Abstract
Purpose: To analyse the response, toxicity, and survival of chemotherapy with gemcitabine and cisplatin for chemotherapy-naive patients with advanced non-small cell lung cancer. Patients and Methods: From 1999 to 2001, thirty one patients with stage IIIB to IV non-small cell lung cancer received chemotherapy. Twenty seven patients (87.1%) presented with locally advanced (stage IIIB - 3 patients, 9.7%) or metastatic (stage IV - 24 patients, 77.4%), and 4 patients (12.9%) had metastases after previous radical surgery. Chemotherapy consisted of intravenous gemcitabine 1250 mg/m2 on days 1 and 8 and cisplatin 80 mg/m2 on day 8 given every 3 weeks for 6 cycles. Results: All patients were evaluable for response and toxicity. The total number of cycles was 157 (mean, 5 cycles). The average given relative dose intensity was 0.91. Therapy was well-tolerated. Grade 3 to 4 toxicities included neutropenia in 9 patients (29%), thrombocytopenia in 3 patients (9.7%), and anaemia in 1 patient (3.2%). No complete responces were documented and 9 patients (29%) achieved a partial response. The disease remained stable for 10 patients (32.3%). The median progression-free survival was 7 months, the median survival was 12.5 months, and 1-year survival was 53%. Conclusion: Chemotherapy with gemcitabine and cisplatin for patients with advanced non-small cell lung cancer is well tolerated and is an appropriate option for first-line therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 8-11 |
| Number of pages | 4 |
| Journal | Oncology Forum |
| Volume | 6 |
| Issue number | 4 |
| State | Published - 30 Oct 2003 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Chemotherapy
- Cisplatin
- Efficacy
- Non small cell lung carcinoma
- Retrospective study
- Survival
- Toxicity
ASJC Scopus subject areas
- Cancer Research
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