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原发性局限性Ⅰ期和Ⅱ期鼻咽非霍奇金淋巴瘤:一项为期17年的单机构回顾性研究经验。

Primary localized stages I and II non-Hodgkin's lymphoma of the nasopharynx: a retrospective 17-year single institutional experience.

作者信息

Mohammadianpanah Mohammad, Ahmadloo Niloofar, Mozaffari Mohammad Amin Nazer, Mosleh-Shirazi Mohammad Amin, Omidvari Shapour, Mosalaei Ahmad

机构信息

Department of Radiation Oncology, Nemazee Hospital, Shiraz University of Medical Science, Iran.

出版信息

Ann Hematol. 2009 May;88(5):441-7. doi: 10.1007/s00277-008-0627-0. Epub 2008 Oct 18.

Abstract

The aim of this retrospective study was to define the natural history, clinicopathological findings, prognostic factors, and treatment outcome of 43 patients with localized stages I and II primary non-Hodgkin's lymphoma (NHL) of the nasopharynx, followed up in a single institution over a 17-year period. Forty-three (13 women and 30 men) consecutive patients with localized stages I (N = 12) and II (N = 31) primary nasopharyngeal NHL were treated in our institution between 1990 and 2007. The pathologic reports were classified according to the International Working Formulation (N = 22) or Revised European-American Lymphoma classification (N = 21). The vast majority of patients (88%) were managed with a sequential combination of chemotherapy and radiation therapy. Chemotherapy mainly consisted of 4-8 (median 6) cycles of CHOP regimen (cyclophosphamide, doxorubicin, vincristine and prednisolone). Involved-field radiation therapy with a median dose of 44 Gy was delivered to the primary site and entire cervical lymph nodes. The median age of the patients was 53 years (range, 6 to 86 years). The majority of the patients (70%) had high-grade histology. B-cell types represented 67% of the cases, among which diffuse large B cell was the most common histological subtype. After a median follow-up of 70 months, the 5-year disease-free survival and overall survival were 58.8% and 70.6%, respectively. In multivariate analysis, age less than or equal to 30 years (hazard ratio (HR) = 5.32, 95% confidence interval (CI) = 1.69-16.76), elevated serum lactate dehydrogenase level (HR = 3.69, 95% CI = 1.43-9.51), and modified International Prognostic Index with more than or equal to two risk factors (HR = 17.99, 95% CI = 2.32-139.30) retained statistical significance. Our limited data suggest that primary nasopharyngeal NHL tends to have aggressive histology and unfavorable clinical course with poor outcome, despite a considerably localized disease at the time of presentation and high frequency of complete initial response rates. Combined modality therapy should be considered for the majority of patients with primary localized nasopharyngeal NHL.

摘要

这项回顾性研究旨在明确43例局限性I期和II期原发性鼻咽非霍奇金淋巴瘤(NHL)患者的自然病程、临床病理特征、预后因素及治疗结果,这些患者在一家机构接受了为期17年的随访。1990年至2007年间,我们机构共治疗了43例(13例女性和30例男性)连续性局限性I期(n = 12)和II期(n = 31)原发性鼻咽NHL患者。病理报告根据国际工作分类法(n = 22)或修订的欧美淋巴瘤分类法(n = 21)进行分类。绝大多数患者(88%)接受了化疗和放疗的序贯联合治疗。化疗主要包括4 - 8个(中位6个)周期的CHOP方案(环磷酰胺、阿霉素、长春新碱和泼尼松龙)。对原发部位和整个颈部淋巴结进行中位剂量为44 Gy的累及野放疗。患者的中位年龄为53岁(范围6至86岁)。大多数患者(70%)为高级别组织学类型。B细胞类型占病例的67%,其中弥漫性大B细胞是最常见的组织学亚型。中位随访70个月后,5年无病生存率和总生存率分别为58.8%和70.6%。多因素分析显示,年龄小于或等于30岁(风险比(HR)= 5.32,95%置信区间(CI)= 1.69 - 16.76)、血清乳酸脱氢酶水平升高(HR = 3.69,95% CI = 1.43 - 9.51)以及具有两个或更多危险因素的改良国际预后指数(HR = 17.99,95% CI = 2.32 - 139.30)具有统计学意义。我们有限的数据表明,原发性鼻咽NHL尽管在初诊时疾病局限且初始完全缓解率较高,但往往具有侵袭性组织学特征和不良临床病程及预后。对于大多数原发性局限性鼻咽NHL患者应考虑采用综合治疗模式。

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