Department of Radiation Oncology, Cancer Hospital and Institute, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Department of Pathology, Cancer Hospital and Institute, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Int J Radiat Oncol Biol Phys. 2014 Mar 15;88(4):806-13. doi: 10.1016/j.ijrobp.2013.12.005. Epub 2014 Feb 1.
To investigate, in a large cohort of patients, the immunophenotypic and clinical differences of nasal and extranasal extranodal nasal-type natural killer/T-cell lymphoma of the upper aerodigestive tract (UADT-NKTCL) and examine the relevance of the immunophenotype on the clinical behavior, prognosis, and treatment.
A total of 231 patients with UADT-NKTCL were recruited. One hundred eighty-one patients had primary location in the nasal cavity (nasal UADT-NKTCL), and 50 patients had primary extranasal UADT-NKTCL.
Patients with extranasal UADT-NKTCL had more adverse clinical features, including advanced-stage disease, regional lymph node involvement, B symptoms, and poor performance status, than patients with nasal UADT-NKTCL. In addition, CD56 and granzyme B were less frequently expressed in extranasal UADT-NKTCL. The 5-year overall survival rate was 74.1% for the entire group and 76.0% for early-stage disease. The 5-year overall survival rate for extranasal UADT-NKTCL was similar or superior to that of nasal UADT-NKTCL for all disease stages (76.9% vs 73.4%, P=.465), stage I disease (75.9% vs 79.2%, P=.786), and stage II disease (83.3% vs 50.3%, P=.018). CD56 expression and a Ki-67 proliferation rate ≥ 50% predicted poorer survival for extranasal UADT-NKTCL but not for nasal UADT-NKTCL.
Patients with nasal and extranasal UADT-NKTCL have significantly different clinical features, immunophenotypes, and prognosis. Extranasal UADT-NKTCL should be considered as a distinct subgroup apart from the most commonly diagnosed prototype of nasal UADT-NKTCL.
在大量患者中研究上呼吸消化道(UADT)鼻型自然杀伤(NK)/T 细胞淋巴瘤(NKTCL)的免疫表型和临床差异,并探讨免疫表型与临床行为、预后和治疗的相关性。
共招募了 231 例 UADT-NKTCL 患者。181 例患者原发部位在鼻腔(鼻腔 UADT-NKTCL),50 例患者原发部位在鼻腔外 UADT-NKTCL。
与鼻腔 UADT-NKTCL 患者相比,鼻腔外 UADT-NKTCL 患者具有更多不良临床特征,包括晚期疾病、区域淋巴结受累、B 症状和较差的体能状态。此外,鼻腔外 UADT-NKTCL 中 CD56 和颗粒酶 B 的表达频率较低。全组患者 5 年总生存率为 74.1%,早期疾病为 76.0%。鼻腔外 UADT-NKTCL 的 5 年总生存率在所有疾病分期(76.9%对 73.4%,P=.465)、Ⅰ期疾病(75.9%对 79.2%,P=.786)和Ⅱ期疾病(83.3%对 50.3%,P=.018)均与鼻腔 UADT-NKTCL 相似或优于鼻腔 UADT-NKTCL。CD56 表达和 Ki-67 增殖率≥50%预测鼻腔外 UADT-NKTCL 患者的生存较差,但对鼻腔 UADT-NKTCL 患者无此预测作用。
鼻腔和鼻腔外 UADT-NKTCL 患者具有显著不同的临床特征、免疫表型和预后。鼻腔外 UADT-NKTCL 应被视为与最常见的鼻腔 UADT-NKTCL 原型不同的独立亚组。