Cisplatin versus Cisplatin plus Doxorubicin for Standard-Risk Hepatoblastoma

被引:205
作者
Perilongo, Giorgio [1 ]
Maibach, Rudolf [2 ]
Shafford, Elisabeth [5 ]
Brugieres, Laurence [9 ]
Brock, Penelope [6 ]
Morland, Bruce [7 ]
de Camargo, Beatriz [10 ]
Zsiros, Jozsef [11 ]
Roebuck, Derek [6 ]
Zimmermann, Arthur [3 ]
Aronson, Daniel [12 ]
Childs, Margaret [5 ]
Widing, Eva [13 ]
Laithier, Veronique [9 ]
Plaschkes, Jack [4 ]
Pritchard, Jon [8 ]
Scopinaro, Marcello [14 ]
MacKinlay, Gordon [8 ]
Czauderna, Piotr [15 ]
机构
[1] Univ Hosp Padua, Dept Pediat, Div Hematol Oncol, I-35128 Padua, Italy
[2] Int Breast Canc Study Grp, Coordinating Ctr, Bern, Switzerland
[3] Univ Bern, Inst Pathol, Dept Surg Pathol, Bern, Switzerland
[4] Univ Childrens Hosp, Dept Surg, Bern, Switzerland
[5] Childrens Canc & Leukaemia Grp, Ctr Data, Leicester, Leics, England
[6] Great Ormond St Hosp Sick Children, London, England
[7] Birmingham Childrens Hosp, Birmingham, W Midlands, England
[8] Royal Hosp Sick Children, Edinburgh EH9 1LF, Midlothian, Scotland
[9] Inst Gustave Roussy, Dept Pediat, Villejuif, France
[10] Hosp Canc, Dept Res, Sao Paulo, Brazil
[11] Univ Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Oncol, NL-1105 AZ Amsterdam, Netherlands
[12] Radboud Univ Nijmegen, Nijmegen Med Ctr, NL-6525 ED Nijmegen, Netherlands
[13] Ullevaal Univ Hosp, Dept Pediat, Oslo, Norway
[14] Prof Dr Juan P Garrahan Childrens Hosp, Serv Hematooncol, Buenos Aires, DF, Argentina
[15] Med Univ Gdansk, Dept Surg & Urol Children & Adolescents, Gdansk, Poland
关键词
PRETREATMENT PROGNOSTIC-FACTORS; PEDIATRIC-ONCOLOGY-GROUP; CHILDHOOD HEPATOBLASTOMA; INTERNATIONAL SOCIETY; LIVER-TUMOR; INFUSION DOXORUBICIN; CHILDREN; CHEMOTHERAPY; TOXICITY; SYSTEM;
D O I
10.1056/NEJMoa0810613
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Preoperative cisplatin alone may be as effective as cisplatin plus doxorubicin in standard-risk hepatoblastoma (a tumor involving three or fewer sectors of the liver that is associated with an alpha-fetoprotein level of >100 ng per milliliter). Methods Children with standard-risk hepatoblastoma who were younger than 16 years of age were eligible for inclusion in the study. After they received one cycle of cisplatin (80 mg per square meter of body-surface area per 24 hours), we randomly assigned patients to receive cisplatin (every 14 days) or cisplatin plus doxorubicin administered in three preoperative cycles and two postoperative cycles. The primary outcome was the rate of complete resection, and the trial was powered to test the noninferiority of cisplatin alone (<10% difference in the rate of complete resection). Results Between June 1998 and December 2006, 126 patients were randomly assigned to receive cisplatin and 129 were randomly assigned to receive cisplatin plus doxorubicin. The rate of complete resection was 95% in the cisplatin-alone group and 93% in the cisplatin-doxorubicin group in the intention-to-treat analysis (difference, 1.4%; 95% confidence interval [CI],-4.1 to 7.0); these rates were 99% and 95%, respectively, in the per-protocol analysis. Three-year event-free survival and overall survival were, respectively, 83% (95% CI, 77 to 90) and 95% (95% CI, 91 to 99) in the cisplatin group, and 85% (95% CI, 79 to 92) and 93% (95% CI, 88 to 98) in the cisplatin-doxorubicin group (median follow-up, 46 months). Acute grade 3 or 4 adverse events were more frequent with combination therapy (74.4% vs. 20.6%). Conclusions As compared with cisplatin plus doxorubicin, cisplatin monotherapy achieved similar rates of complete resection and survival among children with standard-risk hepatoblastoma. Doxorubicin can be safely omitted from the treatment of standard-risk hepatoblastoma. (ClinicalTrials.gov number, NCT00003912.)
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收藏
页码:1662 / 1670
页数:9
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