J Korean Cancer Assoc.
2000 Aug;32(4):690-698.
A Phase II Study with Vinorelbine and Carboplatin in Patients
with Advanced Non-small Cell Lung Cancer
- Affiliations
-
- 1Department of Internal Medicine, Korea Veterans Hospital, Seoul, Korea.
Abstract
-
PURPOSE: To evaluate the efficacy and safety of vinorelbine and carboplatin in advanced non-
small-cell lung cancer (NSCLC).
MATERIALS AND METHODS
Between August 1998 and July 1999, 25 patients were enrolled. The
median age was 68 (range, 46~77) years and male:female ratio was 23:2. Two patients had
stage IIIa, 15 had stage IIIb and 8 had stage IV. Sixteen patients had ECOG performance status
of 0 or 1 and 9 had 2 or 3. Sixteen patients had squamous cell carcinoma, 8 had adenocarcinoma
and 1 had undifferentiated NSCLC. Treatment consists of intravenous carboplatin 400 mg/m2 on
day 1 and vinorelbine 25 mg/m2 on days 1 and 8. The treatment was repeated every 28 days.
RESULTS
Twenty-three of 25 patients were evaluable. Partial response were observed in 11
patients. The overall response rate was 48% (95% confidence interval: 27~69%) and the median
response duration was 19 (range 7 ~44 ) weeks. The median survival of 25 patients was 52
(range 3~53 ) weeks. Toxicities were evaluated by WHO criteria. During a total of 108 cycles,
granulocytopenia worse than WHO grade 3 occurred in 2%, thrombocytopenia in 4% and anemia
in 10%, respectively. Treatment-related death occurred in 1 patient due to sepsis during cytopenic
period. Non-hematologic toxicity was minor and easily controlled.
CONCLUSION
A combination chemotherapy of intravenous vinorelbine and carboplatin has
relatively high activity with acceptable toxicities in patients with advanced NSCLC.