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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

Qvortrup, C. (author)
Department of Oncology, Odense University Hospital, Sdr. Boulevard 29, Odense C 5000, Denmark, Institute of Clinical Research, University of Southern Denmark, Odense, Denmark
Yilmaz, M. (author)
Department of Oncology, Aalborg University Hospital, Aalborg, Denmark
Ogreid, D. (author)
Department of Oncology, Rogaland Central Hospital, Stavanger, Norway
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Berglund, Åke (author)
Uppsala universitet,Enheten för onkologi,Ake Berglund
Balteskard, L. (author)
Department of Oncology, Tromso University Hospital, Tromso, Norway
Ploen, J. (author)
Department of Oncology, Vejle Hospital, Vejle, Denmark
Fokstuen, T. (author)
Department of Oncology and Pathology, Karolinska Hospital, Stockholm, Sweden
Starkhammar, Hans (author)
Östergötlands Läns Landsting,Linköpings universitet,Onkologi,Hälsouniversitetet,Onkologiska kliniken US
Sorbye, H. (author)
Sørbye, H., Department of Oncology, Haukeland University Hospital, Bergen, Norway
Tveit, K. (author)
Department of Oncology, Ullevål University Hospital, Oslo, Norway
Pfeiffer, P. (author)
Department of Oncology, Odense University Hospital, Sdr. Boulevard 29, Odense C 5000, Denmark
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Department of Oncology, Odense University Hospital, Sdr Boulevard 29, Odense C 5000, Denmark, Institute of Clinical Research, University of Southern Denmark, Odense, Denmark Department of Oncology, Aalborg University Hospital, Aalborg, Denmark (creator_code:org_t)
Elsevier BV, 2008
2008
English.
In: Annals of Oncology. - : Elsevier BV. - 0923-7534 .- 1569-8041. ; 19:6, s. 1154-1159
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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 XELOX30 (XELOX30chron): oxaliplatin: 130 mg/m2 on day 1, as a 30-min infusion between 1 and 3 p.m. Capecitabine: total daily dose of 2000 mg/m2, 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: XELOX30chron 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 XELOX30 and XELOX30chron as first-line therapy in patients with mCRC. © The Author 2008. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved.

Keyword

Capecitabine
Chronotherapy
Metastatic colorectal cancer
Oxaliplatin
Short-time infusion
XELOX
NATURAL SCIENCES
NATURVETENSKAP
MEDICINE

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