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多发性骨髓瘤的疾病生物学能改变吗?

Can we change the disease biology of multiple myeloma?

机构信息

The Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.

出版信息

Leuk Res. 2012 Nov;36 Suppl 1(0 1):S3-12. doi: 10.1016/S0145-2126(12)70003-6.

Abstract

Despite improvements in disease management, multiple myeloma (MM) remains incurable. Conventional treatment methods are unsatisfactory, leading to a pattern of regression and remission, and ultimately failure. This pattern suggests that one of the possible strategies for improving outcomes is continuous therapy to maintain suppression of the surviving tumor cells. Optimal management of MM requires potent agents and modalities with direct tumoricidal activity, which can also provide continuous suppression of the residual tumor to prevent disease relapse. Immunomodulatory agents exert immunomodulatory and tumoricidal effects, and cause disruption of stromal cell support from the bone marrow microenvironment. Therefore continuous therapy with immunomodulatory agents may be able to provide both tumor reduction and tumor suppression, enabling physicians to consider the possibility of incorporating continuous therapy into the treatment paradigm of patients with MM.

摘要

尽管疾病管理有所改善,但多发性骨髓瘤 (MM) 仍然无法治愈。常规治疗方法并不令人满意,导致疾病出现复发和缓解的模式,最终治疗失败。这种模式表明,改善预后的可能策略之一是进行持续治疗,以维持对存活肿瘤细胞的抑制作用。MM 的最佳治疗需要具有直接杀瘤活性的强效药物和方法,这些方法还可以持续抑制残留肿瘤,以预防疾病复发。免疫调节剂具有免疫调节和杀瘤作用,并破坏骨髓微环境中基质细胞的支持。因此,免疫调节剂的持续治疗可能能够同时实现肿瘤缩小和肿瘤抑制,使医生能够考虑将持续治疗纳入 MM 患者的治疗模式。

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