摘要
背景:PARP抑制剂似乎在伴随现今使用的许多细胞毒性剂对抗BRCA中的癌症增殖中提供了有希望的作用。缺陷的肿瘤。目前PARP抑制剂的种类在作为单一药剂给药时尚未显示出优于现有治疗的效果;然而,他们似乎放大了这些现有的化疗的影响,当一起使用。这表明PARP抑制剂可以在目前的抗癌策略中发挥有效的维持作用。在不远的将来,PARP抑制剂可能只适用于选择的一组癌症(即由HR途径缺陷引起的那些癌症),尽管正在出现的研究可能表明将适用性扩展到HR熟练的癌症类型。然而,目前的文献表明目前的文献表明,一种可行的PARP抑制剂化疗混合物靶向HR缺乏的癌症很快就会顺利进行。 目的:在这篇手稿中,我们探讨了不同PARP抑制剂正在进行和已完成的临床试验。 结论:自FDA和EMA批准Olaparib以来,进一步的临床试验继续研究使用Olaparib和其他PARP抑制剂。这些试验的预期结果可能会阐明PARP抑制剂在治疗各种BRCA突变实体肿瘤中的益处。
关键词:
图形摘要
Current Drug Targets
Title:PARP Inhibitor Drugs in the Treatment of Breast, Ovarian, Prostate and Pancreatic Cancers: An Update of Clinical Trials
Volume: 19 Issue: 1
关键词:
摘要: Background: PARP inhibitors appear to offer a promising role in the accompaniment of many of the cytotoxic agents used in the present day to combat cancer proliferation in BRCA ½ deficient tumors. Current species of PARP inhibitors have yet to demonstrate a superior effect to that of existing therapies when administered as a single agent; however, they have appeared to amplify the effect of these existing chemotherapies when utilized together. This suggests that PARP inhibitors could play an effective maintenance role in current cancer-combating strategies. In the immediate future, PARP inhibitors may only be applicable to a select group of cancers (i.e., those caused by defective HR pathways), though research is emerging that could indicate an extension of applicability to HR proficient cancer types as well. For the time being, however, the current literature suggests that a viable PARP inhibitorchemotherapy hybrid targeting HR deficient cancers could be well on its way very soon.
Objective: In this manuscript we explores the ongoing and the completed clinical trials for different PARP inhibitors.
Conclusion: Since the approval of Olaparib by both FDA and EMA, further clinical trials continue to investigate the use of Olaparib and other PARP inhibitors. The anticipating outcome of these trials may clarify the benefit of PARP inhibitors in management of various BRCA mutated solid tumors.
Export Options
About this article
Cite this article as:
PARP Inhibitor Drugs in the Treatment of Breast, Ovarian, Prostate and Pancreatic Cancers: An Update of Clinical Trials, Current Drug Targets 2018; 19 (1) . https://dx.doi.org/10.2174/1389450118666170711151518
DOI https://dx.doi.org/10.2174/1389450118666170711151518 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Deep Inspiration Breath-hold (DIBH) Technique to Reduce Cardiac Radiation Dose in the Management of Breast Cancer
Current Cancer Therapy Reviews Targeting RSK: An Overview of Small Molecule Inhibitors
Anti-Cancer Agents in Medicinal Chemistry N-Terminal-Dependent Protein Degradation and Targeting Cancer Cells
Anti-Cancer Agents in Medicinal Chemistry Aromatase Inhibitors for Treatment of Breast Cancer
Current Cancer Therapy Reviews Tetrazole Derivatives as Promising Anticancer Agents
Anti-Cancer Agents in Medicinal Chemistry From Natural Products to Designer Drugs: Development and Molecular Mechanisms Action of Novel Anti-Microtubule Breast Cancer Therapeutics
Current Topics in Medicinal Chemistry Preclinical and Clinical Efficacy of the Bisphosphonate Ibandronate in Cancer Treatment
Current Clinical Pharmacology Genetics and Ulcerative Colitis: What are the Clinical Implications?
Current Drug Targets Non-coding RNAs in Exosomes: New Players in Cancer Biology
Current Genomics Molecular Pathways of Endothelial Cell Activation for (Targeted) Pharmacological Intervention of Chronic Inflammatory Diseases
Current Vascular Pharmacology Synthesis and Anti-Proliferative Activity of New Biphenyle-Benzylidenethiazolidine- 2,4-dione Bis-Adducts Containing Various Heterocyclic Cores
Letters in Drug Design & Discovery Direct Inhibitors of Ras-Effector Protein Interactions
Mini-Reviews in Medicinal Chemistry Overexpression of miR-340-5p Inhibits Skin Fibroblast Proliferation by Targeting Kruppel-like Factor 2
Current Pharmaceutical Biotechnology Regulation of Cell Migration and Invasion by Specific Modules of uPA: Mechanistic Insights and Specific Inhibitors
Current Drug Targets Synthesis and Antitumor Invasive Activity of Novel Ionone Alkaloid Derivatives
Letters in Drug Design & Discovery Quantitative Proteomics Reveals Changes in Transporter Protein Abundance in Liver, Kidney and Brain of Mice by Pregnancy
Drug Metabolism Letters Feud or Friend? The Role of the miR-17-92 Cluster in Tumorigenesis
Current Genomics The Impact of the Activated Stroma on Pancreatic Ductal Adenocarcinoma Biology and Therapy Resistance
Current Molecular Medicine Helical Tomotherapy versus Conventional Technique for Post Mastectomy Left Sided Breast Cancer; Dosimetric Study
Reviews on Recent Clinical Trials Synthesis, Biological and Computational Evaluation of Novel 2,3-dihydro-2-aryl-4-(4- isobutylphenyl)-1,5-benzothiazepine Derivatives as Anticancer and Anti-EGFR Tyrosine Kinase Agents
Anti-Cancer Agents in Medicinal Chemistry