Clinical significance of gene defects in B-cell lymphomas.

Annika Pasanen, Leo Meriranta, Sirpa Leppä
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引用次数: 0

Abstract

Lymphomas are a heterogenous group of malignant diseases. Identification of sub-groups has created pressure for a more detailed diagnosis and individualized treatment. Although the underlying genetic and molecular pathologic factors of the most common B-cell derived lymphomas, i.e. diffuse large B-cell lymphoma and follicular lymphoma, have become more accurate, prognosis is evaluated and treatment options still selected mainly on the basis of clinical variables. In the future, new generation sequencing methods that are becoming more common in clinical practice will allow the assessment of prognosis and treatment on the basis of biologic and genetic risk factors. To achieve this both comprehensive basic research and clinical drug trials taking the pathogenesis of different diseases into consideration are required.

b细胞淋巴瘤基因缺陷的临床意义。
淋巴瘤是一种异质性的恶性疾病。亚群的确定给更详细的诊断和个体化治疗带来了压力。虽然最常见的b细胞源性淋巴瘤,如弥漫性大b细胞淋巴瘤和滤泡性淋巴瘤的潜在遗传和分子病理因素已经变得更加准确,但评估预后和选择治疗方案仍然主要基于临床变量。未来,在临床实践中越来越普遍的新一代测序方法将允许基于生物和遗传风险因素评估预后和治疗。要做到这一点,需要综合考虑不同疾病发病机制的基础研究和临床药物试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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