期刊文献+

利妥昔单抗联合GDP方案治疗复发难治性弥漫大B细胞淋巴瘤的疗效观察 被引量:8

Observation of the curative effect of rituximab combined with GDP regimen in the treatment of recurrent and refractory diffuse large B-cell lymphoma
原文传递
导出
摘要 目的:观察利妥昔单抗联合GDP方案治疗复发难治性弥漫大B细胞淋巴瘤(DLBCL)的疗效和不良反应。方法:2009—01—2013-12在我院住院的复发难治性DLBCL患者28例,采用利妥昔单抗联合GDP方案化疗(利妥昔单抗375mg/m^2d0,吉西他滨1000mg/m^2dl、8,顺铂25mg/m^2d1~3,地塞米松40mg/dd1~4),21d为一个疗程。完成2个疗程后评价疗效及不良反应。结果:随访9~58个月,28例患者中13例获得完全缓解,9例获得部分缓解,1例疾病稳定,5例疾病进展,总有效率为78.6%;常见的不良反应为骨髓抑制和胃肠道反应。结论:利妥昔单抗联合GDP方案是治疗复发难治性DLBCL一个安全有效的挽救方案。 Objective:To explore the effect of rituximab combined with GDP regimen in the treatment of recurrent and refractory diffuse large P-cell lymphoma (DI,BCL) and adverse effect. Method: A total of 28 cases of refractory and relapsed DLBCL from January 2009 to December 2013 in our hospital,we used the combination of rituximab and GDP chemotherapy (rituximab 375 mg/m2 d0, gemcitabine 1 000 mg/m2 d1, 8, cisplatin 25 mg/m2 d1-3,dexamethasone 40 mg/d d1-4), 21 days for a course of treatment. Curative effect and adverse reaction evaluation completed after two courses. Result: Followed up for 9-58 months, 13 cases achieved complete remission,9 cases achieved partial remission, 1 patients with stable disease,5 patients with disease progression,the total efficiency was 78.6%. Common adverse reactions were myelosuppression and gastrointestinal tract reaction. Conclusion:Rituximab combined with GDP is a safe and effective saving scheme for relapsed refractory DLBCL.
出处 《临床血液学杂志》 CAS 2015年第5期764-766,共3页 Journal of Clinical Hematology
关键词 淋巴瘤 大B细胞 弥漫性 利妥昔单抗 GDP diffuse large B-cell lymphoma rituximab GDP
  • 相关文献

参考文献9

二级参考文献56

  • 1黄慧强,卜庆,夏忠军,林旭滨,王风华,李宇红,彭玉龙,潘战和,王树森,林桐榆,姜文奇,管忠震.含美罗华联合方案治疗复发耐药B细胞性非霍奇金淋巴瘤[J].癌症,2006,25(4):486-489. 被引量:9
  • 2石远凯,于燕霞.非霍奇金淋巴瘤治疗进展[J].临床肿瘤学杂志,2006,11(7):481-485. 被引量:11
  • 3程月新,徐卫,李建勇,钱思轩,陆化,吴汉新,陈丽娟.非霍奇金淋巴瘤641例临床分析[J].南京医科大学学报(自然科学版),2006,26(9):837-840. 被引量:15
  • 4Blay J Y, Gomez F, Sebban C, et al. The international prognostic index correlates to survival in patients with aggressive lymphoma in relapse: analysis of the PARMA trial [J]. Blood,1998,92(10): 3562-3568.
  • 5Kimby E, Brandt L, Nygren P, et al. A systematic overview of chemotherapy effects in agrressive non-Hodgkin 's lymphoma [J]. Acta Oncol,2001,40(2-3):198-212.
  • 6Coiffier B. Effective immunoeheotherapy for aggressive non-Hodgkin ' s lyrnphoma[J]. Semin Oneol, 2004,31 ( 1 Suppl 2) : 7-11.
  • 7Crump M, Bartz T, Couban S, et al. Gemictabine, dexamethasone, and cisplatin in patients with recurrent or refractory aggressive histology B-cell non Hodgkin lymphoma:a phase II study by the national cancer institute of canada clinical trials group[J]. Cancer, 2004, 101 (8): 1835-1842.
  • 8Baetz T, Belch A, Couban S, et al. Gemcitabine, dexamethasone and cisplatin is an active and non-toxic chemotherapy regimen in relapsed or refractory Hodgkin' s disease: a phase II study by the national cancer institute of canada clinical trials group[J] . Annals of Oncology,2003,14(12):1762-1767.
  • 9Jaffe ES, Harris NL, Stein H, et al. World Health Organization classification tumours. Pathology and genetics of tumours of haematopoietic and lymphoid tissue [ C ]. IARC Press, 2001.
  • 10Coiffier B. Rituximab in combination with CHOP improves survival in elderly patients with aggressive non-Hodgkin's lymphoma [J]. Semin Oncol, 2002, 29: 18-22.

共引文献92

同被引文献75

引证文献8

二级引证文献57

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部