Recruiting

Factors Increasing Lung Cancer Risk in Never-Smoking Women

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

This observational study aims to identify factors associated with an increased risk of non-small cell lung cancer (NSCLC) in women who have never smoked, using demographic assessments and whole-exome sequencing.

What is being collected

Data Collection

+ other Data

Collected from today forward - Prospective
OtherNo DNA Sample
Who is being recruted

Lung Diseases+4

+ Neoplasms

+ Neoplasms by Site

From 40 to 74 Years
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: June 2026
See protocol details

Summary

Principal SponsorMemorial Sloan Kettering Cancer Center
Study ContactAlexis Chidi, MD, PhDMore contacts
Last updated: July 14, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: June 30, 2026

Actual date on which the first participant was enrolled.

This study focuses on understanding factors that might increase the risk of lung cancer in individuals who have never smoked, specifically women. The goal is to gather insights that could help predict which non-smoking individuals may have a higher likelihood of developing lung cancer. This research is important as it aims to address the unique challenges of lung cancer in never-smokers, a group often overlooked in traditional lung cancer research.

Principal SponsorMemorial Sloan Kettering Cancer Center
Study ContactAlexis Chidi, MD, PhDMore contacts
Last updated: July 14, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

500 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 40 to 74 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Lung DiseasesNeoplasmsNeoplasms by SiteRespiratory Tract DiseasesRespiratory Tract NeoplasmsThoracic NeoplasmsLung Neoplasms

Criteria

Criteria: * Female at birth * Age 40-74 years * No smoking history * Participants must be never-smokers, defined as having smoked \<100 cigarettes in their lifetime * Documentation of disease - case patients o Case patients must have pathologically confirmed primary lung adenocarcinoma. New and prevalent cases will be eligible. Case patients with a history of prior non-lung cancer will be eligible for the study unless actively being diagnosed or treated for another form of cancer at the time of enrollment. * Criteria for control participants * Control participants must have no personal history of lung cancer, symptoms suspicious for lung cancer, or suspicious pulmonary nodules. Participants recruited as controls and found on imaging to have lesions suspicious for lung cancer will be excluded from analysis and followed prospectively. Data regarding these participants will be reported in a sensitivity analysis. Additional control participants will be recruited to ensure balanced age- and race-matched enrollment by frequency matching. Control participants with a history of prior non-lung cancer will be eligible for the study unless actively being diagnosed or treated for another form of cancer at the time of enrollment.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 7 locations

Recruiting

Memorial Sloan Kettering Basking Ridge (All Protocol Activities)

Basking Ridge, United StatesOpen Memorial Sloan Kettering Basking Ridge (All Protocol Activities) in Google Maps
Recruiting

Memorial Sloan Kettering Monmouth (All Protocol Activities)

Middletown, United States
Recruiting

Memorial Sloan Kettering Bergen (All Protocol Activities)

Montvale, United States
Recruiting

Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)

Commack, United States
Recruiting
7 Study Centers