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ABSTRACT: Background
The SCOPE-1 study tested the role of adding cetuximab to conventional definitive chemoradiotherapy (dCRT), and demonstrated greater toxicity and worse survival outcomes. We present the long-term outcomes and patterns of recurrence.Methods
SCOPE-1 was a phase II/III trial in which patients were randomised to cisplatin 60 mg m-2 (day 1) and capecitabine 625 mg m-2 bd (days 1-21) for four cycles +/- cetuximab 400 mg m-2 day 1 then by 250 mg m-2 weekly. Radiotherapy consisted of 50 Gy/25# given concurrently with cycles 3 and 4. Recruitment was between February 2008 and February 2012, when the IDMC recommended closure on the basis of futility.Results
About 258 patients (dCRT=129; dCRT+cetuximab (dCRT+C)=129) were rec
SUBMITTER: Crosby T
PROVIDER: S-EPMC5355926 | biostudies-literature | 2017 Mar
REPOSITORIES: biostudies-literature