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Xeloda

21.11
An oral chemotherapy drug used to treat various types of cancer by targeting rapidly dividing cells.


Ingredient
Availability
In Stock
Delivery
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Capecitabine
Primary Category
Cancer Treatment
Therapeutic Class
Antineoplastic and Immunomodulating Agents, Antineoplastic Agents, Antimetabolites
Pharmacological Class
Pyrimidine Analogues
Indications
Colon cancer, Rectal cancer, Stomach cancer, Breast cancer
Contraindications
Severe kidney impairment, Known DPD deficiency, Severe liver disease, Treatment with sorivudine or brivudine
Minor Side Effects
Tiredness, Weakness, Appetite loss
Moderate Side Effects
Diarrhoea, Hand-foot syndrome (redness/peeling of palms), Nausea, Abdominal pain
Serious Side Effects
Severe dehydration, Heart problems (chest pain), Bone marrow suppression, Severe skin reactions
Dosage Forms
Tablet
Administration Route
Oral
Mechanism of Action
Xeloda is a chemotherapy prodrug that is converted into 5-fluorouracil (5-FU) inside cancer cells by the body's enzymes. Once converted, it interferes with the production of DNA and RNA in cancer cells, preventing them from growing and multiplying.
Prescription Status
Rx
Manufacturer
Roche
Patient Summary
An oral chemotherapy drug used to treat various types of cancer by targeting rapidly dividing cells.
Onset Time
Requires several cycles for observable benefit
Duration
Daily (usually 2 weeks on, 1 week off)
Storage Instructions
Store below 30°C in the original package.
Drug Interactions
Warfarin, Phenytoin, Antacids, Leucovorin, Brivudine
Age Restrictions
Adults only
Pregnancy Use
Do not use during pregnancy. Use effective contraception during and after treatment.
Alternative Drugs
Fluorouracil (IV), Tegafur

Xeloda: Capecitabine Overview

Xeloda is the brand name for the oral chemotherapy agent capecitabine. It belongs to the oncology support category and is supplied as a 500 mg pill. In Hong Kong, Xeloda is a prescription-only medication regulated by the Department of Health.

Capecitabine is a prodrug that is converted inside the body to 5-fluorouracil (5-FU), a chemotherapy compound that interferes with DNA synthesis in rapidly dividing cancer cells. The medication is used in the treatment of several solid tumors and is taken under the close supervision of an oncologist.

How Capecitabine Works in the Body

  • Prodrug conversion - After swallowing the pill, capecitabine is absorbed through the gastrointestinal tract and travels to the liver, where the enzyme carboxylesterase transforms it into 5′-deoxy-5-fluorocytidine (5′-DFCR).
  • Further activation - 5′-DFCR is converted to 5′-deoxy-5-fluorouridine (5′-DFUR) by cytidine deaminase, an enzyme that is especially active in tumor tissue.
  • Final step - The enzyme thymidine phosphorylase (TP) then changes 5′-DFUR into 5-fluorouracil (5-FU) directly inside malignant cells. TP is usually present at higher levels in cancerous tissue, which helps concentrate the active drug where it is needed.

5-FU inhibits the enzyme thymidylate synthase, blocking the formation of thymidine-a nucleotide required for DNA replication. The result is impaired DNA synthesis and cell death, primarily affecting rapidly dividing tumor cells while sparing most normal tissues.

Onset of therapeutic effect typically begins within a few days after starting treatment, with peak plasma concentrations of capecitabine occurring 1-2 hours after ingestion. The drug’s half-life is about 45 minutes, but the active metabolite 5-FU persists longer in tumor cells.

Conditions Treated with Xeloda

Capecitabine is approved by the Hong Kong Department of Health for the following indications:

  • Metastatic colorectal cancer - usually in combination with oxaliplatin (the XELOX regimen).
  • Early-stage (adjuvant) colon cancer - after surgical resection when other high-risk features are present.
  • Metastatic breast cancer - particularly in patients who have previously received anthracycline- and taxane-based therapies.
  • Gastric (stomach) cancer - when the disease is advanced or metastatic.

These uses are based on clinical trials that demonstrated meaningful improvement in progression-free survival and overall survival when capecitabine is incorporated into standard treatment protocols.

