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Phase II clinical trial of alternate-day therapy of S-1 plus carboplatin for squamous cell lung cancer.

Phase II clinical trial of alternate-day therapy of S-1 plus carboplatin for squamous cell lung cancer. - Phase II clinical trial of alternate-day therapy of S-1 plus carboplatin for squamous cell lung cancer.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013613
Enrollment
50
Registered
2014-04-03
Start date
2012-07-05
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

squamous cell lung cancer

Interventions

Carboplatin plus alternative S-1

Sponsors

Shimane university Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Chemotherapy not enforcement cases of stage IV or stage IIIB clinical stage radical irradiation with a diagnosis of squamous cell carcinoma of the lung biopsy or by cytology is not possible.Patients with measurable disease.Performance Status is 0 or 1.WBC more than 4,000 uL,Neutrocyte more than 1,500/uL,Plate more than 100,000/uL,Hb more than 9.0 g/dL,AST/ALT less than 100 IU/L,Total bilirubin less than 1.5 mg/dL,eGFR more than 40 ml/min./1.73m2,SpO2 more than 94 percent.Cases can be expected survival of more than 12 weeks from the start of the administration date.

Exclusion criteria

Exclusion criteria: Case you are planning to radiation concurrent chemotherapy.In addition, patients who had made every irradiation in 2 weeks.Came into force the definitive operation or cases of enforcement plan.Cases are complicated by serious infections.Patients with brain metastases that have clinical symptoms.Cases with pericardial effusion storage chest or ascites requiring drainage.Patients with pulmonary fibrosis or interstitial pneumonia.Mental illness to be a clinical problem.Patients with overlapping cancer activity.Cases there is a possibility that pregnant women, nursing mothers, pregnant.

Design outcomes

Primary

MeasureTime frame
Response rate

Secondary

MeasureTime frame
Adverse event, Biomarker, Dose Intensity

Countries

Japan

Contacts

Public ContactKoba Naoya

Shimane university Hospital Division of Medical Oncology & Respiratory Medicine

smn70329@med.shimane-u.ac.jp0853-20-2580

Outcome results

None listed

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