期刊文献+

以左旋门冬酰胺酶:为基础的方案治疗结外鼻型NK/T细胞淋巴瘤36例 被引量:6

Study of regimen based on L-asparaginase for 36 cases with nasal type extranodal NKFI' celllymphoma
原文传递
导出
摘要 目的观察以左旋门冬酰胺酶(L-ASP)为基础的方案治疗结外鼻型NK/T细胞淋巴瘤(ENKTL)的近期疗效、远期生存和不良反应。方法2008年2月至2011年9月,采用以L-ASP为基础的方案治疗ENKTL36例。20例Ⅰ、Ⅱ期患者采用VLD方案联合放化疗,16例Ⅲ、Ⅳ期患者行改良SMILE方案化疗,其中4例化疗后接受序贯受累野放疗。结果36例患者中35例可评价疗效,完全缓解(CR)率为54.3%(19/35),总有效率为68.6%(24/35)。中位随访13.5个月(3-31个月),全部患者1年总生存率为82%,1年无疾病进展生存率为65%。近期疗效评价有效的患者1年生存率(93%)和无疾病进展生存率(80%)均优于对治疗无应答的患者(35%、33%),差异有统计学意义(X^2=13.909,P=0.000;X^2=8.216,P=0.004)。主要不良反应为骨髓抑制,无化疗相关性死亡。结论以L.ASP为基础的方案治疗ENKTL显示了较好的疗效,且耐受性好。L-ASP用于一线治疗ENKTL的大型前瞻性临床试验值得开展和深入研究。 Object To evaluate the efficacy and toxicity of L-asparaginase based regimen for extranodal nasal type NK/T cell lymphoma (ENKTL). Methods 36 patients were treated with L-asparaginase based regimen from February 2008 to November 2011. 20 stage Ⅰ /Ⅱ patients were administered with VLD regimen based chemo-radiotherapy. 4 of 16 stage Ⅲ/Ⅳ patients received modified SMILE regimen chemotherapy, followed by involved field radiation therapy (IFRT), while othe,'s received modified SMILE regimen chemotherapy alone. Results Among 36 patients, 35 were eligible for treatment response evaluation.The overall response rate (RR) was 68.6% (24/35) with complete response (CR) rate of 54.3% (19/35). Afterthe median follow-up of 13.5 (range 3-31) months, for all patients, the 1-year overall survival (OS) rate was 82 %, and the rate of progression-free survival (PFS) at 1 year was 65 %. The patients who attained responsewith treatment showed better 1-year OS (93 %) and PFS (80 %) as compared with patients without response (35 %; 33 %), and the differences were statistically significant (X^2-13.909, P = 0.000; X^2=8.216, P = 0.004). The major adverse event was myelosuppression. No chemotherapy-related mortality occurred. Conclusiion L-asparaginase based regimen is obviously effective and well tolerant for ENKTL. The large prospective clinical trials of L-asparaginase based regimen in the first-line treatment for ENKTL are worth for further investigation.
出处 《白血病.淋巴瘤》 CAS 2012年第3期153-156,共4页 Journal of Leukemia & Lymphoma
关键词 淋巴瘤 结外NK/T细胞 左旋门冬酰胺酶 药物疗法 联合 Lymphoma, extranodal NK-T cell L-asparaginase Drug therapy, combination
  • 相关文献

