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Chronomodulated capecitabine in combination with short-time oxaliplatin: a Nordic phase II study of second-line therapy in patients with metastatic colorectal cancer after failure to irinotecan and 5-flourouracil

Authors :
Lise Balteskard
J. Ploen
Tone Fokstuen
Halfdan Sorbye
Hans Starkhammar
Mette Karen Yilmaz
Kjell Magne Tveit
Dagfinn Øgreid
Åke Berglund
Camilla Qvortrup
Per Pfeiffer
Source :
Qvortrup, C, Yilmaz, M, Ogreid, D, Berglund, A, Balteskard, L, Ploen, J, Fokstuen, T, Starkhammar, H, Sørbye, H, Tveit, K & Pfeiffer, P 2008, ' Chronomodulated capecitabine in combination with short-time oxaliplatin : a Nordic phase II study of second-line therapy in patients with metastatic colorectal cancer after failure to irinotecan and 5-flourouracil ', Annals of Oncology, vol. 19, no. 6, pp. 1154-1159 . https://doi.org/10.1093/annonc/mdn002, Qvortrup, C, Yilmaz, M, Ogreid, D, Berglund, A, Balteskard, L, Ploen, J, Fokstuen, T, Starkhammar, H, Sørbye, H, Tveit, K & Pfeiffer, P 2008, ' Chronomodulated capecitabine in combination with short-time oxaliplatin: a Nordic phase II study of second-line therapy in patients with metastatic colorectal cancer after failure to irinotecan and 5-flourouracil ', Annals of Oncology, vol. 19, no. 6, pp. 1154-9 . https://doi.org/10.1093/annonc/mdn002
Publication Year :
2008
Publisher :
Elsevier BV, 2008.

Abstract

Udgivelsesdato: 2008-Jun BACKGROUND: Oxaliplatin in combination with capecitabine prolongs survival in patients with metastatic colorectal cancer (mCRC). Chronomodulation might reduce toxicity and improve efficacy. PATIENTS AND METHODS: A phase II study examining chronomodulated XELOX(30) (XELOX(30chron)): oxaliplatin: 130 mg/m(2) on day 1, as a 30-min infusion between 1 and 3 p.m. Capecitabine: total daily dose of 2000 mg/m(2), 20% of the dose between 7 and 9 a.m. and 80% of the dose between 6 and 8 p.m. in patients with mCRC resistant to irinotecan. Seventy-one patients were enrolled. Response rate was 18%; median progression-free survival 5.1 months and median overall survival (OS) 10.2 months. Platelet count and performance status were significantly correlated to OS in multivariate analyses. Neurotoxicity grade 2 and 3 was seen in 25% and 2% of patients, respectively, other grade 3 toxic effects were as follows: nausea 6%, vomiting 3%, diarrhoea 12% (3% experienced grade 4) and palmoplantart erytem 9%. CONCLUSION: XELOX(30chron) is a convenient second-line regimen with efficacy and safety profile similar to other oxaliplatin schedules. To further investigate chronomodulated XELOX, we have started a Nordic randomised phase II study comparing XELOX(30) and XELOX(30chron) as first-line therapy in patients with mCRC.

Details

ISSN :
09237534
Volume :
19
Database :
OpenAIRE
Journal :
Annals of Oncology
Accession number :
edsair.doi.dedup.....1ee9ac1dadeac9f4fe3bd32b8c4f171e