Wilson Matthew R, Barrett Aisling, Cheah Chan Yoon, Eyre Toby A
Beatson West of Scotland Cancer Centre, Glasgow, UK.
Haematology and Cancer Centre, Oxford University Hospitals National Health Service (NHS) Foundation Trust, Oxford, UK.
Br J Haematol. 2023 Apr;201(2):185-198. doi: 10.1111/bjh.18697. Epub 2023 Feb 20.
Mantle cell lymphoma (MCL) is a mature B-cell lymphoma with a variable clinical course and historically poor prognosis. Management is challenging in part due to the heterogeneity of the disease course, with indolent and aggressive subtypes now well recognised. Indolent MCL is often characterised by a leukaemic presentation, SOX11 negativity and low proliferation index (Ki-67). Aggressive MCL is characterised by rapid onset widespread lymphadenopathy, extra-nodal involvement, blastoid or pleomorphic histology and high Ki-67. Tumour protein p53 (TP53) aberrations in aggressive MCL are recognised with clear negative impact on survival. Until recently, trials have not addressed these specific subtypes separately. With the increasing availability of targeted novel agents and cellular therapies, the treatment landscape is constantly evolving. In this review, we describe the clinical presentation, biological factors, and specific management considerations of both indolent and aggressive MCL and discuss current and potential future evidence which may help move to a more personalised approach.
套细胞淋巴瘤(MCL)是一种成熟B细胞淋巴瘤,临床病程多变,历史上预后较差。管理具有挑战性,部分原因是疾病进程的异质性,惰性和侵袭性亚型现已得到充分认识。惰性MCL通常表现为白血病形式、SOX11阴性和低增殖指数(Ki-67)。侵袭性MCL的特征是起病迅速、广泛的淋巴结病、结外受累、母细胞样或多形性组织学以及高Ki-67。侵袭性MCL中的肿瘤蛋白p53(TP53)异常已得到认可,对生存有明显负面影响。直到最近,试验尚未分别针对这些特定亚型。随着靶向新型药物和细胞疗法的可用性不断增加,治疗格局正在不断演变。在本综述中,我们描述了惰性和侵袭性MCL的临床表现、生物学因素和具体管理考虑因素,并讨论了当前和潜在的未来证据,这些证据可能有助于转向更个性化的方法。