A Study of Lung Cancer Screening in People With Unexplained Weight Loss

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-80
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The researchers are doing this study to see if people with unexplained weight loss who have lung cancer screening are more likely to have or develop lung cancer than people without unexplained weight loss. The lung cancer screening will involve use of low-dose computed tomography (LDCT), a CT scan that gives off very low doses of radiation and can make detailed pictures of the lungs to help find tumors. The study researchers will also analyze participants' blood samples to determine if blood testing can be used to help to diagnose lung cancer.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age 50-80 years old

At least 20-pack year history of smoking

Weight loss of 3-10%, defined as UWL, within any timeframe over the past in the 18 months prior to enrollment, that cannot be attributed to an underlying medical condition at the discretion of the enrolling investigator

Note that patients who have 3-10% weight may still be enrolled if the enrolling investigator does not conclude that the weight loss can be attributed to the patient's intentional efforts.

Disqualifiers

Currently pregnant or trying to become pregnant via self-report

Prior history of recent CT scan of the chest either through LDCT screening or with a scan of the chest (standard, not LDCT) performed within the past 12 months

Prior history of NSCLC

Currently undergoing or referred for diagnostic evaluation due to clinical suspicion for malignancy (e.g., referred to a medical or surgical oncologist, or scheduled for biopsy on the basis of a suspicious imaging abnormality).

Trial population

Potential research subjects will be identified at MSKCC largely through survivorship clinics.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Low Dose CT imaging

    Diagnostic test

    at baseline and at Year 1.

  • blood draws

    Other intervention

    at baseline and at Year 1.

  • screening questionnaire

    Other intervention

    at baseline and at 1 year after registration.

Treatment groups

409 Participants
are divided into 1 treatment group
Group A: Patients undergoing Lung cancer screening3 interventions

Trial outcomes

Primary outcomes

1

The incidence of lung cancer in patients with unexplained weight loss

Low Dose CT screening

Time frame
2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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