Status:

COMPLETED

Novel Lung Functional Imaging for Personalized Radiotherapy

Lead Sponsor:

University of California, Davis

Conditions:

Lung Cancer

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

The primary objective of this study is to assess the safety and feasibility of personalized radiotherapy with four-dimensional (4D) computed tomography (CT)-based pulmonary ventilation imaging, which ...

Detailed Description

In this clinical trial, the investigators will assess the safety and feasibility of 4D CT ventilation image-guided personalized radiotherapy. The investigators will deliver personalized radiotherapy t...

Eligibility Criteria

Inclusion

  • Primary lung cancer or metastatic disease to the lungs to be treated with either conventionally-fractionated radiotherapy (CFRT) or hypo-fractionated stereotactic ablative radiotherapy (SABR).
  • Age restriction and/or gender/ethnic restrictions: Patients must be ≥18 years of age. There are no gender or ethnic restrictions.
  • Concurrent chemotherapy is allowed, but not required.
  • Life expectancy with treatment should be ≥6 months in the estimation of the treating physicians.
  • Zubrod performance status ≤2
  • Adequate marrow and hepatic function defined as Hgb ≥8; platelets ≥100k; ANC≥1500; LFTs ≤2x upper limit of normal and creatinine ≤1.3 or creatinine clearance of ≥50
  • Patient must be able to provide study specific informed consent prior to study entry.

Exclusion

  • Prior radiotherapy for thoracic cancer or other malignancy leading to any overlap of planned radiotherapy fields.
  • For patients undergoing definitive CFRT, patients with distant metastatic disease are not eligible.
  • For patients undergoing SABR, both early stage primary lung cancer patients and those with limited metastatic disease to the lungs are eligible; however, patients with oligometastatic disease should have a controlled primary and no more than one other involved organ system.
  • Children (\<18 years of age), pregnant women, University of California employees or students, or prisoners will be excluded from this study.

Key Trial Info

Start Date :

September 15 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 19 2021

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT02308709

Start Date

September 15 2014

End Date

November 19 2021

Last Update

November 10 2022

Active Locations (1)

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1

University of California Davis Medical Center

Sacramento, California, United States, 95817