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细胞动力学驱动的细胞毒化疗后骨髓保护:从旧观念到新的临床方法。

Cytokinetic-driven myeloprotection after cytotoxic chemotherapy: from an old idea to a new clinical approach.

机构信息

Service of Pneumo-Oncology, Pneumology Unit, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.

Department of Surgical, Medical and Molecular Pathology and Critical Care Medicine, University of Pisa, Pisa, Italy.

出版信息

Support Care Cancer. 2022 Sep;30(9):7057-7060. doi: 10.1007/s00520-022-07084-5. Epub 2022 Apr 28.

DOI:10.1007/s00520-022-07084-5
PMID:35484313
Abstract

Chemotherapy is the backbone of the treatment of several solid tumours and lymphomas. Myelotoxicity is often a dose-limiting toxicity and myeloprotection has always been investigated. In fact, over the years, several approaches have been studied in order to reduce the incidence of haematological toxicities and allow patients to receive effective, full-dose, chemotherapy. After the use of stimulating factors, such as granulocyte colony-stimulating factors and erythropoiesis-stimulating agents, in the very last years, a new approach has emerged. Trilaciclib, a cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor, has been studied and it has been demonstrated in several clinical trials to reduce the incidence of myelotoxicity in small-cell lung cancer patients treated with chemotherapy or chemo-immunotherapy. Its potential role has not been fully studied yet, but it represents a highly effective tool to reduce myelotoxicity, widen the applicability of full-dose chemotherapy, even in frailer patients, and finally to increase the efficacy of chemotherapy in those tumours where relative dose intensity is a standard to achieve to get the best clinical results.

摘要

化疗是治疗多种实体瘤和淋巴瘤的基础。骨髓抑制通常是剂量限制毒性,因此一直都在进行骨髓保护的研究。事实上,多年来,为了降低血液学毒性的发生率并使患者能够接受有效、全剂量的化疗,已经研究了几种方法。在过去几年中,除了使用粒细胞集落刺激因子和红细胞生成刺激剂等刺激因子外,还出现了一种新方法。三氯氰胺,一种细胞周期蛋白依赖性激酶 4 和 6(CDK4/6)抑制剂,已在多项临床试验中进行了研究,结果表明它可降低化疗或化疗免疫治疗的小细胞肺癌患者发生骨髓抑制的发生率。其潜在作用尚未得到充分研究,但它是一种非常有效的降低骨髓抑制的工具,可扩大全剂量化疗的适用性,即使在体质较弱的患者中也是如此,最终还可提高那些相对剂量强度是获得最佳临床效果的标准的肿瘤的化疗疗效。

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Support Care Cancer. 2022 Sep;30(9):7057-7060. doi: 10.1007/s00520-022-07084-5. Epub 2022 Apr 28.
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本文引用的文献

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Myeloprotective Effects of Trilaciclib Among Patients with Small Cell Lung Cancer at Increased Risk of Chemotherapy-Induced Myelosuppression: Pooled Results from Three Phase 2, Randomized, Double-Blind, Placebo-Controlled Studies.曲拉西利在化疗引起的骨髓抑制风险增加的小细胞肺癌患者中的骨髓保护作用:三项2期、随机、双盲、安慰剂对照研究的汇总结果
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Trilaciclib prior to chemotherapy reduces the usage of supportive care interventions for chemotherapy-induced myelosuppression in patients with small cell lung cancer: Pooled analysis of three randomized phase 2 trials.化疗前使用 Trilaciclib 可减少小细胞肺癌患者因化疗引起的骨髓抑制的支持性护理干预:三项随机 2 期试验的汇总分析。
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Myelopreservation with the CDK4/6 inhibitor trilaciclib in patients with small-cell lung cancer receiving first-line chemotherapy: a phase Ib/randomized phase II trial.在接受一线化疗的小细胞肺癌患者中,用 CDK4/6 抑制剂替拉西利进行骨髓保护:一项 Ib 期/随机 II 期试验。
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Clinical applications of granulocyte-colony stimulating factor.粒细胞集落刺激因子的临床应用
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Recombinant human erythropoietin in oncology: current status and further developments.重组人促红细胞生成素在肿瘤学中的应用:现状与未来发展
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7
A prospective randomized phase II trial of GM-CSF priming to prevent topotecan-induced neutropenia in chemotherapy-naive patients with malignant melanoma or renal cell carcinoma.一项关于粒细胞巨噬细胞集落刺激因子(GM-CSF)预处理以预防初治恶性黑色素瘤或肾细胞癌患者拓扑替康诱导的中性粒细胞减少的前瞻性随机II期试验。
Blood. 2001 Apr 1;97(7):1942-6. doi: 10.1182/blood.v97.7.1942.
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Cell kinetics of CD34-positive hematopoietic cells following chemotherapy plus colony-stimulating factors in advanced breast cancer.晚期乳腺癌患者化疗联合集落刺激因子后CD34阳性造血细胞的细胞动力学
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