Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
1.
Chinese Medical Journal ; (24): 284-290, 2009.
Article in English | WPRIM | ID: wpr-311875

ABSTRACT

<p><b>BACKGROUND</b>Regional intra-arterial infusion chemotherapy (RIAC) has been more valuable to improve prognosis and quality of life of patients with inoperable pancreatic adenocarcinomas, and adjuvant RIAC plays an important role in prolonging survival and reducing risk of liver metastasis after radical resection of pancreatic cancer, but the effect of preoperative or multiple-phase RIAC (preoperative combined with postoperative RIAC) for resectable pancreatic cancers has not been investigated. In this prospective study, the effect of multiple-phase RIAC for patients with resectable pancreatic head adenocarcinoma was evaluated, and its safety and validity comparing with postoperative RIAC were also assessed.</p><p><b>METHODS</b>Patients with resectable pancreatic head cancer were randomly assigned to two groups. Patients in group A (n=50) were treated with new therapeutic mode of extended pancreaticoduodenectomy combined with multiple-phase RIAC, and those in group B (n=50) were treated with extended pancreaticoduodenectomy combined with postoperative RIAC in the same period. The feasibility, compliance and efficiency of the new therapeutic mode were evaluated by tumor size, serum tumor markers, clinical benefit response (CBR), surgical complications, mortality and toxicity of RIAC. The disease-free survival time, median survival time, incidence of liver metastasis, survival rate at 1, 2, 3 and 5 years were also observed. Life curves were generated by the Kaplan-Meier method.</p><p><b>RESULTS</b>The pain relief rate and CBR in group A was 80% and 84% respectively. Serum tumor markers decreased obviously and tumors size decreased in 26% of patients after preoperative RIAC in group A. No more surgical complications, mortality or severe systemic side effects were observed in group A compared with group B. The incidence of liver metastasis in group A was 34% which was lower than 50% in group B. The disease-free survival time and median survival time in group A were 15.5 months and 18 months respectively. The 1-, 2-, 3- and 5-year survival rates were 54.87%, 34.94%, 24.51% and 12.25% respectively. There was no significant difference of survival time or survival rates between two groups.</p><p><b>CONCLUSIONS</b>Multiple-phase RIAC is effective in combined therapy of resectable pancreatic head carcinomas by enhancing inhibition of tumor growth and reduction of liver metastasis, without negative effect on patients' safety or surgical procedure.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Adenocarcinoma , Drug Therapy , Mortality , Pathology , General Surgery , Deoxycytidine , Therapeutic Uses , Disease-Free Survival , Fluorouracil , Therapeutic Uses , Infusions, Intra-Arterial , Methods , Liver Neoplasms , Mitomycin , Therapeutic Uses , Neoplasm Metastasis , Pancreas , Pathology , General Surgery , Pancreatic Neoplasms , Drug Therapy , Mortality , Pathology , General Surgery , Pancreaticoduodenectomy
2.
Chinese Journal of Oncology ; (12): 618-620, 2004.
Article in Chinese | WPRIM | ID: wpr-254271

ABSTRACT

<p><b>OBJECTIVE</b>To determine the contents of thymidine phosphorylase (TP) and dihydropyrimidine dehydrogenase (DPD) in pancreatic cancer to provide a basis for the clinical use of capecitabine in pancreatic cancer patients.</p><p><b>METHODS</b>The contents of TP and DPD in pancreatic cancer and adjacent normal tissues from 20 patients were determined by ELISA and the TP to DPD ratios in the cancer and adjacent normal tissue were compared.</p><p><b>RESULTS</b>TP content was 5- to 283-fold higher in tumor tissue (mean 74-fold) than in the adjacent normal tissue (P < 0.01). DPD in the cancer tissue increased significantly. So did the TP to DPD ratio, when compared to that in normal pancreatic tissue (P < 0.01).</p><p><b>CONCLUSION</b>The increased TP to DPD ratio in pancreatic cancer suggests that capecitabine could be activated by the cancer, these capable of selectively kill the tumor cells.</p>


Subject(s)
Humans , Dihydrouracil Dehydrogenase (NADP) , Metabolism , Enzyme-Linked Immunosorbent Assay , Pancreas , Pancreatectomy , Pancreatic Neoplasms , General Surgery , Thymidine Phosphorylase , Metabolism
SELECTION OF CITATIONS
SEARCH DETAIL