Functional Imaging in Lung SBRT

Sponsor
University of Michigan Rogel Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT03121300
Collaborator
Department of Health and Human Services (U.S. Fed)
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Study Details

Study Description

Brief Summary

Little is known about the safety of body radiation therapy (SBRT), especially the impact on pulmonary function, quality of life, and on functional changes within the lung itself. Radiation dose constraints and capturing functional changes on imaging are not well studied in this setting.

The current study aims to evaluate the utility of advanced imaging to measure lung function prior to and after treatment and to assess the feasibility of using this data to adapt SBRT planning.

Condition or Disease Intervention/Treatment Phase
  • Other: CT Scan
  • Other: Lung CT
  • Other: MRI
  • Other: Walk Test
  • Other: SGRQ
  • Other: Biological Sample Collection
  • Other: Toxicity
  • Other: Cardiac Assessment

Detailed Description

Stereotactic body radiation therapy (SBRT) is becoming a new standard for unresectable lung metastases and primary lung cancers.

However, it is becoming increasingly common for patients to undergo multiple courses of lung SBRT to synchronous and/or metachronous lung lesions. Further, the indications for SBRT are being expanded to patients who have very poor pulmonary function such as FEV1 < 0.5 L or DLCO < 35% predicted, who have large tumors (>3 cm), or who have centrally located lesions that abut great vessels and mainstem bronchi. Little is known about the safety of such treatments, especially the impact on pulmonary function, quality of life, and on functional changes within the lung itself. Radiation dose constraints and capturing functional changes on imaging are not well studied in this setting.

The current study aims to evaluate the utility of advanced imaging to measure lung function prior to and after treatment and to assess the feasibility of using this data to adapt SBRT planning. SPECT/CT will be used to measure ventilation and perfusion changes while. CT ventilation scans will be used to correlate functional changes observed on diagnostic SPECT/CT. Dynamic contrast enhanced MRI (DCE-MRI) will also be used to explore local vascular changes in the treated tumor. In patients whose tumors lie close to the heart, cardiac MRI will be used to investigate whether high doses of radiation per fraction are associated with changes in cardiac function. These imaging modalities may be used to potentially predict toxicity and patient response with the ultimate goal of prospectively adapt dose to individual patient and tumor characteristics. Lung function prior to and post-treatment will also be measured as a correlate of functional imaging changes. Identifying areas of the lung that are sub-functional or low-functioning may offer an opportunity to adapt stereotactic ablations that spare functional lung thereby making SBRT treatments to higher risk patients safer.

Study Design

Study Type:
Observational
Actual Enrollment :
33 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Functional Outcomes for Stereotactic Body Radiotherapy of Lung Lesions in High Risk Patients
Actual Study Start Date :
Feb 6, 2017
Actual Primary Completion Date :
Aug 30, 2019
Actual Study Completion Date :
Aug 30, 2019

Arms and Interventions

Arm Intervention/Treatment
High Risk Lung Cancer Patients

Other: CT Scan
Quantitative lung SPECT-CT

Other: Lung CT
CT lung ventilation

Other: MRI
DCE MRI

Other: Walk Test
6 minute hall walk test

Other: SGRQ
St. George Respiratory Questionnaire

Other: Biological Sample Collection
Blood Draw

Other: Toxicity
Toxicity Evaluation

Other: Cardiac Assessment
Cardiac MRI Scan

Outcome Measures

Primary Outcome Measures

  1. Longitudinal Changes in Lung Function [From baseline to 6 months post Radiation Treatment]

    To characterize longitudinal changes in lung function using SPECT/CT and CT ventilation scans in "high risk" patients undergoing standard SBRT treatments.

Secondary Outcome Measures

  1. Dosimetric Predictors to Assess Changes in Toxicity [From baseline to 6 months post Radiation Treatment]

    To explore radiation dosimetric predictors and correlates of SPECT-CT and CT ventilation functional imaging that predict toxicity in these patients.

  2. Changes in SPECT-CT Correlate with Changes in CT Ventilation [From baseline to 6 months post Radiation Treatment]

    To determine if early functional changes in SPECT-CT correlate with changes in CT ventilation, pulmonary function and patient reported decrements in lung function on the St. George Respiratory Questionnaire (SGRQ).

  3. To Assess Early Vascular Changes Using DCE-MRI [From baseline to 6 months post Radiation Treatment]

    To assess early vascular changes using DCE-MRI in the lung tumor treated with SBRT as a possible predictor of tumor response.

Other Outcome Measures

  1. Changes in Cardiac Function [From baseline to 6 months post Radiation Treatment]

    To explore if SBRT tumors that lie within 2 cm of the heart cause any changes in cardiac function on cardiac MRI

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients receiving SBRT lung treatment and who have any one of the following high risk features:

  • Lung lesion > 5 cm

  • DLCO < 35%

  • FEV1 < 0.5 L

  • Central lung tumors (defined as within 2 cm from the proximal bronchial tree)

  • Tumors that abut the great vessels, trachea, spinal cord, or esophagus

  • Prior lobectomy or pneumonectomy

  • Prior lung radiation (SBRT or conventional definitive lung radiation)

  • Patients must be 18 years of age or older

Exclusion Criteria:
  • Patients who have received targeted agents or systemic potentially radiosensitizing chemotherapy within 2 weeks of lung SBRT start

  • Pregnancy or lactation

  • Unable to tolerate MRI without anesthesia

  • Inability cooperate with the scans

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Michigan Ann Arbor Michigan United States 48109

Sponsors and Collaborators

  • University of Michigan Rogel Cancer Center
  • Department of Health and Human Services

Investigators

  • Principal Investigator: Shruti Jolly, M.D., University of Michigan

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Michigan Rogel Cancer Center
ClinicalTrials.gov Identifier:
NCT03121300
Other Study ID Numbers:
  • UMCC 2015.146
First Posted:
Apr 20, 2017
Last Update Posted:
Oct 17, 2019
Last Verified:
Oct 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Oct 17, 2019