Neoadjuvant continuous infusion of weekly 5-fluorouracil and escalating doses of oxaliplatin plus concurrent radiation in locally advanced oesophageal squamous cell carcinoma: Results of a phase I/II trial

S. Lorenzen, B. Brücher, F. Zimmermann, H. Geinitz, J. Riera, T. Schuster, N. Roethling, H. Höfler, K. Ott, C. Peschel, J. R. Siewert, M. Molls, F. Lordick

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26 Scopus citations

Abstract

Oxaliplatin and 5-fluorouracil have a significant activity in locally advanced oesophageal squamous cell cancer (OSCC). However, their optimal dosage and efficacy when combined with concurrent radiotherapy as neoadjuvant treatment are unknown. This non-randomised, phase I/II study aimed to define the maximum tolerated dose (MTD) and assessed the histopathological tumour response rate to neoadjuvant oxaliplatin in weekly escalating doses (40, 45, 50 mg m -2) and continuous infusional 5-fluorouracil (CI-5FU; 225 mg m -2) plus concurrent radiotherapy. Patients had resectable OSCC. Resection was scheduled for 4-6 weeks after chemoradiotherapy. During phase I (dose escalation; n=19), weekly oxaliplatin 45 mg m-2 plus CI-5FU 225 mg m-2 was established as the MTD and was the recommended dosage for phase II. Oesophageal mucositis was the dose-limiting toxicity at higher doses. During phase II, histopathological responses (<10% residual tumour cells within the specimen) were observed in 10 of 16 patients (63%; 95% confidence interval: 39-82%). Overall, 16 of the 25 patients (64%) who underwent resection had a histopathological response; tumour-free resection (R0) was achieved in 80%. Neoadjuvant weekly oxaliplatin 45 mg m-2 plus CI-5FU 225 mg m-2 with concurrent radiotherapy provides promising histological response rates and R0 resection rates in locally advanced OSCC.

Original languageEnglish
Pages (from-to)1020-1026
Number of pages7
JournalBritish Journal of Cancer
Volume99
Issue number7
DOIs
StatePublished - 7 Oct 2008

Keywords

  • 5-fluorouracil
  • Chemoradiotherapy
  • Neoadjuvant
  • Oesophageal carcinoma
  • Oxaliplatin
  • Response

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