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套细胞淋巴瘤是否应该有标准疗法?

Should there be a standard therapy for mantle cell lymphoma?

机构信息

Department of Medical Oncology, Fox Chase Cancer Center, 333 Cottman Avenue, PA 19111 USA.

出版信息

Future Oncol. 2011 Feb;7(2):227-37. doi: 10.2217/fon.10.189.

Abstract

Mantle cell lymphoma (MCL) is an uncommon subtype of B-cell lymphoma that is characterized by monoclonal B cells that express CD5 on their surface, but not CD23, and harbor the t(11:14) chromosomal translocation that leads to dysregulated expression of cyclin D1. MCL is a biologically and clinically heterogeneous disease. It has the unfavorable characteristics of both aggressive and indolent lymphoma in that MCL is not curable with current standard therapy, yet patients have a shorter survival compared with other indolent histology. MCL is incurable, yet more intensive therapy does lead to longer disease-free intervals; therefore, treatment must be designed to optimize survival while maintaining quality of life. Thus, therapy should be individualized based on both the clinical behavior of the lymphoma and the patient's status. While there is no clear standard therapy that can be recommended for all patients, there may be an optimal choice for each patient. Knowledge of the expected clinical benefits and toxicities of various approaches will allow the physician and patient to appropriately select the therapy.

摘要

套细胞淋巴瘤(MCL)是一种罕见的 B 细胞淋巴瘤亚型,其特征为表面表达 CD5 的单克隆 B 细胞,但不表达 CD23,并存在导致 cyclin D1 失调表达的 t(11:14)染色体易位。MCL 是一种生物学和临床异质性疾病。它具有侵袭性和惰性淋巴瘤的不利特征,即目前的标准治疗无法治愈 MCL,但与其他惰性组织学相比,患者的生存期更短。MCL 无法治愈,但更强化的治疗确实会导致无病间期延长;因此,治疗必须在优化生存的同时维持生活质量。因此,治疗应根据淋巴瘤的临床行为和患者的状况进行个体化。虽然没有可以推荐给所有患者的明确标准治疗方法,但可能对每个患者都有最佳选择。了解各种方法的预期临床益处和毒性将使医生和患者能够适当地选择治疗方法。

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