Stereotactic Body Radio Therapy (SBRT) for Early-stage Non Small Cell Lung Cancer (NSCLC) (SBRT-NSCLC)
Primary Purpose
Non Small Cell Lung Cancer
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
SBRT by cyberknife
SBRT by linear accelerator
Conformational radiotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Non Small Cell Lung Cancer focused on measuring SBRT, non-operated, non-metastatic, non-small-cell lung cancer, conformational radiotherapy, non-operated non-metastatic non-small-cell lung cancer
Eligibility Criteria
Inclusion Criteria:
Non-operated non-small-cell lung cancer (NSCLC) (inoperable tumor or patient refusal of surgery)
- cytologically or histologically proven NSCLC Or
- primitive pulmonary tumor of unproven malignancy
- macroscopically normal bronchial endoscopy, negative cytology and biopsies
- AND size increase on 2 successive scans (at 10-12 weeks interval)
- AND hypermetabolic PET-CT pattern
- AND absence of other proven etiology
- Tumor < 5cm, distant (> 1.5 cm) from large vessels, principally in the bronchus and spinal-cord
- No metastasis: M0
- No lymph node involvement: N0
- Functional respiratory evaluation (FRE) compatible with thoracic irradiation
- Maximum expiratory flow-volume > 30% theoretical value
- Age >= 18
- ECOG PS <= 2
- Female patients of childbearing potential: effective method of contraception
- Written advice of the RCP (conciliation meeting) present in the patient file
- Mandatory affiliation with a social security system
- Written, signed informed consent
Exclusion Criteria:
- Previously operated tumors
- Previous thoracic irradiation
- Previous or concurrent primary malignancies at other sites (except basocellular skin cancer or cervical cancer in situ or complete remission for more than 5 years)
- Life expectancy < 6 months
- Pregnant or lactating woman
- Difficult follow-up
- Patient deprived of freedom
Sites / Locations
- Centre Georges François Leclerc
- Centre Oscar Lambret
- Centre Leon Berard
- Centre Val d'Aurelle Paul Lamarque
- Centre Antoine Lacassagne
- Hôpital Tenon
- CHLS
- Centre René Gauducheau
- Centre Alexis Vautrin
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Other
Other
Other
Arm Label
1 - SBRT using cyberknife
2 - SBRT using linear accelerator
3 - Conformational radiotherapy
Arm Description
SBRT using cyberknife: treatment = 2x15 Gy during 2 weeks
SBRT using linear accelerator: treatment = 2x15 Gy during 2 weeks
Conformational radiotherapy: treatment = 5x2 Gy during 7 weeks
Outcomes
Primary Outcome Measures
Evaluation of local control in patients with non-operated, non-metastatic non-small-cell lung cancer treated by radiotherapy
Secondary Outcome Measures
Health economic evaluation of the various methods used for stereotactic radiotherapy
Prospective evaluation of acute and late toxicities of SBRT
Study of quality of life in the 3 groups
Evaluation of progression-free survival and overall survival in the 3 groups
Full Information
NCT ID
NCT00870116
First Posted
March 25, 2009
Last Updated
March 5, 2013
Sponsor
Centre Leon Berard
Collaborators
The Biostatistics and Therapy Evaluation Unit, National Cancer Institute, France
1. Study Identification
Unique Protocol Identification Number
NCT00870116
Brief Title
Stereotactic Body Radio Therapy (SBRT) for Early-stage Non Small Cell Lung Cancer (NSCLC)
Acronym
SBRT-NSCLC
Official Title
SBRT Radiotherapy for Non-operated Non-small-cell Lung Cancer (NSCLC), T1-T2, N0, M0
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Unknown status
Study Start Date
April 2009 (undefined)
Primary Completion Date
March 2013 (Anticipated)
Study Completion Date
March 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Leon Berard
Collaborators
The Biostatistics and Therapy Evaluation Unit, National Cancer Institute, France
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate local disease control after 2 years in patients with non-metastatic, non-operated non-small-cell lung cancer treated by radiotherapy.
Eligible patients will be recruited and registered consecutively (no randomization). The estimated inclusion period is approximately 24 months. The duration of the research is 4 years.
The number of patients required in this multicentric prospective study is 120:
20 patients in the SBRT-1 arm (cyberknife),
80 patients in the SBRT-2 arm (linear accelerator-based)
20 patients in the conformational radiotherapy arm.
This is a prospective, multicentric, non comparative and non randomized study.
Detailed Description
The main objective of this study is to do a health economic evaluation of innovating techniques in radiotherapy.
SBRT is the very precise delivery of high-powered radiation to small target volumes, using multiple low-intensity beams. Extremely precise patient positioning and target location is essential for accurate treatment delivery.
Several studies have shown a benefit of SBRT in terms of local control and progression-free survival, in particular for the treatment of cerebral metastases of limited number and size.
