Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Year range
1.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 2905-2909, 2017.
Article in Chinese | WPRIM | ID: wpr-609398

ABSTRACT

Objective To explore the clinical efficacy and safety of panaxadiol saponins for the treatment of non-small cell lung cancer(NSCLC) with chemotherapy-induced leukopenia.Methods 92 NSCLC patients with leukopenia after chemotherapy were selected and divided into the observation group (46 cases) and the control group (46 cases) by random number table method.On the second day after the chemotherapy,the observation group was given panaxadiol saponins capsules,3 tablets/time,2 times/day.The control group was orally given placebo or reserpine,4 weeks for one course of treatment,the two groups were continuously treated for two courses.The clinical efficacy,number of leukocytes,improvement of TCM symptoms and adverse reactions were evaluated.Results After treatment for 4 weeks and 8 weeks,the WBC counts of the observation group were (4.48 ±0.77) × 109/L and (4.92 ± 0.89) × 109/L,respectively,which were significantly higher than those of the control group[(4.02 ± O.93) × 109/L and (4.57 ± 0.86) × 109/L],the differences were statistically significant(t =8.24,8.41,all P < 0.05).After treatment for 4 weeks and 8 weeks,the TCM syndrome scores of the observation group were (24.02 ± 5.91)points and (21.73 ± 4.14) points,respectively,which were lower than those of the control group [(26.33 ± 5.08) points and (23.14 ± 3.90) points],the differences were statistically significant (t =9.68,9.63,all P < 0.05).After treatment for 4 weeks and 8 weeks,the total effective rates of TCM were 76.09% (35/46) and 82.61% (38/46),respectively,which were significantly higher than those of the control group [63.04% (29/46) and 63.04% (29/46)],the differences were statistically significant(x2 =10.32,8.61,all P < 0.05).The effective rates of leukopenia improvement of the observation group after treatment for 4 weeks and 8 weeks were 69.57% (32/46) and 78.26% (36/46),respectively,which were higher than those of the control group [56.52% (26/46) and 65.22% (30/46)],the differences were statistically significant(t =9.38,9.51,all P < 0.05).There were no significant differences in adverse reactions between the two groups (P > 0.05).Conclusion Panaxadiol saponins in the treatment of NSCLC chemotherapy-induced leukopenia can significantly improve the number of white blood cells,improve the clinical symptoms,and it has good safety.

2.
Pakistan Journal of Medical Sciences. 2014; 30 (6): 1270-1272
in English | IMEMR | ID: emr-148778

ABSTRACT

This study is to determine the curative effect of beta-elemene emulsion on chemotherapy in the treatment of refractory/relapsed acute myeloid leukemia [AML]. In the beta-elemene emulsion plus HAA chemotherapy [harringtonine, aclacinomycin, Ara-c group] group, 120 cases received beta-elemene emulsion [400 mg] plus the HAA treatment. A 14-day treatment was a course of treatment, followed by an 8-14 day pause, and then the next course of treatment. The HAA treatment included Ara-c, 100 mg/m2, once every 12 h from day 1 to day 7; aclacinomycin, 20 mg/m2, from day 1 to day 7; and homoharringtonine, 4 mg/m2, from day 1 to day 7. The patients in the control HAA group received HAA treatment only. For both groups, effective antibiotics were given to patients when it was necessary. The total effective rate in the beta-elemene emulsion plus HAA group was 80.8%. But the total effective rate in the HAA only group was 52.9%. These results suggest that the beta-elemene emulsion plus HAA treatment has a much better curative effect in comparison with the HAA only treatment [P < 0.05]. Furthermore, beta-elemene emulsion has slightly adverse response, without causing blood and bone marrow depression. Beta-elemene emulsion has a curative effect in treatment of refractory/relapsed AML in combination with harringtonine, aclacinomycin, and Ara-c


Subject(s)
Humans , Male , Female , Sesquiterpenes , Antineoplastic Agents , Harringtonines , Aclarubicin/analogs & derivatives , Cytarabine
SELECTION OF CITATIONS
SEARCH DETAIL