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“双打击”细胞遗传学状态可能无法通过基线临床病理特征预测,并且与 B 细胞淋巴瘤患者的总生存高度相关。

'Double-Hit' cytogenetic status may not be predicted by baseline clinicopathological characteristics and is highly associated with overall survival in B cell lymphoma patients.

机构信息

Lymphoma Program, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Br J Haematol. 2014 Aug;166(3):369-74. doi: 10.1111/bjh.12901. Epub 2014 Apr 25.

Abstract

'Double-Hit' (DH) B cell non-Hodgkin lymphomas are characterized by the presence of a MYC rearrangement and additional rearrangement(s) most commonly involving BCL2 and/or BCL6. Patients with DH lymphomas are unlikely to achieve long-term survival when treated with standard immunochemotherapy alone. DH gene rearrangements can be identified through metaphase karyotyping or more sensitive fluorescence in situ hybridization (FISH), although the latter is not routinely performed. We report 53 cases of B cell lymphoma that underwent diagnostic metaphase karyotying or FISH for MYC rearrangements. DH lymphoma was detected in 17 cases. No baseline factor, including age, serum lactate dehydrogenase, stage, International Prognostic Index or histology predicted for DH status. The median overall survival was significantly shorter for DH compared to non-DH lymphoma patients (8·2 vs. 56·8 months, P < 0·001). DH status retained the most statistically significant association with overall survival on multivariate Cox regression analysis. DH status could not be inferred by baseline disease- or patient-related characteristics and was most predictive of overall survival in this cohort of B cell lymphoma patients. These findings support the practice of routine performance of FISH for DH gene rearrangements on B cell lymphoma specimens in order to effectively identify DH patients who may benefit from risk-adapted therapy.

摘要

“双打击”(DH)B 细胞非霍奇金淋巴瘤的特征是存在 MYC 重排,以及常见的额外重排(s),最常涉及 BCL2 和/或 BCL6。单独采用标准免疫化疗治疗 DH 淋巴瘤患者,长期生存的可能性较低。DH 基因重排可以通过中期核型分析或更敏感的荧光原位杂交(FISH)来识别,尽管后者并非常规进行。我们报告了 53 例接受诊断性中期核型分析或 MYC 重排 FISH 的 B 细胞淋巴瘤病例。在 17 例中检测到 DH 淋巴瘤。没有基线因素,包括年龄、血清乳酸脱氢酶、分期、国际预后指数或组织学,可预测 DH 状态。与非 DH 淋巴瘤患者相比,DH 患者的总生存期明显更短(8.2 与 56.8 个月,P<0.001)。多变量 Cox 回归分析显示,DH 状态与总生存期的相关性最具统计学意义。DH 状态不能通过基线疾病或患者相关特征推断,在该队列的 B 细胞淋巴瘤患者中,它是总生存期的最具预测性因素。这些发现支持在 B 细胞淋巴瘤标本中常规进行 FISH 以检测 DH 基因重排的做法,以便有效识别可能从风险适应治疗中受益的 DH 患者。

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