Long-term fostamatinib treatment of adults with immune thrombocytopenia during the phase 3 clinical trial program
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
Grantová podpora
Rigel Pharmaceuticals, Inc - International
PubMed
30784097
PubMed Central
PMC6594140
DOI
10.1002/ajh.25444
Knihovny.cz E-zdroje
- MeSH
- aminopyridiny MeSH
- časové faktory MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- idiopatická trombocytopenická purpura krev farmakoterapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- morfoliny MeSH
- oxaziny * aplikace a dávkování škodlivé účinky MeSH
- počet trombocytů MeSH
- pyridiny * aplikace a dávkování škodlivé účinky MeSH
- pyrimidiny MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- aminopyridiny MeSH
- fostamatinib MeSH Prohlížeč
- morfoliny MeSH
- oxaziny * MeSH
- pyridiny * MeSH
- pyrimidiny MeSH
Two randomized, double-blind, placebo-controlled studies demonstrated responses (≥50 000/μL) to fostamatinib in adults with long-standing immune thrombocytopenia (ITP). The long-term safety and efficacy of fostamatinib were evaluated in a follow-on, open-label extension (OLE) study. Patients received double-blind fostamatinib in the randomized trials, and responders continued the same dose, 100 to 150 mg BID, in the OLE study. Nonresponders received 100 mg BID for 4 weeks and could escalate to 150 mg BID at week 4. Endpoints included stable response, platelet count ≥50 000/μL at 4/6 biweekly (randomized trials) or 2/3 monthly visits (OLE), and overall response, ≥1 platelet count ≥50 000/μL during weeks 1 to 12. A total of 146 patients received fostamatinib including 123 in the OLE study. Median treatment duration was 6.7 months. Baseline median ITP duration was 8 years and median platelet count was 16 000/μL; prior treatments included thrombopoietic (TPO) agents (47%), splenectomy (35%), and rituximab (32%). Twenty-seven (18%) patients achieved a stable response with median duration of >28 months and a median platelet count of 89 000/μL. Sixty-four (44%) patients achieved an overall response (including stable responders) with a median platelet count of 63 000/μL and a median response duration of >28 months. Twenty-four of 71 (34%) patients who had failed TPO agents achieved overall responses to fostamatinib. The most common adverse events (AEs) were diarrhea, hypertension, nausea, epistaxis, and abnormal liver function tests. Most AEs were mild/moderate and resolved or were managed with dose reduction, dose interruption, and/or secondary medication. Almost half of the patients achieved an overall response, and most of these maintained their responses for >2 years. No new or increased frequency of AEs was seen at up to 31 months of treatment.
Arizona Oncology Associates Tucson Arizona
Canadian Blood Services Hamilton Ontario Canada
Fakultni nemocnice Brno Brno Czech Republic
Imperial College Healthcare NHS Trust Hammersmith Hospital London United Kingdom
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