A Study to Assess DNA Tumor Markers in Whole Blood Specimens of Patients with Newly Diagnosed Lung Cancer

Overview

Información sobre este estudio

The purpose of this study is to assess Methylated DNA tumor markers distributed in blood samples of patients newly diagnosed with different types of lung cancer. The goal is to develop new blood screening tests that can identify the type and primary site of cancer.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • From Lung Archive - IBB # 442-99
    • Cancer cases, n=100 (adeno 50, squamous 40, other 10)
    • Disease controls (benign lung nodules), n=50
  • From Prospective Case Cohort
    • Cancer cases, n=150 (distribution roughly same as for archival cases)
  • From Parallel Control Study, n=2000 - IRB #15-006191
    • Controls matched on age, sex, and smoking history will be selected from this larger parallel study (at least 300 independent controls for each case group).
  • For exploratory Disease Control group (Aim 4), 4 ml (minimum of 2 ml) plasma will be requested for each of following tumor subsets:
    • Lymphoma, n=20 (any stage or site, at least 10 non-Hodgkins)
      • Obtained from Dr. Thomas Witzig’s Lymphoma SPORE registry (IRB # 118-01)
    • Thyroid, n=20 (any stage, at least half non-papillary)
      • Obtained prospectively from Oncology calendars
    • Breast, n=20 (stage (half I-II, half III-IV), ER status (half positive, half negative)
      • Obtained from Dr. Fergus Couch and Janet Olson’s Breast Cancer Registry (IRB # 1815-04)
    • Prostate, n=20 (half Gleason’s 6 or less, half Gleason’s 7 or higher)
      • Obtained from Dr. Matthew Gettman’s Prostate protocol (IRB # 15-009309)
    • Gynecologic, n=20 (Ovarian, n=10 (any stage or type); Uterine, n=10 (any stage or type))
      • Ovarian obtained from Dr. Kimberly Kalli’s Ovarian Cancer registry (IRB#08-005749)
      • Uterine obtained from Dr. Sean Dowdy’s Endometrial cancer bank (IRB # 2405-04)
    • Kidney, n=20 (any stage or type)
      • Obtained from Dr. R. Houston Thompson’s (IRB # 14-03)
    • Esophagus, n=20 (any stage, type (10 adeno, 10 squamous cell))
      • Obtained from Dr. Navtej Buttar’s Esophageal Biospecimen Registry (IRB #495-01)
    • Stomach, n=20 (any stage or type)
      • Obtained from Dr. Lisa Boardman’s GI Tumor Registry (IRB # 622-00)
    • Liver, n=20 (any stage)
      • Obtained from Dr. Lewis Roberts’ Liver Registry (RB # 707-03)
    • Pancreas, n=20 (any stage)
      • Obtained from Dr. David Ahlquist’s Compartmentalization study (IRB # 15-001127)
    • Colorectum, n=20 (stage (half I-II, half III-IV)
      • Obtained from Dr. Lisa Boardman’s GI Tumor Registry (IRB # 622-00) or Dr. David Ahlquist’s Compartmentalization study (IRB # 15-001127)

Exclusion Criteria:

  • Known primary cancer outside of the lungs within the last 5 years (not including basal cell or squamous cell skin cancers) (primary aim only)
  • Current target pathology is a recurrence
  • Prior or active chemotherapy or radiation for the primary lung cancer (primary aim only)
  • Patient has had a transplant
  • Inability to give informed consent (prospective groups only)

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

John Kisiel, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20232527

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