Primary non-Hodgkin's lymphoma of the nose and nasopharynx: Clinical features, tumor immunophenotype, and treatment outcome in 113 patients

被引:318
作者
Cheung, MMC
Chan, JKC
Lau, WH
Foo, W
Chan, PTM
Ng, CS
Ngan, RKC
机构
[1] Queen Elizabeth Hosp, Dept Radiotherapy & Oncol, Kowloon, Hong Kong
[2] Queen Elizabeth Hosp, Dept Pathol, Kowloon, Hong Kong
[3] Caritas Med Ctr, Dept Pathol, Hong Kong, Hong Kong
关键词
D O I
10.1200/JCO.1998.16.1.70
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To study the clinical features and outcome for primary non-Hodgkin's lymphomas of the nose/nasopharynx (NNP-NHLs) according to immunophenotype. Patients and Methods: One hundred thirteen Chinese patients with primary NNP-NHLs that belonged to the categories E, F, G, or H according to the Working Formulation (WF), with full immunophenotypic data and complete clinical follow-up data, were analyzed in this retrospective study. Results: Ninety (79.6%) patients had localised (stage I or II) disease, while 23 (20.4%) had stage III or IV disease. The lymphomas in 51 (45.1%), 24 (21.3%), and 38 (33.6%) patients showed natural kilter (NK)/T-(CD56-positive), T-cell, and B-cell immunophenotype, respectively, Seventy-three patients (65.8%) achieved a complete remission, of whom 34 (46.6%) subsequently relapsed. The median follow-up time for those alive was 88 months, The 5-year actuarial disease-free and overall survival rates were 34.4% and 37.9%, respectively. Multivariate analysis showed that only stage and immunophenotype were significant for survival. NK/T lymphomas were distinctive among the three immunophenotypes in the following aspects: the highest male-to-female ratio, more frequent involvement of the nasal cavity alone, higher risk of dissemination to the skin, more frequent development of hemophagocytic syndrome, and the worst prognosis (overall median survival, 12.5 months). Conclusion: The three immunophenotypes studied ape shown to exhibit different clinical patterns, Since the NK/T phenotype carries the worst prognosis, patients who present with NNP-NHL, should have their tumors analyzed for CD56 expression. (C) 1998 by American Society of Clinical Oncology.
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页码:70 / 77
页数:8
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