[Combination chemotherapy with gemcitabine plus cisplatin in the treatment of advanced non-small cell lung cancer.].
L Li, L Zhang, J Li, M Wang, Zhengjiu Cui
Abstract
L Li, L Zhang, J Li, M Wang, Zhengjiu Cui
Abstract
BACKGROUND: To determine the clinical activity and toxicity of a novel combination chemotherapy with gemcitabine and cisplatin in the treatment of non-small cell lung cancer (NSCLC) . METHODS: We chose 12 previously untreated patients with NSCLC in stages III (41. 7 %) and IV (58. 3 %) . Gemcitabine was given on day 1 , 8 and 15 at a dose of 1 000 mg/m(2) and cisplatin at a dose of 100 mg/m(2) on day 1. The chemotherapy was repeated every 28 days. RESULTS: Eleven patients were evaluable for response. Six patients (54. 5 %) achieved partial response. The overall response rate was 54. 5 %. The main toxicity was hematological : neutropenia and thrombocytopenia at WHO-CTC grade III-IV occured in 33. 3 % and 41. 7 % of the patients respectively. The non-hematological toxicity was mild and tolerable. Only 15. 2 % of total patients were dose-reduced or omitted due to toxicity. Within follow-up 3 patients were still alive and 8 died. The median overall survival period was 8 months. CONCLUSIONS: This regimen of gemcitabine and cisplatin is effective and well-tolerated in the treatment of NSCLC , especially in the elderly patients. The clinical symptoms relieve and the living quality improves significantly.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
BACKGROUND: To determine the clinical activity and toxicity of a novel combination chemotherapy with gemcitabine and cisplatin in the treatment of non-small cell lung cancer (NSCLC) . METHODS: We chose 12 previously untreated patients with NSCLC in stages III (41. 7 %) and IV (58. 3 %) . Gemcitabine was given on day 1 , 8 and 15 at a dose of 1 000 mg/m(2) and cisplatin at a dose of 100 mg/m(2) on day 1. The chemotherapy was repeated every 28 days. RESULTS: Eleven patients were evaluable for response. Six patients (54. 5 %) achieved partial response. The overall response rate was 54. 5 %. The main toxicity was hematological : neutropenia and thrombocytopenia at WHO-CTC grade III-IV occured in 33. 3 % and 41. 7 % of the patients respectively. The non-hematological toxicity was mild and tolerable. Only 15. 2 % of total patients were dose-reduced or omitted due to toxicity. Within follow-up 3 patients were still alive and 8 died. The median overall survival period was 8 months. CONCLUSIONS: This regimen of gemcitabine and cisplatin is effective and well-tolerated in the treatment of NSCLC , especially in the elderly patients. The clinical symptoms relieve and the living quality improves significantly.
Key concepts: Gemcitabine, Medicine, Cisplatin, Lung cancer, Neutropenia, Toxicity, Regimen, Chemotherapy