Skip to content

The Utility of PET/CT in Erlotinib treatment for Non-Small Cell cancer

The Utility of PET/CT in Erlotinib treatment for Non-Small Cell cancer - The Utility of PET/CT in Erlotinib treatment for Non-Small Cell cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002044
Enrollment
20
Registered
2009-06-08
Start date
2009-06-01
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

PET/CT 2 days after erlotinib administration

Sponsors

Department of Respiratory Medicine, Allergy and Rheumatic Diseases, Osaka University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) NSCLC 2) no history of treatment of EGFR-TKI 3) At least one measurable lesion 4) Age>20 years 5) Performance status(PS) of 0 to 2 6) Written informed consent

Exclusion criteria

Exclusion criteria: 1)History of radiation therapy for primary site 2)Severe infection 3)Bowel obstruction 4)Interstitioal pneumonia or lung fibrosis 5)History of any thoracic radiation therapy 6)Active concomitant malignancy 7)Sever heart disease 8)No regulatory condition because of psychological disease 9)Pregnant women or somen willing child-bearing 10)inadequate condition siagnosed by primary physician

Design outcomes

Primary

MeasureTime frame
Relationship between uptake of FDG 2 days after the erlotinib administration and tumor size on CT

Secondary

MeasureTime frame
OS, PFS

Countries

Japan

Contacts

Public ContactIsao Tachibana

Osaka University Graduate School of Medicine Department of Respiratory Medicine, Allergy and Rheumatic Diseases

itachi02@imed3.med.osaka-u.ac.jp06-6879-3831

Outcome results

None listed

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