Skip to content

Phase II study of carboplatin-gemcitabine combination chemotherapy in elderly patients with advanced non–small cell lung cancer

Phase II study of carboplatin-gemcitabine combination chemotherapy in elderly patients with advanced non–small cell lung cancer - Phase II study of carboplatin-gemcitabine combination chemotherapy in elderly patients with advanced non–small cell lung cancer

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-C000000112
Enrollment
55
Registered
2005-09-04
Start date
2004-10-01
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

day 1: CBDCA 4AUC GEM 1000mg/m2 day 8: GEM 1000mg/m2

Sponsors

Kumamoto University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with histologically or cytologically confirmed NSCLC who were 70 years or older at diagnosis, had measurable disease on thoracic computed tomography (CT) scans, and had not previously received chemotherapy were eligible for enrollment in the study. An additional requirement was that the disease was inoperable as a result of substantial comorbidity, impairment of respiratory function, or anatomic contraindication. Patients who relapsed after complete tumor resection or in whom resection was incomplete were also eligible. Further entry criteria included an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 as well as adequate bone marrow (leukocyte count, 4000 to 12,000/µL; hemoglobin concentration, >9.0 g/dL; platelet count, >100,000/µL), renal (serum creatinine concentration, 70 torr) function.

Exclusion criteria

Exclusion criteria: Individuals with active infection, severe heart disease, active concomitant malignancy, or pleural or pericardial effusion requiring drainage were excluded.

Design outcomes

Primary

MeasureTime frame
response rate

Countries

Japan

Contacts

Public ContactJi-ichiro Sasaki

Kumamoto University School of Medicine Department of Respiratory Medicine

saji@gpo.kumamoto-u.ac.jp

Outcome results

None listed

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