Related Experiment Videos
Phase 2 randomized study of enzastaurin (LY317615) for lung cancer prevention in former smokers
Jhanelle E Gray1, Soner Altiok, Mark G Alexandrow
1Moffitt Cancer Center, Tampa, FL, USA.
Background:
Chemoprevention for lung cancer with nutraceutical or anti-inflammatory agents has had mixed clinical benefit. Novel targeted agents hold the promise of greater efficacy and selectivity. The authors of this report evaluated enzastaurin, a selective protein kinase C-β (PKC-β) inhibitor with antiproliferative and proapoptotic properties, in former smokers.
Methods:
The primary objective of this study was to compare the average fraction of Ki-67-stained cells (the Ki-67 labeling index [LI]) in bronchial biopsy specimens that were collected before and after treatment. Participants were randomized (2:1) to receive either 6 months of daily oral enzastaurin (500 mg) or placebo. Stratification was based on morphology, history of lung cancer, and airway obstruction.
Results:
In pretrial investigations, the rationale for PKC-β inhibition and pathway interrogation was established in premalignant lesions and early stage lung cancer. In an intent-to-treat analysis, of 40 randomized participants, there was no significant difference in the pretreatment/post-treatment change in the Ki-67 LI between the enzastaurin group and the placebo group (P = .53). Six participants discontinued enzastaurin, including 4 participants who had adverse events, including abdominal distension, deep vein thrombosis, hyponatremia, and rash, and 2 participants who decided to discontinue. One participant in the placebo group was discontinued on the study because of noncompliance. Two participants had ≥1 serious adverse event (bradycardia, deep vein thrombosis, and hypotension).
Conclusions:
To the authors' knowledge, this represents the first chemoprevention trial with a non-US Food and Drug Administration-approved, oral, small-molecule-targeted agent. Although the primary endpoint was not met, enzastaurin was tolerable for 6 months by 75% of participants, and there was a suggestion of response in a subset analysis that was restricted to those who had metaplastic or dysplastic lesions.
Insights
Enzastaurin, a targeted agent, did not significantly reduce cell proliferation in former smokers' bronchial tissues. However, it was generally well-tolerated, showing potential in a subset with precancerous lesions.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Lung cancer chemoprevention has yielded mixed results with traditional agents.
- Targeted therapies offer potential for improved efficacy and selectivity.
- Enzastaurin, a protein kinase C-beta (PKC-β) inhibitor, exhibits antiproliferative and proapoptotic properties.
Purpose of the Study:
- To evaluate enzastaurin's efficacy in lung cancer chemoprevention among former smokers.
- To assess the impact of enzastaurin on bronchial cell proliferation using the Ki-67 labeling index (LI).
Main Methods:
- A randomized, double-blind, placebo-controlled trial was conducted.
- Participants received daily oral enzastaurin (500 mg) or placebo for six months.
- Changes in the Ki-67 LI in bronchial biopsy specimens were compared pre- and post-treatment.
Main Results:
- No significant difference in the change of Ki-67 LI was observed between the enzastaurin and placebo groups (P = .53).
- Enzastaurin was generally tolerable, with 75% of participants completing the 6-month treatment.
- Adverse events led to discontinuation in some participants; serious adverse events were reported in two participants.
Conclusions:
- The study did not meet its primary endpoint of significantly reducing cell proliferation.
- This trial represents the first chemoprevention study of an oral, small-molecule targeted agent not approved by the FDA.
- A subset analysis suggested potential benefit in individuals with metaplastic or dysplastic lesions.
Related Concept Videos
Chronic Obstructive Pulmonary Disease II: Emphysema
Cancer Prevention
Some...
Clinical Trials: Overview
Clinical Trials
There are four phases in a clinical trial. A phase one...