Short-Time Infusion of Oxaliplatin (Eloxatin®) in Combination with Capecitabine (Xeloda®) in Patients with Advanced Colorectal Cancer

Authors

  • Per Pfeiffer Department of Oncology, Odense University Hospital
  • Pernille Hahn Department of Oncology, Odense University Hospital
  • Helle Anita Jensen Department of Oncology, Odense University Hospital

DOI:

https://doi.org/10.1080/02841860310015894

Abstract

Neuropathy exacerbated by exposure to cold is a dose-limiting toxicity of oxaliplatin. The incidence of this side effect is claimed to dependent on infusion rate and therefore a 2-h infusion is often recommended. For practical reasons and for the convenience of the patient, we used XELOX (Xeloda 2000 mg/m2orally on days 1–14 and oxaliplatin 130 mg/m2as a 30-min infusion on day 1) in patients with advanced colorectal cancer resistant to irinotecan and 5-fluorouracil. Thirty-four consecutive patients received a median of 5 courses of XELOX. Nine patients obtained partial response (PR) (response rate (RR) 26%), 11 patients no change (NC), 7 patients disease progression (PD) and 7 patients were not evaluable. Median time to progression was 4.7 (2.6–7.6) months and median survival was 7.4 (6.0–11.3) months. Sixteen patients had neuropathy grade 1, four patients grade 2 and two patients grade 3. Short-time infusion of oxaliplatin and capecitabine is an active and convenient second-line regimen with a safety profile similar to that of other oxaliplatin schedules.

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Published

2003-12-01

How to Cite

Pfeiffer, P. ., Hahn, P. ., & Anita Jensen, H. . (2003). Short-Time Infusion of Oxaliplatin (Eloxatin®) in Combination with Capecitabine (Xeloda®) in Patients with Advanced Colorectal Cancer. Acta Oncologica, 42(8), 832–836. https://doi.org/10.1080/02841860310015894