Adherence to ruxolitinib, an oral JAK1/2 inhibitor, in patients with myelofibrosis: interim analysis from an Italian, prospective cohort study (ROMEI).


Journal

Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422

Informations de publication

Date de publication:
01 2022
Historique:
pubmed: 16 9 2021
medline: 18 3 2022
entrez: 15 9 2021
Statut: ppublish

Résumé

ROMEI, a prospective, observational study in patients with myelofibrosis receiving the oral JAK1/2 inhibitor ruxolitinib in real-world practice, assesses treatment adherence based on the 8-item Morisky Medication Adherence Scale (MMAS-8). Here, we present MMAS-8 results at week 24. Overall, 101 of 188 evaluable patients completed the questionnaire at every visit (full completers). Mean (±standard deviation) total MMAS-8 scores remained stable from week 4 to week 24 in the overall population (7.54 ± 0.77 and 7.67 ± 0.70, respectively) and full completers (7.53 ± 0.79 and 7.67 ± 0.73, respectively). Rates of low (MMAS-8 ˂6) or medium (MMAS-8 ≥ 6 to ˂8) adherence were 25-40% and 26-36%, respectively. Fifty-five full completers (54%) reported ≥1 change in adherence category (improvement and/or worsening), most of which were associated with unintentional behavior. The data suggest that one-third of patients receiving ruxolitinib may be undertreated due to non-adherence, potentially undermining disease control, and indicate a need for better interventions addressing noncompliance to oral therapies.

Identifiants

pubmed: 34521299
doi: 10.1080/10428194.2021.1969388
doi:

Substances chimiques

Nitriles 0
Pyrazoles 0
Pyrimidines 0
ruxolitinib 82S8X8XX8H
JAK1 protein, human EC 2.7.10.2
JAK2 protein, human EC 2.7.10.2
Janus Kinase 1 EC 2.7.10.2
Janus Kinase 2 EC 2.7.10.2

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-198

Auteurs

Paola Guglielmelli (P)

CRIMM, Center for Research and Innovation of Myeloproliferative Neoplasms, AOU Careggi, Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Francesca Palandri (F)

Policlinico S.Orsola-Malpighi, Dipartimento di Oncologia e di Ematologia, Azienda Ospedaliero-Universitaria di Bologna, IRCCS Istituto di Ricovero e Cura a Carattere Scientifico, Bologna, Italy.

Carmine Selleri (C)

UOC di Ematologia e Trapianti di Cellule Staminali Emopoietiche, Dipartimento di Medicina, Università di Salerno, AOU San Giovanni di Dio e Ruggi D'Aragona, Salerno, Italy.

Daniela Cilloni (D)

Department of Clinical and Biological Sciences, University of Turin, Turin, Italy.

Francesco Mendicino (F)

U.O.C. di Ematologia, Azienda Ospedaliera "Annunziata", Cosenza, Italy.

Patrizio Mazza (P)

C/O Ospedale Moscati, Department of Hematology-Oncology, Taranto, Italy.

Domenico Pastore (D)

Hematology, Hospital A. Perrino Hospital, Brindisi, Italy.

Giuseppe A Palumbo (GA)

Dipartimento di Scienze Mediche Chirurgiche e Tecnologie Avanzate "G.F. Ingrassia", Unità Operativa di Ematologia con TMO AOU "Policlinico - San Marco", Università degli Studi di Catania, Catania, Italy.

Marco Santoro (M)

Dipartimento di Chirurgia, Stomatologia e Oncologia Sperimentale (DiChirOnS), Università degli Studi di Palermo, Palermo, Italy.

Vincenzo Pavone (V)

Haematology, "G.Panico" Hospital, Tricase, LE, Italy.

Stefana Impera (S)

UOC Ematologia, ARNAS Garibaldi, Catania, Italy.

Mara Morelli (M)

Novartis Oncology, Novartis Farma SpA, Varese, Italy.

Paola Coco (P)

Novartis Oncology, Novartis Farma SpA, Varese, Italy.

Diletta Valsecchi (D)

Novartis Oncology, Novartis Farma SpA, Varese, Italy.

Francesco Passamonti (F)

Università degli Studi dell'Insubria, Ospedale di Circolo - ASST Sette Laghi, Varese, Italy.

Massimo Breccia (M)

Hematology, Department of Translational and Precision Medicine, Azienda Policlinico Umberto I, Sapienza University, Rome, Italy.

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Classifications MeSH