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一种预防老年患者癌症化疗期间造血功能衰竭的积极方法:临时细胞周期阻滞。

A Proactive Approach to Prevent Hematopoietic Exhaustion During Cancer Chemotherapy in Older Patients: Temporary Cell-Cycle Arrest.

作者信息

Balducci Lodovico, Falandry Claire, List Alan

机构信息

Emeritus Moffitt Cancer Center, 12902 Usf Magnolia Dr, Tampa, FL, 33612, USA.

Service de Gériatrie, Centre Hospitaliser Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

出版信息

Drugs Aging. 2023 Mar;40(3):263-272. doi: 10.1007/s40266-022-01005-1. Epub 2023 Jan 30.

Abstract

Age is associated with the decline of multiple organ systems. In older patients, hematological toxicities associated with chemotherapy are often dose limiting, impairing dose intensity and treatment efficacy. Contrary to the classical path using growth factors to activate tissue regeneration, a novel strategy is emerging to prevent chemotherapy toxicity that involves temporary cell-cycle arrest of normal cells, such as hematopoietic or epithelial precursors. This proactive approach may allow the sparing of the stem cell reserve of these tissues. Two molecules are included in this new category, trilaciclib and ALRN-6924, which induce cell-cycle arrest by two different pathways. Previous approaches, such as the use of myelopoietic growth factors, were reactive and they might even have accelerated the depletion of stem cells by enhancing the commitment of these elements. Trilaciclib causes cell-cycle arrest by CDK 4/6 inhibition and ALRN-6924 by p53 activation. In a pooled analysis of three randomized phase II studies of patients with small cell lung cancer, trilaciclib prevented neutropenia, thrombocytopenia, and anemia. Similar chemoprotective results were observed with ALRN-6924 in an open-label phase Ib study of patients with p53-mutated small cell lung cancer. Trilaciclib is now approved as a myelopreservation agent in patients with extensive-stage small cell lung cancer. ALRN-6924 is currently in phase Ib clinical development in patients with p53-mutated cancer. In addition to preserving the normal hemopoietic pool, these drugs promise to preserve the stem cell reserve of other normal tissues with high turnover, preventing potentially other dose-limiting toxicities, such as mucositis and diarrhea. An "ex vivo" study provided early evidence that ALRN-6924 may prevent chemotherapy-induced alopecia. By affording protection from multiple toxicities with a single drug, trilaciclib and ALRN-6924 have the potential to transform the current standards of supportive care for oncology patients and may prevent the depletion of tissue stem cells already compromised with age.

摘要

年龄与多个器官系统的衰退相关。在老年患者中,化疗相关的血液学毒性往往会限制剂量,损害剂量强度和治疗效果。与使用生长因子激活组织再生的传统途径相反,一种新的预防化疗毒性的策略正在兴起,该策略涉及使正常细胞(如造血或上皮前体细胞)暂时停滞于细胞周期。这种积极主动的方法可能会使这些组织的干细胞储备得以保留。这一新类别中包括两种分子,即曲拉西利和ALRN-6924,它们通过两种不同途径诱导细胞周期停滞。以前的方法,如使用骨髓生长因子,是被动反应性的,甚至可能通过增强这些细胞成分的分化而加速干细胞的耗竭。曲拉西利通过抑制CDK 4/6使细胞周期停滞,而ALRN-6924则通过激活p53使细胞周期停滞。在一项对三项小细胞肺癌患者随机II期研究的汇总分析中,曲拉西利预防了中性粒细胞减少、血小板减少和贫血。在一项针对p53突变的小细胞肺癌患者的开放标签Ib期研究中,使用ALRN-6924也观察到了类似的化学保护结果。曲拉西利现已被批准作为广泛期小细胞肺癌患者的骨髓保护剂。ALRN-6924目前正处于针对p53突变癌症患者的Ib期临床开发阶段。除了保留正常的造血池外,这些药物有望保留其他更新换代快的正常组织的干细胞储备,预防潜在的其他剂量限制性毒性,如粘膜炎和腹泻。一项“离体”研究提供了早期证据,表明ALRN-6924可能预防化疗引起的脱发。通过用单一药物提供针对多种毒性的保护,曲拉西利和ALRN-6924有可能改变目前肿瘤患者支持性护理的标准,并可能防止已经因年龄增长而受损的组织干细胞耗竭。

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