Prospective observational study to evaluate the persistence of treatment with denosumab in patients with bone metastases from solid tumors in routine clinical practice: final analysis
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, pozorovací studie
Grantová podpora
Not applicable
Amgen (Europe North East)
PubMed
31350601
PubMed Central
PMC7036060
DOI
10.1007/s00520-019-04988-7
PII: 10.1007/s00520-019-04988-7
Knihovny.cz E-zdroje
- Klíčová slova
- Bone metastases, Denosumab, Observational study, Persistence, Solid tumors,
- MeSH
- denosumab aplikace a dávkování škodlivé účinky MeSH
- dospělí MeSH
- inhibitory kostní resorpce aplikace a dávkování škodlivé účinky MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- nádory kostí farmakoterapie sekundární MeSH
- nádory farmakoterapie patologie MeSH
- osteonekróza chemicky indukované MeSH
- prospektivní studie MeSH
- rozvrh dávkování léků MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- Názvy látek
- denosumab MeSH
- inhibitory kostní resorpce MeSH
PURPOSE: In the integrated analysis of phase III head-to-head trials in patients with advanced solid tumors, denosumab demonstrated superiority over zoledronic acid in preventing skeletal-related events (SREs). Regular and continued drug use (persistence) is a precondition of clinical efficacy; persistence in real-life is yet undetermined for denosumab. METHODS: This was a single-arm, prospective, observational, non-interventional study in 598 patients with bone metastases from breast, prostate, lung, or other solid tumors treated with denosumab every four weeks in real-world clinical practice in Austria, Czech Republic, Hungary, Slovakia, and Bulgaria. Persistence was defined as denosumab administration at ≤ 35-day intervals over 24 or 48 weeks, respectively. RESULTS: Previous SREs were found in 10.9% of patients. 62.6% were persistent over 24 weeks and 40.1% over 48 weeks. The Kaplan-Meier median (95% CI) time to non-persistence was 274.0 days (232.0, 316.0). The most frequent reason for non-persistence was delayed administration. There was a trend towards weaker analgesics over time, with approximately 60% of patients not requiring any analgesics. Serum calcium remained within the normal range throughout the study. Adjudicated osteonecrosis of the jaw was documented in three patients with an incidence per patient-year (95% CI) of 0.012 (0.004, 0.029). CONCLUSIONS: Most patients received denosumab regularly once every four weeks over 24 weeks of treatment. Non-persistence was mainly due to delayed administration. The incidence of adverse drug reactions, especially of osteonecrosis of the jaw, was in line with expectations from previous studies.
Complex Oncology Center Plovdiv EOOD Plovdiv Bulgaria
Global Medical Affairs Amgen GmbH Europe HQ Rotkreuz Switzerland
Medical Affairs Amgen GmbH Vienna Austria
Medical Affairs Amgen Rotkreuz Switzerland
Nemocnice Na Homolce Prague Czech Republic
Onkologicky ustav Sv Alzbety Bratislava Slovak Republic
Ordensklinikum Linz Barmherzige Schwestern Elisabethinen Linz Austria
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