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Two different first-line 5-fluorouracil regimens with or without oxaliplatin in patients with metastatic colorectal cancer

  • David Cunningham*
  • , B. Sirohi
  • , A. Pluzanska
  • , B. Utracka-Hutka
  • , J. Zaluski
  • , R. Glynne-Jones
  • , P. Koralewski
  • , J. Bridgewater
  • , P. Mainwaring
  • , H. Wasan
  • , J. Y. Wang
  • , C. Szczylik
  • , P. Clingan
  • , R. T.T. Chan
  • , I. Tabah-Fisch
  • , J. Cassidy
  • *此作品的通信作者
  • Royal Marsden NHS Foundation Trust
  • Medical University of Łódź
  • Maria Sklodowska-Curie Institute of Oncology
  • Klinika Chemioterapii
  • The Hillingdon Hospitals NHS Foundation Trust
  • Rydygier Memorial Hospital
  • North Middlesex University Hospital NHS Trust
  • Mater Group
  • Imperial College Healthcare NHS Trust
  • Wojskowy Instytut Medyczny
  • Southern Medical Day Care Centre
  • The University of Hong Kong
  • Sanofi-Aventis
  • University of Glasgow

研究成果: 期刊稿件文章同行評審

54 引文 斯高帕斯(Scopus)

摘要

Background: Oxaliplatin, 5-fluorouracil (5-FU), and leucovorin (LV) are standard first-line treatments for patients with metastatic colorectal cancer (mCRC). The aim of this multicentre, open-label, phase IIIb study was to assess the addition of oxaliplatin to two different 5-FU regimens. Patients and methods: Patients with previously untreated mCRC were randomised to arm A [two-weekly oxaliplatin 85 mg/m2 + either continuous intravenous infusion (CIV) of 5-FU without LV or two-weekly bolus and CIV 5-FU + LV (LV5FU2)] or arm B (5-FU CIV or LV5FU2 alone). Irinotecan monotherapy was planned on progression. Results: A total of 725 patients were enrolled. After a fixed follow-up of 2 years for each patient, 2-year survival rates were 27.3% and 24.8% in arms A and B, respectively (hazard ratio 0.93; 95% confidence interval 0.78-1.10). The addition of oxaliplatin significantly improved response rates (54.1 versus 29.8%; P < 0.0001) and median progression-free survival (7.9 versus 5.9 months; P < 0.0001). The most common grade 3-4 toxic effects were neutropenia (arm A, 33%; arm B, 5%), diarrhoea (arm A, 14%; arm B, 8%), and fatigue (arm A, 9%; arm B, 8%). Conclusions: Despite improved rates of tumour control, these results failed to demonstrate a survival benefit from the addition of oxaliplatin to infused 5-FU and lend further support to the use of sequential monotherapy in some patients with mCRC.

原文英語
頁(從 - 到)244-250
頁數7
期刊Annals of Oncology
20
發行號2
DOIs
出版狀態已出版 - 2009

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    SDG3 健康與福祉

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