Patient preference for deferasirox film-coated versus dispersible tablet formulation: a sequential-design phase 2 study in patients with thalassemia

dc.contributor.authorViprakasit, Vip
dc.contributor.authorHamdy, Mona Mohamed
dc.contributor.authorHassab, Hoda Mohammed Abo El Fotoh
dc.contributor.authorSherief, Laila Metwaly
dc.contributor.authorAl-Bagshi, Muneer
dc.contributor.authorKhattab, Mohammed
dc.contributor.authorChuncharunee, Suporn
dc.contributor.authorDung, Phu Chi
dc.contributor.authorKüpesiz, Alphan O.
dc.contributor.authorShekhawat, Ankita
dc.contributor.authorSonawane, Yamini
dc.contributor.authorPerez, Laura Torres
dc.contributor.authorSlader, Cassandra
dc.contributor.authorTaher, Ali T.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:46:13Z
dc.date.available2025-01-24T11:46:13Z
dc.date.issued2023
dc.description.abstractIron chelation therapy (ICT) is the mainstay of treatment in patients with thalassemia requiring blood transfusions. This phase 2 JUPITER study evaluated patient preference between film-coated tablet (FCT) and dispersible tablet (DT) in transfusion-dependent thalassemia (TDT) or non-TDT (NTDT) patients treated with both formulations in a sequential manner. The primary endpoint was patient-reported preference for FCT over DT, while secondary outcomes included patient reported outcomes (PROs) evaluated by overall preference, and by age, thalassemia transfusion status, and previous ICT status. Out of 183 patients screened, 140 and 136 patients completed the treatment periods 1 and 2 of the core study, respectively. At week 48, the majority of patients preferred FCT over DT (90.3 vs. 7.5%; difference of percentage: 0.83 [95% confidence interval (CI), 0.75–0.89; P < 0.0001]). FCT scored better on secondary PROs and showed less severe gastrointestinal symptoms than DT, except in the change of modified Satisfaction with Iron Chelation Therapy (mSICT) preference scores, which were similar for both the formulations. Patients with TDT had stable ferritin levels, while it showed a downward trend up to week 48 in patients with NTDT on deferasirox treatment. Overall, 89.9% of patients reported ≥ 1 adverse event (AE), of which 20.3% experienced ≥ 1 serious AE. The most common treatment-emergent AEs were proteinuria, pyrexia, urine protein/creatinine ratio increase, diarrhea, upper respiratory tract infections, transaminase increase, and pharyngitis. Overall, this study reinforced the observations from the previous study by showing a distinct patient preference for FCT over DT formulation and further supported the potential benefits of life-long compliance with ICT. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
dc.identifier.doihttps://doi.org/10.1007/s00277-023-05240-3
dc.identifier.eid2-s2.0-85160286785
dc.identifier.pmid37227493
dc.identifier.urihttp://hdl.handle.net/10938/30640
dc.language.isoen
dc.publisherSpringer Science and Business Media Deutschland GmbH
dc.relation.ispartofAnnals of Hematology
dc.sourceScopus
dc.subjectAdherence
dc.subjectCompliance
dc.subjectDeferasirox
dc.subjectDispersible tablets
dc.subjectFilm-coated tablet
dc.subjectPalatability
dc.subjectPatient preference
dc.subjectPatient-reported outcome
dc.subjectBenzoates
dc.subjectHumans
dc.subjectIron
dc.subjectIron chelating agents
dc.subjectIron overload
dc.subjectTablets
dc.subjectThalassemia
dc.subjectAminotransferase
dc.subjectFerritin
dc.subjectLiver enzyme
dc.subjectBenzoic acid derivative
dc.subjectIron chelating agent
dc.subjectAdolescent
dc.subjectAge
dc.subjectArticle
dc.subjectBicarbonate blood level
dc.subjectChild
dc.subjectControlled study
dc.subjectDiarrhea
dc.subjectDispersible tablet formulation
dc.subjectDose response
dc.subjectDrug dose increase
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectFemale
dc.subjectFerritin blood level
dc.subjectFever
dc.subjectFilm coated tablet formulation
dc.subjectGastrointestinal symptom
dc.subjectHepatomegaly
dc.subjectHuman
dc.subjectIron chelation
dc.subjectMajor clinical study
dc.subjectMale
dc.subjectModified satisfaction with iron chelation therapy preference score
dc.subjectMulticenter study
dc.subjectOpen study
dc.subjectOutcome assessment
dc.subjectPatient compliance
dc.subjectPatient satisfaction
dc.subjectPatient satisfaction assessment
dc.subjectPharyngitis
dc.subjectPhase 2 clinical trial
dc.subjectPreschool child
dc.subjectProtein creatinine ratio
dc.subjectProteinuria
dc.subjectRandomized controlled trial
dc.subjectRhinopharyngitis
dc.subjectSchool child
dc.subjectSide effect
dc.subjectTablet formulation
dc.subjectTonsillitis
dc.subjectTransfusion dependent thalassemia
dc.subjectTreatment duration
dc.subjectTrend study
dc.subjectUpper respiratory tract infection
dc.subjectClinical trial
dc.subjectComplication
dc.subjectTablet
dc.titlePatient preference for deferasirox film-coated versus dispersible tablet formulation: a sequential-design phase 2 study in patients with thalassemia
dc.typeArticle

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