Hepatocellular carcinoma in children and adolescents: Results from the Pediatric Oncology Group and the Children's Cancer Group intergroup study

被引:96
|
作者
Katzenstein, HM
Krailo, MD
Malogolowkin, MH
Ortega, JA
Liu-Mares, W
Douglass, EC
Feusner, JH
Reynolds, M
Quinn, JJ
Newman, K
Finegold, MJ
Haas, JE
Sensel, MG
Castleberry, RP
Bowman, LC
机构
[1] Univ Tennessee, Dept Pediat, Memphis, TN USA
[2] Univ Alabama Birmingham, Dept Pediat, Birmingham, AL USA
[3] Childrens Hosp, Dept Pathol, Denver, CO 80218 USA
[4] Baylor Coll Med, Houston, TX 77030 USA
[5] Childrens Natl Med Ctr, Dept Pediat Surg, Washington, DC 20010 USA
[6] AstraZeneca Pharmaceut LP, Wilmington, DE USA
[7] Childrens Hosp, Dept Hematol Oncol, Oakland, CA 94609 USA
[8] Childrens Oncol Grp, Grp Operat Ctr, Arcadia, CA 91066 USA
[9] Childrens Hosp Los Angeles, Dept Pediat, Los Angeles, CA 90027 USA
[10] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
[11] Childrens Mem Hosp, Chicago, IL 60614 USA
[12] Northwestern Univ, Dept Surg, Chicago, IL 60611 USA
[13] Northwestern Univ, Dept Pediat, Chicago, IL 60611 USA
关键词
D O I
10.1200/JCO.2002.06.155
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine surgical resectability, event-free survival (EFS), and toxicity in children with hepatocellular carcinoma (HCC) randomized to treatment with either cisplatin (CDDP), vincristine, and fluorouracil (regimen A) or CDDP and continuous-infusion doxorubicin (regimen B). Patients and Methods: Forty-six patients were enrolled onto Pediatric Intergroup Hepatoma Protocol INT-0098 (Pediatric Oncology Group (POG) 8945/Children's Cancer Group (CCG) 8881). After initial surgery or biopsy, children with stage I (n = 8), stage III (n = 25), and stage IV (n = 13) HCC were randomly assigned to receive regimen A (n = 20) or regimen B (n = 26). Results: For the entire cohort, the 5-year EFS estimate was 19% (SD = 6%). Patients with stage I, III, and IV had 5-year EFS estimates of 88% (SD = 12%), 8% (SD = 5%), and 0%, respectively. Five-year EFS estimates were 20% (SD = 9%) and 19% (SD = 8%) for patients on regimens A and B, respectively (P = .78), with a relative risk of 1.2 (95% confidence interval, 0.60 to 2.3) for regimen B when compared with regimen A. Outcome was similar for either regimen within disease stages. Events occurred before postinduction surgery 1 in 18 (47%)of 38 patients with stage III or IV disease, and tumor resection was possible in two (10%) of the remaining 20 children with advanced stage disease after chemotherapy. Conclusion: Children with initially resectable HCC have a good prognosis and may benefit from the use of adjuvant chemotherapy. Outcome was uniformly poor for children with advanced-stage disease treated with either regimen. New therapeutic strategies are needed for the treatment of advanced-stage pediatric HCC.
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收藏
页码:2789 / 2797
页数:9
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