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Feasibility study of adjuvant chemotherapy with S-1 in elderly patients with non-small-cell lung cancer

Feasibility study of adjuvant chemotherapy with S-1 in elderly patients with non-small-cell lung cancer - Feasibility study of adjuvant chemotherapy with S-1 in elderly patients with non-small-cell lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002383
Enrollment
25
Registered
2009-08-25
Start date
2009-04-01
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

Adjuvant chemotherapy of eight courses (2-week administration and 1-week withdrawal): S-1 dose of 67mg/m2 twice daily

Sponsors

Lung Oncology Group in Kyushu, Japan (LOGIK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically confirmed NSCLC 2)p-Stage IB, II and III & complete resection 3)No prior treatment 4)Adjuvant chemotherapy within 4-8 weeks 5)ECOG PS 0-1 6)Age 70 or older 7)Adequate organ function 8)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Past history of drug hypersensitivity 2)Past history of myocardial infarction within 6 months 3)Interstitial pneumonia or active lung fibrosis 4)Uncontrolled heart diseases 5)Uncontrolled psychiatric disorders 6)Uncontrolled diabetes 7)Bowel problems 8)Active infection 9)Severe complications 10)Active concomitant malignancy

Design outcomes

Primary

MeasureTime frame
The percentage of patients who accomplished S-1 therapy of eight courses.

Secondary

MeasureTime frame
Adverse events The relative total administration dose of S-1

Countries

Japan

Contacts

Public ContactNoriyuki Ebi

Iizuka Hospital Department of respiratory medicine

0948-22-3800

Outcome results

None listed

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