TENIPOSIDE FOR BRAIN METASTASES OF SMALL-CELL LUNG-CANCER - A PHASE-II STUDY

被引:51
作者
POSTMUS, PE
SMIT, EF
HAAXMAREICHE, H
VANZANDWIJK, N
ARDIZZONI, A
QUOIX, E
KIRKPATRICK, A
SAHMOUD, T
GIACCONE, G
机构
[1] UNIV GRONINGEN HOSP, GRONINGEN, NETHERLANDS
[2] INST NAZL RIC CANC, GENOA, ITALY
[3] HOP UNIV STRASBOURG, STRASBOURG, FRANCE
[4] EUROPEAN ORG RES TREATMENT CANC, CTR DATA, BRUSSELS, BELGIUM
关键词
D O I
10.1200/JCO.1995.13.3.660
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Here we report the results of a phase II study of teniposide, one of the most active drugs against small-cell lung cancer (SCLC), in patients with brain metastases. Patients and Methods: Patients with SCLC who presented with brain metastases at diagnosis (n = 11) or during follow-up evaluation after treatment (n = 69) were treated with teniposide at a dose of 150 mg/m(2) intravenously on days 1, 3, and 5 at 3-week intervals in an outpatient setting. Response in the brain was evaluated by brain computed tomography (CT) after two, six, and 12 courses. Results: In 26 of 80 assessable patients, an intracranial response was seen, with a response rate of 33% (95% confidence interval, 22% to 44%). The median response duration was 5.4 months for patients with a complete response (CR) and 4.2 months for patients with a partial response (PR). Patients who required corticosteroids for peritumoral edema had a significantly lower response rate than patients who did not receive corticosteroids. Neurologic function at the start of treatment had a significant influence (neurologic function 1 better than 2, respectively, better than 3 and 4; P < .001), as did the number of cycles of previous chemotherapy (0 better than 1 to 5 cycles, respectively, better than > 5 cycles; P = .043). Grade 3/4 leukocytopenia and thrombocytopenia were seen in 3% and 39%, respectively, of 80 patients. Toxicity-related death was seen in eight patients, seven of whom were previously treated with chemotherapy Conclusion: Teniposide is active against brain metastases of SCLC. It is a suitable drug for palliation, especially of patients without extensive pretreatment and with a good neurologic function and performance status. Patients previously treated with cranial radiotherapy are also candidates for this therapy. If systemic chemotherapy is considered for tumor progression outside the brain, radiotherapy of brain metastases might be omitted or delayed pending the effect of chemotherapy. The use of corticosteroids in patients with brain metastases treated with chemotherapy might influence the efficacy of the chemotherapy. (C) 1995 by American Society of Clinical Oncology.
引用
收藏
页码:660 / 665
页数:6
相关论文
共 44 条
[1]  
BAGLAN RJ, 1981, CANCER, V47, P41, DOI 10.1002/1097-0142(19810101)47:1<41::AID-CNCR2820470109>3.0.CO
[2]  
2-M
[3]   TENIPOSIDE (VM-26), AN OVERLOOKED HIGHLY-ACTIVE AGENT IN SMALL-CELL LUNG-CANCER - RESULTS OF A PHASE-II TRIAL IN UNTREATED PATIENTS [J].
BORK, E ;
HANSEN, M ;
DOMBERNOWSKY, P ;
HANSEN, SW ;
PEDERSEN, AG ;
HANSEN, HH .
JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (04) :524-527
[4]   RESULTS OF THERAPEUTIC CRANIAL IRRADIATION IN SMALL CELL LUNG-CANCER [J].
CARMICHAEL, J ;
CRANE, JM ;
BUNN, PA ;
GLATSTEIN, E ;
IHDE, DC .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1988, 14 (03) :455-459
[5]  
COHEN MH, 1977, CANCER TREAT REP, V61, P349
[6]  
COHEN MH, 1979, CANCER TREAT REP, V63, P163
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]  
Cox DR, 2018, ANAL BINARY DATA
[9]  
COX JD, 1980, CANCER TREAT REP, V64, P957
[10]  
CREAVEN PJ, 1982, CANCER CHEMOTH PHARM, V7, P133