Chemotherapy for advanced CNS ependymoma

被引:44
作者
Gornet, MK
Buckner, JC
Marks, RS
Scheithauer, BW
Erickson, BJ
机构
[1] Mayo Clin & Mayo Fdn, Div Med Oncol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Radiol, Rochester, MN 55905 USA
关键词
ependymoma; chemotherapy; CNS; advanced;
D O I
10.1023/A:1006394407245
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. The role of chemotherapy in recurrent ependymoma is poorly defined. This study was performed to help clarify the benefits of chemotherapy in this setting. Patients and methods. We retrospectively reviewed the charts of patients with advanced ependymoma of the CNS who received chemotherapy in our institution between 1974 and 1993, inclusive. Sixteen consecutive patients were treated with regimens containing either nitrosourea, platinum, or other combinations exclusive of nitrosourea or platinum. No patient received nitrosourea and platinum concurrently. Two methods were used to define response. The first was a direct comparison of radiographic images before and after chemotherapy more than one month apart. A second broader definition of response that employed four other criteria in addition to imaging studies (symptoms, signs, performance status, and neurologic functional status) was also used. Results. Results were as follows (response rate by imaging studies followed by response rate by scoring in parenthesis): Platinum-based chemotherapy resulted in a 67% (83%) response rate with 33% (0%) remaining stable. Nitrosourea-based regimens resulted in a 25% (60%) response rate with 50% (10%) remaining stable. When combinations other than platinum or nitrosourea were used, 11% (22%) responded and 56% (44%) remained stable. Relative differences in response rates between chemotherapy regimens persisted when the data were analyzed by grade. Median time to progression was 6, 10, and 3 months, respectively. Conclusion. Platinum-based chemotherapy regimens appear to result in higher response rates with lower rates of progression than nitrosourea-based regimens. Other regimens that do not include cisplatinum or nitrosourea appear to be even less effective.
引用
收藏
页码:61 / 67
页数:7
相关论文
共 18 条
[1]   A PHASE-II STUDY OF CISPLATIN THERAPY IN RECURRENT CHILDHOOD BRAIN-TUMORS - A REPORT FROM THE CHILDRENS-CANCER-STUDY-GROUP [J].
BERTOLONE, SJ ;
BAUM, ES ;
KRIVIT, W ;
HAMMOND, GD .
JOURNAL OF NEURO-ONCOLOGY, 1989, 7 (01) :5-11
[2]  
DeVita VT., 1997, CANC PRINCIPLES PRAC, V5th
[3]   A PHASE-II STUDY OF DIAZIQUONE IN CHILDREN WITH RECURRENT OR PROGRESSIVE PRIMARY BRAIN-TUMORS - A REPORT FROM THE CHILDRENS CANCER STUDY-GROUP [J].
ETTINGER, LJ ;
RU, N ;
KRAILO, M ;
RUCCIONE, KS ;
KRIVIT, W ;
HAMMOND, GD .
JOURNAL OF NEURO-ONCOLOGY, 1990, 9 (01) :69-76
[4]  
GAYNON PS, 1990, CANCER, V66, P2465, DOI 10.1002/1097-0142(19901215)66:12<2465::AID-CNCR2820661204>3.0.CO
[5]  
2-N
[6]   SURVIVAL OF INFANTS WITH PRIMITIVE NEUROECTODERMAL TUMORS OR MALIGNANT EPENDYMOMAS OF THE CNS TREATED WITH 8 DRUGS IN 1 DAY - A REPORT FROM THE CHILDRENS CANCER GROUP [J].
GEYER, JR ;
ZELTZER, PM ;
BOYETT, JM ;
RORKE, LB ;
STANLEY, P ;
ALBRIGHT, AL ;
WISOFF, JH ;
MILSTEIN, JM ;
ALLEN, JC ;
FINLAY, JL ;
AYERS, GD ;
SHURIN, SB ;
STEVENS, KR ;
BLEYER, WA .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (08) :1607-1615
[7]  
GOLDWEIN JW, 1990, CANCER-AM CANCER SOC, V66, P557, DOI 10.1002/1097-0142(19900801)66:3<557::AID-CNCR2820660325>3.0.CO
[8]  
2-8
[9]  
KLEIHUES P, 1993, HISTOLOGICAL TYPING, P17
[10]   RADIATION-THERAPY FOR NEOPLASMS OF THE BRAIN [J].
LEIBEL, SA ;
SHELINE, GE .
JOURNAL OF NEUROSURGERY, 1987, 66 (01) :1-22