Off-Label and Investigational Applications

Evidence from peer-reviewed studies and guideline panels suggests that capecitabine may be used off-label for:

  • Pancreatic cancer - often combined with gemcitabine; however, this indication is not approved by Hong Kong regulators.
  • Head and neck squamous cell carcinoma - as part of concomitant chemoradiation protocols in selected patients.

Disclaimer: Off-label use of capecitabine requires careful medical supervision, individualized risk assessment, and adherence to local regulatory guidance.

Who Should or Should Not Use Xeloda?

Ideal Candidates

  • Adults with the approved cancer types listed above.
  • Patients with adequate liver and kidney function (creatinine clearance ≥ 50 mL/min) unless dose adjustments are planned.
  • Individuals who can reliably adhere to an oral medication schedule and attend regular monitoring visits.

Absolute Contraindications

  • Known hypersensitivity to capecitabine, 5-FU, or any excipients in the pill.
  • Dihydropyrimidine dehydrogenase (DPD) deficiency - a rare genetic condition that impairs 5-FU metabolism and can cause severe toxicity.
  • Pregnancy - capecitabine is teratogenic and contraindicated in all trimesters.
  • Breastfeeding - the drug is excreted in breast milk and may harm the infant.

Relative Contraindications

  • Severe renal impairment (creatinine clearance < 30 mL/min) - dose reduction may be needed.
  • Significant hepatic disease (elevated bilirubin > 1.5 × upper limit of normal).
  • Concomitant use of other fluoropyrimidines (e.g., 5-FU) without dose adjustment.

Special Populations

  • Elderly patients - may require lower starting doses and closer toxicity monitoring.
  • Patients with mild to moderate renal or hepatic dysfunction - dose adjustments are generally recommended, but exact reductions should be prescribed by the treating oncologist.

If you fall into any of the contraindication categories, discuss alternative treatment options with your healthcare team.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Nausea or loss of appetite.
  • Hand-foot syndrome (palmar-plantar erythrodysesthesia) - redness, swelling, or tenderness of the palms and soles.
  • Diarrhea or loose stools.
  • Fatigue or generalized weakness.
  • Mild skin rash or itching.

Most of these reactions are manageable with supportive care and dose adjustments.

Serious Adverse Events

  • Severe hand-foot syndrome - may require temporary drug interruption.
  • Grade 3-4 neutropenia or other blood-cell count reductions, increasing infection risk.
  • Mucositis - painful inflammation of the mouth or gastrointestinal lining.
  • Cardiotoxicity (rare) - chest pain, arrhythmias, or heart failure symptoms.
  • Severe allergic reactions - rash, swelling, breathing difficulty; seek emergency care.

Any sign of a serious reaction should prompt immediate medical evaluation.

Drug Interactions

  • Warfarin - capecitabine can enhance anticoagulant effects, increasing bleeding risk; more frequent INR monitoring is advised.
  • CYP2C9 inhibitors (e.g., fluconazole, amiodarone) - may raise capecitabine plasma levels, warranting dose modification.
  • Other fluoropyrimidines (5-FU, tegafur) - combined use can lead to excess toxicity; usually avoided.
  • Immunosuppressants (e.g., azathioprine) - heightened risk of bone-marrow suppression.

Patients should provide a complete medication list-including over-the-counter drugs, herbal supplements, and vitamins-to their oncologist before starting Xeloda.

Food and Lifestyle Interactions

  • Take with food - capecitabine absorption is increased when taken with meals, which also helps reduce gastrointestinal upset.
  • Alcohol - moderate consumption is acceptable, but excessive intake may worsen liver toxicity.
  • Driving - most patients can safely operate a vehicle, but those experiencing severe fatigue or neuropathy should exercise caution.
  • Sun exposure - hand-foot syndrome can be aggravated by heat; protect hands and feet from extreme temperatures and direct sunlight.

How to Take Xeloda

  • Formulation - Xeloda is supplied as a 500 mg tablet. Swallow the tablet whole with a full glass of water; do not crush or chew.
  • Typical schedule - The drug is usually prescribed in a two-weeks-on, one-week-off cycle, but the exact dosing schedule, total daily dose, and number of tablets per dose are individualized based on body-surface area, cancer type, and treatment goals.
  • Administration with food - Take each dose within 30 minutes after a meal to improve absorption and lessen stomach irritation.
  • Missed dose - If you forget a dose, take it as soon as you remember provided it is still within the same dosing day. Do not double the next scheduled dose.
  • Overdose - Symptoms may include severe nausea, vomiting, diarrhea, and confusion. Seek emergency medical attention; supportive care and, if available, leucovorin rescue may be used.
  • Discontinuation - Stopping capecitabine abruptly is generally safe, but any change in therapy should be directed by the oncologist, who may recommend a taper or transition to another regimen.

