The effect and influence factor analysis ofⅠandⅡ stage DLBCL patients who receive radiotherapy after chemotherapy
10.3969/J.ISSN.1672-8270.2016.10.020
- VernacularTitle:Ⅰ期和Ⅱ期弥漫大B细胞淋巴瘤化疗后完全缓解患者接受放射治疗的效果及影响因素分析
- Author:
Huipin LI
;
Zhen QI
;
Da GAO
- Publication Type:Journal Article
- Keywords:
Diffuse large B cell lymphoma;
Survival rate;
Rituximab;
Radiotherapy
- From:
China Medical Equipment
2016;13(10):68-71
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To study the effect and influence factor analysis of DLBCL patient with early stage who receive radiotherapy after chemotherapy.Methods: 374 cases of patients with DLBCL was selected from January 2010 to December 2015 in our hospital. By random number table method, the patients were divided into CHOP group (n=104), R-CHOP+RT group (n=93), R-CHOP group (n=80), CHOP+RT group (n=97). CHOP chemotherapy was given to all patients, 180 patients received radiotherapy after chemotherapy, and 169 patients received rituximab. Survival rates were compared between the 4 groups.Results: The survival rate of R-CHOP group in 12 months, 24 months, 50 months and 100 months were lower than R-CHOP+RT group, but the difference was not statistically significant in twelfth months(x2=2.02,P>0.05). The differences of 24 months, 50 months and 100 months were statistically significant (x2=4.08,x2=4.03,x2=8.79;P<0.05); The survival rate of CHOP group was 12 months and 24 months was higher than CHOP+RT group which the difference was not statistically significant (x2=1.05,x2=0.22;P>0.05); The survival rate of CHOP group in 50 months and 100th months was lower than CHOP+RT, but the difference was no significant difference (x2=1.62,x2=0.03;P>0.05). Smoking index, whether the use of rituximab, the age associated with the survival of patients, the difference was statistically significant.Conclusion: Early DLBCL patients with R-CHOP and radiotherapy combined treatment can be effective in patients with survival, while the use of rituximab chemotherapy, in addition to smoking on the prognosis of patients with serious adverse effects.