Nomura Yuko, Yoshida Shiro, Karube Kennosuke, Takeshita Morishige, Hirose Shinichi, Nakamura Shigeo, Yoshino Tadashi, Kikuchi Masahiro, Ohshima Koichi
Department of Pathology, School of Medicine, Kurume University, Asahimati 67, Kurume, Japan.
Cancer Sci. 2008 Aug;99(8):1564-9. doi: 10.1111/j.1349-7006.2008.00851.x.
Burkitt's lymphoma and atypical Burkitt/Burkitt-like lymphoma (BL/BLL) are considered highly aggressive B-cell lymphomas with a rapid proliferative rate and high rate of apoptosis. The aim of the present study was to confirm whether apoptotic and cell proliferative factors affect BL/BLL clinical outcomes. We retrospectively analyzed the relationship between the clinical and immunophenotypic features of 43 BL/BLL patients by immunohistochemical staining for bcl-2 and double staining for Ki-67 plus caspase-3. In double staining experiments, all patients were divided into high and low groups for the expression of caspase-3, Ki-67, and both Ki-67 and caspase-3, by using the medians of their percentages as limits. The 43 BL/BLL patients were divided into high caspase-3 (n = 19) and low caspase-3 (n = 24) groups. There was a significant difference in the overall survival between the high (77%) and low caspase-3 (33%) groups; the survival rate of patients in the low caspase-3 group who received aggressive short-term chemotherapy (58%) was significantly better than that of patients who received cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP) therapy (17%). All patients positive for bcl-2 were in the low caspase-3 group (high caspase-3 group, 0%; low caspase-3 group, 42%). The overall survival tended to be better in the high caspase-3 and bcl-2-negative group (76%) than in the low caspase-3 and bcl-2-negative (50%) group. In addition, the low caspase-3 and bcl-2-positive group tended to show the worst prognosis (16%). We suggest that caspase-3 may function as an indicator of the prognosis of BL/BLL. Furthermore, intensive short-term chemotherapeutic regimens may improve the prognosis of the patients in the low caspase-3 group.
伯基特淋巴瘤和非典型伯基特/伯基特样淋巴瘤(BL/BLL)被认为是具有快速增殖率和高凋亡率的高度侵袭性B细胞淋巴瘤。本研究的目的是确认凋亡和细胞增殖因子是否影响BL/BLL的临床结局。我们通过免疫组化染色检测bcl-2以及Ki-67和caspase-3双重染色,回顾性分析了43例BL/BLL患者的临床和免疫表型特征之间的关系。在双重染色实验中,以各指标百分比的中位数为界,将所有患者分为caspase-3、Ki-67以及Ki-67和caspase-3高表达组和低表达组。43例BL/BLL患者被分为caspase-3高表达组(n = 19)和caspase-3低表达组(n = 24)。caspase-3高表达组(77%)和低表达组(33%)的总生存率存在显著差异;接受积极短期化疗的caspase-3低表达组患者的生存率(58%)显著高于接受环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)方案治疗的患者(17%)。所有bcl-2阳性患者均在caspase-3低表达组(caspase-3高表达组为0%;caspase-3低表达组为42%)。caspase-3高表达且bcl-2阴性组的总生存率(76%)倾向于高于caspase-3低表达且bcl-2阴性组(50%)。此外,caspase-3低表达且bcl-2阳性组的预后往往最差(16%)。我们认为caspase-3可能作为BL/BLL预后的一个指标。此外,强化短期化疗方案可能改善caspase-3低表达组患者的预后。