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PhaseII study of maintenance S-1 after chemotherapy with platinium+pemetrexed in advanced nonsquamous NSCLC.

PhaseII study of maintenance S-1 after chemotherapy with platinium+pemetrexed in advanced nonsquamous NSCLC. - PhaseII study of maintenance S-1 after chemotherapy with platinium+pemetrexed in advanced nonsquamous NSCLC.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009275
Enrollment
22
Registered
2012-11-06
Start date
2012-11-06
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 Squamous Non Small Cell Lung Cancer

Interventions

Sponsors

Kansai Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically or cytologically confirned advanced non-small-cell lung cancer (NSCLC) 2)stage IV or postoperative recurrence patients 3)Patients previously treated with platinum- based chemotherapy for four cycles and except PD cases 4)more than 20 years old 5)ECOG PS 0-2 6)Measurable lesion 7)Adequate organ function 8)patients who can take orally 9)Signed informed consent

Exclusion criteria

Exclusion criteria: 1)Interstitial pneumonia or pulmonary fibrosis on chest X-ray 2) History of serious drug allergy 3)Patients with active double cancer 4)Patients with pleural or pericardial effusion ,or ascites 5)Being treated with flucytosine. 6) History of serious infection 7)History of HBs antigen 8)Patients with significant complications a) Uncontrolled angina pectoris, myocardial infarction, heart failure within 3 months b)Uncontrolled diabetes or hypertension c)Current severe infection, or suspicious of severe infection d) Patients whose participation in the trial is judged to be inappropriate by the attending doctor. (e.g., ileus, bleeding tendency, diarrhea and varicella) 9 )Symptomatic brain metastases 10)Patients with pregnancy or lactation 11)patients whom it is judged to have difficulty in participation in study because of psychosis or neurologic disease 12)Patients whose participation in the trial is judged to be inappropriate by the attending doctor.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival

Secondary

MeasureTime frame
Overall Survival, Response Rate, Safety

Countries

Japan

Outcome results

None listed

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