Performance of capecitabine in novel combination therapies in colorectal cancer.
Fahima Danesh PouyaYousef RasmiIrem Yalim CamciYusuf TutarMohadeseh NematiPublished in: Journal of chemotherapy (Florence, Italy) (2021)
Colorectal cancer is one of the most common cancers throughout the world, and no definitive cure has ever been found. Perhaps a new insight into the effectiveness of chemotherapy drugs could help better treat patients. Targeted therapies have significantly improved the median overall survival of colorectal cancer patients. One of the standard chemotherapy regimens used for colorectal cancer is capecitabine, which is important in monotherapy and combination therapies. Capecitabine, with other chemotherapeutic agents (irinotecan, oxaliplatin, perifosine, 17-allylamino-17-demethoxygeldanamycin, aspirin, celecoxib, statins, quinacrine, inositol hexaphosphate and inositol, cystine/theanine, curcumin, and isorhamnetin), and biological ones (antibodies) plays an important role in the inhibition of some signaling pathways, increasing survival, reducing tumor growth and side effects of capecitabine. However, some drugs, such as proton pump inhibitors, are negatively related to capecitabine; therefore, the purpose of this work is to review and discuss the performance of capecitabine combination therapies in colorectal cancer.
Keyphrases
- locally advanced
- phase ii study
- rectal cancer
- metastatic breast cancer
- metastatic colorectal cancer
- squamous cell carcinoma
- phase iii
- radiation therapy
- open label
- end stage renal disease
- signaling pathway
- randomized controlled trial
- systematic review
- low dose
- chronic kidney disease
- ejection fraction
- newly diagnosed
- prognostic factors
- clinical trial
- antiplatelet therapy
- free survival
- oxidative stress
- cell proliferation
- acute coronary syndrome
- endoplasmic reticulum stress
- atrial fibrillation