Aflibercept Plus FOLFIRI vs. Placebo Plus FOLFIRI in Second-Line Metastatic Colorectal Cancer: a Post Hoc Analysis of Survival from the Phase III VELOUR Study Subsequent to Exclusion of Patients who had Recurrence During or Within 6 Months of Completing Adjuvant Oxaliplatin-Based Therapy
Jazyk angličtina Země Francie Médium print
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie
PubMed
26706237
DOI
10.1007/s11523-015-0402-9
PII: 10.1007/s11523-015-0402-9
Knihovny.cz E-zdroje
- MeSH
- analýza přežití MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- fluoruracil aplikace a dávkování farmakologie terapeutické užití MeSH
- kamptothecin aplikace a dávkování analogy a deriváty farmakologie terapeutické užití MeSH
- kolorektální nádory farmakoterapie mortalita MeSH
- leukovorin aplikace a dávkování farmakologie terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- lokální recidiva nádoru farmakoterapie MeSH
- organoplatinové sloučeniny aplikace a dávkování farmakologie terapeutické užití MeSH
- oxaliplatin MeSH
- protokoly protinádorové kombinované chemoterapie aplikace a dávkování farmakologie terapeutické užití MeSH
- receptory vaskulárního endoteliálního růstového faktoru aplikace a dávkování terapeutické užití MeSH
- rekombinantní fúzní proteiny aplikace a dávkování farmakologie terapeutické užití 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
- aflibercept MeSH Prohlížeč
- fluoruracil MeSH
- kamptothecin MeSH
- leukovorin MeSH
- organoplatinové sloučeniny MeSH
- oxaliplatin MeSH
- receptory vaskulárního endoteliálního růstového faktoru MeSH
- rekombinantní fúzní proteiny MeSH
The aim of this post hoc analysis of the VELOUR study (ClinicalTrials.gov NCT00561470) was to investigate the treatment effect of adding aflibercept to second-line infusional 5-fluorouracil (5-FU), leucovorin and irinotecan (FOLFIRI) in patients with metastatic colorectal cancer (mCRC) who had failed any prior oxaliplatin-containing regimen. Adjuvant rapid relapsers (ARR), who were enrolled directly following relapse during or within 6 months of completion of oxaliplatin-containing adjuvant chemotherapy (N = 124, including 17 patients who also received bevacizumab as part of their adjuvant therapy), were excluded from the original VELOUR intention-to-treat (ITT) population (N = 1226). After exclusion of the ARR, overall survival (OS) in the ITT minus ARR (ITT-ARR) population (N = 1102) was longer in the aflibercept plus FOLFIRI arm than in the placebo plus FOLFIRI arm [hazard ratio (HR) 0.78, 95 % confidence interval (CI) 0.68-0.90; median survival difference 1.87 months]. In the subgroup of patients assigned to the prior bevacizumab stratum at randomization, OS was numerically longer in the aflibercept plus FOLFIRI arm than in the placebo plus FOLFIRI arm (HR 0.81; 95 % CI 0.63-1.04; median survival difference 2.14 months). Comparison of the post hoc analysis results with the primary analysis from VELOUR suggests that the inclusion of the directly enrolled ARR may have understated the aflibercept treatment benefit for both bevacizumab-pretreated and bevacizumab-naïve patients in the strictly second-line setting although no definitive conclusion may be inferred. The benefit associated with the addition of aflibercept to second-line FOLFIRI in patients with mCRC was observed whatever the timing of first-line disease progression. There were no unexpected safety concerns.
Amphia Hospital Breda The Netherlands
Centro De Oncologia Hospital Sirio Libanes São Paulo Brazil
Department of Medical Oncology Tumor Biology Center Freiburg Germany
Digestive Oncology University Hospitals Gasthuisberg Leuven Leuven Belgium
Faculty of Health Sciences University of Witwatersrand Johannesburg South Africa
Fakultni nemocnice v Motole Prague Czech Republic
Kimmel Cancer Center at Jefferson Jefferson University Hospitals Philadelphia PA USA
Martin Luther University Halle Wittenberg Halle Germany
Masaryk Memorial Cancer Institute Brno Czech Republic
Medical Oncology Department University Hospital 12 de Octubre Madrid Spain
Monash University Melbourne Victoria Australia
Regeneron Pharmaceuticals Inc Tarrytown NY USA
Sanofi Aventis Belgium Diegem Belgium
Sanofi Global Oncology Medical Affairs Cambridge MA USA
Schwerpunktpraxis für Hämatologie und Onkologie Magdeburg Germany
Scientific Research Institute of Oncology n a N N Petrov St Petersburg Russian Federation
St Luc University Hospital Brussels Belgium
The Royal Marsden Hospital Sutton Surrey UK
University of Western Australia Perth Western Australia Australia
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ClinicalTrials.gov
NCT00561470