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Guangdong Provincial Hospital of TCM,Guangzhou
Published:2001,
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Cheng, Jh., Chang, G., Wu, Wy. et al. Study on treatment of primary hepatic carcinoma by arterial perfusion embolization with zedoary turmeric oil., CJIM 7, 261–267 (2001). https://doi.org/10.1007/BF02934366
Jian-hua Cheng, Gang Chang, Wan-yin Wu, et al. Study on treatment of primary hepatic carcinoma by arterial perfusion embolization with zedoary turmeric oil. [J]. Chinese Journal of Integrative Medicine 7(4):261-267(2001)
Cheng, Jh., Chang, G., Wu, Wy. et al. Study on treatment of primary hepatic carcinoma by arterial perfusion embolization with zedoary turmeric oil., CJIM 7, 261–267 (2001). https://doi.org/10.1007/BF02934366 DOI:
Jian-hua Cheng, Gang Chang, Wan-yin Wu, et al. Study on treatment of primary hepatic carcinoma by arterial perfusion embolization with zedoary turmeric oil. [J]. Chinese Journal of Integrative Medicine 7(4):261-267(2001) DOI: 10.1007/BF02934366.
To evaluate the effect
side-effect and prospect of hepatic arterial perfusion embolization (HAPE) with Zedoary turmeric oil (ZTO) in treating primary hepatic carcinoma (PHC). Clinical study was carried out by administration of 1/2-3 ml ZTO through arterial catheter to induce embolism in 32 patients of PHC
and compared with 32 patients treated by hepatic arterial perfusion embolization with chemical agents (HAPE-C) in the control group. The Chinese herbal medicine was given orally to both groups according to Syndrome Differentiation of TCM. In the experimental study
transplantation hepatic carcinoma model was established in 40 rats. They were randomly divided into the treated group and the control group
20 in each group
and were perfused with 10 mg/kg ZTO and 0.2/2-0.3 ml normal saline respectively to observe the effect of treatment. The effect of treatment in the ZTO group was CR in 1 case and PR in 13 cases
the total effective rate being 43.75%
with AFP negative reversed in 7 cases
titer decreased in 7; while in the control group it was PR in 10 cases
the total effective rate being 31. 25%
AFP negative reversed in 5
titer decreased in 2
and the difference of therapeutic effect between the two groups was insignificant (P>0.05). The post-perfusion thrombotic syndrome occurrence
with the symptoms of fever
abdominal pain
vomiting
etc. in the two groups was similar
but no bone marrow inhibition occurred in the ZTO group
which was different from the control group (P<0. 01
P<0.05). The mean survival time
median survival time
1-
2-
3- and 4-year survival rate in the ZTO group was 13.84 months
10 months
37.5%
18.87%
9.70% and 6.4% respectively
and in the control group
8.03 months
6 months
15.6%
6. 27%
0% and 0% respectively
the mean survival time
median survival time and 1-year survival rate in the ZTO group were significantly superior to those in the control group (P<0.05). Experimental study showed that the effect in the treated group was better than that in the control group in tumor growth inhibition with the tumor growth rate as 10.8±4.5%% vs 20.6±12.7%
P<0.05
tumor necrosis degree (P<0.01) and survival time prolonged (14.8±3.4 days vs 11.7±1. 9 days
P<0.05) HAPE-ZTO in treating PHC showed the therapeutic effect similar to that of HAPE-C
but superior to the latter in survival time prolongation and bone marrow inhibition.
