Zucca E, Roggero E, Pinotti G, Pedrinis E, Cappella C, Venco A, Cavalli F
Servizio Oncologico Cantonale, Ospedale San Giovanni, Bellinzona, Switzerland.
Ann Oncol. 1995 Mar;6(3):257-62. doi: 10.1093/oxfordjournals.annonc.a059155.
The term mantle cell lymphoma (MCL) describes a subtype of non-Hodgkin's lymphoma that includes those lymphomas previously defined as centrocytic lymphoma, intermediate lymphocytic lymphoma, and mantle zone lymphoma. Since MCL has only recently been recognised as a distinct entity, the clinical literature is sparse and very little information is available about its treatment.
We retrospectively attempted to analyse the clinical features and outcome of 65 patients with mantle cell lymphoma (MCL) treated from 1979 to 1993 at two institutions in the same geographic area. Univariate (Log-rank test) and multivariate (Cox regression) analyses of the major prognostic factors were performed.
At the time of analysis the median follow-up was 49 months. Median age was 64 years with a range of 27-85 years. The male to female ratio was 2:1. Forty-seven patients (72%) had stage IV at presentation and 20 (31%) had B-symptoms at presentation. The patients usually presented with generalised adenopathy (78% of cases) and bone marrow involvement (58%). Serum LDH were analysed at diagnosis in 61 patients and found to be elevated in 30%. beta 2-Microglobulin was determined at presentation in 42 patients and was higher than normal in 54% of them. In comparison with the other subtypes of NHLs in our series, MCL appears to have a very poor survival pattern. The median overall survival was 42 months. The CR rate was 51% with a median DFS of 44 months. Good performance status, normal LDH, normal beta 2-microglobulin, younger age (< 65 years), and a low prognostic risk according to the International Index were significantly associated (p < 0.05) with a better outcome.
The characteristics of the patients in this study appear to be in general agreement with those in most of the previously reported series except for the somewhat lower rate of bone marrow infiltration observed in this series. Despite the limitations of a retrospective analysis and the lack of randomization between the treatment options, this study seems to suggest a survival advantage with anthracycline-containing regimens in some patients with MCL. However, this benefit was evident only for the patients with favourable International Index prognostic scores (i.e., low- and to low-intermediate-risk disease) who may already have a better prognosis. Patients with intermediate-high and high-risk disease according to the International Index have a poor prognosis regardless of the type of therapy given.
套细胞淋巴瘤(MCL)这一术语描述了非霍奇金淋巴瘤的一种亚型,其中包括那些先前被定义为中心细胞性淋巴瘤、中间淋巴细胞性淋巴瘤和套区淋巴瘤的淋巴瘤。由于MCL直到最近才被确认为一种独特的实体,临床文献稀少,关于其治疗的信息非常有限。
我们回顾性地分析了1979年至1993年在同一地理区域的两家机构接受治疗的65例套细胞淋巴瘤(MCL)患者的临床特征和预后。对主要预后因素进行了单因素(对数秩检验)和多因素(Cox回归)分析。
在分析时,中位随访时间为49个月。中位年龄为64岁,范围为27至85岁。男女比例为2:1。47例患者(72%)初诊时为IV期,20例患者(31%)初诊时有B症状。患者通常表现为全身淋巴结肿大(78%的病例)和骨髓受累(58%)。对61例患者诊断时的血清乳酸脱氢酶(LDH)进行分析,发现30%升高。对42例患者初诊时测定β2-微球蛋白,其中54%高于正常。与我们系列中的其他非霍奇金淋巴瘤亚型相比,MCL的生存模式似乎很差。中位总生存期为42个月。完全缓解(CR)率为51%,中位无病生存期(DFS)为44个月。良好的身体状况、正常的LDH、正常的β2-微球蛋白、较年轻的年龄(<65岁)以及根据国际预后指数(IPI)的低预后风险与较好的预后显著相关(p<0.05)。
本研究中患者的特征似乎与大多数先前报道的系列研究中的特征总体一致,只是本系列中观察到的骨髓浸润率略低。尽管存在回顾性分析的局限性以及治疗方案之间缺乏随机分组,但本研究似乎表明含蒽环类药物方案对某些MCL患者有生存优势。然而,这种益处仅在国际预后指数预后评分良好(即低危和低中危疾病)的患者中明显,这些患者可能本来预后就较好。根据国际预后指数属于中高危和高危疾病的患者,无论接受何种治疗类型,预后都很差。