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Adjuvant therapy in pathological stage IA2-IIA EGFR-mutated NSCLC: a multicenter prospective observational study

Adjuvant therapy in pathological stage IA2-IIA EGFR-mutated NSCLC: a multicenter prospective observational study - WJOG17123L

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000054291
Enrollment
800
Registered
2024-05-07
Start date
2024-05-07
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(non-squamous cell cancer)

Interventions

None listed

Sponsors

National Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Non-squamous non-small cell lung cancer Pathological stage IA2 and high risk, or stage IA3, IB, IIA Entire lesion diameter 5cm or less Complete resection by lobectomy or segmentectomy EGFR gene mutation has been confirmed Postoperative adjuvant therapy with tegafur/uracil or osimertinib, or observation without treatment is planned. 18 years or older ECOG performance status 0-1 Written consent has been obtained from the patient

Exclusion criteria

Exclusion criteria: Cases that fall under any of the following items will be excluded. 1) Have active multiple cancers*1 2) Have a local or systemic active infection that requires treatment 3) Pregnant women, lactating women, and women who may be currently pregnant. 4) Registration in this study is judged to be difficult due to a clinically problematic mental illness. 5) Receiving continuous systemic administration of steroids or immunosuppressants 6) Have a history of severe hypersensitivity 7) Exclusion provisions regarding complications (a) Have a history of ILD, drug-induced ILD, radiation pneumonitis requiring steroid treatment, or have active ILD. (b) Viral hepatitis HBs antigen positive or HCV antibody positive (c) HIV positive (however, negative confirmation by serum test is not required). 8) Other cases deemed inappropriate by the attending physician

Design outcomes

Primary

MeasureTime frame
Disease-free survival

Countries

Japan

Contacts

Public ContactTomohiro Miyoshi

National Cancer Center Hospital East Division of Thoracic Surgery

tmiyoshi@east.ncc.go.jp0471331111

Outcome results

None listed

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