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OPALS:使用五种重新定位药物的奥希替尼辅助治疗肺腺癌或胶质母细胞瘤的新方法。

OPALS: A New Osimertinib Adjunctive Treatment of Lung Adenocarcinoma or Glioblastoma Using Five Repurposed Drugs.

机构信息

IIAIGC Study Center, Burlington, VT 05408, USA.

Department of Neurosurgery, Cantonal Hospital of Winterthur, 8400 Winterthur, Switzerland.

出版信息

Cells. 2021 May 10;10(5):1148. doi: 10.3390/cells10051148.

Abstract

BACKGROUND

Pharmacological targeting aberrant activation of epidermal growth factor receptor tyrosine kinase signaling is an established approach to treating lung adenocarcinoma. Osimertinib is a tyrosine kinase approved and effective in treating lung adenocarcinomas that have one of several common activating mutations in epidermal growth factor receptor. The emergence of resistance to osimertinib after a year or two is the rule. We developed a five-drug adjuvant regimen designed to increase osimertinib's growth inhibition and thereby delay the development of resistance. Areas of Uncertainty: Although the assembled preclinical data is strong, preclinical data and the following clinical trial results can be discrepant. The safety of OPALS drugs when used individually is excellent. We have no data from humans on their tolerability when used as an ensemble. That there is no data from the individual drugs to suspect problematic interaction does not exclude the possibility.

DATA SOURCES

All relevant PubMed.org articles on the OPALS drugs and corresponding pathophysiology of lung adenocarcinoma and glioblastoma were reviewed. Therapeutic Opinion: The five drugs of OPALS are in wide use in general medicine for non-oncology indications. OPALS uses the anti-protozoal drug pyrimethamine, the antihistamine cyproheptadine, the antibiotic azithromycin, the antihistamine loratadine, and the potassium sparing diuretic spironolactone. We show how these inexpensive and generically available drugs intersect with and inhibit lung adenocarcinoma growth drive. We also review data showing that both OPALS adjuvant drugs and osimertinib have data showing they may be active in suppressing glioblastoma growth.

摘要

背景

靶向表皮生长因子受体酪氨酸激酶信号的异常激活是治疗肺腺癌的一种既定方法。奥希替尼是一种酪氨酸激酶抑制剂,已被批准用于治疗具有表皮生长因子受体几种常见激活突变的肺腺癌,并且疗效显著。奥希替尼治疗一两年后出现耐药是常见现象。我们开发了一种五药辅助治疗方案,旨在增强奥希替尼的生长抑制作用,从而延缓耐药的发生。不确定性领域:尽管已有的临床前数据很强,但临床前数据和随后的临床试验结果可能存在差异。OPALS 药物单独使用时的安全性非常好。我们没有人类使用它们作为一个整体的耐受性数据。没有来自单个药物的数据表明存在有问题的相互作用,并不能排除这种可能性。

数据来源

所有关于 OPALS 药物和肺腺癌及胶质母细胞瘤相应病理生理学的相关 PubMed.org 文章都进行了回顾。治疗意见:OPALS 中的五种药物在普通医学中非肿瘤适应症中广泛使用。OPALS 使用抗寄生虫药物乙胺嘧啶、抗组胺药赛庚啶、抗生素阿奇霉素、抗组胺药氯雷他定和保钾利尿剂螺内酯。我们展示了这些廉价且通用的药物如何与抑制肺腺癌生长的机制相互作用和抑制。我们还回顾了数据,表明 OPALS 辅助药物和奥希替尼都有数据表明它们可能对抑制胶质母细胞瘤生长有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbb/8151869/cd89e7457f25/cells-10-01148-g001.jpg

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