Response rate and prognostic factors of recurrent oligodendroglioma treated with procarbazine, CCNU, and vincristine chemotherapy

被引:141
作者
van den Bent, MJ
Kros, JM
Heimans, JJ
Pronk, LC
van Groeningen, CJ
Krouwer, HGJ
Taphoorn, MJB
Zonnenberg, BA
Tijssen, CC
Twijnstra, A
Punt, CJA
Boogerd, W
机构
[1] Dr Daniel Den Hoed Canc Ctr, Dept Neurooncol, NL-3008 AE Rotterdam, Netherlands
[2] Dr Daniel Den Hoed Canc Ctr, Dept Med Oncol, NL-3008 AE Rotterdam, Netherlands
[3] Univ Hosp Dijkzigt, Dept Pathol, NL-3015 GD Rotterdam, Netherlands
[4] Vrije Univ Amsterdam, Univ Hosp, Dept Neurol & Med Oncol, Amsterdam, Netherlands
[5] Univ Utrecht Hosp, Dept Neurol & Internal Med, Utrecht, Netherlands
[6] St Elisabethgasthuis, Dept Neurol, Tilburg, Netherlands
[7] Univ Hosp Maastricht, Dept Neurol, Maastricht, Netherlands
[8] Univ Nijmegen Hosp, Dept Med Oncol, Nijmegen, Netherlands
[9] Antoni Van Leeuwenhoek Huis, Netherlands Canc Inst, Dept Neurooncol, Amsterdam, Netherlands
关键词
D O I
10.1212/WNL.51.4.1140
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To determine the response rate and factors correlated with response of oligodendroglial tumors to procarbazine, lomustine (CCNU), and vincristine (PCV) chemotherapy. Design: Retrospective, observational multicenter study. Methods: Patients treated with PCV or intensified PCV chemotherapy for a recurrent oligodendroglial tumor after surgery and radiation therapy with measurable disease were retrospectively evaluated for response. A 50% reduction in cross-sectional enhancing tumor area was considered a partial response. Stabilized or responding patients received six cycles of PCV unless unacceptable toxicity occurred. Results: Fifty-two patients were included; median time to progression (MTP) for the entire group was 10 months. In 17% of patients a complete response (MTP, 25 months) was obtained, and in 46% a partial response (MTP, 12 months) was obtained. Median overall survival was 20 months. Although treatment was discontinued for toxicity in seven patients, it was generally well tolerated. The intensified PCV regimen was more toxic. Patients initially presenting with seizures and patients with tumor necrosis in histologic specimens had a better response rate in contrast to patients who had their first relapse within 1 year of first treatment (surgery and radiation therapy). Conclusions: Oligodendroglial tumors are chemosensitive, but most patients will have relapsed after 12 to 16 months. New studies must aim at improving initial treatment and second-line chemotherapy.
引用
收藏
页码:1140 / 1145
页数:6
相关论文
共 34 条
[1]  
Bakardjiev AI, 1996, CANCER, V78, P864
[2]   O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE ACTIVITY CORRELATES WITH THE THERAPEUTIC RESPONSE OF HUMAN RHABDOMYOSARCOMA XENOGRAFTS TO 1-(2-CHLOROETHYL)-3-(TRANS-4-METHYLCYCLOHEXYL)-1-NITROSOUREA [J].
BRENT, TP ;
HOUGHTON, PJ ;
HOUGHTON, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2985-2989
[3]  
BROWN M, 1990, Neurology, V40, P397
[4]  
BULLARD DE, 1987, CANCER-AM CANCER SOC, V60, P2179, DOI 10.1002/1097-0142(19871101)60:9<2179::AID-CNCR2820600912>3.0.CO
[5]  
2-G
[6]   CHEMOTHERAPY FOR ANAPLASTIC OLIGODENDROGLIOMA [J].
CAIRNCROSS, G ;
MACDONALD, D ;
LUDWIN, S ;
LEE, D ;
CASCINO, T ;
BUCKNER, J ;
FULTON, D ;
DROPCHO, E ;
STEWART, D ;
SCHOLD, C ;
WAINMAN, N ;
EISENHAUER, E .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (10) :2013-2021
[7]   CHEMOTHERAPY FOR OLIGODENDROGLIOMA - PROGRESS REPORT [J].
CAIRNCROSS, JG ;
MACDONALD, DR .
ARCHIVES OF NEUROLOGY, 1991, 48 (02) :225-227
[8]   Salvage chemotherapy with paclitaxel for recurrent oligodendrogliomas [J].
Chamberlain, MC ;
Kormanik, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (12) :3427-3432
[9]  
Coons SW, 1997, CANCER, V79, P1381, DOI 10.1002/(SICI)1097-0142(19970401)79:7<1381::AID-CNCR16>3.0.CO
[10]  
2-W