HIGH-DOSE CYCLOPHOSPHAMIDE, ADRIAMYCIN, AND VINCRISTINE (HD-CAV) IN CHILDREN WITH RECURRENT SOLID TUMOR

被引:14
作者
ZOUBEK, A
HOLZINGER, B
MANN, G
PETERS, C
EMMINGER, W
PERNECZKYHINTRINGER, E
GADNER, H
MOSTBECK, G
HORCHER, E
DOBROWSKY, W
机构
[1] ST ANNA CHILDRENS HOSP,A-1090 VIENNA,AUSTRIA
[2] UNIV VIENNA,DEPT RADIOL,VIENNA,AUSTRIA
[3] LUDWIG BOLTZMANN INST RADIOL PHYS TUMOR DIAG,VIENNA,AUSTRIA
[4] SOZIALMED ZENTRUM OST,DEPT PEDIAT SURG,VIENNA,AUSTRIA
[5] UNIV VIENNA,DEPT RADIOTHERAPY & RADIOBIOL,VIENNA,AUSTRIA
关键词
AUTOLOGOUS STEM CELL REINFUSION; HIGH-DOSE CAV; HIGH-DOSE CHEMOTHERAPY; RECURRENT CHILDHOOD TUMORS;
D O I
10.3109/08880019409141808
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A dose-intensive regimen of cyclophosphamide (140 mg/kg over 2 days), doxorubicin (Adriamycin, 75 mg/m(2) over 3 days), and vincristine (1 mg/m(2) on days 1, 2, and 3 and 1.5 mg/m(2) on day 9) war tested in 18 children and adolescents with poor-prognosis recurrent: or refractory solid tumors. Nine were affected by neuroblastoma, 3 by Ewing's tumors, 2 by rhabdomyosarcoma, 2 by synovial sarcoma, 1 by hepatocellular carcinoma, and 1 by osteogenic sarcoma. All enrolled patients were heavily pretreated, including 2 patients after bone marrow transplantation. Forty courses were applied (median, 2). The overall response rate was 33% (2 complete remissions and 4 partial remissions). Responses were obtained in children with neuroblastoma, Ewing's tumors, and hepatocellular carcinoma. Myelosuppression [World Health Organization (WHO) grade IV after all courses] and cardiac toxicity (3 WHO grade I, 5 WHO grade III, and 3 WHO grade IV) were the main side effects. Nephrotoxicity and hepatoxicity were not observed. With further therapy consisting of surgery, radiotherapy, and high-dose chemotherapy [cisplatin, carboplatin/etoposide (VP16), or ifosfamide/VP16 with or without autologous stem cell reinfusion after conditioning with melphalan/VP16/carboplatin], 3 complete remissions and 5 very good partial remissions were obtained. Ten of 18 patients are alive after a median follow-up of 16 months.
引用
收藏
页码:613 / 623
页数:11
相关论文
共 17 条
[11]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
[12]  
2-6
[13]   IFOSFAMIDE WITH MESNA UROPROTECTION AND ETOPOSIDE - AN EFFECTIVE REGIMEN IN THE TREATMENT OF RECURRENT SARCOMAS AND OTHER TUMORS OF CHILDREN AND YOUNG-ADULTS [J].
MISER, JS ;
KINSELLA, TJ ;
TRICHE, TJ ;
TSOKOS, M ;
JAROSINSKI, P ;
FORQUER, R ;
WESLEY, R ;
MAGRATH, I .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (08) :1191-1198
[14]  
RANEY RB, 1983, CANCER-AM CANCER SOC, V52, P44, DOI 10.1002/1097-0142(19830701)52:1<44::AID-CNCR2820520110>3.0.CO
[15]  
2-V
[16]   HIGH-DOSE CYCLOPHOSPHAMIDE (7G/M2) WITH OR WITHOUT AUTOLOGOUS BONE-MARROW RESCUE AFTER CONVENTIONAL CHEMOTHERAPY IN THE TREATMENT OF PATIENTS WITH SMALL CELL LUNG-CANCER [J].
SMITH, IE ;
EVANS, BD ;
HARLAND, SJ .
CANCER TREATMENT REVIEWS, 1983, 10 :79-81
[17]   AUTOLOGOUS BONE-MARROW TRANSPLANTATION IN PEDIATRIC SOLID TUMORS [J].
YANIV, I ;
BOUFFET, E ;
IRLE, C ;
NEGRIER, S ;
BIRON, P ;
FAVROT, M ;
PHILIP, I ;
BRUNATMENTIGNY, M ;
PHILIP, T .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1990, 7 (01) :35-46