TREATMENT OF OSTEOSARCOMA WITH IFOSFAMIDE - COMPARISON OF RESPONSE IN PEDIATRIC-PATIENTS WITH RECURRENT DISEASE VERSUS PATIENTS PREVIOUSLY UNTREATED - A PEDIATRIC-ONCOLOGY-GROUP STUDY

被引:82
作者
HARRIS, MB
CANTOR, AB
GOORIN, AM
SHOCHAT, SJ
AYALA, AG
FERGUSON, WS
HOLBROOK, T
LINK, MP
机构
[1] UNIV MED & DENT NEW JERSEY,HACKENSACK MED CTR,TOMORROWS CHILDRENS INST,HACKENSACK,NJ
[2] POG,STAT OFF,GAINESVILLE,FL
[3] CHILDRENS HOSP,DANA FARBER CANC INST,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,BOSTON,MA
[5] STANFORD UNIV,SCH MED,STANFORD,CA 94305
[6] MD ANDERSON CANC CTR,HOUSTON,TX
[7] MASSACHUSETTS GEN HOSP,BOSTON,MA 02114
[8] E CAROLINA UNIV,SCH MED,GREENVILLE,NC
来源
MEDICAL AND PEDIATRIC ONCOLOGY | 1995年 / 24卷 / 02期
关键词
OSTEOSARCOMA; IFOSFAMIDE; PHASE II STUDY; METASTATIC OSTEOSARCOMA AT DIAGNOSIS;
D O I
10.1002/mpo.2950240205
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was designed to test if the activity of a phase II agent, ifosfamide, would have been underestimated if it was tested exclusively in a population of children and young adults with recurrent osteosarcoma. The response rate to ifosfamide was compared in patients younger than 30 years of age with previously untreated osteosarcoma with metastases at diagnosis and/or unresectable primary tumors (stratum 1) with that of patients with recurrent osteosarcoma following adjuvant chemotherapy who were not previously exposed to ifosfamide (stratum 2). Evaluation of response was conducted 3 weeks after two courses of ifosfamide (2400 mg/m(2) x 5 days) were administered 3 weeks apart. Nine of 33 (27%) evaluable patients in stratum 1 responded (1 complete and 8 partial responses) to ifosfamide. Among 30 evaluable patients in stratum 2, only 3 (10%) responded (1 complete and 2 partial responses; P=.04) Both groups of patients received equal doses of ifosfamide and experienced comparable toxicities. Results from this study suggest that the activity of new agents will be underestimated if tested in a population of heavily pretreated patients with recurrent disease. When possible, new chemotherapeutic agents should be tested in patients with a poor prognosis who have not been exposed to chemotherapy. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:87 / 92
页数:6
相关论文
共 17 条
[1]  
ANTMAN KH, 1990, SEMIN ONCOL, V17, P68
[2]   RESPONSE TO IFOSFAMIDE AND MESNA - 124 PREVIOUSLY TREATED PATIENTS WITH METASTATIC OR UNRESECTABLE SARCOMA [J].
ANTMAN, KH ;
RYAN, L ;
ELIAS, A ;
SHERMAN, D ;
GRIER, HE .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (01) :126-131
[3]   OSTEOSARCOMA OF THE EXTREMITY METASTATIC AT PRESENTATION - RESULTS ACHIEVED IN 26 PATIENTS TREATED WITH COMBINED THERAPY (PRIMARY CHEMOTHERAPY FOLLOWED BY SIMULTANEOUS RESECTION OF THE PRIMARY AND METASTATIC LESIONS) [J].
BACCI, G ;
PICCI, P ;
BRICCOLI, A ;
AVELLA, M ;
FERRARI, S ;
FEMINO, FP ;
MONTI, C ;
RUGGIERI, P ;
RIZZENTE, AG ;
CASADEI, R .
TUMORI, 1992, 78 (03) :200-206
[4]   HIGH-DOSE IFOSFAMIDE WITH MESNA UROPROTECTION - A PHASE-I STUDY [J].
ELIAS, AD ;
EDER, JP ;
SHEA, T ;
BEGG, CB ;
FREI, E ;
ANTMAN, KH .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (01) :170-178
[5]   JUSTIFICATION FOR EVALUATING NEW ANTICANCER DRUGS IN SELECTED UNTREATED PATIENTS WITH EXTENSIVE-STAGE SMALL-CELL LUNG-CANCER - AN EASTERN-COOPERATIVE-ONCOLOGY-GROUP RANDOMIZED STUDY [J].
ETTINGER, DS ;
FINKELSTEIN, DM ;
ABELOFF, MD ;
SKEEL, RT ;
STOTT, PB ;
FRONTIERA, MS ;
BONOMI, PD .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (14) :1077-1084
[6]  
GASPARINI M, 1987, ECCO, V4, P233
[7]  
GOLDIN A, 1982, SEMIN ONCOL, V9, P14
[8]   OSTEO-SARCOMA - 15 YEARS LATER [J].
GOORIN, AM ;
ABELSON, HT ;
FREI, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (26) :1637-1643
[9]  
JAFFE N, 1989, CANCER, V63, P63, DOI 10.1002/1097-0142(19890101)63:1<63::AID-CNCR2820630110>3.0.CO
[10]  
2-O