Monitoring and Follow-Up

  • Complete blood count (CBC) - before treatment, then weekly during the first two cycles, and as clinically indicated thereafter.
  • Renal function (serum creatinine, eGFR) - baseline and at regular intervals; dose adjustments are made for reduced clearance.
  • Liver function tests (ALT, AST, bilirubin) - baseline and periodic monitoring.
  • Physical examination - assessment of hand-foot syndrome, mucosal health, and any signs of infection.
  • Imaging studies (CT, MRI, or PET scans) - per oncologist’s schedule to evaluate tumor response.

Regular follow-up visits allow the treatment team to modify dosing, manage toxicities, and assess therapeutic effectiveness.

Storage and Handling

  • Keep the tablets in the original container, tightly closed, at room temperature (15 °C-30 °C).
  • Protect from moisture, direct sunlight, and heat.
  • Do not store in the bathroom or near the kitchen sink.
  • Keep out of reach of children and pets.
  • Discard any expired or unused tablets according to local pharmaceutical waste guidelines or return them to a pharmacy for safe disposal.

Medication-Specific Glossary

Hand-Foot Syndrome
A toxicity characterized by redness, swelling, and tenderness of the palms and soles, commonly seen with capecitabine therapy.
DPD Deficiency
A hereditary lack of the enzyme dihydropyrimidine dehydrogenase, leading to impaired breakdown of 5-fluorouracil and heightened risk of severe chemotherapy toxicity.
Prodrug
An inactive compound that is metabolized in the body to produce an active therapeutic agent; capecitabine is a prodrug of 5-fluorouracil.

Medical Disclaimer

This article provides educational information about Xeloda (capecitabine) and is not a substitute for professional medical advice. Treatment decisions, including use for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Xeloda FAQ

What should I do if I develop hand-foot syndrome while taking Xeloda?

Hand-foot syndrome is managed by dose reduction, temporary drug interruption, and using soothing skin care measures such as lubricating creams and avoiding hot water or tight footwear. Report symptoms promptly to your oncologist for individualized advice.

Can I travel internationally with Xeloda tablets, and will they be inspected at customs?

Yes, you may travel with Xeloda, but keep the medication in its original labeled container, carry a copy of the prescription, and be prepared to show the prescription if requested by customs or airline security.

Will Xeloda appear on a standard workplace drug test?

Capecitabine is not a controlled substance and is not typically screened for in routine workplace drug-testing panels. However, specialized testing can detect it if specifically requested.

Are there any dietary restrictions while taking Xeloda?

There are no specific foods that must be avoided, but maintaining a balanced diet helps support overall health. Limit excessive alcohol and avoid very spicy or acidic foods if they worsen nausea.

How does Xeloda compare to intravenous 5-fluorouracil?

Both deliver the same active chemotherapy (5-FU). Xeloda offers the convenience of oral administration and can be tailored to patient weight, while intravenous 5-FU provides controlled dosing in a clinical setting. Efficacy is comparable when used in appropriate regimens.

Is it safe to receive the flu vaccine while on capecitabine treatment?

Inactivated vaccines, such as the seasonal flu shot, are generally safe for patients receiving capecitabine. Live-attenuated vaccines should be avoided. Discuss timing with your oncologist.

What should I know about using other medications, like herbal supplements, with Xeloda?

Herbal products can affect liver enzymes that process capecitabine. For example, St. John’s wort may increase metabolism, potentially reducing effectiveness. Always disclose any supplements to your treatment team.

Can capecitabine cause long-term fertility issues?

Capecitabine may affect sperm production in men and ovarian function in women, especially with high cumulative doses. Discuss fertility preservation options before starting therapy if future childbearing is a concern.

How is Xeloda disposed of after the treatment course ends?

Unused tablets should be returned to a pharmacy or a community drug-take-back program. Do not flush medications down the toilet or throw them in household trash, as this can contaminate the water supply.

What are the cost considerations for Xeloda in Hong Kong?

Xeloda is a patented oncology product; price varies by pharmacy and insurance coverage. Generic capecitabine tablets of the same strength may be less expensive, but the decision to switch should be made by your oncologist based on clinical suitability.

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