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非亚洲人群中鼻型结外NK/T细胞淋巴瘤治疗的鼓舞人心的经验。

Encouraging experience in the treatment of nasal type extra-nodal NK/T-cell lymphoma in a non-Asian population.

作者信息

Qi Shunan, Yahalom Joachim, Hsu Meier, Chelius Monica, Lunning Matthew, Moskowitz Alison, Horwitz Steven

机构信息

a Department of Radiation Oncology , Memorial Sloan Kettering Cancer Center , New York , NY , USA ;

b Department of Radiation Oncology , Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing , China ;

出版信息

Leuk Lymphoma. 2016 Nov;57(11):2575-83. doi: 10.1080/10428194.2016.1180689. Epub 2016 May 17.

Abstract

Extra-nodal NK/T-cell lymphoma, nasal type (EN-NK/TCL-NT), is rare in the Western world. We launched the current single-institutional retrospective study with Institutional Review Board approval to better understand the disease. 43 EN-NK/TCL-NT patients treated from 1996 to 2014 were analyzed, including 10 (23%) Asians and 33 (76%) non-Asians. 19/26 (73%) early-stage patients received short-course chemotherapy followed by radiotherapy. 14/17 (82%) advanced-stage patients received primary chemotherapy. Complete response rate was significantly higher in the modified-SMILE group than the accelerated-CHOP group (80% vs. 30%, p = 0.015). The 2-year overall survival (OS) and progression-free survival (PFS) were 60% and 40%, respectively. Early-stage disease had significantly higher 2-year OS (87% vs. 21%) and PFS (56% vs.18%) than advanced-stage (p < 0.001). Ethnicity had no prognostic difference. EN-NK/TCL-NT in non-Asians shared similar disease characteristics and treatment outcomes with Asians. Most early-stage patients have achieved durable remissions. Management of advanced-stage disease remains challenging, with frequent progression and high mortality.

摘要

结外NK/T细胞淋巴瘤,鼻型(EN-NK/TCL-NT)在西方世界较为罕见。我们在获得机构审查委员会批准后开展了当前这项单机构回顾性研究,以更好地了解该疾病。分析了1996年至2014年期间接受治疗的43例EN-NK/TCL-NT患者,其中包括10例(23%)亚洲人和33例(76%)非亚洲人。26例早期患者中有19例(73%)接受了短程化疗,随后进行放疗。17例晚期患者中有14例(82%)接受了一线化疗。改良SMILE组的完全缓解率显著高于加速CHOP组(80%对30%,p = 0.015)。2年总生存率(OS)和无进展生存率(PFS)分别为60%和40%。早期疾病的2年OS(87%对21%)和PFS(56%对18%)显著高于晚期(p < 0.001)。种族在预后方面无差异。非亚洲人的EN-NK/TCL-NT与亚洲人具有相似的疾病特征和治疗结果。大多数早期患者已实现持久缓解。晚期疾病的管理仍然具有挑战性,常有进展且死亡率高。

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