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Master Protocol to Evaluate Biomarker-Driven Therapies and Immunotherapies In Previously-Treated Non-Small Cell Lung Cancer (Lung-MAP Screening Study)

Objective

The primary objective of this screening study is to test patient specimens to determine eligibility for participation in the biomarker-driven and non-matched sub-studies included within the Lung-MAP umbrella protocol.

Protocol #

LUNGMAP

Trial Phase:

Phase II/III

Principal Investigator:

Martins, Renato

Cancer Type
  • Lung
Study Site
  • Hunter Holmes McGuire VAMC
  • Hunter Holmes McGuire VAMC RTOG Institution #
  • Lynchburg Hematology Oncology Clinic
  • Inc.
  • Shenandoah Oncology
  • Shenandoah Oncology
  • PC
  • Stony Point
  • VCU Community Memorial Healthcenter
  • Virginia Cancer Institute
  • Virginia Commonwealth University

- Patients must have Stage IV or recurrent disease as outlined below (AJCC Cancer Staging Manual, 8th Edition, 2017)
- Patients registered to Step 0 are not registered to the LungMAP protocol. To participate in LungMAP, patients must be registered to Step 1 after evaluation of patient
eligibility, including tumor tissue adequacy, per protocol
- Patients registered at Step 0 must use the same SWOG patient ID for registration at Step 1.
- Step 1:
- Patients must have pathologically proven non-small cell lung cancer (all histologic types) confirmed by tumor biopsy and/or fine-needle aspiration. Disease must be
Stage IV, or recurrent. The primary diagnosis of non-small cell lung cancer should be established using the current WHO/IASLC- classification of Thoracic
Malignancies. (13) All histologies, including mixed, are allowed.

Get more detailed information at ClinicalTrials.gov

  • Enrollment Status 1
  • Age Group Adult
  • Protocol Type Screening
  • Research Study Team Carrie Donovan, RN
    Phone: +1 804-628-3836
    Email Study Contact

Click "I'm Interested" to get started. If you have questions, call our study contact.

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