A phase II study of VM-26 plus lonidamine in pretreated small cell lung cancer

被引:0
|
作者
Gridelli, C
DeMarinis, F
Rossi, A
Tucci, E
Daprile, M
Cioffi, R
Cortesi, E
Migliorino, R
Pisano, A
Scognamiglio, F
DiGiacomo, R
Bianco, AR
机构
[1] AZIENDA OSPED SENESE,DIV RADIOTERAPIA,SIENA,ITALY
[2] OSPED FORLANINI,DIV PNEUMOL 3,ROME,ITALY
[3] OSPED S MARIA GORETTI,DIV MED ONCOL,LATINA,ITALY
[4] OSPED CIVILE,DIV PNEUMOL,CASERTA,ITALY
[5] UNIV ROMA LA SAPIENZA,DIV MED ONCOL,ROME,ITALY
[6] OSPED S MARIA DEILE GRAZIE,DIV MED,POZZUOLO FRIULI,NA,ITALY
[7] IST NAZL TUMORI,DIV CHIRURG TORAC,NAPLES,ITALY
[8] UNIV FEDERICO 2,CATTEDRA ONCOL MED,NAPLES,ITALY
关键词
small cell lung cancer; salvage chemotherapy; VM-26; lonidamine;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. SCLC relapsing or refractory after induction chemotherapy is a chemoresistant tumor. The outcome of salvage chemotherapy is poor, with low response rates (< 30%) and short survival times (3-4 months). The development of drug resistance is considered the major cause of failure of treatment. VM-26 is one of the most active drugs in SCLC. Lonidamine has shown to enhance in both vivo and vitro antitumor activity of several cytotoxic drugs acting on drug resistance mechanisms. Materials and methods: VM-26 and lonidamine were employed as salvage chemotherapy in 30 small cell hmg cancer patients. The doses of chemotherapy used were: VM-26 100 mg/m(2), i.v., days I to 3; lonidamine 600 mg, p.o., days I to 5, recycled every 3 weeks. Results: We observed 13.3% of objective response and a median survival of 4 months. All the responses were obtained inpatients relapsing after a response to induction chemotherapy. Toxicity was moderate with no toxic death. Conclusions: our study shows that Lonidamine failed to increase the VM-26 activity in pretreated small cell lung cancer patients.
引用
收藏
页码:1277 / 1279
页数:3
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