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Phase II study of alternate-day treatment with S-1 as adjuvant chemotherapy for patients with lung cancer.

Phase II study of alternate-day treatment with S-1 as adjuvant chemotherapy for patients with lung cancer. - Phase II study of alternate-day treatment with S-1 as adjuvant chemotherapy for patients with lung cancer.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011370
Enrollment
25
Registered
2013-08-05
Start date
2013-05-01
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

lung cancer

Interventions

Adjuvant treatment of S-1 is administered on alternate-day for 1 year after surgery.

Sponsors

Chiba University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. histologically proven non-small cell lung cancer with stage IB to IIIA 2. curative resection (R0) at the prior surgery 3.without any prior radiation therapy, chemotherapy for primary lung cancer. 4. age: 20< years old 5. PS(ECOG): 0 or 1 6. without any other severe diseases WBC 3,000<= and => 12,000/mm3 Platelet 100,000/mm3 <= Hemoglobin 9.0 g.dl <= Total bilirubin 1.5 mg/dl => AST, ALT 100 IU/L <= SPO2 90% <= or PaO2 60mmHg <= Creatinin clearance 40 ml/min/body <= **Cockcroft-Gault method is available 7.patients who can start adjuvant treatment within 8 weeks postoperatively. 8. written informed consents

Exclusion criteria

Exclusion criteria: 1) patients who cannot take S-1 1.with severe allergic history against the ingredients of S-1. 2. with sever bone marrow suppression, renal or liver dysfunction 3. patients who need other fluorouracil 4. patients who need flucitosine. 2) with severe allergic history against medicines 3) with history of myocardial infarction in 6 months. 4)with other severe diseases (cardiac failure,mental disorder, infection or other severe complications) 5) with uncontrolled DM 6) with watery diarrhea 7) with double cancer and or multiple cancer 8)doctors' stop not to register to the study

Design outcomes

Primary

MeasureTime frame
The ratio of the patients who completed the course

Countries

Japan

Contacts

Public ContactHidemi Suzuki

Chiba University Graduate School of Medicine Department of General Thoracic Surgery

hidemisuzukidesu@yahoo.co.jp043-222-7171

Outcome results

None listed

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