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Methylated Genes in Blood as Biomarkers for Advanced Lung Cancer

Memorial Sloan Kettering Cancer Center (MSK) logo

Memorial Sloan Kettering Cancer Center (MSK)

Status

Completed

Conditions

Lung Cancer

Treatments

Other: Blood and Tissue studies

Study type

Observational

Funder types

Other
NIH

Identifiers

Details and patient eligibility

About

The purpose of this study is to study whether the presence of lung cancer in your body can be detected by testing the blood, and if the results of these blood tests change as your tumor shrinks or grows.

Full description

This is a cooperative research project involving patients on the Thoracic Oncology Service at Memorial Sloan-Kettering Cancer Center, and the laboratory of Dr. Peter Danenberg, Professor of Biochemistry and Molecular Biology, University of Southern California / Norris Comprehensive Cancer Center in Los Angeles, California. The primary objectives are to measure the proportion of patients with advanced (stage III-IV) lung cancer with methylated genes in their blood, and to determine if response to chemotherapy (complete or partial radiologic response) in patients with advanced lung cancer renders methylated genes undetectable in the blood. This research project will enroll approximately 80 patients per year over 4 years to generate a sample size of approximately 320 patients.Blood will be collected from participating patients at baseline, as close as possible to the date of their baseline radiologic assessment. Three follow-up blood collections will be drawn, each within 7-10 days of each follow-up radiologic evaluation.

Enrollment

281 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pathologically proven advanced (stage III-IV) lung cancer
  • Measurable and/or evaluable disease
  • Enrollment in an MSKCC protocol of experimental chemotherapy with radiologic response rate as an efficacy outcome variable, or prescription of standard chemotherapy in which the patient will be receiving routine radiological scans (every 4-8 weeks) as standard clinical practice.
  • Signed written informed consent

Exclusion criteria

-None

Trial design

281 participants in 1 patient group

1
Description:
Patients with advanced lung cancer.
Treatment:
Other: Blood and Tissue studies

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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