Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.

Capecitabine (Xeloda) and irinotecan (CPT-11, Camptosar) exhibit single-agent activity in colorectal cancer, have nonoverlapping major toxicities, and exhibit a synergistic effect in tumor xenograft models. European early-phase trials of the combination in patients with metastatic colorectal cancer...

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Main Author: Kerr, D
Format: Journal article
Language:English
Published: 2002
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author Kerr, D
author_facet Kerr, D
author_sort Kerr, D
collection OXFORD
description Capecitabine (Xeloda) and irinotecan (CPT-11, Camptosar) exhibit single-agent activity in colorectal cancer, have nonoverlapping major toxicities, and exhibit a synergistic effect in tumor xenograft models. European early-phase trials of the combination in patients with metastatic colorectal cancer indicate good response rates across doses tested and manageable toxicities, with available data supporting use of a regimen of oral capecitabine at 1,000 mg/m2 twice daily on days 1 to 14 plus IV irinotecan at 250 mg/m2 on day 1 every 21 days in this setting. The European Organisation for Research and Treatment of Cancer has planned a phase III trial (EORTC 40015) comparing this regimen of capecitabine/irinotecan with infusional fluorouracil (5-FU)/leucovorin plus irinotecan in approximately 700 patients with metastatic colorectal cancer. The QUASAR (Quick and Simple and Reliable) 2 adjuvant trial will compare 5-FU/leucovorin with capecitabine/irinotecan given over 6 months as adjuvant therapy in patients with stage II/III colorectal cancer. These trials will help define the roles of this combination in the treatment of colorectal cancer.
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spelling oxford-uuid:1d7b27e9-f4ed-42d6-af6d-f27b911a3bb32022-03-26T11:11:00ZCapecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:1d7b27e9-f4ed-42d6-af6d-f27b911a3bb3EnglishSymplectic Elements at Oxford2002Kerr, DCapecitabine (Xeloda) and irinotecan (CPT-11, Camptosar) exhibit single-agent activity in colorectal cancer, have nonoverlapping major toxicities, and exhibit a synergistic effect in tumor xenograft models. European early-phase trials of the combination in patients with metastatic colorectal cancer indicate good response rates across doses tested and manageable toxicities, with available data supporting use of a regimen of oral capecitabine at 1,000 mg/m2 twice daily on days 1 to 14 plus IV irinotecan at 250 mg/m2 on day 1 every 21 days in this setting. The European Organisation for Research and Treatment of Cancer has planned a phase III trial (EORTC 40015) comparing this regimen of capecitabine/irinotecan with infusional fluorouracil (5-FU)/leucovorin plus irinotecan in approximately 700 patients with metastatic colorectal cancer. The QUASAR (Quick and Simple and Reliable) 2 adjuvant trial will compare 5-FU/leucovorin with capecitabine/irinotecan given over 6 months as adjuvant therapy in patients with stage II/III colorectal cancer. These trials will help define the roles of this combination in the treatment of colorectal cancer.
spellingShingle Kerr, D
Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.
title Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.
title_full Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.
title_fullStr Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.
title_full_unstemmed Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.
title_short Capecitabine/irinotecan in colorectal cancer: European early-phase data and planned trials.
title_sort capecitabine irinotecan in colorectal cancer european early phase data and planned trials
work_keys_str_mv AT kerrd capecitabineirinotecanincolorectalcancereuropeanearlyphasedataandplannedtrials