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18F-Fluoroazomycin Arabinoside (18F-FAZA) in Lung Cancer

A Feasibility Study of Hypoxia Imaging in Patients With Lung Cancer Using Positron Emission Tomography (PET) With 18F-Fluoroazomycin Arabinoside (18F-FAZA)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02701699
Acronym
FAZA Lung
Enrollment
36
Registered
2016-03-08
Start date
2014-12-01
Completion date
2027-06-01
Last updated
2026-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Lung Cancer, FAZA PET Imaging, Lung Radiotherapy

Brief summary

The purpose of this study is to look for low levels of oxygen (hypoxia) in lung cancer using a positron emission tomography (PET) scan. Hypoxia can influence how lung cancer grows and responds to treatments like radiotherapy and chemotherapy. The use of PET scans to measure hypoxia may be better and simpler than the approaches used previously. This study will assess whether or not PET scans can provide useful information about hypoxia in lung cancer. In this study, a radiotracer called Fluoroazomycin Arabinoside (FAZA) will be used to measure hypoxia in the patient's tumour. FAZA has already been used in many cancers including lung cancer. Patients who consent to participate in this trial will receive 1 FAZA PET Scan prior to their first radiotherapy treatment

Interventions

BIOLOGICAL18-F-FAZA

All patients enrolled in this study will receive a FAZA PET Scan prior to their first radiation therapy fraction

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years 2. Patients with stage II or III lung cancer (both NSCLC and SCLC) qualifying for radiotherapy to the primary tumor, with or without treatment of mediastinal or hilar lymph nodes 3. Intention to treat using radiotherapy according to the current treatment policies of the PMH Lung Group 4. Concurrent systemic therapy allowed 5. A negative serum pregnancy test within the two week interval immediately prior to PET-CT imaging, in women of child-bearing age 6. Ability to provide written informed consent to participate in the study

Exclusion criteria

1. Previous radiotherapy to intended treatment volumes. 2. Previous systemic therapy 3. Active malignancy other than lung cancer 4. Unable to remain supine for more than 60 minutes 5. Pregnancy 6. Age less than 18 years old 7. Failure to provide written informed consent

Design outcomes

Primary

MeasureTime frame
Number of patients with lung cancer using the PET tracer FAZA to image primary tumor hypoxia prior to treatment with radiotherapy5 years
Number of patients with lung cancer using 4D (gated) and static PET imaging of FAZA uptake5 years

Secondary

MeasureTime frame
Proportion of the volume of injected FAZA tracer taken up in the tumor prior to treatment with radiotherapy5 years

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORAlex Sun, MD

The Princess Margaret Cancer Foundation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026