Treatment of high-risk neuroblastoma with intensive chemotherapy, radiotherapy, autologous bone marrow transplantation, and 13-cis-retinoic acid

被引:1465
作者
Matthay, KK
Villablanca, JG
Seeger, RC
Stram, DO
Harris, RE
Ramsay, NK
Swift, P
Shimada, H
Black, CT
Brodeur, GM
Gerbing, RB
Reynolds, CP
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Radiat Oncol, San Francisco, CA 94143 USA
[3] Univ So Calif, Sch Med, Dept Pediat, Los Angeles, CA USA
[4] Univ So Calif, Sch Med, Dept Pathol, Los Angeles, CA USA
[5] Univ So Calif, Sch Med, Dept Prevent Med, Los Angeles, CA USA
[6] Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
[7] Childrens Hosp, Med Ctr, Dept Pediat, Cincinnati, OH USA
[8] Univ Minnesota, Sch Med, Dept Pediat, Minneapolis, MN 55455 USA
[9] MD Anderson Hosp & Tumor Inst, Dept Surg, Houston, TX USA
[10] Childrens Canc Grp, Arcadia, CA 91066 USA
[11] Univ Penn, Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
关键词
D O I
10.1056/NEJM199910143411601
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Children with high-risk neuroblastoma have a poor outcome. In this study, we assessed whether myeloablative therapy in conjunction with transplantation of autologous bone marrow improved event-free survival as compared with chemotherapy alone, and whether subsequent treatment with 13-cis-retinoic acid (isotretinoin) further improves event-free survival. Methods All patients were treated with the same initial regimen of chemotherapy, and those without disease progression were then randomly assigned to receive continued treatment with myeloablative chemotherapy, total-body irradiation, and transplantation of autologous bone marrow purged of neuroblastoma cells or to receive three cycles of intensive chemotherapy alone. All patients who completed cytotoxic therapy without disease progression were then randomly assigned to receive no further therapy or treatment with 13-cis-retinoic acid for six months. Results The mean (+/-SE) event-free survival rate three years after the first randomization was significantly better among the 189 patients who were assigned to undergo transplantation than among the 190 patients assigned to receive continuation chemotherapy (34+/-4 percent vs. 22+/-4 percent, P = 0.034). The event-free survival rate three years after the second randomization was significantly better among the 130 patients who were assigned to receive 13-cis-retinoic acid than among the 128 patients assigned to receive no further therapy (46+/-6 percent vs. 29+/-5 percent, P = 0.027). Conclusions Treatment with myeloablative therapy and autologous bone marrow transplantation improved event-free survival among children with highrisk neuroblastoma. In addition, treatment with 13-cis-retinoic acid was beneficial for patients without progressive disease when it was administered after chemotherapy or transplantation. (N Engl J Med 1999; 341:1165-73.) (C)1999, Massachusetts Medical Society.
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页码:1165 / 1173
页数:9
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