Capecitabine is administered in the treatment of different cancer types, most commonly as part of a combination of other treatments. Some major indications include:
Breast Cancer: Capecitabine is administered in early or advanced stages of breast cancer, especially in cases that are HER2-negative or have metastasized.
Colorectal Cancer: Capecitabine is administered to treat advanced or metastatic colorectal cancer. It is administered in combination with other chemotherapy and drugs,
Gastric Cancer: Capecitabine is also administered to treat advanced or metastatic gastric cancer, especially when given in combination with other drugs, such as cisplatin.
Other Cancer Types: Capecitabine is sometimes used off-label for cancer types like pancreatic or esophageal cancer, but it is not approved for any other cancer type.
Capecitabine is a prodrug, where once it enters the body, it undergoes conversion into its active form, 5-FU. The primary location of this conversion process occurs in the liver and in the tumor tissue. 5-FU is an antimetabolite drug that works to interfere with normal metabolic pathways in cancer cells.
It is the active form of 5-FU, which inhibits thymidine synthesis, a required DNA building block. Without thymidine, cancer cells cannot successfully replicate and divide, leading to cell death. This process helps in slowing the growth of the tumors and preventing the metastasis of cancer. As such, since capecitabine is metabolized within the tumor tissue, the drug tends to act within a localized area; as such, it reduces side effects from systemic compared to traditional chemotherapy agents, including 5-FU applied through IV.
As with any chemotherapy drug, capecitabine can cause side effects. These can be mild, moderate, or severe, depending on a person’s health, dosage, and length of treatment. Some common side effects of capecitabine are:
Nausea and Vomiting: These are common side effects, especially in the beginning stages of treatment.
Diarrhea: Capecitabine can cause gastrointestinal symptoms, such as diarrhea that may need to be managed with anti-diarrheal medications.
Fatigue: Most patients feel tired or weak while on treatment with capecitabine.
Loss of Appetite: Some patients may develop an aversion to food or experience weight loss.
Mouth Sores: Painful sores can develop in the mouth and throat that make it painful to eat or swallow.
Low Blood Counts: Capecitabine can cause low levels of red blood cells, white blood cells, or platelets, making it easier to get infections, become anemic, or experience bleeding.
Liver Toxicity: In some instances, capecitabine can cause problems in the liver, including elevated liver enzymes, jaundice, or hepatitis.
There are a number of important warnings and precautions to consider when using capecitabine:
Pregnancy and Breastfeeding: Capecitabine can cause harm to the fetus. Therefore, pregnant women should not use it during pregnancy. Also, the medicine is not prescribed for lactating mothers because it may pass into the breast milk.
Kidney or Liver Conditions: Patients with kidney or liver conditions should exercise utmost care when using capecitabine because this drug may worsen their conditions.
Blood Disorders: Capecitabine can cause bone marrow suppression, which may lead to low blood cell counts. Patients are required to have regular blood tests to monitor their blood counts during treatment.
Capecitabine, an oral chemotherapy drug, interacts with other medications, affecting its efficacy and safety.
- Anticoagulants (e.g., warfarin) – Capecitabine increases bleeding risk by enhancing the effects of blood thinners, requiring close monitoring.
- Phenytoin – It can elevate phenytoin levels, leading to toxicity, including neurological side effects.
- Leucovorin (Folinic Acid) – Enhances capecitabine’s effects but also raises toxicity risks, such as gastrointestinal distress.
- Proton Pump Inhibitors (e.g., omeprazole) – May alter capecitabine absorption, potentially reducing effectiveness. Patients should inform their healthcare provider about all medications to manage interactions and minimize adverse effects.
The dosage of capecitabine varies depending on the type of cancer being treated, the patient’s overall health, and their response to the drug. The usual dose is taken twice a day for two weeks, followed by a one-week break. The dosage is typically based on body surface area (BSA) and may be adjusted depending on the patient’s tolerance to the drug and any side effects experienced.
It is essential to follow your doctor’s instructions regarding dosage to ensure the effectiveness of the drug while minimizing side effects.
Capecitabine is available only by prescription. It should only be used under the guidance of an oncologist or a healthcare provider familiar with cancer treatments. Regular monitoring, including blood tests, may be necessary to assess the drug’s effectiveness and detect any side effects.