期刊文献+

美罗华联合Hyper-CVAD/MTX+Ara-C方案治疗高危青年伯基特淋巴瘤的疗效观察(附6例) 被引量:2

Observation on the efficacy of rituximab combined with Hyper-CVAD/MTX+Ara-C regimen in the treatment of 6 cases of high-risk young Burkitt lymphoma
下载PDF
导出
摘要 目的:分析美罗华联合Hyper-CVAD/MTX+Ara-C方案治疗高危青年伯基特淋巴瘤的治疗效果。方法:总结2014年10月至2016年10月,我院收治的6例伯基特淋巴瘤患者的特征,均采用美罗华联合Hyper-CVAD/MTX+Ara-C方案化疗,历时4个周期共8个疗程,病程中腰穿及鞘注。结果:6例初诊患者临床分期(Arbor分期)Ⅲ期1例,Ⅳ期5例;首发部位多见于腹部包块及浅表淋巴结,均有B症状,乳酸脱氢酶(LDH)水平偏高,骨髓侵犯3例,中枢神经系统侵犯1例,有结外侵犯者3例。总疗程结束后评估,CR 5例,PR 1例,平均缓解期2.3个月。随访2.5年,5例患者病情稳定,1例死亡。结论:美罗华联合Hyper-CVAD/MTX+Ara-C方案治疗高危青年伯基特淋巴瘤有一定效果,患者对联合化疗的耐受性尚可。 Objective:To analyse the therapeutic effect of rituximab combined with Hyper-CVAD/MTX+Ara-C regimen in the treatment of high-risk young Burkitt lymphoma.Methods:To summarize the characteristics of 6 patients with Burkitt lymphoma treated in hospital from October 2014 to October 2016,rituximab combined with Hyper-CVAD/MTX+Ara-C regimen was used in all patients,which total of 8 courses of treatment lasted 4 cycles.Lumbar puncture and sheath injection were used.Results:Clinical staging(Arbor staging)of 6 newly diagnosed patients:1 case in stageⅢand 5 cases in stageⅣ.The primary site was abdominal mass and superficial lymph nodes,all with B symptoms,high lactate dehydrogenase,bone marrow invasion in 3 cases,central nervous system invasion in 1 case,3 cases with extranodal invasion.There were 5 cases with CR and 1 case with PR,with an average median remission period of 2.3 months.Follow-up of 2.5 years showed that 5 patients were in stable condition and 1 was died.Conclusion:Rituximab combined with Hyper-CVAD/MTX+Ara-C regimen has a certain effect in the treatment of high-risk young Burkitt lymphoma,and the patient's tolerance to combined chemotherapy is acceptable.
作者 周倩 阿茹娜 Zhou Qian;Aruna(Department of Hematology,Inner Mongolia People's Hospital,Inner Mongolia Hohhot 010017,China)
出处 《现代肿瘤医学》 CAS 2020年第14期2490-2493,共4页 Journal of Modern Oncology
基金 内蒙古自治区自然科学基金项目(编号:2018MS08070)。
关键词 伯基特淋巴瘤 美罗华 Hyper-CVAD/MTX+Ara-C方案 效果 Burkitt lymphoma rituximab Hyper-CVAD/MTX+Ara-C regimen effect
  • 相关文献

参考文献8

二级参考文献72

  • 1李家驹 王东方 等.伯基特淋巴瘤10例[J].中华小儿外科杂志,1994,15(2):109-109.
  • 2李家驹,中华小儿外科杂志,1994年,15卷,2期,109页
  • 3Swerdlow S H, Campo E, Harris N L, et al. World Health Org- nization classification of turnouts of haematopoietic and lymphoid tissues[M]. 4th ed. Lyon: IARC Press, 2008:262 -4.
  • 4Lu B B, Zhou C J, Yang W P, et al. Morphological, immunophe- notypic and molecular eb.araeterizati-oa of raatttre aggressive B-cell lymphomas in Chinese pediatric patients [ J ]. Leuk Lymphoma, 2011,52(12) :2356 -64.
  • 5Sampson V B, Rong N H, Han J, et al. MicroRNA let-7a down- regulates MYC and reverts MYC-induced growth in Burkitt lympho- ma cells [ J ]. Cancer Res, 2007,67 (20) :9762 - 70.
  • 6Leucci E, Cocco M, Onnis A, et al. MYC translocation-negative classical Burkitt lymphoma cases: an alternative pathogenetic mechanism involving miRNA deregulation [ J ]. J Pathol, 2008, 216(4) :440 -50.
  • 7Onnis A, Falco G D, Antonicelli G, et al. Alteration of MicroR- NAs regulated by c-Myc in Burkitt lymphoma [ J]. PLoS One, 2010,5(9) :e12960.
  • 8Privado I M, Martinez M R, Rebollo P, et al. E2F1 expression is deregulated and plays al oncogenic role in sporadic Burkitt' s lym- phoma [ J ]. Cancer Res, 2009,69 (9) :4052 - 8.
  • 9Chen S H, Wang Z Q, Dai X Z, et al. Re-expression of microR- NA-150 induces EBV-positive Burkitt lymphoma differentiation by modulating c-Myb in vitro[ J ]. Cancer Sci, 2013,104 (7) :826 - 34.
  • 10Leucci E, Onnis A, Cocco M, et al. B-cell differentiation in EBV-positive Burkitt lymphoma is impaired at posttranscriptional level by miRNA-ahered expression [J]. Int J Cancer, 2010,126 (6) :1316 -26.

共引文献31

同被引文献26

引证文献2

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