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Intensity Modulated Radiotherapy (IMRT) in Stage III Non Small Cell Lung Cancer (NSCLC) - A Feasibility Study

Intensity Modulated Radiotherapy (IMRT) in Stage III Non Small Cell Lung Cancer (NSCLC) - A Feasibility Study - A feasibikity study of IMRT for locally advanced NSCLC

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000017780
Enrollment
22
Registered
2015-06-06
Start date
2015-08-01
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

Non-small cell lung cancer

Interventions

Chemotherapy and IMRT

Sponsors

Shizuoka Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically or cytologically confirmed NSCLC 2) Inoperable 3) Stage III NSCLC patients who are suitable for definitive RT 4) No previous chemotherapy and thoracic radiotherapy 5) Who have measurable lesions 6) Age 20-74 years old 7) Performance status 0,1 8) Who are able to eat by oral intake 9) Who are without severe co-morbid conditions 10) Informed consent

Exclusion criteria

Exclusion criteria: 1)Active double cancer 2)History of severe infections or complications 3)HBs antigen positive 4)History of thoracic radiotherapy 5)Radiographically (chest CT image) confirmed interstitial pneumonitis or pulmonary fibrosis 6)Severe emphysema, chronic bronchitis, asthma 7)History of drug-induced pneumonia or severe drug allergies 8)Uncontrolled diabetes despite continuing treatment of insulin 9)Unstable angina, cardiac infarction within 6 months before enrollment 10)A fever of over 38 degrees 11)Continuous systemic administration of steroid or immunosuppressant 12)Pregnant women 13)Patients with severe mental illness 14)Unsuitable patients judged by the attending physician

Design outcomes

Primary

MeasureTime frame
The ratio of the patients who completed chemoradiotherapy using IMRT

Secondary

MeasureTime frame
safety, progression free survival, overall survival, first relapse site

Countries

Japan

Contacts

Public ContactHideyuki Harada

Shizuoka Cancer Center Radiation Oncology

h.harada@scchr.jp81559895222

Outcome results

None listed

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