Difference between revisions of "Capecitabine (Xeloda)"

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* 9/7/2001: New indication in combination with [[Docetaxel (Taxotere) | docetaxel]] is indicated for the treatment of patients with metastatic [[Breast cancer | breast cancer]] after failure of prior [[Regimen_classes#Anthracycline-based_regimen|anthracycline containing chemotherapy]].
 
* 9/7/2001: New indication in combination with [[Docetaxel (Taxotere) | docetaxel]] is indicated for the treatment of patients with metastatic [[Breast cancer | breast cancer]] after failure of prior [[Regimen_classes#Anthracycline-based_regimen|anthracycline containing chemotherapy]].
  
===[[Colon cancer|Colorectal cancer]]===
+
===[[:Category:Colorectal_cancers|Colorectal cancer]]===
* 4/30/2001: New indication as first-line treatment of patients with metastatic [[Colon cancer | colorectal carcinoma]] when treatment with [[:Category:Fluoropyrimidines|fluoropyrimidine]] therapy alone is preferred.
+
* 4/30/2001: New indication as first-line treatment of patients with metastatic [[:Category:Colorectal_cancers| colorectal carcinoma]] when treatment with [[:Category:Fluoropyrimidines|fluoropyrimidine]] therapy alone is preferred.
 
* 6/15/2005: New indication as a single agent for adjuvant treatment in patients with Dukes’ C [[Colon cancer | colon cancer]] who have undergone complete resection of the primary tumor when treatment with [[:Category:Fluoropyrimidines|fluoropyrimidine]] therapy alone is preferred.
 
* 6/15/2005: New indication as a single agent for adjuvant treatment in patients with Dukes’ C [[Colon cancer | colon cancer]] who have undergone complete resection of the primary tumor when treatment with [[:Category:Fluoropyrimidines|fluoropyrimidine]] therapy alone is preferred.
  

Revision as of 16:31, 3 February 2020

General information

Class/mechanism: Pyrimidine analog, antimetabolite, inhibitor of thymidylate synthase. Converted in vivo to fluorouracil (5-FU), which is metabolized to 5-fluoro-2'-deoxyuridine monophosphate (FdUMP) and 5-fluorouridine triphosphate (FUTP). FdUMP inhibits DNA synthesis by binding to thymidylate synthase and inhibiting production of thymidylate; FUTP interferes with RNA processing when it is mistakenly incorporated in place of uridine triphosphate (UTP).[1][2][3]
Route: PO
Extravasation: n/a

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, Medscape, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

Breast cancer

Colorectal cancer

  • 4/30/2001: New indication as first-line treatment of patients with metastatic colorectal carcinoma when treatment with fluoropyrimidine therapy alone is preferred.
  • 6/15/2005: New indication as a single agent for adjuvant treatment in patients with Dukes’ C colon cancer who have undergone complete resection of the primary tumor when treatment with fluoropyrimidine therapy alone is preferred.

Also known as

  • Code name: Ro 09-1978/000
  • Generic names: capecitabine RDT, kapesitabin
  • Brand names: Cabita, Capebin, Capegard, Capnat, Caposib, Capsy, Caxeta, Citabin, Flagoda, Naprocap, Skemca, Xeloda, Xlotabin

References