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Phase I/II Study of Fractionated Stereotactic Radiotherapy for Medically Inoperable NSCLC or Metastatic Lung Tumours

Primary Purpose

Lung Neoplasms, Lung Cancer

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Fractionated Stereotactic Radiotherapy
Sponsored by
AHS Cancer Control Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Neoplasms focused on measuring lung neoplasms, metastatic lung cancer, stereotactic radiation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: non-small cell lung cancer less than 6cm; no mediastinal or distant metastases Open to Alberta,Canada Residents Exclusion Criteria: tumour size greater than 6cm; inadequate pulmonary function(ie. FEV1 less than 0.8 L), Karnofsky performance status less than 70, multiple co-morbid conditions

Sites / Locations

  • Tom Baker Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Schedule I (10 fractions)

Schedule II (4 fractions)

Arm Description

Subjects will receive a total of 10 stereotactic radiation treatments, given over 3 weeks.

Subjects will receive a total of 4 stereotactic radiation treatments, given over 2 weeks.

Outcomes

Primary Outcome Measures

Dose-limiting toxicity as defined by CTCAE V3 grade 4 or 5.
Each schedule will be evaluated according to the occurrence of DLTs observed.

Secondary Outcome Measures

Full Information

First Posted
July 11, 2006
Last Updated
September 20, 2017
Sponsor
AHS Cancer Control Alberta
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1. Study Identification

Unique Protocol Identification Number
NCT00351962
Brief Title
Phase I/II Study of Fractionated Stereotactic Radiotherapy for Medically Inoperable NSCLC or Metastatic Lung Tumours
Official Title
Phase I/II Study of Fractionated Stereotactic Radiotherapy for Medically Inoperable Non-Small Cell Lung Cancer (NSCLC) or Metastatic Lung Tumours
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Completed
Study Start Date
September 2006 (Actual)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2, 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AHS Cancer Control Alberta

4. Oversight

5. Study Description

Brief Summary
Medically inoperable lung cancer or metastatic lung tumours will be treated with fractionated stereotactic radiation using a schedule of 1) 12 Gy x 4 treatments or 2) 6 Gy x 10 treatments.
Detailed Description
You will be positioned in a special body mould while you are lying in the treatment position. This ensures that you are treated in the exact position each time. A soft plastic sheet may be placed over your body from the chest down. A vacuum device may be used to apply the sheet gently over you. This mild compression will ensure that you can breathe comfortably but will minimize any movement which may affect the accuracy of your treatments. A CT (computed tomography) scan will be done for your treatment planning. The CT scan will take approximately 45 minutes. In some cases, intravenous dye may be administered during the CT scan. You will be asked to hold your breath for a short time during the CT scan. If you are unable to hold your breath comfortably, the scan will be performed during your normal breathing cycle. In some cases, your doctor may also order a PET (positron emission tomography) scan. The treatment planning to be done by your oncologist and physicist will take approximately one to two weeks. After that is completed, your treatments will begin. Each treatment will take about 30 minutes. If the CT scans show that there is a lot of movement of your lung cancer due to breathing motion, your oncologist may recommend the insertion of a "fiducial" marker to help guide your treatments. An additional consent form will be obtained prior to this procedure. The "fiducial" marker is a tiny gold or stainless steel coil measuring about one inch long. It would be inserted into your lung in or next to the tumour by a respirologist via bronchoscopy under sedation. The procedure would take approximately 30 minutes, and you would be in hospital for about 4 hours. You would meet the respirologist in the clinic in consultation prior to the procedure so that he/she can tell you more about the procedure and assess your case in details to determine if it is safe for you to undergo the procedure. The insertion of the fiducial marker is considered part of your clinical care and a separate consent will be required prior to this procedure. You may choose not to undergo this procedure but still participate in this study. In some cases, your respirologist may have already inserted a fiducial marker at the time of diagnostic bronchoscopy after discussions with yourself and your radiation oncologist. The "fiducial" marker would be used to guide your radiation treatments during your normal breathing cycle. You will be assigned into one of the two study groups described below depending on the location of your tumour: Schedule I (10 fractions): You will receive a total of 10 stereotactic radiation treatments, given over 3 weeks. Schedule II (4 fractions): You will receive a total of 4 stereotactic radiation treatments, given over 2 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Neoplasms, Lung Cancer
Keywords
lung neoplasms, metastatic lung cancer, stereotactic radiation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
58 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Schedule I (10 fractions)
Arm Type
Experimental
Arm Description
Subjects will receive a total of 10 stereotactic radiation treatments, given over 3 weeks.
Arm Title
Schedule II (4 fractions)
Arm Type
Experimental
Arm Description
Subjects will receive a total of 4 stereotactic radiation treatments, given over 2 weeks.
Intervention Type
Procedure
Intervention Name(s)
Fractionated Stereotactic Radiotherapy
Primary Outcome Measure Information:
Title
Dose-limiting toxicity as defined by CTCAE V3 grade 4 or 5.
Description
Each schedule will be evaluated according to the occurrence of DLTs observed.
Time Frame
At the completion of accrual, an analysis with respect to acute toxicity will be performed after all patients have been followed a minimum of 90 days from the start of RT.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: non-small cell lung cancer less than 6cm; no mediastinal or distant metastases Open to Alberta,Canada Residents Exclusion Criteria: tumour size greater than 6cm; inadequate pulmonary function(ie. FEV1 less than 0.8 L), Karnofsky performance status less than 70, multiple co-morbid conditions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harold P Lau, MD
Organizational Affiliation
Tom Baker Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tom Baker Cancer Center
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 4N2
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Phase I/II Study of Fractionated Stereotactic Radiotherapy for Medically Inoperable NSCLC or Metastatic Lung Tumours

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