Nomura Yuko, Karube Kennosuke, Suzuki Ritsuro, Ying Guo, Takeshita Morishige, Hirose Shinichi, Nakamura Shigeo, Yoshino Tadashi, Kikuchi Masahiro, Ohshima Koichi
Department of Pathology, School of Medicine, Kurume University, Asahimati 67, Kurume 830-0011, Japan.
Cancer Sci. 2008 Feb;99(2):246-52. doi: 10.1111/j.1349-7006.2007.00681.x.
The aim of the present study was to estimate optimum chemotherapeutic regimens for high-grade mature B-cell lymphoma cases with Burkitt-like morphology (Burkitt's lymphoma [BL]/Burkitt-like lymphoma [BLL]) patients. We analyzed 72 BL/BLL, including 36 with the c-myc translocation (molecular BL [mBL]), 20 without it (mBL-like), and 16 in whom we were uncertain regarding the existence of the c-myc translocation, and compared them with 182 diffuse large B-cell lymphoma (DLBCL) cases. On clinical and immunophenotypic analysis, the typical BL immunophenotype (CD10 positive, bcl-2 negative, and Ki-67 index >or=95%) was noted in 23 (66%) and 11 (55%) of the 35 mBL and 20 mBL-like patients, respectively. The presence of the c-myc translocation and typical immunophenotype in BL did not affect the overall survival of BL/BLL. There were no significant differences between the overall survival of DLBCL (45%) and BL/BLL (50%, P = 0.85). However, the overall survival of BL/BLL patients who received cyclophosphamide, doxorubicin, vincristine, and prednisolone-related therapy (22%) was significantly lower than that of DLBCL patients (P = 0.01). In contrast, the overall survival of BL/BLL patients who received aggressive short-term chemotherapy (75%) was better than that of the patients who received cyclophosphamide, doxorubicin, vincristine, and prednisolone therapy (P < 0.01). The finding was confirmed by multivariate analysis (hazard ratio 4.4; confidence interval 2.0-9.7; P = 0.0003). We concluded that aggressive short-term chemotherapy improves survival in BL/BLL, regardless of its genetic and immunophenotypic features.
本研究的目的是评估针对具有伯基特样形态的高级别成熟B细胞淋巴瘤病例(伯基特淋巴瘤[BL]/伯基特样淋巴瘤[BLL])患者的最佳化疗方案。我们分析了72例BL/BLL患者,其中36例存在c-myc易位(分子学BL [mBL]),20例不存在c-myc易位(mBL样),16例无法确定是否存在c-myc易位,并将他们与182例弥漫性大B细胞淋巴瘤(DLBCL)病例进行比较。在临床和免疫表型分析中,35例mBL患者中的23例(66%)和20例mBL样患者中的11例(55%)表现出典型的BL免疫表型(CD10阳性、bcl-2阴性且Ki-67指数≥95%)。BL中c-myc易位和典型免疫表型的存在并不影响BL/BLL的总生存期。DLBCL的总生存期(45%)与BL/BLL的总生存期(50%,P = 0.85)之间无显著差异。然而,接受环磷酰胺、阿霉素、长春新碱和泼尼松龙相关治疗的BL/BLL患者的总生存期(22%)显著低于DLBCL患者(P = 0.01)。相比之下,接受积极短期化疗的BL/BLL患者的总生存期(75%)优于接受环磷酰胺、阿霉素、长春新碱和泼尼松龙治疗的患者(P < 0.01)。多因素分析证实了这一发现(风险比4.4;置信区间2.0 - 9.7;P = 0.0003)。我们得出结论,积极的短期化疗可提高BL/BLL患者的生存率,无论其基因和免疫表型特征如何。