RECORD-2: phase II randomized study of everolimus and bevacizumab versus interferon α-2a and bevacizumab as first-line therapy in patients with metastatic renal cell carcinoma
Language English Country Great Britain, England Media print-electronic
Document type Clinical Trial, Phase II, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
25851632
DOI
10.1093/annonc/mdv170
PII: S0923-7534(19)34495-3
Knihovny.cz E-resources
- Keywords
- bevacizumab, combination targeted therapy, everolimus, first-line, metastatic renal cell carcinoma,
- MeSH
- Bevacizumab administration & dosage MeSH
- Adult MeSH
- Everolimus administration & dosage MeSH
- Interferon-alpha administration & dosage MeSH
- Carcinoma, Renal Cell drug therapy mortality secondary MeSH
- Middle Aged MeSH
- Humans MeSH
- Neoplasm Metastasis MeSH
- Survival Rate MeSH
- Young Adult MeSH
- Kidney Neoplasms drug therapy mortality pathology MeSH
- Follow-Up Studies MeSH
- Carcinoma, Papillary drug therapy mortality secondary MeSH
- Prognosis MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Neoplasm Staging MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase II MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Comparative Study MeSH
- Names of Substances
- Bevacizumab MeSH
- Everolimus MeSH
- IFNA2 protein, human MeSH Browser
- Interferon-alpha MeSH
BACKGROUND: The open-label, phase II RECORD-2 trial compared efficacy and safety of first-line everolimus plus bevacizumab (EVE/BEV) with interferon plus bevacizumab (IFN/BEV) in patients with metastatic renal cell carcinoma. PATIENTS AND METHODS: Previously untreated patients were randomized 1:1 to bevacizumab 10 mg/kg every 2 weeks with either everolimus 10 mg/day (EVE/BEV) or interferon (9 MIU 3 times/week, if tolerated) (IFN/BEV). Tumor assessments occurred every 12 weeks. The primary objective was the assessment of treatment effect on progression-free survival (PFS), based on an estimate of the chance of a subsequent phase III trial success (50% threshold for phase II success). RESULTS: Baseline characteristics were balanced between the EVE/BEV (n = 182) and IFN/BEV (n = 183) arms. The median PFS was 9.3 and 10.0 months in the EVE/BEV and IFN/BEV arms, respectively (P = 0.485). The predicted probability of phase III success was 5.05% (hazard ratio = 0.91; 95% confidence interval 0.69-1.19). The median duration of exposure was 8.5 and 8.3 months for EVE/BEV and IFN/BEV, respectively. The percentage of patients discontinuing because of adverse events (AEs) was 23.4% for EVE/BEV and 26.9% for IFN/BEV. Common grade 3/4 AEs included proteinuria (24.4%), stomatitis (10.6%), and anemia (10.6%) for EVE/BEV and fatigue (17.1%), asthenia (14.4%), and proteinuria (10.5%) for IFN/BEV. The median overall survival was 27.1 months in both arms. CONCLUSIONS: The efficacy of EVE/BEV and IFN/BEV appears similar. No new or unexpected safety findings were identified and, with the exception of proteinuria in about one-fourth of the population, EVE/BEV was generally well tolerated. CLINICAL TRIAL REGISTRY AND TRIAL REGISTRATION NUMBER: ClinicalTrials.gov: NCT00719264.
Department of Medical Oncology Hopital Saint Andre Bordeaux University Hospital Bordeaux France
Department of Medicine PUCRS School of Medicine Porto Alegre Brazil
Department of Oncology National Taiwan University Hospital Taipei Taiwan
Hertzen Cancer Research Institute Moscow Russia
Leningrad Regional Oncology Center St Petersburg
Medical Oncology Department Hacettepe University Institute of Oncology Ankara Turkey
Novartis Oncology East Hanover USA
Novartis Pharma AG Basel Switzerland
Novartis Pharma Novartis Oncology BDM Paris France
OncoCare Cancer Centre Singapore
Russian Research Center for Radiology and Surgical Technologies St Petersburg Russia
St Luke's University Hospital and Health Network Bethlehem USA
References provided by Crossref.org
ClinicalTrials.gov
NCT00719264