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Neoadjuvant Finasteride for Patients With Non-small Cell Lung Cancer

Neoadjuvant Finasteride for Patients With Non-small Cell Lung Cancer

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02055170
Enrollment
4
Registered
2014-02-05
Start date
2014-06-30
Completion date
2018-03-27
Last updated
2018-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer

Brief summary

The purpose of this study is to study the effect of hormone therapies (androgen pathway modification) on the outcomes of patients with lung cancer. This information may be of benefit for future treatment strategies, prevention and control. In this study, the protein where testosterone binds, called the androgen receptor (AR), will be measured in samples from the patient's biopsy and surgical tumor samples. The investigators will look at a marker of how fast the cancer is growing (Ki67) before using finasteride from your biopsy specimen. Finasteride will be taken from the day of consent until the day of the patient's surgery. This marker will be measured again after using finasteride from the surgical specimen. The investigators will be looking for a decrease in the Ki67 from the patient's biopsy specimen to the surgical specimen as an indicator that this medication is blocking tumour growth.

Interventions

DRUGfinasteride 5mg oral daily

Sponsors

CancerCare Manitoba
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* male * age \>18 * biopsy-proven non-small cell lung cancer * surgical intervention planned

Exclusion criteria

* current use of 5-alpha reductase inhibitor * previous diagnosis of prostate cancer * previous hypersensitivity to 5-alpha reductase inhibitor

Design outcomes

Primary

MeasureTime frameDescription
Change in proliferationOriginal biopsy to surgical specimen (approx 6 weeks)Patients will be followed from time of consent (around the time of consultation with a Thoracic Surgeon) to date of surgery (on average, approximately 4-6 weeks following Thoracic Surgeon consultation).

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026