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Lomustine with or without reirradiation for first progression of glioblastoma, LEGATO, EORTC-2227-BTG: study protocol for a randomized phase III study
M. Preusser, T. Kazda, E. Le Rhun, F. Sahm, M. Smits, J. Gempt, JA. Koekkoek, AF. Monti, M. Csanadi, JG. Pitter, H. Bulbek, B. Fournier, C. Quoilin, T. Gorlia, M. Weller, G. Minniti, European Organisation for Research, Treatment of Cancer (EORTC)...
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, protokol klinické studie
Grantová podpora
101103655
Horizon 2020 Framework Programme
NLK
BioMedCentral
od 2000-04-01
BioMedCentral Open Access
od 2006
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2000-04-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2006-01-01
Medline Complete (EBSCOhost)
od 2009-01-01
Nursing & Allied Health Database (ProQuest)
od 2000-04-01
Health & Medicine (ProQuest)
od 2000-04-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
Springer Nature OA/Free Journals
od 2000-04-01
- MeSH
- alkylační protinádorové látky * terapeutické užití MeSH
- časové faktory MeSH
- chemoradioterapie metody MeSH
- doba přežití bez progrese choroby * MeSH
- glioblastom * patologie farmakoterapie mortalita radioterapie terapie MeSH
- klinické zkoušky, fáze III jako téma MeSH
- kvalita života MeSH
- lidé MeSH
- lomustin * aplikace a dávkování terapeutické užití škodlivé účinky MeSH
- multicentrické studie jako téma * MeSH
- nádory mozku * radioterapie patologie mortalita terapie MeSH
- pragmatické klinické studie jako téma MeSH
- progrese nemoci * MeSH
- randomizované kontrolované studie jako téma MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- protokol klinické studie MeSH
BACKGROUND: Chemotherapy with lomustine is widely considered as standard treatment option for progressive glioblastoma. The value of adding radiotherapy to second-line chemotherapy is not known. METHODS: EORTC-2227-BTG (LEGATO, NCT05904119) is an investigator-initiated, pragmatic (PRECIS-2 score: 34 out of 45), randomized, multicenter phase III trial in patients with first progression of glioblastoma. A total of 411 patients will be randomized in a 1:1 ratio to lomustine (110 mg/m2 every 6 weeks) or lomustine (110 mg/m2 every 6weeks) plus radiotherapy (35 Gy in 10 fractions). Main eligibility criteria include histologic confirmation of glioblastoma, isocitrate dehydrogenase gene (IDH) wild-type per WHO 2021 classification, first progression at least 6 months after the end of prior radiotherapy, radiologically measurable disease according to RANO criteria with a maximum tumor diameter of 5 cm, and WHO performance status of 0-2. The primary efficacy endpoint is overall survival (OS) and secondary endpoints include progression-free survival, response rate, neurocognitive function, health-related quality of life, and health economic parameters. LEGATO is funded by the European Union's Horizon Europe Research program, was activated in March 2024 and will enroll patients in 43 sites in 11 countries across Europe with study completion projected in 2028. DISCUSSION: EORTC-2227-BTG (LEGATO) is a publicly funded pragmatic phase III trial designed to clarify the efficacy of adding reirradiation to chemotherapy with lomustine for the treatment of patients with first progression of glioblastoma. TRIAL REGISTRATION: ClinicalTrials.gov NCT05904119. Registered before start of inclusion, 23 May 2023.
Brainstrust the brain cancer people Isle of Wight Cowes UK
Department of Medical Physics ASST GOM Niguarda Milano Italy
Department of Neurology Leiden University Medical Centre Leiden The Netherlands
Department of Neurology University Hospital and University of Zurich Zurich Switzerland
Department of Neurosurgery University Medical Centre Hamburg Eppendorf Hamburg Germany
Department of Radiology and Nuclear Medicine Erasmus MC Rotterdam The Netherlands
Citace poskytuje Crossref.org
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