Everolimus in advanced, progressive, well-differentiated, non-functional neuroendocrine tumors: RADIANT-4 lung subgroup analysis
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie
PubMed
29055056
PubMed Central
PMC5765303
DOI
10.1111/cas.13427
Knihovny.cz E-zdroje
- Klíčová slova
- RADIANT-4, everolimus, lung carcinoid, neuroendocrine tumors, progression-free survival,
- MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- everolimus aplikace a dávkování škodlivé účinky MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory plic farmakoterapie MeSH
- neuroendokrinní nádory farmakoterapie MeSH
- přežití bez známek nemoci MeSH
- prospektivní studie MeSH
- protinádorové látky aplikace a dávkování škodlivé účinky MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- výsledek terapie 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
- randomizované kontrolované studie MeSH
- Názvy látek
- everolimus MeSH
- protinádorové látky MeSH
In the phase III RADIANT-4 study, everolimus improved median progression-free survival (PFS) by 7.1 months in patients with advanced, progressive, well-differentiated (grade 1 or grade 2), non-functional lung or gastrointestinal neuroendocrine tumors (NETs) vs placebo (hazard ratio, 0.48; 95% confidence interval [CI], 0.35-0.67; P < .00001). This exploratory analysis reports the outcomes of the subgroup of patients with lung NETs. In RADIANT-4, patients were randomized (2:1) to everolimus 10 mg/d or placebo, both with best supportive care. This is a post hoc analysis of the lung subgroup with PFS, by central radiology review, as the primary endpoint; secondary endpoints included objective response rate and safety measures. Ninety of the 302 patients enrolled in the study had primary lung NET (everolimus, n = 63; placebo, n = 27). Median PFS (95% CI) by central review was 9.2 (6.8-10.9) months in the everolimus arm vs 3.6 (1.9-5.1) months in the placebo arm (hazard ratio, 0.50; 95% CI, 0.28-0.88). More patients who received everolimus (58%) experienced tumor shrinkage compared with placebo (13%). Most frequently reported (≥5% incidence) grade 3-4 drug-related adverse events (everolimus vs. placebo) included stomatitis (11% vs. 0%), hyperglycemia (10% vs. 0%), and any infections (8% vs. 0%). In patients with advanced, progressive, well-differentiated, non-functional lung NET, treatment with everolimus was associated with a median PFS improvement of 5.6 months, with a safety profile similar to that of the overall RADIANT-4 cohort. These results support the use of everolimus in patients with advanced, non-functional lung NET. The trial is registered with ClinicalTrials.gov (no. NCT01524783).
Charité University Medicine Berlin Campus Virchow Klinikum Berlin Germany
Dana Farber Cancer Institute Boston MA USA
European Institute of Oncology IRCCS Milan Italy
Faculty of Medicine Masaryk Memorial Cancer Institute Masaryk University Brno Czech Republic
Fondazione IRCCS Foundation The National Institute of Tumors Milan Italy
Hospital Sant'Andrea La Sapienza University Rome Italy
Moffitt Cancer Center Tampa FL USA
Montefiore Einstein Center for Cancer Care Bronx NY USA
Netherlands Cancer Institute Antoni van Leeuwenhoek Amsterdam the Netherlands
Novartis Pharma AG Basel Switzerland
Novartis Pharma S A S Rueil Malmaison France
Novartis Pharmaceuticals Corporation East Hanover NJ USA
Sunnybrook Health Sciences Centre Toronto ON Canada
University Hospitals Gasthuisberg Leuven and KU Leuven Leuven Belgium
University of Texas MD Anderson Cancer Center Houston TX USA
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ClinicalTrials.gov
NCT01524783