复发/难治性多发性骨髓瘤:目前的发展状况

M. Mateos, E. Ocio, V. Gonzalez, J. Dávila
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引用次数: 0

摘要

多发性骨髓瘤(MM)通常对治疗有反应,但无法治愈。在大多数患者中,临床病程的特点是一系列的缓解和复发。对于年轻患者,目前的初始治疗通常包括诱导使用蛋白酶体抑制剂硼替佐米(BOR),单独或联合,然后进行自体干细胞移植(ASCT)。通常只有临床复发才需要治疗;治疗方案应个性化,以考虑诸如对先前治疗的反应、缓解持续时间、所经历的不良反应和可用的治疗方案等因素。有证据表明,许多对BOR有反应的患者将再次对其有反应。初次复发的患者也应考虑进行进一步的ASCT或同种异体移植。临床研究已经导致其他药物被批准用于治疗复发性MM,其中包括来那度胺(一种免疫调节药物),卡非佐米(另一种蛋白酶体抑制剂),波马度胺(一种免疫调节药物),以及最近的帕比诺他(一种去乙酰化酶抑制剂)。这些药物的可用性大大增加了治疗进一步复发的治疗选择。此外,还有一系列令人眼花缭乱的新型药物正处于不同的测试阶段。它们包括上述类别的其他药物,以及单克隆抗体、作用于细胞周期的药物、激酶抑制剂和信号转导途径抑制剂。在未来几年,这些药物的引入可能会进一步提高MM患者的生存率,甚至可能导致治愈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relapsed/Refractory Multiple Myeloma: The Current State of Play
Multiple myeloma (MM) usually responds to treatment but is incurable. The clinical course is characterised, in most patients, by a series of remissions and relapses. For younger patients, the initial treatment currently usually involves induction with the proteasome inhibitor bortezomib (BOR), alone or in combination, followed by an autologous stem cell transplant (ASCT). Usually only clinical relapses require treatment; the treatment plan should be individualised to take into account factors such as response to previous treatment, duration of the remission, adverse effects experienced, and available treatment options. Evidence suggests that many patients who have responded to BOR will respond to it again. Patients at first relapse should also be considered for a further ASCT or an allotransplant. Clinical studies have led to other drugs being approved for treatment of relapsed MM. These include lenalidomide (an immunomodulatory drug), carfilzomib (another proteasome inhibitor), pomalidomide (an immunomodulatory drug), and most recently panobinostat (a deacetylase inhibitor). The availability of these drugs greatly enhances the therapeutic options available to treat further relapses. Moreover, a bewildering array of other novel agents are at various stages in testing. They include other drugs from the classes already mentioned, as well as monoclonal antibodies, drugs acting on the cell cycle, kinase inhibitors, and signal transduction pathway inhibitors. It seems probable that the introduction of these agents in the coming years will further improve the survival of patients with MM, and may even lead to a cure.
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