ChemotherapyFDA-approvedSecond-line

Capecitabine

How it works

Converts into a chemotherapy agent that kills rapidly dividing cancer cells.

Cancer types

Colorectal CancerAll patients
Pancreatic CancerAll patients
Breast CancerAll patients

Efficacy

In clinical trials, around 24% of patients achieved an objective response, with median progression-free survival of approximately 5 months.

Side effects

Moderate

Side effects can be significant and may require dose adjustments or supportive medication, but the treatment is usually continued.

Evidence from research

StudyCancer typeStageEfficacy
Testing Capecitabine for Metastatic ER Positive Breast CancerBreast Cancerphase-2Source →
Rectal Cancer Trial Examines New Treatment CombinationColorectal Cancerphase-2Source →
Testing Atezolizumab and Capecitabine for Triple Negative Breast CancerBreast Cancerphase-2Source →
Combination Therapy Shows Promise for Advanced Breast CancerBreast Cancerphase-2The objective response rate was 25.8%, with 17 partial responses.Source →
Evaluating a Combination Treatment for Metastatic Colorectal Cancer in Elderly PatientsColorectal Cancerphase-2Source →
Study Examines Effectiveness of Capecitabine in Triple-Negative Breast CancerBreast CancerobservationalAdjuvant capecitabine did not improve disease-free survival (HR = 0.96; 95% CI 0.52-1.78) or overall survival (HR = 0.70; 95% CI 0.33-1.46) in univariable analyses.Source →
Genetic Testing for Breast Cancer Patients on Capecitabine May Be Cost-EffectiveBreast Cancerphase-3The genotyping strategy yielded 1.16 QALYs at a cost of $2,832, compared to $2,677 and 1.15 QALYs for the no-genotyping strategy.Source →
Methylcobalamin May Help Prevent Hand-Foot Syndrome in Breast Cancer PatientsBreast Cancerphase-3Grade ≥2 hand-foot syndrome occurred in 14.5% of patients in the methylcobalamin group, compared to 29.1% in the placebo group.Source →
Capecitabine plus Temozolomide Therapy for Pancreatic TumorsPancreatic CancerobservationalThe objective response rates and disease control rates were 26.7 and 66.7%, respectively.Source →
Lu-DOTATATE with Capecitabine Tested in Advanced Gastroenteropancreatic Neuroendocrine TumorsPancreatic Cancerphase-2The objective response rate was 33.3% in the experimental arm versus 30.6% in the control arm.Source →
Predicting Capecitabine-Induced Diarrhea in Cancer PatientsColorectal Cancerlab-studyThe area under curve of the model was 0.907, with a specificity of 100.0% and a sensitivity of 71.4% for predicting diarrhea in colorectal cancer patients.Source →
New Treatment Options for Advanced HER2-Positive Breast CancerBreast Cancerphase-3Median overall survival for patients in the tucatinib arm was 21.9 months compared with 17.4 months for patients in the control arm.Source →
Long-Term Outcomes of Pancreatic Cancer TreatmentPancreatic Cancerphase-3The median overall survival was 31.6 months in patients given GemCap.Source →
Phenytoin Interaction with Capecitabine in Cancer TreatmentColorectal CancerobservationalSource →
Tailoring Cancer Treatment for Triple-Negative Breast Cancer PatientsBreast Cancerphase-3Among immune-hot patients, the 5-year disease-free survival rate was 96.9% in the capecitabine group and 79.4% in the control group.Source →
Neoadjuvant Chemotherapy for Rare Lung Tumors Shows PromiseLung CancerobservationalThere was a 21% regression in the primary tumor size.Source →
Combining two treatments for hormone receptor positive breast cancerBreast Cancerphase-2The estimated median progression-free survival for the combination was 17.7 months versus 14.6 months for letrozole alone.Source →
Targeted Cancer Treatment Using Carbohydrate-Based NanoparticlesColorectal Cancerlab-studySource →
Rare Case of Ependymoma Shows Long-Term Remission with Combination ChemotherapyLung CancerobservationalThe patient remained in remission for approximately 29 months.Source →

This information is provided for general education only and is not medical advice. Always consult a qualified healthcare professional before making treatment decisions.