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©The Author(s) 2022.
World J Gastrointest Oncol. Jan 15, 2022; 14(1): 110-123
Published online Jan 15, 2022. doi: 10.4251/wjgo.v14.i1.110
Published online Jan 15, 2022. doi: 10.4251/wjgo.v14.i1.110
Cancer type | Study type | Statin (dose) | Combination therapies | Outcome |
Gastric cancer | Phase III | Simvastatin (40 mg/d) | Capecitabine andcisplatin | Simvastatin + capecitabine-cisplatin did not increase progression-free survival compared with capecitabine-cisplatin alone |
Phase II | Pravastatin (40 mg/d) | Epirubicin, cisplatinand capecitabine | Pravastatin + standard chemotherapy was well tolerated, but did not improve progression-free survival at 6 months compared with chemotherapy alone | |
Colorectal | Phase III | Simvastatin (40 mg/d) | FOLFIRI/XELIRI | Simvastatin + FOLFIRI/XELIRI did not increase progression-free survival compared with FOLFIRI/XELIRI alone |
Hepatocellular | Phase III | Pravastatin (40 mg/d) | Sorafenib | Pravastatin + sorafenib did not improve overall or progression-free survival compared with sorafenib alone |
Phase II | Pravastatin (40 mg/d) | Transcatheter arterialembolization followedby fluorouracil | Pravastatin + standard therapy prolonged overall survival compared with standard therapy alone | |
Pancreatic | Phase II | Simvastatin (40 mg/d) | Gemcitabine | Simvastatin + gemcitabine was well tolerated, but did not decrease time to progression compared with gemcitabine alone |
- Citation: Uemura N, Hayashi H, Baba H. Statin as a therapeutic agent in gastroenterological cancer. World J Gastrointest Oncol 2022; 14(1): 110-123
- URL: https://www.wjgnet.com/1948-5204/full/v14/i1/110.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v14.i1.110