王迎, 李业楠, 邹德慧, 王亚非, 秦铁军, 赵耀中, 钱林生, 邱录贵. 美罗华联合化疗治疗侵袭性B细胞非霍奇金淋巴瘤的临床分析[J]. 中国肿瘤临床, 2008, 35(8): 421-423.
引用本文: 王迎, 李业楠, 邹德慧, 王亚非, 秦铁军, 赵耀中, 钱林生, 邱录贵. 美罗华联合化疗治疗侵袭性B细胞非霍奇金淋巴瘤的临床分析[J]. 中国肿瘤临床, 2008, 35(8): 421-423.
WANG Ying, LI Yenan, ZOU Dehui, WANG Yafei, QIN Tiejun, ZHAO Yaozhong, QIAN Linsheng, QIU Lugui. The Efficacy of Rituximab Combined with Chemotherapy in Treating Aggressive B-Cell Non-Hodgkin's Lymphoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2008, 35(8): 421-423.
Citation: WANG Ying, LI Yenan, ZOU Dehui, WANG Yafei, QIN Tiejun, ZHAO Yaozhong, QIAN Linsheng, QIU Lugui. The Efficacy of Rituximab Combined with Chemotherapy in Treating Aggressive B-Cell Non-Hodgkin's Lymphoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2008, 35(8): 421-423.

美罗华联合化疗治疗侵袭性B细胞非霍奇金淋巴瘤的临床分析

The Efficacy of Rituximab Combined with Chemotherapy in Treating Aggressive B-Cell Non-Hodgkin's Lymphoma

  • 摘要: 目的: 评价美罗华联合化疗治疗侵袭性B细胞非霍奇金淋巴瘤的疗效,分析影响疗效的相关因素。 方法: 回顾性分析我科采用美罗华联合化疗治疗32例侵袭性B细胞非霍奇金淋巴瘤的疗效及影响因素。 结果: 31例可评价疗效,完全缓解(CR)20例(64.5%),部分缓解(PR)7例(22.6%)。总有效率(CR+PR)87.1%。其中25例初治患者CR20例(80.0%),PR5例(20.0%),总有效率100%;6例难治复发患者PR2例(33.3%),SD2例(33.3%),PD2例(33.3%),总有效率33.3%。初治患者和复发难治患者中位无进展生存(Progression-free Survival,PFS)时间分别为72.0(2~74)个月、7.2(1~12)个月。治疗前按东部肿瘤协作组(Eastern Cooperative Oncology Group,ECOG)标准评定的体力评分对疗效有明显影响(P<0.05)。单因素分析表明血清乳酸脱氢酶水平、ECOG体力评分、国际预后指数(International Prognosis Index,IPI)评分和染色体核型异常与总体生存(Overall Survival,OS)时间和PFS均有关(P<0.05),B症状与PFS有关(P<0.05)。COX回归多因素分析发现只有IPI评分对PFS的影响有统计学意义(P=0.01),相对危险度(RR)为9.34。 结论: 美罗华联合化疗治疗初治侵袭性B细胞性非霍奇金淋巴瘤疗效显著,可作为CD20阳性侵袭性B细胞非霍奇金淋巴瘤的首选治疗。

     

    Abstract: Objective: To evaluate the efficacy of the combination of Rituximab and chemotherapy in treating aggressive B-cell non-Hodgkin's lymphoma (B-NHL), and to analyze correlation factors of the response. Methods: We retrospectively ana-lyzed the data from 32 patients with aggressive B-NHL who underwent Rituximab combined with chemotherapy in our hospital. Results: Thirty-one patients were evaluable for objective response. The complete response(CR) rate was 64.5%,the partial response(PR) rate was 22.6%, and the overall response(OR) rate was 87.1%. In the 25 de novo patients, the CR rate was 80.0%, the PR rate was 20.0%, and the OR rate was 100%. While in the 6 recurrent or relapsed patients, the combination therapy achieved an OR rate of 33.3% and a PR rate of 33.3%. The median progression-free survival (PFS) time of the de novo patients and the recurrent or relapsed patients were 72.0(2~74) months and 7.2(1~12) months, respec-tively. The efficacy of treatment was influenced by Eastern Cooperative Oncology Group(ECOG) score(P<0.05). Serum lac-tate dehydrogenase(LDH) level, ECOG score, international prognostic index(IPI) score and chromosomal abnormalities were correlated with overall survival(OS) and PFS(P<0.05). B symptoms were correlated to PFS(P<0.05). Through COX regres-sion analysis, we found that PFS was influenced significantly by IPI score(P=0.01), and relative risk(RR) was 9.34. Con-clusion: Rituximab-containing chemotherapeutic regimens are effective for naive aggressive B-NHL and should be the first choice in the treatment for aggressive B-NHL with CD20 expression.

     

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