical outcomes. Thus, effective management of CML requires assessing the impact of treatment-emergent AEs on QOL. ASC, the first BCR::ABL1 inhibitor to Specifically Target the ABL Myristoyl Pocket, is approved in several countries for pts with newly diagnosed CML in chronic phase (CP) based on superior clinical outcomes vs IS-TKIs in the pivotal phase 3 ASC4FIRST trial (NCT04971226). In the wk 48 ASC4FIRST PRO analysis, ASC vs IS-TKIs was associated with improved health-related QOL (HRQOL) and reduced symptom burden. Here, we present PROs from the wk 96 analysis (data cutoff: Oct 22, 2024). Methods Adults with newly diagnosed CML-CP were randomized 1:1 to receive ASC or an IS-TKI, stratified by ELTS risk category and prerandomization-selected TKI (imatinib [IMA]/second-generation [2G] TKI). Wk 96 PRO secondary endpoints were change from baseline (BL) in scores and individual scales for EORTC QLQ-C30 and EORTC QLQ-CML24; improvement corresponded to a change from BL in functional/satisfaction and global health status/QOL scales (increase of >5) or symptom/item scores (decrease of >5). PRO-CTCAE items and FACIT-GP5 will be reported separately by Hughes et al. Pts completed questionnaires on electronic devices at BL and scheduled study visits. Results A total of 405 pts were randomized to ASC (ASCIMA, n=101; ASC2G, n=100) or IS-TKIs (IS-TKIIMA, n=102; IS-TKI2G, n=102); median duration of follow-up was 26.9 and 26.3 months per arm, respectively. Completion rates were balanced with ASC vs IS-TKI for EORTC QLQ-C30 (BL, 57.7% vs 59.0%; wk 96, 76.2% vs 65.2%) and EORTC QLQ-CML24 (BL, 56.2% vs 56.4%; wk 96, 75.5% vs 65.2%). Per EORTC QLQ-C30 at wk 96 vs BL, the following proportions of pts on ASCIMA and IS-TKIIMAand on ASC2G and IS-TKI2G had improvement in the physical (31.3% and 17.6%; 43.5% and 40.0%), role (18.8% and 5.9%; 20.6% and 8.6%), cognitive (18.7% and 5.9%; 18.0% and 8.6%), social (25.0% and 17.7%; 33.3% and 22.9%), and emotional (40.7% and 23.5%; 35.9% and 34.2%) functional scales, respectively.The proportions of pts reporting improvement with ASCIMA and IS-TKIIMAand with ASC2G and IS-TKI2G across symptoms included: fatigue (43.8% and 11.8%; 43.6% and 28.5%), nausea/vomiting (15.6% and 0.0%; 7.7% and 2.9%), diarrhea (18.8% and 17.6%; 10.3% and 11.4%), pain (15.7% and 5.9%; 33.4% and 14.3%), dyspnea (9.4% and 0.0%; 12.8% and 5.7%), insomnia (18.8% and 5.9%; 12.8% and 20.0%), appetite loss (25.0% and 5.9%; 25.6% and 11.4%), and constipation (18.8% and 11.8%; 7.7% and 20.0%), respectively. The proportion of pts on ASCIMA and IS-TKIIMAand on ASC2G and IS-TKI2Gwho had improvement with financial difficulties was (18.8% and 29.4%; 23.1% and 20.0%). Overall, 37.5% vs 17.7% of pts receiving ASCIMA vs IS-TKIIMA and 58.9% vs 28.6% receiving ASC2G vs IS-TKI2G, respectively, had improvements in global health status/QOL. Change from BL to wk 96 in EORTC QLQ-CML24 satisfaction/symptom scale scores with ASCIMA vs IS-TKIIMAand with ASC2G vs IS-TKI2G, respectively, showed that higher proportions of pts had improvements in symptom burden (27.5% vs 0.0%; 46.1% vs 20.6%), impact on daily life (62.0% vs 23.5%; 58.9% vs 47.1%), impact on worry/mood (48.2% vs 29.5%; 58.9% vs 41.2%), body image problems (27.6% vs 0.0%; 28.2% vs 11.8%), and satisfaction with care and information (41.4% vs 29.4%; 53.8% vs 29.4%). Improvement in satisfaction with social life was reported by 24.1% and 23.5% of pts on ASCIMA and IS-TKIIMA,and 41.0% and 20.6% on ASC2G and IS-TKI2G, respectively. Exploratory sensitivity analyses evaluating the impact of missing BL PRO data concluded that there was no substantial impact on observed PROs. Conclusions Overall,ASC continued to be associated with improved HRQOL and reduced symptom burden vs IS-TKIs, regardless of strata, in the wk 96 PRO analysis of ASC4FIRST. Considering the superior efficacy and favorable safety and tolerability of ASC in ASC4FIRST observed at wk 96, these PRO findings reinforce ASC as a standard of care for pts with newly diagnosed CML-CP. Longer follow-up of PRO evaluations is warranted and may support long-term QOL benefit of ASC in pts with CML-CP.

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)0,004
score de la tête « metaresearch » (Gemma)0,002
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Essai non randomisé · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,007
Score d'incertitude au seuil0,023

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0040,002
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0020,004
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0010,001
Science ouverte0,0010,001
Intégrité de la recherche0,0010,002
Charge utile insuffisante (le modèle a refusé de juger)0,0070,001

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 Opus0,009
Tête enseignante GPT0,245
Écart entre enseignants0,236 · 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'étudeEssai non randomisé
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

Citations1
Publié2025
Routes d'admission1
Résumé présentoui

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