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OPALS: A New Osimertinib Adjunctive Treatment of Lung Adenocarcinoma or Glioblastoma Using Five Repurposed Drugs
Richard E Kast1, Marc-Eric Halatsch2, Rafael Rosell3
1IIAIGC Study Center, Burlington, VT 05408, USA.
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.
Insights
A novel five-drug regimen (OPALS) may delay resistance to osimertinib in lung adenocarcinoma by inhibiting tumor growth. Further trials are needed to confirm safety and efficacy in combination therapy.
Area of Science:
- Oncology
- Pharmacology
Background:
- Targeting epidermal growth factor receptor (EGFR) tyrosine kinase is key for lung adenocarcinoma treatment.
- Osimertinib is effective against EGFR-mutated lung adenocarcinomas but resistance emerges.
- Developing strategies to overcome osimertinib resistance is crucial.
Purpose of the Study:
- To develop and evaluate a novel five-drug adjuvant regimen (OPALS) to enhance osimertinib's efficacy and delay resistance.
- To investigate the potential of repurposed generic drugs for lung adenocarcinoma treatment.
Main Methods:
- Literature review of PubMed articles on OPALS drugs, lung adenocarcinoma, and glioblastoma pathophysiology.
- Analysis of preclinical data on the proposed five-drug regimen.
Main Results:
- The OPALS regimen includes pyrimethamine, cyproheptadine, azithromycin, loratadine, and spironolactone.
- These inexpensive, generic drugs inhibit lung adenocarcinoma growth.
- Preclinical data suggests potential activity against glioblastoma as well.
Conclusions:
- The OPALS regimen shows promise in preclinical studies for overcoming osimertinib resistance in lung adenocarcinoma.
- Further clinical investigation is required to establish safety and efficacy of the combined regimen.
- Repurposed generic drugs offer a cost-effective approach to cancer therapy.
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