High-dose sequential chemotherapy and autologous stem cell reinfusion in advanced pediatric solid tumors

被引:17
作者
Chan, KW
Petropoulos, D
Choroszy, M
Herzog, C
Jaffe, N
Ater, J
Korbling, M
机构
[1] Univ Texas, MD Anderson Cancer Ctr, Dept Clin Pediat, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Cancer Ctr, Dept Nursing, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Cancer Ctr, Dept Hematol, Houston, TX 77030 USA
关键词
sequential chemotherapy; autologous stem cell reinfusion; neuroblastoma; thiotepa; high-dose cyclophosphamide; melphalan;
D O I
10.1038/sj.bmt.1701014
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Between January 1993 and December 1996, 21 children with advanced solid tumors were entered in a dose-escalating study of high-dose sequential chemotherapy followed by autologous stem cell transplantation. The diagnoses included neuroblastoma (NB) for 13 patients; Ewing's sarcoma (ES) for six patients and osteosarcoma for two patients, Nine patients received therapy as consolidation for primary metastatic disease, and 12 patients had had previous relapses, Treatment consisted of CY given i.v. at a dose of 7 g/m(2) on day 1, followed by G-CSF until myeloid recovery, After 3 weeks of rest, all patients were given thiotepa i.v. on days 22-24. The total dose of thiotepa was 450 mg/m(2) in three patients, 600 mg/m(2) in six patients, and 750 mg/m(2) in 12 patients, Melphalan was given i.v. at a dose of 180 mg/m(2) i.v. on day 27 followed by stem cell infusion on day 28, Major toxic reactions included stomatitis, esophagitis, diarrhea and dermatitis, Three patients died of treatment-related complications, Twelve patients have had a relapse, Six patients (five with NB and one with ES) are alive in continuous remission 5-50 months (median 36) after transplantation. The results of this study show that it is feasible to administer high-dose sequential chemotherapy to children with advanced solid tumors.
引用
收藏
页码:1039 / 1043
页数:5
相关论文
共 22 条
[1]  
ANTMAN K, 1990, SEMIN ONCOL, V17, P33
[2]   Double dose-intensive chemotherapy with autologous stem-cell support for metastatic breast cancer: No improvement in progression-free survival by the sequence of high-dose melphalan followed by cyclophosphamide, thiotepa, and carboplatin [J].
Ayash, LJ ;
Elias, A ;
Schwartz, G ;
Wheeler, C ;
Ibrahim, J ;
Teicher, BA ;
Reich, E ;
Warren, D ;
Lynch, C ;
Richardson, P ;
Schnipper, L ;
Frei, E ;
Antman, K .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (11) :2984-2992
[3]   REGIMEN-RELATED TOXICITY IN PATIENTS UNDERGOING BONE-MARROW TRANSPLANTATION [J].
BEARMAN, SI ;
APPELBAUM, FR ;
BUCKNER, CD ;
PETERSEN, FB ;
FISHER, LD ;
CLIFT, RA ;
THOMAS, ED .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (10) :1562-1568
[4]  
EMMINGER W, 1991, BONE MARROW TRANSPL, V8, P119
[5]   BONE-MARROW TRANSPLANTATION FOR HIGH-RISK NEUROBLASTOMA AT THE CHILDRENS-HOSPITAL-OF-PHILADELPHIA - AN UPDATE [J].
EVANS, AE ;
AUGUST, CS ;
KAMANI, N ;
BUNIN, N ;
GOLDWEIN, J ;
ROSS, AJ ;
DANGIO, GJ .
MEDICAL AND PEDIATRIC ONCOLOGY, 1994, 23 (04) :323-327
[6]   PREVENTION OF ACUTE DEATHS IN MICE AFTER VERY HIGH-DOSE CYCLOPHOSPHAMIDE BY DIVIDED DOSE SCHEDULE [J].
EVANS, BD ;
SMITH, IE ;
CLUTTERBUCK, RD ;
MILLAR, JL .
BRITISH JOURNAL OF CANCER, 1984, 49 (01) :43-47
[7]  
Garaventa A, 1996, BONE MARROW TRANSPL, V18, P125
[8]   HIGH-DOSE CHEMO-RADIOTHERAPY FOR SENSITIVE TUMORS - IS SEQUENTIAL BETTER THAN CONCURRENT DRUG DELIVERY [J].
GIANNI, AM ;
BONADONNA, G .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1989, 25 (07) :1027-1030
[9]   HIGH-DOSE SEQUENTIAL CHEMORADIOTHERAPY, A WIDELY APPLICABLE REGIMEN, CONFERS SURVIVAL BENEFIT TO PATIENTS WITH HIGH-RISK MULTIPLE-MYELOMA [J].
GIANNI, AM ;
TARELLA, C ;
BREGNI, M ;
SIENA, S ;
LOMBARDI, F ;
GANDOLA, L ;
CARACCIOLO, D ;
STERN, A ;
BONADONNA, G ;
BOCCADORO, M ;
PILERI, A .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (03) :503-509
[10]   PROLONGED DISEASE-FREE SURVIVAL AFTER HIGH-DOSE SEQUENTIAL CHEMORADIOTHERAPY AND HEMATOPOIETIC AUTOLOGOUS TRANSPLANTATION IN POOR PROGNOSIS HODGKINS-DISEASE [J].
GIANNI, AM ;
SIENA, S ;
BREGNI, M ;
LOMBARDI, F ;
GANDOLA, L ;
VALAGUSSA, P ;
BONADONNA, G .
ANNALS OF ONCOLOGY, 1991, 2 (09) :645-653