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Biweekly Paclitaxel+Carboplatin for elderly patients with untreated nonresectable non-small cell lung cancer

Biweekly Paclitaxel+Carboplatin for elderly patients with untreated nonresectable non-small cell lung cancer - Biweekly Paclitaxel+Carboplatin for elderly patients with untreated nonresectable non-small cell lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001328
Enrollment
65
Registered
2008-08-23
Start date
2007-01-01
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

Paclitaxel and carboplatin are given on day1 and day15 every 28days.

Sponsors

Keio University School of Medicine Division of Pulmonary Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients who were histologically or cytologically confirmed non-small cell lung cancer. 2)Patients who have measurable lesion. 3)No prior chemotherapy. 4)Stage IIIB or IV. 5)ECOG PS 0-2 6)Older than 70years old. 7)Patients who have adequate organ function. WBC>=4000/mm3 neutrophil count>=2000/mm3 Platelet count>=100,000/mm3 Hemoglobin>=9.0g/dl GOT,GPT within twice the upper limit of normal of institution Serum creatinine <=1.5mg/dl Normal ECG or UCG 8)Patients who have no severe complication. 9)Patients who have estimated life expectancy longer than 1 month. 10)Written informed consent.

Exclusion criteria

Exclusion criteria: 1)Patients with severe heart disease. 2)Patients with recent history of myocardial infarction. 3)Patients with liver cirrhosis. 4)Patients with pulmonary fibrosis or interstitial pneumonitis with symptoms or apparent abnormalities on chest X-ray. 5)Patients with severe diabetis mellitus. 6)Patients with ileus. 7)Patients with infection. 8)Patients with severe complications. 9)Patients with peripheral neuropathy. 10)Patients with severe mental disorder. 11)Patients with severe drug allergy. 12)Patients judged unfit to be enrolled in the study by the investigator .

Design outcomes

Primary

MeasureTime frame
Response Rate

Countries

Japan

Outcome results

None listed

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