Lung Cancer - Standard Therapy and the Use of a Novel, Highly Effective, Well Tolerated, Treatment With Progesterone

Jerome H Check1,2, Trina Poretta3, Diane Check2

  • 1Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology & Infertility, Cooper Medical School of Rowan University, Camden, NJ, U.S.A.; laurie@ccivf.com.

Anticancer Research
|February 28, 2023
PubMed

Insights

Recent lung cancer therapies target tumor mutations for better outcomes. A novel approach using progesterone receptor antagonists shows potential for advanced lung cancer, warranting further clinical studies.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Lung cancer treatment advances focus on personalized profiling (genetic, epigenetic, immunologic).
  • Targeted therapies and immunotherapies (e.g., EGFR, KRAS, ALK inhibitors, PD-1/ligand blockade) have improved survival and palliation for specific patient groups.

Purpose of the Study:

  • To review lung cancer drug efficacy up to 2022.
  • To introduce progesterone receptor (PR) antagonists targeting progesterone induced blocking factor (PIBF) as a novel therapeutic strategy.
  • To encourage large-scale clinical trials to validate PR antagonist efficacy in advanced lung cancer.

Main Methods:

  • Review of existing literature on lung cancer therapies and drug efficacy.
  • Analysis of preliminary data from one murine study and five human cases on PR antagonists.
  • Proposal for future well-powered clinical studies.

Main Results:

  • Established targeted therapies and immunotherapies have demonstrated significant benefits for specific lung cancer mutations.
  • Preliminary data suggest PR antagonists may offer palliative and longevity benefits in advanced lung cancer patients with limited options.
  • Further research is needed to confirm these findings in larger patient cohorts.

Conclusions:

  • Personalized medicine has revolutionized lung cancer treatment.
  • PR antagonists represent a potential new avenue for treating advanced lung cancer, but require robust clinical validation.
  • Oncologists are encouraged to investigate PR antagonist therapy through well-designed clinical trials.

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