CARBOPLATIN AND VINCRISTINE FOR RECURRENT AND NEWLY DIAGNOSED LOW-GRADE GLIOMAS OF CHILDHOOD

被引:270
作者
PACKER, RJ
LANGE, B
ATER, J
NICHOLSON, HS
ALLEN, J
WALKER, R
PRADOS, M
JAKACKI, R
REAMAN, G
NEEDLES, MN
PHILLIPS, PC
RYAN, J
BOYETT, JM
GEYER, R
FINLAY, J
机构
[1] GEORGE WASHINGTON UNIV, CHILDRENS NATL MED CTR, DEPT PEDIAT, WASHINGTON, DC 20052 USA
[2] GEORGE WASHINGTON UNIV, CHILDRENS NATL MED CTR, DEPT ONCOL, WASHINGTON, DC 20052 USA
[3] UNIV PENN, CHILDRENS HOSP PHILADELPHIA, DIV HEMATOL ONCOL, PHILADELPHIA, PA 19104 USA
[4] UNIV PENN, CHILDRENS HOSP PHILADELPHIA, DIV NEUROL, PHILADELPHIA, PA 19104 USA
[5] MD ANDERSON CANC CTR, DEPT PEDIAT, HOUSTON, TX USA
[6] NYU MED CTR, DEPT NEUROL, NEW YORK, NY 10016 USA
[7] MEM SLOAN KETTERING CANC CTR, DEPT NEUROL, NEW YORK, NY 10021 USA
[8] MEM SLOAN KETTERING CANC CTR, DEPT PEDIAT, NEW YORK, NY 10021 USA
[9] UNIV CALIF SAN FRANCISCO, BRAIN TUMOR RES CTR, SAN FRANCISCO, CA 94143 USA
[10] UNIV CALIF SAN FRANCISCO, DEPT NEUROSURG, SAN FRANCISCO, CA 94143 USA
[11] INDIANA UNIV, JAMES WHITCOMB RILEY HOSP CHILDREN, DEPT ONCOL, INDIANAPOLIS, IN 46223 USA
[12] ST JUDE CHILDRENS RES HOSP, DEPT BIOSTAT, MEMPHIS, TN 38101 USA
关键词
D O I
10.1200/JCO.1993.11.5.850
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study investigates the response rate to and toxicity of carboplatin and vincristine in children with recurrent low-grade gliomas (LGGs) or patients younger than 60 months with newly diagnosed LGGs. Patients and Methods: Twenty-three children with recurrent and 37 children with newly diagnosed LGGs were treated with a 10-week induction cycle of carboplatin and vincristine, followed by maintenance treatment with the same drugs. Patients were evaluated for response to treatment and toxicity. Results: Twelve of 23 (52% ± 10%; 95% confidence interval [CI], 0.32 to 0.72) assessable children with recurrent disease had an objective response to treatment, which included a greater than 50% reduction in tumor size in seven of 23 (30% ± 10%; 95% CI, 0.10 to 0.50). Twenty-three of 37 (62% ± .08; 95% CI, 0.46 to 0.78) of newly diagnosed patients had an objective response, 16 of 37 (43% ± 0.08%; 95% CI, 0.27 to 0.59) with greater than 50% reduction in tumor size. The majority of those with an objective response had diencephalic tumors (n = 29), but children with thalamic (n = 2), cortical (n = 1), and brain stem (n = 2) LGGs also responded to treatment. Of the 35 patients with objective response to treatment, the maximum response was seen in 25 after completion of induction and in the remaining 10 after two to six cycles of maintenance treatment. Fortynine of 53 (92% ± .04%) patients who were stable or improved after induction remain without progressive disease (PD). Hematologic toxicity was common, but resulted in cessation of therapy in only one patient. Six children have been removed from the study because of allergic reactions, which were considered to be carboplatin-associated. Conclusion: Carboplatin and vincristine have activity in children with recurrent and newly diagnosed progressive LGGs. Objective responses to treatment after chemotherapy can be seen. This drug regimen is relatively well tolerated, and further studies are indicated to define the role of this combination of drugs in children with newly diagnosed LGGs.
引用
收藏
页码:850 / 856
页数:7
相关论文
共 24 条
[1]   CARBOPLATIN AND RECURRENT CHILDHOOD BRAIN-TUMORS [J].
ALLEN, JC ;
WALKER, R ;
LUKS, E ;
JENNINGS, M ;
BARFOOT, S ;
TAN, C .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (03) :459-463
[2]  
BACHA DM, 1986, CANCER TREAT REP, V70, P865
[3]   INTRA-CRANICAL TUMORS - RESPONSE AND RESISTANCE TO THERAPEUTIC ENDEAVORS, 1970-1980 [J].
BLOOM, HJG .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1982, 8 (07) :1083-1113
[4]   THE BIOLOGICAL AND CLINICAL BEHAVIOR OF PILOCYTIC ASTROCYTOMAS OF THE OPTIC PATHWAYS [J].
BORIT, A ;
RICHARDSON, EP .
BRAIN, 1982, 105 (MAR) :161-187
[5]   COMBINATION CHEMOTHERAPY WITH MOPP IN CHILDREN WITH RECURRENT BRAIN TUMORS [J].
CANGIR, A ;
VANEYS, J ;
BERRY, DH ;
HVIZDALA, E ;
MORGAN, SK .
MEDICAL AND PEDIATRIC ONCOLOGY, 1978, 4 (03) :253-261
[6]  
DANGIO GJ, 1962, AMER J ROENTGENOL RA, V87, P106
[7]  
EDWARDS MS, 1980, CHILD BRAIN, V7, P252
[8]   TREATMENT OF CHILDREN WITH PROGRESSIVE OR RECURRENT BRAIN-TUMORS WITH CARBOPLATIN OR IPROPLATIN - A PEDIATRIC ONCOLOGY GROUP RANDOMIZED PHASE-II STUDY [J].
FRIEDMAN, HS ;
KRISCHER, JP ;
BURGER, P ;
OAKES, WJ ;
HOCKENBERGER, B ;
WEINER, MD ;
FALLETTA, JM ;
NORRIS, D ;
RAGAB, AH ;
MAHONEY, DH ;
WHITEHEAD, MV ;
KUN, LE .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (02) :249-256
[9]  
GILLES FH, 1988, J NEURO-ONCOL, V6, P9
[10]  
HEIDEMAN RL, 1989, PRINCIPLES PRACTICE, P505