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Front-line therapies for elderly patients with transplant-ineligible multiple myeloma and high-risk cytogenetics in the era of novel agents

机译:新药时代下老年不适合移植的多发性骨髓瘤和高危细胞遗传学患者的一线治疗

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In multiple myeloma, certain cytogenetic abnormalities, such as t(4;14), t(14;16), and del(17p), are considered high risk and are associated with worse prognosis. Patients with these high-risk cytogenetic abnormalities, as well as those who are elderly and transplant ineligible, have not experienced the same degree of improved survival outcomes that other patients have seen with recent advances in the treatment of multiple myeloma. To date, no treatment regimen has demonstrated sustained and consistent survival benefits in elderly, transplant-ineligible patients with high-risk cytogenetic abnormalities and newly diagnosed multiple myeloma. Thus, there is an unmet need to identify effective treatment options for these patients and achieve outcomes parity with standard-risk patients. In this review, we assessed clinical trials of both doublet and triplet regimens for newly diagnosed multiple myeloma that included elderly, transplant-ineligible patients with high-risk cytogenetic abnormalities and that provided outcomes data stratified by cytogenetic risk status. We concluded that regimens containing an IMiD agent as the foundation of therapy, combined with agents that have synergistic mechanisms of action—including novel therapies—may in future investigations help overcome the poor prognosis of high-risk cytogenetic abnormalities in this vulnerable patient population.
机译:在多发性骨髓瘤中,某些细胞遗传学异常,例如t(4; 14),t(14; 16)和del(17p),被认为是高风险的,并且与预后较差有关。患有这些高风险细胞遗传学异常的患者,以及那些年老且不适合移植的患者,其生存结果的改善程度未达到其他患者在多发性骨髓瘤治疗方面的最新进展。迄今为止,尚无治疗方案可证明具有高风险细胞遗传学异常和新诊断的多发性骨髓瘤的老年,不适合移植的老年患者具有持续稳定的生存获益。因此,迫切需要为这些患者确定有效的治疗方案,并与标准风险患者取得同样的结果。在这篇综述中,我们评估了新诊断的多发性骨髓瘤的双重和三次治疗方案的临床试验,其中包括老年,不适合移植的高危细胞遗传学异常患者,并提供了以细胞遗传学风险状态分层的结局数据。我们得出的结论是,包含IMiD药物作为治疗基础的方案,以及具有协同作用机制的药物(包括新疗法),可能在未来的研究中有助于克服这一脆弱患者群体中高危细胞遗传学异常的不良预后。

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