Skip to content

Feasibility study of dose eslation and concentration in stereotactic body radiotherapy (SBRT) for lung tumors

Feasibility study of dose eslation and concentration in stereotactic body radiotherapy (SBRT) for lung tumors - Feasibility study of dose eslation and concentration in SBRT for lung tumors

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006172
Enrollment
15
Registered
2011-08-16
Start date
2011-08-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

T1-4N0M0 non-small cell lung cancer solitary or ipsilateral two lung metastasis

Interventions

Stereotactic body radiotherapy

Sponsors

Ofuna SBRT study group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1-1.Histologically or cytologically (class IV or V) diagnosed NSCLC or solitary or ipsilateral two lung metastasis 1-2.radiographically diagnosed NSCLC (with no elevation of NSE or proGRP) or solitary or ipsilateral two lung metastasis 2.CT diagnosis within 60 days and FDG-PET diagnosis within 90 days 3.No other intrathoracic lesions 4.Dose constraints of the organs at risk seem to be limited within range 5.No previous thoracic radiation 6.No previous chemotherapy 7.ECOG PS=0-2 8.GOLD stage 0-II 9.Written informed consent

Exclusion criteria

Exclusion criteria: 1. apparent interstitial pneumonitis and fibrosis 2. active inflamation without oral drugs 3. double cancer 4. pregnancy 5. psychiatric disorder 6. steroid administration 7. oxygen administration 8. fever of 38.0 degrees centigrade or higher 9. narcotics administration for coughing

Design outcomes

Primary

MeasureTime frame
incidence of Grade 2 or more radiation pneumonits within 180 days after stereotactic radiotherapy

Secondary

MeasureTime frame
incidence of Grade 3 or more radiation pneumonitis, adverse events, severe adverse events, local progression free survival, 3-year local progression free survival, event free survival

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026