Abstract | PURPOSE: METHODS: Treatment consisted of paclitaxel 80 mg/m(2) on days 1, 8, 15 and gemcitabine 1,000 mg/m(2) on days 1 and 8 every 3 weeks. Of the 31 patients enrolled, 10 had refractory and 21 had sensitive disease. Objective responses occurred in 8 patients (26%), including 2 out of 10 patients with refractory- and 6 out of 21 patients with sensitive SCLC. Median time to progression and median survival were 9.4 and 32 weeks, respectively. RESULTS: The schedule was very well tolerated, with grade 3-4 thrombocytopenia in 26% of the patients, grade 3 neutropenia in 26%, grade 3-4 asthenia in 13% and grade 1-2 sensory neuropathy in 32%. CONCLUSION:
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Authors | Vincenzo Dongiovanni, Lucio Buffoni, Alfredo Berruti, Diego Dongiovanni, Raffaella Grillo, Carla Barone, Alfredo Addeo, Camilla Fissore, Oscar Bertetto |
Journal | Cancer chemotherapy and pharmacology
(Cancer Chemother Pharmacol)
Vol. 58
Issue 2
Pg. 203-9
(Aug 2006)
ISSN: 0344-5704 [Print] Germany |
PMID | 16331497
(Publication Type: Clinical Trial, Phase II, Journal Article)
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Chemical References |
- Deoxycytidine
- Etoposide
- Carboplatin
- Paclitaxel
- Cisplatin
- Gemcitabine
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Topics |
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(adverse effects, therapeutic use)
- Carboplatin
(administration & dosage)
- Carcinoma, Small Cell
(drug therapy)
- Cisplatin
(administration & dosage)
- Deoxycytidine
(administration & dosage, analogs & derivatives)
- Etoposide
(administration & dosage)
- Female
- Humans
- Lung Neoplasms
(drug therapy)
- Male
- Middle Aged
- Paclitaxel
(administration & dosage)
- Gemcitabine
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