PET/CT Changes During Chemoimmunotherapy and Radiation Therapy in Patients With Stage IV Non-small Cell Lung Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Washington

About this trial

This study investigates the changes in positron emission tomography (PET)/computed tomography (CT) imaging scans during chemoimmunotherapy and radiation therapy treatment in patients with stage IV non-small cell lung cancer. Analyzing changes in PET/CT imaging scans may help doctors assess and predict patterns of cancer response to chemoimmunotherapy and radiation therapy.

Eligibility criteria

Qualifiers

Histologically-confirmed or cytologically-confirmed metastatic NSCLC in patients who have not received chemotherapy or immunotherapy for their advanced disease (stage IV or recurrent, using the American Joint Committee on Cancer [AJCC]/Union for International Cancer Control [UICC] 8th edition for staging)

Evidence of stage IV disease on imaging by CT, PET/CT, or magnetic resonance imaging (MRI)

Plan to treat with a platinum doublet with a PD1 or PDL1 inhibitor

Adjuvant chemotherapy or concurrent chemoradiation for early stage disease does not count as prior therapy unless subject progressed within 6 months of completion of regimen.

Disqualifiers

Any known additional malignancy (with exception of non-melanoma skin cancer, in-situ breast cancer, low risk prostate cancer, or a malignancy diagnosed >= 3 years prior to the current NSCLC diagnosis and with no evidence of requiring active treatment)

Had prior treatment with an anti-PD-1, or PD-L1 or PD-L2 agent or an antibody targeting other immuno-regulatory receptors or mechanisms

Has any serious or uncontrolled active infection that could create false positives on a PET/CT scan, in the opinion of the treating investigator

Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator

Trial design

Treatments tested in this trial

  • Positron Emission Tomography
  • Computed Tomography
  • Chemotherapy
  • Immunotherapy
  • Radiation Therapy
  • Biospecimen Collection
  • Magnetic Resonance Imaging

Treatment groups

80 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Washington

Lead sponsor

National Cancer Institute (NCI)

Collaborator