Overview of studies investigating the efficacy of using MEK inhibitors combined with hydroxychloroquine in pre-treated patients
Tumor type | Study design | Number | MEK inhibitor | Endpoints | Reference |
---|---|---|---|---|---|
Biliary tract cancer | Phase II trial | 2 | Trametinib | PFS: 2.48 months;OS: 3.1 months. | [32] |
Colorectal cancer | Case report | 1 | Binimetinib (+ bevacizumab) | Best response: stable disease;Duration: approximately 4 months. | [28] |
Pancreatic cancer | Case report | 1 | Trametinib | Best response: partial response;Duration: approximately 4 months. | [26] |
Pancreatic cancer | Case report | 2 | Trametinib | Best response: stable disease;Duration: approximately 4 months and 7 months. | [33] |
Pancreatic cancer | Case report | 1 | Trametinib | Best response: stable disease;Duration: approximately 7 months. | [34] |
Pancreatic cancer | Case report | 1 | Trametinib | Best response: progressive disease;Duration: approximately 2 months. | [35] |
Pancreatic cancer | Retrospective | 9 | Trametinib | DCR: 63%;PFS: 5.7 months;OS: 6.6 months. | [20] |
1 | Cobimetinib | ||||
Pancreatic cancer | Retrospective | 8 | Trametinib | Best response: stable disease (16.7%);PFS: 2.0 months;OS: 4.2 months. | [16] |
NSCLC | Phase II trial | 9 | Binimetinib | Best response: stable disease (11.1%);PFS: 1.9 months;OS: 5.3 months. | [18] |
NSCLC: non-small cell lung cancer; DCR: disease control rate; PFS: progression-free survival; OS: overall survival
We are cordially thankful to Dr. Priscilla S. Amankwah for the critical reading and editing of this manuscript.
AAM: Writing—original draft, Writing—review & editing, Data curation, Visualization, Formal analysis. EMA and AIT: Data curation, Investigation. NVM and ANE: Resources, Formal analysis. ADS and ARV: Visualization. ENI and SVO: Writing—review & editing, Project administration, Supervision. AAM and SVO confirm the authenticity of all the raw data. All authors read and approved the final version of the manuscript.
The authors declare that they have no conflicts of interest.
The study was approved (approval no. 02/231) by the Ethics Committee of N.N. Petrov National Medical Research Center of Oncology (Saint Petersburg, Russia), and was conducted in compliance with the Helsinki Declaration of 1975.
Informed consent to participate in the study was obtained from relevant participants.
Informed consent to publication was obtained from relevant participants.
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.
This work has been supported by the Russian Science Foundation [22-15-00487]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
© The Author(s) 2024.