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以培门冬酶为基础的GELOX方案治疗结外鼻型NK/T细胞淋巴瘤 被引量:3

The pegaspargase-based GELOX regimen for treatment of extranodal NK-T-cell lymphoma, nasal type
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摘要 目的:评价以培门冬酶替代左旋门冬酰胺酶的GELOX方案(吉西他滨、奥沙利铂、培门冬酶)治疗结外鼻型NK/T细胞淋巴瘤的疗效及安全性。方法:回顾分析经病理确诊为鼻型NK/T细胞淋巴瘤患者15例,均接受了4个疗程以上的含有培门冬酶的GELOX方案化疗,即第1、8天静脉滴注吉西他滨1 000mg/(m^2·d),第1天肌肉注射培门冬酶2 500 IU/(m^2·d),第1天静脉滴注奥沙利铂130 mg/(m^2·d),每3周为1个周期。结果:化疗后GELOX完全缓解(CR)率为66.7%,总体有效率(ORR)为100%,2年的无进展生存率为60%,2年的总生存率为80%,GELOX方案毒性反应轻微,除2例患者因肠道浸润,在初次化疗中出现肠穿孔,其他病例无严重不良事件。结论:含有培门冬酶的GELOX方案治疗NK/T细胞淋巴瘤临床疗效好,毒副作用轻,联合局部侵犯放疗后,将有利于患者的远期生存。 Objective To evaluate the safety profile and the efficacy of a pegaspargase-based GELOX regimen (gemcitabine, oxaliplatin and pegaspargase) in patients with nasal-type extranodal natural killer (NK) cell lymphoma (ENKTL). Methods 15 patients with newly diagnosed ENKTL were treated with more than four cycles of GELOX chemotherapy (gemcitabine 1000 mg/m^2 on dayl and day 8, oxaliplatin 100 mg/m^2 on dayl, pegaspargase 2500 IU/m^2 on dayl and repeated every 3 weeks) are included in the study. Results Upon completion of treatment, the complete response rate (CR) were 66.7% and the overall response rate (ORR) was 100.0% while the 2-year PFS and OS rates were 60% and 80% respectively. The GELOX regimen had been well tolerated in all of patients, and only 2 patients with intestinal tract infiltration suffered enterobrosis during the first induction chemotherapy. Conclusion For patients with newly diagnosed ENKTL, the pegaspargase-based GELOX regimen is a safe and effective treatment, and benefits for long term survival if combined with radiotherapy.
出处 《实用医学杂志》 CAS 北大核心 2016年第21期3566-3569,共4页 The Journal of Practical Medicine
基金 广东省科技计划项目(编号:2013B21800103)
关键词 结外NK/T细胞淋巴瘤 GELOX 疗效 生存 Extranodal NK-T-cell lymphoma GELOX Efficacy Survival
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  • 1姚青,何杰,钱宏,郭庆明,魏晓莹.鼻NK/T细胞淋巴瘤的临床病理特征[J].东南大学学报(医学版),2005,24(2):101-104. 被引量:3
  • 2高立永,卢敏华,李敏,高子芬.鼻NK/T细胞淋巴瘤临床病理学观察[J].河北医药,2005,27(5):360-361. 被引量:2
  • 3李忠实,金恒顺.鼻腔T/NK细胞淋巴瘤4例报告[J].中国眼耳鼻喉科杂志,2006,6(4):261-261. 被引量:3
  • 4金恒顺.8例鼻腔T/NK细胞淋巴瘤临床病理[J].肿瘤学杂志,2007,13(3):255-255. 被引量:1
  • 5Jaffe E, Harris N L, Stein H, et al. Pathology and gentics of tumors of haematopoietic and lymphoid tissues [ M ]. Lyon : IARC Press, France, 2001 : 204-207.
  • 6Kuo T T, Shih L Y, Tsang N M. Nasal NK/T cell lymphoma in Taiwan: a clinicopathologic study of 22 cases, with analysis of histologic subtypes, Epstein-Barr virus LMP- 1 gene association, and treatment modalities [J]. Int J Surg Pathol, 2004,2(4) :375-387.
  • 7KoY H, ChoEY, KimJ E, et al. NKand NK-likeT-cell lymphoma in extranasal sites: a comparative clinicopathological study according to site and EBV status [J]. Histopathology,2004, 44(5) : 480-489.
  • 8Kato N, Yasukawa K, Onozuka T, et al. Nasal and nasal-type T/ NK-cell lymphoma with cutaneous involvement [J]. J Am Acad Dermatol, 1999,40 (5 Pt 2 ) : 850-856.
  • 9LI C C, TIEN H F, TANG J L, et al. Treatment outcome and pat- tern of failure in 77 patients with sinonasal natural killer/T - cell or T-cell lymphoma[J]. Cancer, 2004, 100(2): 366-375.
  • 10LI Y X, YAO B, JIN J, et al. Radiotherapy as primary treatment for stage I E and IIE nasal natural killer/T- cell lymphoma[ J]. J Clin Oncol, 2006, 24(1) : 181 -189.

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