To evaluate the effect
side-effect and prospect of hepatic arterial perfusion embolization (HAPE) with Zedoary turmeric oil (ZTO) in treating primary hepatic carcinoma (PHC). Clinical study was carried out by administration of 1/2-3 ml ZTO through arterial catheter to induce embolism in 32 patients of PHC
and compared with 32 patients treated by hepatic arterial perfusion embolization with chemical agents (HAPE-C) in the control group. The Chinese herbal medicine was given orally to both groups according to Syndrome Differentiation of TCM. In the experimental study
transplantation hepatic carcinoma model was established in 40 rats. They were randomly divided into the treated group and the control group
20 in each group
and were perfused with 10 mg/kg ZTO and 0.2/2-0.3 ml normal saline respectively to observe the effect of treatment. The effect of treatment in the ZTO group was CR in 1 case and PR in 13 cases
the total effective rate being 43.75%
with AFP negative reversed in 7 cases
titer decreased in 7; while in the control group it was PR in 10 cases
the total effective rate being 31. 25%
AFP negative reversed in 5
titer decreased in 2
and the difference of therapeutic effect between the two groups was insignificant (P>0.05). The post-perfusion thrombotic syndrome occurrence
with the symptoms of fever
abdominal pain
vomiting
etc. in the two groups was similar
but no bone marrow inhibition occurred in the ZTO group
which was different from the control group (P<0. 01
P<0.05). The mean survival time
median survival time
1-
2-
3- and 4-year survival rate in the ZTO group was 13.84 months
10 months
37.5%
18.87%
9.70% and 6.4% respectively
and in the control group
8.03 months
6 months
15.6%
6. 27%
0% and 0% respectively
the mean survival time
median survival time and 1-year survival rate in the ZTO group were significantly superior to those in the control group (P<0.05). Experimental study showed that the effect in the treated group was better than that in the control group in tumor growth inhibition with the tumor growth rate as 10.8±4.5%% vs 20.6±12.7%
P<0.05
tumor necrosis degree (P<0.01) and survival time prolonged (14.8±3.4 days vs 11.7±1. 9 days
P<0.05) HAPE-ZTO in treating PHC showed the therapeutic effect similar to that of HAPE-C
but superior to the latter in survival time prolongation and bone marrow inhibition.
Zedoary turmeric oilhepatic arterial perfusion embolizationPrimary Hepatocarcinoma
Zedoary turmeric oilhepatic arterial perfusion embolizationPrimary Hepatocarcinoma
Medical Affair Department of Ministry of Health, PRC. Norm of Diagnosis and Treatment of Often Encountered Malignant Tumor. Second fascicle. Primary Carcinoma. 2nd edition. Beijing: Combined Publishing House of Beijing Medical University and PUMC 1991: 54–55.
Yang JJ, Zhu YF, Zuo CJ, et al. Establishment of rat model of transplantation hepatocarcinoma. Chin J Radiol 1993; 27(2): 122–123.
Garsson G, Gullbery B, Hafstrom L. Estimation of liver tumor volume using different formulas — an experimental study in rats. J Cancer Res Clin Oncol 1983; 105(l): 20.
Lindell B, Aronson KF, Nosslin B. Repeated arterial embolization of rat liver by degradable microspheres. Eur Sur Res 1988; 9: 347.
Jia YC. Progression of intervention therapy of hepatocarcinoma. Chin J Practical Surg 1995; 15(3): 175–178.
Chen XM, Luo PF, Hu JL, et al. Postpone adverse effect of hepatic arterial anti-tumor iodized oil suspension embolization on liver of patients with hepatocarcinoma. Cancer 1994; 13(1): 50–52.
Groupe d’Etude et de Traitement du Carcinome Hepatocellulaire. A comparison of lipiodol chemoembolization and conservative treatment for unresectable hepatocellular carcinoma. New Engl J Med 1995; 332(19): 1256–1261.
Jia YC, Tian JM, Wang ZT. To make efforts on further elevating the therapeutic effect of intervention therapy in treating hepatocarcinoma. Chin J Radiol 1996; 30(2): 77–78.
Yang Y, Wang XP, Yu LL, et al. Effects of elemene in anti-tumor and tumor cell apoptosis induction. Chin J Oncol 1996; 18(3): 169–172.
Qian J, Tai QZ, Yang AL, et al. Experimental study on effect of elemene emulsion in reversing cells of human lung cancer. Cancer Research on Prevention and Treatment 1996; 23(5): 299–301.
Wu WG, Luo YJ, Chen JH, et al. Image analysis of effect of Zedoary turmeric oil on hepatocarcinoma cell DNA in mice. Chin J Integrated Traditional and Western Medicine on Liver Dis 1999;9(1): 18–20.
Dong S, Xiao XS, Chen QH, et al. Study on therapeutic effect of hepatic arterial perfusion of hydroxycamptothecine gelatin microencapsule on transplantation hepatocarcinoma in rats. Chin J Radiol 1996;30(1): 45–48.
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