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靶向治疗后残留病灶。

Targeting therapy-persistent residual disease.

机构信息

Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.

Massachusetts General Hospital Cancer Center, Boston, MA, USA.

出版信息

Nat Cancer. 2024 Sep;5(9):1298-1304. doi: 10.1038/s43018-024-00819-9. Epub 2024 Sep 17.

DOI:10.1038/s43018-024-00819-9
PMID:39289594
Abstract

Disease relapse driven by acquired drug resistance limits the effectiveness of most systemic anti-cancer agents. Targeting persistent cancer cells in residual disease before relapse has emerged as a potential strategy for enhancing the efficacy and the durability of current therapies. However, barriers remain to implementing persister-directed approaches in the clinic. This Perspective discusses current preclinical and clinical complexities and outlines key steps toward the development of clinical strategies that target therapy-persistent residual disease.

摘要

获得性耐药驱动的疾病复发限制了大多数全身性抗癌药物的疗效。在复发前针对残留疾病中的持久性癌细胞进行靶向治疗,已成为提高现有疗法疗效和持久性的潜在策略。然而,在临床上实施针对持久性细胞的方法仍然存在障碍。本文观点讨论了当前临床前和临床的复杂性,并概述了开发针对治疗后持久性残留疾病的临床策略的关键步骤。

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Targeting therapy-persistent residual disease.靶向治疗后残留病灶。
Nat Cancer. 2024 Sep;5(9):1298-1304. doi: 10.1038/s43018-024-00819-9. Epub 2024 Sep 17.
2
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[Tumor resistance to HER2 inhibitors: the drug sedimentation concept].[肿瘤对HER2抑制剂的耐药性:药物沉积概念]
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Targeting PRMT1 Reduces Cancer Persistence and Tumor Relapse in EGFR- and KRAS-Mutant Lung Cancer.靶向PRMT1可降低EGFR和KRAS突变型肺癌的癌症持续性和肿瘤复发率。
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本文引用的文献

1
Liquid biopsy epigenomic profiling for cancer subtyping.液体活检的表观基因组特征分析用于癌症分型。
Nat Med. 2023 Nov;29(11):2737-2741. doi: 10.1038/s41591-023-02605-z. Epub 2023 Oct 21.
2
Drug-tolerant persister cells in cancer: the cutting edges and future directions.耐药性癌细胞:前沿与未来方向。
Nat Rev Clin Oncol. 2023 Nov;20(11):799-813. doi: 10.1038/s41571-023-00815-5. Epub 2023 Sep 25.
3
Persister cell phenotypes contribute to poor patient outcomes after neoadjuvant chemotherapy in PDAC.在 PDAC 患者接受新辅助化疗后,持久细胞表型导致预后不良。
应对肺癌治疗中耐药性的复杂性:机制、类器官模型及克服治疗失败的策略
Cancers (Basel). 2024 Nov 28;16(23):3996. doi: 10.3390/cancers16233996.
Nat Cancer. 2023 Sep;4(9):1362-1381. doi: 10.1038/s43018-023-00628-6. Epub 2023 Sep 7.
4
Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells.药物治疗同质癌细胞会出现不同的克隆命运。
Nature. 2023 Aug;620(7974):651-659. doi: 10.1038/s41586-023-06342-8. Epub 2023 Jul 19.
5
Therapy-induced APOBEC3A drives evolution of persistent cancer cells.治疗诱导的 APOBEC3A 驱动持续性癌细胞的进化。
Nature. 2023 Aug;620(7973):393-401. doi: 10.1038/s41586-023-06303-1. Epub 2023 Jul 5.
6
Early Clearance of Plasma Epidermal Growth Factor Receptor Mutations as a Predictor of Outcome on Osimertinib in Advanced Non-Small Cell Lung Cancer; Exploratory Analysis from AURA3 and FLAURA.血浆表皮生长因子受体突变的早期清除作为奥希替尼治疗晚期非小细胞肺癌疗效的预测指标;来自AURA3和FLAURA的探索性分析
Clin Cancer Res. 2023 Sep 1;29(17):3340-3351. doi: 10.1158/1078-0432.CCR-22-3146.
7
Liquid Biopsy in Early-Stage Lung Cancer: Current and Future Clinical Applications.早期肺癌的液体活检:当前及未来的临床应用
Cancers (Basel). 2023 May 10;15(10):2702. doi: 10.3390/cancers15102702.
8
Early Changes in Circulating Cell-Free KRAS G12C Predict Response to Adagrasib in KRAS Mutant Non-Small Cell Lung Cancer Patients.循环无细胞 KRAS G12C 早期变化可预测 KRAS 突变型非小细胞肺癌患者对阿达格拉西布的反应。
Clin Cancer Res. 2023 Aug 15;29(16):3074-3080. doi: 10.1158/1078-0432.CCR-23-0795.
9
SHP2 Inhibition Sensitizes Diverse Oncogene-Addicted Solid Tumors to Re-treatment with Targeted Therapy.SHP2 抑制增强了多种致癌基因依赖的实体肿瘤对靶向治疗的再治疗敏感性。
Cancer Discov. 2023 Aug 4;13(8):1789-1801. doi: 10.1158/2159-8290.CD-23-0361.
10
N-of-1 Trials in Cancer Drug Development.癌症药物研发中的 N-of-1 试验
Cancer Discov. 2023 Jun 2;13(6):1301-1309. doi: 10.1158/2159-8290.CD-22-1377.