参考文献29

  • 1Li YX,Coucke PA,Li JY. Primary non-Hodgkin's lymphoma of the nasal cavity:prognostic significance of paranasal extension and the role of radiotherapy and chemotherapy[J].Cancer,1998.449-456.
  • 2Cheung MM,Chan JK,Lau WH. Early stage nasal NK/T cell lymphoma:clinical outcome,prognostic factors,and the effect of treatment modality[J].International Journal of Radiation Oncology,Biology,Physics,2002,(2):182-190.doi:10.1038/scientificamerican0297-83.
  • 3Vose Armitage J,Weisenburger D. International peripheral T-cell and natural killer/T-cell lymphoma study:pathology findings and clinical outcomes[J].Journal of Clinical Oncology,2008.4124-4130.
  • 4Koom WS,Chung EJ,Yang WI. Angiocentric T-cell and NK/T-cell lymphomas:radiotherapeutic viewpoints[J].International Journal of Radiation Oncology,Biology,Physics,2004.1127-1137.
  • 5Lee J,Kim WS,Park YH. Nasal-type NK/T cell lymphoma:clinical features and treatment outcome[J].British Journal of Cancer,2005.1226-1230.
  • 6Kim BS,Kim TY,Kim CW. Therapeutic outcome of extranodal NK/T-cell lymphoma initially treated with chemotherapy-result of chemotherapy in MKIT-cell lymphoma[J].Acta Oncologica,2003.779-783.
  • 7Cheung MM,Chan JK,Lau WH. Early stage nasal NK-Tcell lymphoma:clinical outcome,prognostic factors,and the effect of treatment modality[J].International Journal of Radiation Oncology,Biology,Physics,2002,(2):182-190.doi:10.1038/scientificamerican0297-83.
  • 8Kim WS,Song SY,Ahn YC. CHOP followed by involved field radiation:is it optimal for localized nasal natural killer / T-cell lymphoma[J].Annals of Oncology,2001.349-352.
  • 9Yong W,Zheng W,Zhu J. Midline NK / T-cell lymphoma nasaltype:treatment outcome,the effect of L-asparaginase based regimen,and prognostic factors[J].Hematological Oncology,2006.28-32.
  • 10Yong W,Zheng W,Zhu J. L-Asparaginase in the treatment of refractory and relapsed extranodal NK/T-cell lymphoma,nasal type[J].Annals of Hematology,2009.647-652.

二级参考文献18

共引文献20

同被引文献80

  • 1黄慧强,彭玉龙,潘战和,蔡清清,林旭滨,蔡绮纯.CTOP与CHOP方案治疗外周T细胞淋巴瘤的疗效比较[J].中国肿瘤临床,2006,33(11):638-640. 被引量:10
  • 2饶晓松,刘翠苓,李敏,崔岩,李宏宇,董格红,黄欣,郑杰,高子芬.TSLC1和BLU基因在鼻NK/T细胞淋巴瘤中CpG岛甲基化研究[J].肿瘤研究与临床,2006,18(8):534-537. 被引量:3
  • 3Cho EY, Kim KH, Kim WS, et al. The spectrum of Epstein-Barr virus- associated lymphoproliferative disease in Korea: incidence of disease entities by age groups. J Korean Med Sci, 2008, 23:185-192.
  • 4Zhang Y, Ohyashiki JH, Takaku T, et al. Transcriptional profiling of Epstein-Barr virus (EBV) genes and host cellular genes in nasal NK/T- cell lymphoma and chronic active EBV infection. Br J Cancer, 2006, 94: 599-608.
  • 5Kanemitsu N, Isobe Y, Masuda A, et al. Expression of Epstein-Barr virus-encoded proteins in extranodal NK/T-cell lymphoma, nasal type (ENKL): differences in biologic and clinical behaviors of LMPI- positive and -negative ENKL. Clin Cancer R es, 2012, 18:2164-2172.
  • 6Pang MF, Lin KW, Peh SC. The signaling pathways of Epstein-Barr virus-encoded latent membrane protein 2A (LMP2A) in latency and cancer. Cell Mol Biol Lett, 2009, 14: 222-247.
  • 7Nagamine M, Kishibe K, Takahara M, et al. Selected amino acid change encoding Epstein-Barr virus-specific T cell epitope of the LMP2A gene in Japanese nasal NK/T cell lymphoma patients. Intervirology, 2007, 50:319-322.
  • 8Kim do N, Lee SK. Biogenesis of Epstein-Barr virus microRNAs. Mol Cell Bioehem, 2012, 365: 203-210.
  • 9Ramakrishnan R, Donahue H, Garcia D, ct at. Epstein-Ban" virus BART9 miRNA modulates LMP1 levels and affects growth rate of nasal NK T cell lymphomas. PLoS One, 2011, 6: e27271.
  • 10Motsch N, Alles J, Imig J, et at. MicroRNA profiling of Epstcin-Barr virus-associated NK/T-cell lymphomas by deep sequencing. PLoS One, 2012, 7: e42193.

引证文献6

二级引证文献12

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