D'Amore F, Christensen B E, Thorling K, Pedersen M, Jensen M K, Boesen A M, Andersen E, Johansen P, Mortensen L S
Department of Haematology, Odense University Hospital, Denmark.
Leuk Lymphoma. 1993 Dec;12(1-2):69-77. doi: 10.3109/10428199309059573.
During the period January 1983 to January 1988 1597 newly diagnosed cases of non-Hodgkin's lymphoma (NHL) were included in a Western Danish population-based NHL registry. Of these, 31% (N = 496) were low-grade NHL (LG-NHL) consisting of (Kiel): 9% lymphocytic (LY), 27% lymphoplasmacytic/-cytoid (IC), 53% follicular centroblastic/-centrocytic (CB/CCf) and 11% unclassifiable low-grade. LG-NHL (age range: 26-94 yrs, median: 64 yrs; M/F ratio: 0.8) had an age-standardised incidence rate (IR) of 2.7/10(5)/yr. Age-specific IR's showed an age-related exponential rise in all subtypes except for CB/CCf. Compared with the intermediate (IG)- and high-grade (HG) group, LG-NHL had more female cases (M/F ratio: 0.79 vs. 1.2; p = 0.0002), a higher frequency of stage III-IV disease (66% vs. 53%; p < 0.00005) and of bone marrow involvement (39% vs. 19%; p < 0.00005). A later revision of all IC cases (N = 132) distinguished 79 non-polymorphic (ICnp) from 25 polymorphic (ICp) cases; 28 cases were differently classified. In 34 LG-NHL patients histologic transformation was verified: CB/CCf to CB diffuse (22 pts) and LY to immunoblastic or CB type (6 pts). The 7-yr survival for LG-NHL was 63% (IG: 48%, HG: 38%; p < 0.00005). A Cox-regression analysis identified the following adverse prognostic factors for survival in LG-NHL: age > 50 with a relative risk (RR) of 3.2, hepatic involvement (RR = 2.1), elevated s-LDH (RR = 1.9), B-symptoms (RR = 1.8) and IC histology (ICnp+ICp) (RR = 1.7).(ABSTRACT TRUNCATED AT 250 WORDS)
在1983年1月至1988年1月期间,1597例新诊断的非霍奇金淋巴瘤(NHL)病例被纳入丹麦西部基于人群的NHL登记处。其中,31%(N = 496)为低级别NHL(LG - NHL),包括(基尔分类):9%淋巴细胞型(LY)、27%淋巴浆细胞/细胞样型(IC)、53%滤泡中心母细胞/中心细胞型(CB/CCf)和11%无法分类的低级别类型。LG - NHL(年龄范围:26 - 94岁,中位数:64岁;男/女比例:0.8)的年龄标准化发病率(IR)为2.7/10⁵/年。除CB/CCf外,所有亚型的年龄特异性发病率均呈现与年龄相关的指数上升。与中级(IG)和高级别(HG)组相比,LG - NHL女性病例更多(男/女比例:0.79对1.2;p = 0.0002),III - IV期疾病(66%对53%;p < 0.00005)和骨髓受累(39%对19%;p < 0.00005)的频率更高。对所有IC病例(N = 132)的后期修订区分出79例非多形性(ICnp)和25例多形性(ICp)病例;28例分类不同。在34例LG - NHL患者中证实有组织学转化:CB/CCf转化为弥漫性CB(22例),LY转化为免疫母细胞型或CB型(6例)。LG - NHL的7年生存率为63%(IG:48%,HG:38%;p < 0.00005)。Cox回归分析确定了LG - NHL生存的以下不良预后因素:年龄>50岁,相对风险(RR)为3.2,肝脏受累(RR = 2.1),血清乳酸脱氢酶(s - LDH)升高(RR = 1.9),B症状(RR = 1.8)和IC组织学(ICnp + ICp)(RR = 1.7)。(摘要截断于250字)