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Enregistrement W4310112932 · doi:10.1182/blood-2022-156749

Quality of Life in Patients with Chronic Lymphocytic Leukemia Initiating Venetoclax in Routine Clinical Practice across Canada: Results from the Devote Study

2022· article· en· W4310112932 sur OpenAlexaffabout
Andrew Aw, Versha Banerji, Sarah-Jane Bull, Pierre‐André Fournier, Anthea Peters, Carolyn Owen

Notice bibliographique

RevueBlood · 2022
Typearticle
Langueen
DomaineMedicine
ThématiqueChronic Lymphocytic Leukemia Research
Établissements canadiensUniversity of CalgaryUniversity of AlbertaABB (Canada)CancerCare ManitobaAlberta Health ServicesOttawa Hospital
Organismes subventionnairesnon disponible
Mots-clésVenetoclaxChronic lymphocytic leukemiaMedicineLeukemiaQuality of life (healthcare)Family medicineGerontologyInternal medicineIntensive care medicineOncologyImmunologyNursing

Résumé

récupéré en direct d'OpenAlex

Clinical trials have shown venetoclax (VEN) has a positive impact on health-related quality of life (HRQoL) in patients with relapsed/refractory (R/R) CLL, as well as being an effective and well tolerated intervention (Cochrane T, et al. Leukemia & Lymphoma 2022; Weirda W, et al. Presented at EHA 2017).Currently, real-world data describing the impact of VEN on HRQoL in patients with R/R CLL are lacking. This abstract focuses on the HRQoL data from the DEVOTE study, a Canadian multicenter, open label, single arm, 24-week observational study which examined the real-world characteristics of patients with R/R CLL who initiated VEN treatment. Eligible patients were >18 years old, provided written informed consent, had CLL and had received ≥1 prior line of therapy, and whose physician had decided to prescribe VEN (± rituximab) as routine clinical care. Those participating in an interventional study were excluded. The HRQoL assessments were performed at baseline (B/L), the end of the VEN ramp-up phase (R/U), and at the end of observation period, either end of study (EoS) visit at 24 weeks or early discontinuation (WD) visit. Assessments included the EORTC-QLQ-C30, a 30-item cancer questionnaire with 5 functional scales (cognitive, social, physical, emotional, and role functioning), a global health status/QoL scale, 3 symptom scales (fatigue, nausea and vomiting, and pain) and 6 single items (insomnia, appetite loss, constipation, diarrhea, dyspnea, and financial difficulties), and the EORTC QLQ-CLL17, a 17-item module specific to CLL consisting of three multi-item scales (symptom burden, physical condition/fatigue, and worries/fears health and functioning). Scores for both questionnaires, and their functional/symptoms scales, range from 0-100. For functional scales, a higher score represents an improvement in HRQoL while for symptom scales, a higher score denotes more intense symptoms. The minimum important difference (MID) from B/L was defined for both questionnaires as a 5-point change, the lower bound of the 5-10 point range considered a "small" change for EORTC-QLQ-C30 (Osoba D, et al. J Clin Oncol 1998; Osoba D, et.al. Qual Life Res 1994). Overall, 89 patients were enrolled in the DEVOTE study and received ≥1 dose of VEN. Median (range) age was 73.0 (39-91) years, 67 (75.3%) were male and 78 (87.6%) were Caucasian. Patients had undergone a median (range) of 2 (0-7) prior lines of therapy with 79.8% previously treated with ibrutinib. Eighty-one completed R/U and 74 reached EoS. Questionnaire completion rates were high for both the EORTC-QLQ-C30 (86/89 at baseline, 66/81 at R/U and 60/79 at EoS/WD) and EORTC-QLQ-CLL17 (86/89 at baseline, 67/81 at R/U and 62/79 at EoS/WD). Baseline EORTC-QLQ-C30 scores were aligned with previous reports for a pre-treated CLL population (Holzner B, et al. Eur J Haematol 2004). Treatment with VEN was associated with improvements in HRQoL overall, across all five EORTC-QLQ-C30 functioning scales and most of the symptom scales, which were sustained from the end of R/U to the EoS/WD (Fig 1A). Mean improvement in scores surpassed the MID of 5 for all functioning scales other than cognitive functioning, and the fatigue, pain, dyspnea and insomnia symptom scales. The nausea and vomiting and the constipation symptom scores both worsened marginally, and the diarrhea score was variable (Fig 1B). Similar results were observed for all 3 EORCT-QLQ-CLL17 domains (Fig 2A and B). This pre-treated population showed a rapid improvement in HRQoL following initiation of VEN both in terms of functional and symptom scales, with most improvements sustained from the end of R/U until EoS/WD. There was no negative impact on HRQoL observed in association with the VEN ramp-up period. These real-world results corroborate the findings from clinical trials and the high response rates suggest observational studies are an effective forum for assessing the impact of interventions on HRQoL. Figure 1View largeDownload PPTFigure 1View largeDownload PPT Close modal

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)0,002
score de la tête « metaresearch » (Gemma)0,005
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 enseignants0,030
Score d'incertitude au seuil0,157

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0020,005
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0010,001
Bibliométrie0,0010,004
Études des sciences et des technologies0,0020,001
Communication savante0,0010,000
Science ouverte0,0010,001
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0010,000

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 Opus0,044
Tête enseignante GPT0,362
Écart entre enseignants0,318 · 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

Citations1
Publié2022
Routes d'admission2
Résumé présentoui

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