COMPARATIVE EFFECTIVENESS OF 2 COMBINED MODALITY REGIMENS IN THE TREATMENT OF SURGICAL STAGE III HODGKINS-DISEASE IN CHILDREN - AN 8-YEAR FOLLOW-UP-STUDY BY THE PEDIATRIC-ONCOLOGY-GROUP

被引:0
作者
SULLIVAN, MP
FULLER, LM
BERARD, C
TERNBERG, J
CANTOR, AB
LEVENTHAL, BG
机构
[1] UNIV TEXAS, MD ANDERSON CANC CTR, HOUSTON, TX 77025 USA
[2] PEDIAT ONCOL GRP, STAT OFF, GAINESVILLE, FL USA
[3] ST JUDE CHILDRENS RES HOSP, MEMPHIS, TN 38101 USA
[4] WASHINGTON UNIV, MED CTR, ST LOUIS, MO 63130 USA
[5] JOHNS HOPKINS UNIV, BALTIMORE, MD 21218 USA
来源
AMERICAN JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 1991年 / 13卷 / 04期
关键词
HODGKINS DISEASE; STAGE-III; MOPP + BLEO; A-COPP; PEDIATRIC ONCOLOGY GROUP;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Pediatric Oncology Group compared two regimens that employed involved field radiotherapy 3,500 rad and either MOPP + Bleo or A-COPP chemotherapy, given in a sandwich fashion, as treatments for stage III Hodgkin's disease in children under the age of 18 years. Eighty-four surgically staged children from the United States and Mexico who had been randomly assigned to treatment during the period from July 1976 through October 1982 were evaluated. Unfavorable disease characteristics were distributed equally between the treatment groups. The percentages of children achieving complete remission by regimen were 84% for MOPP + Bleo and 92% for A-COPP. For those continuing in complete remission, the percentages were 71% for MOPP + Bleo and 72% for A-COPP. For those surviving 9 years, the percentage was 84% for MOPP + Bleo and 85% for A-COPP. The presence of low abdominal disease at diagnosis did not adversely influence response to therapy or survival. All deaths among MOPP + Bleo cases occurred within 4 years of study entry; 3 late deaths in A-COPP cases at 8-10 years were due to osteosarcoma, cardiopathy, and recurrent Hodgkin's disease. The preferred treatment regimen for future use cannot be determined until the cardiotoxicity of Adriamycin is eliminated by the development of drug delivery techniques that reduce cardiotoxicity or anthacycline congeners that are not cardiotoxic.
引用
收藏
页码:450 / 458
页数:9
相关论文
共 43 条
[1]  
CANELLOS GP, 1988, P AN M AM SOC CLIN, V7, P230
[2]   MALE GONADAL DYSFUNCTION IN HODGKINS-DISEASE - A PROSPECTIVE-STUDY [J].
CHAPMAN, RM ;
SUTCLIFFE, SB ;
MALPAS, JS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1981, 245 (13) :1323-1328
[3]  
COLEMAN CA, 1978, BLEOMYCIN CURRENT ST, P227
[4]   SECONDARY MALIGNANCY AFTER TREATMENT OF HODGKINS-DISEASE - AN EVOLVING PICTURE [J].
COLEMAN, CN .
JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (06) :821-824
[5]  
DEVITA VT, 1972, CANCER, V30, P1495, DOI 10.1002/1097-0142(197212)30:6<1495::AID-CNCR2820300613>3.0.CO
[6]  
2-I
[7]   COMBINED MODALITY TREATMENT WITH LOW-DOSE RADIATION AND MOPP CHEMOTHERAPY FOR CHILDREN WITH HODGKINS-DISEASE [J].
DONALDSON, SS ;
LINK, MP .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (05) :742-749
[8]  
DONALDSON SS, 1982, CANCER TREAT REP, V66, P977
[9]  
DUCUNHA MF, 1984, J CLIN ONCOL, V2, P571
[10]   PULMONARY-FUNCTION FOLLOWING MANTLE-FIELD IRRADIATION FOR HODGKINS-DISEASE [J].
EVANS, RF ;
SAGERMAN, RH ;
RINGROSE, TL ;
AUCHINCLOSS, JH ;
BOWMAN, J .
RADIOLOGY, 1974, 111 (03) :729-731