Clinical trial · Observational
Pilot Study of a Novel Type of CT Scan to Assess Treatment Response During Chemoradiotherapy for Stage III Non-Small Cell Lung Cancer
Pilot Study of Dual-Energy Computed Tomography in Stage III Non-Small Cell Lung Cancer
NCT02053285CI-TRIAL-00061008completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Dual-energy CT (DECT) provides information on the blood volume in tumors and lymph nodes. As tumors respond to treatment, preliminary data suggests that the blood volumes changes as well. Investigators are therefore using DECT to test whether it can be used on radiation treatment to rapidly assess response to treatment.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small Cell Lung Cancer Stage III | Lung Non-Small Cell Carcinoma | CURATED_BROADER | 0.78 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Change in the tumor's maximum iodine related attenuation (IRA) from baseline to on-treatment DECT.
- timeFrame
- 0, 1, 3, 5
- description
- This change in the maximum IRA will be compared with the change in the maximum standardized uptake value (SUV max) between baseline PET-CT and follow-up PET-CT at 3 months after treatment. For patients undergoing surgery, this change in the maximum IRA will be compared between patients who have a complete pathologic response, and those patients who do not.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients aged greater than 18 years with a diagnosis of stage III non-small cell lung cancer. * Planned treatment with either definitive chemoradiotherapy or preoperative chemoradiotherapy followed by surgical resection. * PET-CT study within 4 weeks of next available DECT study. * Patients must have measurable primary and nodal disease, defined by at least one lesion (primary and lymph node) greater than 1 cm. * Kidney function sufficient to tolerate iodine-based CT contrast. * No allergy to iodine-based contrast. * Ability to understand and the willingness to sign informed consent. Exclusion Criteria: * Participants with a prior history of thoracic radiotherapy. * Participants may not be receiving any other study agents. * Inability to tolerate CT contrast * Pregnant women are excluded from this study because radiotherapy has the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk of adverse events in nursing infants secondary to treatment of the mother with radiotherapy, breastfeeding should be discontinued if the mother is treated with radiotherapy. These potential risks may also apply to other agents used in this study.
References
Publications (0)
Data not yet available
No reference posted for this study.