Oncology Letters · 2018 · 10 citations · 10 references
MedicineOncologySurgeryChemotherapyGastrointestinal OncologyMedical OncologyAdverse Effects Of ChemotherapyChemotherapy Toxicity ManagementCombination ChemotherapyGastric CancerGastrointestinal Cancer SurgeryToxicity ManagementAnticancer ChemotherapyChemotherapy-induced Gastrointestinal ToxicityClinical Survival RatesGastric Cancer PharmacotherapyGastrointestinal Oncologic SurgeryOncologic Gastrointestinal SurgeryOxaliplatin-based TherapySurvival Rates
Clinical effects of FOLFOX4 and TPF chemotherapy regimen on postoperative gastric cancer patients were investigated. A total of 60 patients admitted to the First People's Hospital of Changzhou receiving gastric cancer operation were selected and they were divided into two groups at random. Thirty patients in the FOLFOX4 group were treated with oxaliplatin, fluorouracil and leucovorin, while 30 patients in the TPF group were treated with paclitaxel, fluorouracil and cisplatin. The therapeutic effects, adverse reactions, quality of life and survival time of patients in the two groups were observed. The total effective rate of the FOLFOX4 group was 73.3%, which was significantly higher than that of the TPF group (43.3%), and the difference was statistically significant (P<0.05). The proportions of neurotoxicity and thrombocytopenia in the FOLFOX4 group were 56.7 and 33.3%, while those in the TPF group were 26.7 and 60%, respectively, and the differences were statistically significant (P<0.05). The increasing proportion of postoperative scores of the FOLFOX4 group was 46.7%, which was significantly higher than that of the TPF group (20%), and the difference was statistically significant (P<0.05). The 2- and 3-year survival rates of the FOLFOX4 group were 63.3 and 50%, which were significantly higher than those of the TPF group (36.7 and 23.3%), and the differences were statistically significant (P<0.05). Therefore, the effective rate of FOLFOX4 regimen is high in the treatment of gastric cancer with relatively fewer adverse reactions, which has a certain advantage.
10
Ferdinando De Vita, Michele Orditura, Elide Matano et al. · British Journal of Cancer · 2005 · 181 citations · Full text
Medicine, Oncology, Pharmacotherapy +17
Jérôme Fayette, C. Fontaine-Delaruelle, A. Ambrun et al. · Oncotarget · 2016 · 39 citations · Full text
Medicine, Oncology, Pharmacology +12
Ralf‐Dieter Hofheinz, Johannes Clouth, J. Borchardt-Wagner et al. · BMC Cancer · 2016 · 37 citations · Full text