Department of Pathology, School of Medicine, Kurume University, Kurume, Japan.
Cancer Sci. 2010 Mar;101(3):806-14. doi: 10.1111/j.1349-7006.2009.01433.x. Epub 2009 Nov 13.
Although the 2008 World Health Organization classification defines two subtypes of mantle cell lymphoma (MCL), classical and aggressive, we often encounter MCL with both features in the same site. We named this feature "MCL with focal aggressive form (intermediate MCL)". In the present study, we reclassified 237 patients with cyclin D1 (CCND1)-positive MCL on the basis of the concept of intermediate MCL, and analyzed the correlation of this reclassification with immunohistochemical detection of CCND1, Ki-67, p53, p27(Kip1), and p21(WAF/Cip1). The median overall survival was 77, 31, and 18 months for classical, intermediate, and aggressive MCL, respectively, showing a statistically significant difference (P < 0.0001). The expression levels of CCND1, Ki-67, p53, and p21(WAF/Cip1) in aggressive MCL (mean 80.1 +/- 27.8%, 73.7 +/- 28.9%, 31.0 +/- 69.0%, and 10.4 +/- 24.8%, respectively) were higher than those in classical MCL (mean 58.1 +/- 36.7%, 25.2 +/- 25.5%, 6.5 +/- 24.3%, and 2.5 +/- 13.0%, respectively) and intermediate MCL (mean 75.7 +/- 31.4%, 30.8 +/- 33.3%, 21.0 +/- 57.4%, and 4.8 +/- 16.5%, respectively). Significantly different levels of Ki-67 and p21(WAF/Cip1) were only recognized between intermediate and aggressive (P < 0.05 and P < 0.0001, respectively), whereas those of CCND1 and p53 were only between classical and intermediate (P < 0.0001 and P < 0.05, respectively). There were no significant differences in p27(Kip1) among the three groups. The subsequent discriminant analysis with independent prognostic factors clearly demonstrated that the morphological evolution of MCL occurs in parallel with increased labeling index of CCND1 and Ki-67. The diagnosis of intermediate MCL thus proved to be of major significance and should enable the design of more tailored therapies.
虽然 2008 年世界卫生组织(WHO)分类定义了两种套细胞淋巴瘤(MCL)亚型,即经典型和侵袭性,但我们经常在同一部位遇到同时具有这两种特征的 MCL。我们将这种特征命名为“具有局灶性侵袭形式的 MCL(中间型 MCL)”。在本研究中,我们基于中间型 MCL 的概念,对 237 例 cyclin D1(CCND1)阳性 MCL 患者进行了重新分类,并分析了这种重新分类与 CCND1、Ki-67、p53、p27(Kip1)和 p21(WAF/Cip1)免疫组化检测的相关性。经典型、中间型和侵袭性 MCL 的中位总生存期分别为 77、31 和 18 个月,差异具有统计学意义(P<0.0001)。侵袭性 MCL 的 CCND1、Ki-67、p53 和 p21(WAF/Cip1)表达水平(平均值分别为 80.1±27.8%、73.7±28.9%、31.0±69.0%和 10.4±24.8%)高于经典型 MCL(平均值分别为 58.1±36.7%、25.2±25.5%、6.5±24.3%和 2.5±13.0%)和中间型 MCL(平均值分别为 75.7±31.4%、30.8±33.3%、21.0±57.4%和 4.8±16.5%)。中间型和侵袭性 MCL 之间仅 Ki-67 和 p21(WAF/Cip1)的水平有显著差异(P<0.05 和 P<0.0001),而 CCND1 和 p53 仅在经典型和中间型之间有差异(P<0.0001 和 P<0.05)。三组之间 p27(Kip1)无显著差异。随后对独立预后因素进行判别分析,结果表明 MCL 的形态学演变与 CCND1 和 Ki-67 标记指数的增加平行发生。因此,中间型 MCL 的诊断具有重要意义,应能设计更适合的治疗方案。