Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?

Fluorouracil (5-FU) remains the most widely used agent for colorectal cancer. Capecitabine is a rationally designed 5-FU pro-drug developed to mimic the continuous infusion of 5-FU while avoiding complications and inconvenience of intravenous administration. Capecitabine is absorbed intact from the...

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Main Authors: Lakshmi Chintala, Susmitha Vaka, Joaquina Baranda, Stephen K. Williamson
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-06-01
Series:Oncology Reviews
Subjects:
Online Access:http://www.oncologyreviews.org/index.php/or/article/view/26
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author Lakshmi Chintala
Susmitha Vaka
Joaquina Baranda
Stephen K. Williamson
author_facet Lakshmi Chintala
Susmitha Vaka
Joaquina Baranda
Stephen K. Williamson
author_sort Lakshmi Chintala
collection DOAJ
description Fluorouracil (5-FU) remains the most widely used agent for colorectal cancer. Capecitabine is a rationally designed 5-FU pro-drug developed to mimic the continuous infusion of 5-FU while avoiding complications and inconvenience of intravenous administration. Capecitabine is absorbed intact from the gastrointestinal tract, converted enzymatically to active 5-FU, and released directly into the tumor. Capecitabine’s efficacy and safety are shown in multiple phase III trials across different disease stages and therapy lines. Three randomized phase III trials demonstrated the equivalence of capecitabine plus oxaliplatin (XELOX) versus 5-FU/leucovorin (LV)/oxaliplatin (FOLFOX). The safety of capecitabine compared with 5-FU depends on the regimen of 5-FU used. The adverse event rate with oxaliplatin in combination with infusional 5-FU is similar to that of capecitabine plus oxaliplatin but is associated with more neutropenia and venous thrombotic events; capecitabine plus oxaliplatinbased regimens tend to be associated with more grade 3 diarrhea and hand-foot skin reaction. Combination therapy with capecitabine and irinotecan (CapeIRI) versus 5-FU/ LV and irinotecan (FOLFIRI) had more variable results; some former schedules resulted in excessive treatmentrelated toxicity. More recent data show that lower capecitabine and irinotecan doses, different schedules, and combination with targeted agents (e.g, bevacizumab) have resulted in more favorable outcomes.
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spelling doaj.art-42318c25350f4a4582168a721602820d2023-01-03T10:55:35ZengFrontiers Media S.A.Oncology Reviews1970-55571970-55652011-06-015210.4081/oncol.2011.12921Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?Lakshmi Chintala0Susmitha Vaka1Joaquina Baranda2Stephen K. Williamson3Division of Hematology/Oncology, University of Kansas Cancer CenterDivision of Hematology/Oncology, University of Kansas Cancer CenterDivision of Hematology/Oncology, University of Kansas Cancer CenterDivision of Hematology/Oncology, University of Kansas Cancer CenterFluorouracil (5-FU) remains the most widely used agent for colorectal cancer. Capecitabine is a rationally designed 5-FU pro-drug developed to mimic the continuous infusion of 5-FU while avoiding complications and inconvenience of intravenous administration. Capecitabine is absorbed intact from the gastrointestinal tract, converted enzymatically to active 5-FU, and released directly into the tumor. Capecitabine’s efficacy and safety are shown in multiple phase III trials across different disease stages and therapy lines. Three randomized phase III trials demonstrated the equivalence of capecitabine plus oxaliplatin (XELOX) versus 5-FU/leucovorin (LV)/oxaliplatin (FOLFOX). The safety of capecitabine compared with 5-FU depends on the regimen of 5-FU used. The adverse event rate with oxaliplatin in combination with infusional 5-FU is similar to that of capecitabine plus oxaliplatin but is associated with more neutropenia and venous thrombotic events; capecitabine plus oxaliplatinbased regimens tend to be associated with more grade 3 diarrhea and hand-foot skin reaction. Combination therapy with capecitabine and irinotecan (CapeIRI) versus 5-FU/ LV and irinotecan (FOLFIRI) had more variable results; some former schedules resulted in excessive treatmentrelated toxicity. More recent data show that lower capecitabine and irinotecan doses, different schedules, and combination with targeted agents (e.g, bevacizumab) have resulted in more favorable outcomes.http://www.oncologyreviews.org/index.php/or/article/view/26Capecitabine - Chemotherapy - Colorectal cancer - Combination therapy - Fluorouracil
spellingShingle Lakshmi Chintala
Susmitha Vaka
Joaquina Baranda
Stephen K. Williamson
Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?
Oncology Reviews
Capecitabine - Chemotherapy - Colorectal cancer - Combination therapy - Fluorouracil
title Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?
title_full Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?
title_fullStr Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?
title_full_unstemmed Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?
title_short Capecitabine versus 5-fluorouracil in colorectal cancer: where are we now?
title_sort capecitabine versus 5 fluorouracil in colorectal cancer where are we now
topic Capecitabine - Chemotherapy - Colorectal cancer - Combination therapy - Fluorouracil
url http://www.oncologyreviews.org/index.php/or/article/view/26
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