ALTERNATING CHEMOTHERAPY FOR SMALL-CELL LUNG-CANCER - A 12-WEEK SCHEDULE OF 6 DRUGS

被引:7
作者
ALBA, E
BRETON, JJ
ALONSO, L
PAREDES, G
BELON, J
BALLESTEROS, P
机构
[1] HOSP REG MALAGA,PORTUGAL 4,E-29017 MALAGA,SPAIN
[2] HOSP CLIN MALAGA,MALAGA,SPAIN
[3] HOSP REG JAEN,JAEN,SPAIN
[4] HOSP REG GRANADA,GRANADA,SPAIN
关键词
LUNG CANCER; SMALL-CELL; TREATMENT; WEEKLY CHEMOTHERAPY;
D O I
10.1093/oxfordjournals.annonc.a058062
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have treated sixty-two patients (21 with limited disease, 41 with extensive disease), on an outpatient-basis schedule of six drugs administered weekly for twelve weeks. Cyclophosphamide, 400 mg/m2, adriamycin, 20 mg/m2 and vincristine, 2 mg, full dose, were administered during weeks 1, 5 and 9; cisplatin, 50 mg/m2 and etoposide, 100 mg/m2 during weeks 2, 6 and 10; adriamycin and vincristine at the same doses during weeks 3, 7 and 11; methotrexate 30 mg/m2, during weeks 4, 8 and 12. After the first 28 patients vincristine was replaced by teniposide (VM-26) due to neurotoxicity. The overall response rate was 64.5% (complete remission 13 p., partial remission 27 p.). Toxicity grade 3-4, mainly nausea and vomiting or neutropenia, was recorded in 17 patients. Alopecia grade 1-2 was universal. One toxic death occurred from sepsis. The overall survival was 8 months (range 1-40), (95% CL: 53-77%); 8 months in limited disease (range 1-40), and 7 months in extensive disease (range 1 23). Time to treatment failure was 6 months (7 limited disease, 5 extensive disease). In conclusion, the results of this alternating schedule are poorer than those attained with standard, high-dose treatments, mainly in limited disease, but could be a less toxic option for patients with extensive disease.
引用
收藏
页码:31 / 35
页数:5
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