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1.
China Journal of Chinese Materia Medica ; (24): 510-512, 2006.
Article in Chinese | WPRIM | ID: wpr-356778

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of Yanshu injection on the combined treatment in the advanced primary liver cancer.</p><p><b>METHOD</b>Eighty-five cases of advanced primary liver cancer were treated with Yanshu injection combining with chemotherapy or only chemotherapy. The curative effects, pain genesic rate, one year survival rate, survival quality of life and cell immune functions were observed.</p><p><b>RESULT</b>The remission rate and one year survival rate of the trial group were 60.5% and 51.2%, respectively, and were significantly higher than those (45.2% and 40.5%) of the control group (P < 0.05). The pain relief rate of the trial group was significantly higher than that of the control group (P < 0.05). The improvement of the quality of life was higher than that of the contral group (P < 0.01). The ability of the T-cell subgroup and NK-cell of the trail group were significantly difference between pre-and post-treatment (P < 0.01 or 0.05); however, that of the control group was no obviously change.</p><p><b>CONCLUSION</b>Yanshu injection combination with chemotherapy can raise the curative effect, one year survival rate and cellular immune function, reduce pain genesic rate and toxicity of chemotherapy, and improve the quality of life of the patients with advanced primary liver cancer, which is worthy to be recommended for clinical application.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Antineoplastic Agents, Phytogenic , Therapeutic Uses , Antineoplastic Combined Chemotherapy Protocols , Therapeutic Uses , Drug Therapy, Combination , Drugs, Chinese Herbal , Therapeutic Uses , Injections, Intravenous , Liver Neoplasms , Drug Therapy , Pathology , Neoplasm Staging , Phytotherapy , Plants, Medicinal , Chemistry , Quality of Life , Sophora , Chemistry , Survival Rate
2.
Chinese Journal of Oncology ; (12): 214-216, 2006.
Article in Chinese | WPRIM | ID: wpr-308379

ABSTRACT

<p><b>OBJECTIVE</b>To detect changes of serum soluble Apo-1/Fas (sApo-1/Fas) in pancreatic cancer patients and to investigate its clinical value in assessing the effect of chemotherapy.</p><p><b>METHODS</b>The serum level of sApo-1/Fas in 30 normal control subjects and 58 pancreatic cancer patients were detected using enzyme-linked immunosorbent assay (ELISA), and the sApo-1/Fas level of 48 pancreatic cancer patients, before and after chemotherapy was compared.</p><p><b>RESULTS</b>Compared with the level of the control group, the level of serum soluble Apo-1/Fas was significantly correlated with clinical stage but not with age, sex or pathologic type of pancreatic cancer. It was elevated gradually from stage II to IV (P < 0.01). However, it would obviously decrease in pancreatic cancer patients after chemotherapy (P < 0.01).</p><p><b>CONCLUSION</b>The serum soluble Apo-1/Fas may be involved in the development of pancreatic cancer, and it may be used as one parameter to assess the disease status and prognosis of pancreatic cancer patient.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Adenocarcinoma, Mucinous , Blood , Drug Therapy , Antineoplastic Combined Chemotherapy Protocols , Therapeutic Uses , Carcinoma, Pancreatic Ductal , Blood , Drug Therapy , Cisplatin , Deoxycytidine , Disease Progression , Neoplasm Staging , Pancreatic Neoplasms , Blood , Drug Therapy , Prognosis , Remission Induction , fas Receptor , Blood
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