RANDOMIZED PHASE-III TRIAL IN CHILDHOOD HIGH-GRADE ASTROCYTOMA COMPARING VINCRISTINE, LOMUSTINE, AND PREDNISONE WITH THE 8-DRUGS-IN-1-DAY REGIMEN

被引:268
作者
FINLAY, JL
BOYETT, JM
YATES, AJ
WISOFF, JH
MILSTEIN, JM
GEYER, JR
BERTOLONE, SJ
MCGUIRE, P
CHERLOW, JM
TEFFT, M
TURSKI, PA
WARA, WM
EDWARDS, M
SUTTON, LN
BERGER, MS
EPSTEIN, F
AYERS, G
ALLEN, JC
PACKER, RJ
机构
[1] MEM SLOAN KETTERING CANC CTR, NEW YORK, NY 10021 USA
[2] NYU, MED CTR, NEW YORK, NY 10016 USA
[3] ST JUDE CHILDRENS RES HOSP, MEMPHIS, TN 38105 USA
[4] CLEVELAND CLIN FDN, CLEVELAND, OH 44195 USA
[5] OHIO STATE UNIV, COLUMBUS, OH 43210 USA
[6] CHILDRENS HOSP & MED CTR, SEATTLE, WA 98105 USA
[7] KOSAIR CHILDRENS HOSP, LOUISVILLE, KY USA
[8] PRESBYTERIAN ST LUKES MED CTR, DENVER, CO USA
[9] LONG BEACH MEM MED CTR, LONG BEACH, CA USA
[10] UNIV CALIF SAN FRANCISCO, SAN FRANCISCO, CA 94143 USA
[11] UNIV WISCONSIN, MADISON, WI USA
[12] CHILDRENS HOSP PHILADELPHIA, PHILADELPHIA, PA 19104 USA
[13] CHILDRENS NATL MED CTR, WASHINGTON, DC 20010 USA
关键词
D O I
10.1200/JCO.1995.13.1.112
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: In a previous randomized trial, the addition of adjuvant chemotherapy to postoperative radiotherapy proved beneficial in the treatment of childhood high-grade astrocytomas. The present study tests the hypothesis sis that an eight-drug adjuvant chemotherapy regimen would improve survival in such children compared with the three-drug regimen of the prior study. Patients and Methods: Between April 1985 and May 1990, patients between the ages of 18 months and 21 years with newly diagnosed high-grade astrocytomas were eligible for this study, as determined by the treating institution's histopathologic diagnosis. Treatment consisted of postoperative local-field radiotherapy and adjuvant chemotherapy, either lomustine (CCNU), vincristine, and prednisone (control regimen) or eight-drugs-in-1-day chemotherapy (experimental regimen). Two cycles of postoperative preirradiation chemotherapy were administered in the experimental regimen. Patients were evaluated radiographically every 3 months after irradiation. Results: Eighty-five eligible patients were randomized to the control regimen and 87 to the experimental regimen. The progression-free survival (PFS) and overall survival (OS) at 5 years were 33% (SE = 5%) and 36% (SE = 6%), respectively. There was no statistical difference in outcome between the two chemotherapy regimens. In patients with confirmed diagnoses of anaplastic astrocytoma (AA) or glioblastoma multiforme (GEM), anaplastic astrocytoma, greeter than 90% resection, and nonmidline tumor location were characteristics predictive of an improved PFS. There was a difference in toxicity between the two chemotherapeutic regimens, with greeter myelosuppression and hearing loss in the experimental regimen. Tumor recurrence occurred primarily within the primary tumor site. Conclusions: There is no benefit to the treatment of high rode astrocytomas in children with eight-drugs-in-1-day chemotherapy compared with CCNU, vincristine, and prednisone. Extent of tumor resection and histopathologic diagnosis are significant prognostic variables. The overall outcome for children with high-grade astrocytomas remains poor.
引用
收藏
页码:112 / 123
页数:12
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