Kim Gwi Eon, Koom Woong Sub, Yang Woo-Ick, Lee Sang-Wook, Keum Ki Chang, Lee Chang Geol, Suh Chang Ok, Hahn Jee Sook, Roh Jae Kyung, Kim Joo Hang
Department of Radiation Oncology, Yonsei Cancer Center, Yonsei University, College of Medicine, Brain Korea 21 Project for Medical Science, Seodaemoon-Gu, Shinchon-Dong 134, Seoul 120-752, Korea.
Head Neck. 2004 Jul;26(7):584-93. doi: 10.1002/hed.20015.
The purpose of this study was to investigate the clinical relevance of subtypes categorized by immunophenotypic analysis in primary sinonasal lymphomas.
Eighty patients with localized non-Hodgkin's lymphoma involving the nasal cavity and/or paranasal sinuses were divided into three subtypes on the basis of their immunohistochemical findings: (A) B-cell lymphoma (n = 19), (B) T-cell lymphoma (n = 27), and (C) natural killer (NK)/T-cell lymphoma (n = 34). The clinicopathologic profiles, immunophenotypic data, patterns of treatment failure, and survival data among the three patient groups were retrospectively compared.
The nasal cavity was the predominant site of involvement in T-cell and NK/T-cell lymphoma, whereas sinus involvement without nasal disease was common in B-cell lymphoma. Systemic B symptoms were frequently observed in NK/T-cell lymphoma. Almost all patients with NK/T-cell lymphoma showed a strong association with the Epstein-Barr virus by in situ hybridization studies. Sixty-five patients (81%) patients achieved complete remission after initial treatment, but 36 (55%) of these subsequently experienced treatment failure. Although there were no significant differences in locoregional failure rates among the patients of the three groups, distant failure was far more common in B-cell or NK/T-cell lymphoma than in T-cell lymphoma (p =.005). Most B-cell lymphoma cases showed a predilection for sites of systemic failure in the nodal and extranodal sites below the diaphragm, such as the paraaortic lymph nodes or the gastrointestinal (GI) tract, whereas patients with NK/T-cell lymphoma showed an increased risk of systemic dissemination to the skin, testes, or GI tract, including the development of hemophagocytic syndrome. The 5-year actuarial and disease-free survival rates for all patients were 57% and 51%, respectively. Of the three subtypes of primary sinonasal lymphomas, T-cell lymphoma seemed to carry the most favorable prognosis and NK/T-cell lymphoma the worst. (The 5-year actuarial survival rate was 57% for B-cell lymphoma, 80% for T-cell lymphoma, 37% for NK/T-cell lymphoma; p =.02, log-rank.) By univariate and multivariate analyses, immunophenotype was identified as the most important prognostic factor.
Our data indicate that the three subtypes of primary sinonasal lymphomas classified by immunohistochemical studies exhibit different clinical profiles, different patterns of failure, and different treatment outcomes. Given these observations, it is concluded that the recognition of these distinct subsets, diagnosed on the basis of immunophenotypic study, is very important and clinically relevant in predicting their potential behavior and prognosis.
本研究旨在探讨原发性鼻窦淋巴瘤免疫表型分析所分类别的临床相关性。
80例局限于鼻腔和/或鼻窦的非霍奇金淋巴瘤患者根据免疫组化结果分为三个亚型:(A)B细胞淋巴瘤(n = 19),(B)T细胞淋巴瘤(n = 27),以及(C)自然杀伤(NK)/T细胞淋巴瘤(n = 34)。回顾性比较三组患者的临床病理特征、免疫表型数据、治疗失败模式及生存数据。
鼻腔是T细胞和NK/T细胞淋巴瘤的主要受累部位,而鼻窦受累且无鼻腔病变在B细胞淋巴瘤中较为常见。全身B症状在NK/T细胞淋巴瘤中经常出现。通过原位杂交研究,几乎所有NK/T细胞淋巴瘤患者均显示与EB病毒有强关联。65例(81%)患者初始治疗后达到完全缓解,但其中36例(55%)随后出现治疗失败。尽管三组患者局部区域失败率无显著差异,但远处失败在B细胞或NK/T细胞淋巴瘤中比在T细胞淋巴瘤中更为常见(p = 0.005)。大多数B细胞淋巴瘤病例倾向于在横膈以下的淋巴结和结外部位出现全身衰竭,如腹主动脉旁淋巴结或胃肠道,而NK/T细胞淋巴瘤患者出现全身播散至皮肤、睾丸或胃肠道的风险增加,包括噬血细胞综合征的发生。所有患者的5年精算生存率和无病生存率分别为57%和51%。在原发性鼻窦淋巴瘤的三种亚型中,T细胞淋巴瘤似乎预后最佳,NK/T细胞淋巴瘤最差。(B细胞淋巴瘤的5年精算生存率为57%,T细胞淋巴瘤为80%,NK/T细胞淋巴瘤为37%;p = 0.02,对数秩检验。)通过单因素和多因素分析,免疫表型被确定为最重要的预后因素。
我们的数据表明,通过免疫组化研究分类的原发性鼻窦淋巴瘤的三种亚型表现出不同的临床特征、不同的失败模式和不同的治疗结果。基于这些观察结果,得出结论:基于免疫表型研究诊断出的这些不同亚组对于预测其潜在行为和预后非常重要且具有临床相关性。