The development of this technique is recent. The number of treatment sessions is low: 1 to 4.
But the patient is exposed to a major risk of toxicity in several organs: the bronchi, the lungs, large vessels, the oesophagus and the spinal-cord.
Pulmonary SBRT imposes strict rules and the use of specific equipment.
Extra-cranial SBRT can be realized using either:
Conventional linear-accelerator equipped SBRT,
Cyberknife SBRT.
3 groups of treatment will be evaluated in this study:
SBRT by cyberknife,
SBRT by linear accelerator,
Conformational radiotherapy (free breathing or breath holding).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non Small Cell Lung Cancer
Keywords
SBRT, non-operated, non-metastatic, non-small-cell lung cancer, conformational radiotherapy, non-operated non-metastatic non-small-cell lung cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1 - SBRT using cyberknife
Arm Type
Other
Arm Description
SBRT using cyberknife: treatment = 2x15 Gy during 2 weeks
Arm Title
2 - SBRT using linear accelerator
Arm Type
Other
Arm Description
SBRT using linear accelerator: treatment = 2x15 Gy during 2 weeks
Arm Title
3 - Conformational radiotherapy
Arm Type
Other
Arm Description
Conformational radiotherapy: treatment = 5x2 Gy during 7 weeks
Intervention Type
Radiation
Intervention Name(s)
SBRT by cyberknife
Intervention Description
treatment = 2x15 Gy during 2 weeks
Intervention Type
Radiation
Intervention Name(s)
SBRT by linear accelerator
Intervention Description
treatment = 2x15 Gy during 2 weeks
Intervention Type
Radiation
Intervention Name(s)
Conformational radiotherapy
Intervention Description
treatment = 5x2 Gy during 7 weeks (free breathing or breath holding)
Primary Outcome Measure Information:
Title
Evaluation of local control in patients with non-operated, non-metastatic non-small-cell lung cancer treated by radiotherapy
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Health economic evaluation of the various methods used for stereotactic radiotherapy
Time Frame
during treatment / post treatment
Title
Prospective evaluation of acute and late toxicities of SBRT
Time Frame
M1, M3, M6, M12, M18 and M24
Title
Study of quality of life in the 3 groups
Time Frame
inclusion, M1, M3, M12
Title
Evaluation of progression-free survival and overall survival in the 3 groups
Time Frame
No time
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Non-operated non-small-cell lung cancer (NSCLC) (inoperable tumor or patient refusal of surgery)
cytologically or histologically proven NSCLC Or
primitive pulmonary tumor of unproven malignancy
macroscopically normal bronchial endoscopy, negative cytology and biopsies
AND size increase on 2 successive scans (at 10-12 weeks interval)
AND hypermetabolic PET-CT pattern
AND absence of other proven etiology
Tumor < 5cm, distant (> 1.5 cm) from large vessels, principally in the bronchus and spinal-cord
No metastasis: M0
No lymph node involvement: N0
Functional respiratory evaluation (FRE) compatible with thoracic irradiation
Maximum expiratory flow-volume > 30% theoretical value
Age >= 18
ECOG PS <= 2
Female patients of childbearing potential: effective method of contraception
Written advice of the RCP (conciliation meeting) present in the patient file
Mandatory affiliation with a social security system
Written, signed informed consent
Exclusion Criteria:
Previously operated tumors
Previous thoracic irradiation
Previous or concurrent primary malignancies at other sites (except basocellular skin cancer or cervical cancer in situ or complete remission for more than 5 years)
Life expectancy < 6 months
Pregnant or lactating woman
Difficult follow-up
Patient deprived of freedom
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Line CLAUDE, MD
Organizational Affiliation
Centre Léon Bérard, LYON
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Georges François Leclerc
City
Dijon
ZIP/Postal Code
21000
Country
France
Facility Name
Centre Oscar Lambret
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
Centre Leon Berard
City
Lyon
ZIP/Postal Code
69008
Country
France
Facility Name
Centre Val d'Aurelle Paul Lamarque
City
Montpellier
ZIP/Postal Code
34000
Country
France
Facility Name
Centre Antoine Lacassagne
City
Nice
ZIP/Postal Code
06000
Country
France
Facility Name
Hôpital Tenon
City
Paris
ZIP/Postal Code
75012
Country
France
Facility Name
CHLS
City
Pierre Bénite
ZIP/Postal Code
69495
Country
France
Facility Name
Centre René Gauducheau
City
Saint Herblain
ZIP/Postal Code
44000
Country
France
Facility Name
Centre Alexis Vautrin
City
Vandoeuvre les Nancy
ZIP/Postal Code
54511
Country
France
12. IPD Sharing Statement
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Stereotactic Body Radio Therapy (SBRT) for Early-stage Non Small Cell Lung Cancer (NSCLC)
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