Abstract
Purpose
Hepatoblastoma (HB) is a relatively rare pediatric malignancy. In this study, we present demographic data and a survival analysis from the largest patient cohort with HB reported to date.
Methods
The surveillance, epidemiology, and end results database was queried from 1973 to 2005 for all patients diagnosed with HB. Kaplan–Meier survival analysis was conducted to determine actuarial survival. Cox regression analysis was performed to determine hazard ratios (HR) for prognostic variables.
Results
During the study period, 459 patients with HB were identified. Overall 1-, 3-, and 5-year survival rates for the entire patient cohort were 76, 63, and 60%, respectively. Five-year survival improved over time from 36 (1973–1982) to 63% (1983–2005). Predictors of poor survival include: age 2 years and greater (HR 1.566), black race (HR 1.910), diagnosis prior to 1983 (HR 3.327), inability to perform surgical resection (HR 3.857), regional disease (HR 1.939), and distant disease (HR 3.196).
Conclusions
Hepatoblastoma continues to challenge surgeons and oncologists. Most children are diagnosed early in life and undergo surgical resection whenever possible. With the advent of efficacious chemotherapy, survival has improved. Older children, black patients, and those who present with advanced disease tend to have poor outcomes. Surgical resection is the single most important predictor of survival.
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References
Meyers RL (2007) Tumors of the liver in children. Surg Oncol 16(3):195–203. doi:10.1016/j.suronc.2007.07.002
Darbari A, Sabin KM, Shapiro CN, Schwarz KB (2003) Epidemiology of primary hepatic malignancies in U.S. children. Hepatology 38(3):560–566. doi:10.1053/jhep.2003.50375
Perilongo G, Shafford E, Maibach R et al (2004) Risk-adapted treatment for childhood hepatoblastoma final report of the second study of the International Society of Paediatric Oncology–SIOPEL 2. Eur J Cancer 40(3):411–421. doi:10.1016/j.ejca.2003.06.003
Sasaki F, Matsunaga T, Iwafuchi M et al (2002) Outcome of hepatoblastoma treated with the JPLT-1 (Japanese Study Group for Pediatric Liver Tumor) Protocol-1: a report from the Japanese Study Group for Pediatric Liver Tumor. J Pediatr Surg 37(6):851–856. doi:10.1053/jpsu.2002.32886
Schnater JM, Aronson DC, Plaschkes J et al (2002) Surgical view of the treatment of patients with hepatoblastoma: results from the first prospective trial of the International Society of Pediatric Oncology Liver Tumor Study Group. Cancer 94(4):1111–1120. doi:10.1002/cncr.10282
Ortega JA, Douglass EC, Feusner JH et al (2000) Randomized comparison of cisplatin/vincristine/fluorouracil and cisplatin/continuous infusion doxorubicin for treatment of pediatric hepatoblastoma: a report from the Children’s Cancer Group and the Pediatric Oncology Group. J Clin Oncol 18(14):2665–2675
Czauderna P, Otte JB, Aronson DC et al (2005) Guidelines for surgical treatment of hepatoblastoma in the modern era—recommendations from the Childhood Liver Tumour Strategy Group of the International Society of Paediatric Oncology (SIOPEL). Eur J Cancer 41(7):1031–1036. doi:10.1016/j.ejca.2005.02.004
von Schweinitz D (2006) Management of liver tumors in childhood. Semin Pediatr Surg 15(1):17–24. doi:10.1053/j.sempedsurg.2005.11.004
Warren JL, Klabunde CN, Schrag D, Bach PB, Riley GF (2002) Overview of the SEER-Medicare data: content, research applications, and generalizability to the United States elderly population. Med Care 40(Suppl 8):IV3–IV8
Surveillance E, End Results (SEER) Program Public Use Data (1973–2005) Washington, DC: National Cancer Institute, DCCPS, Surveillance Research Program, Cancer Statistics Branch, April 2008 [based on April 2008 submission]. Available on the Web at: www.seer.cancer.gov.
Evans AE, Land VJ, Newton WA, Randolph JG, Sather HN, Tefft M (1982) Combination chemotherapy (vincristine, adriamycin, cyclophosphamide, and 5-fluorouracil) in the treatment of children with malignant hepatoma. Cancer 50(5):821–826. doi:10.1002/1097-0142(19820901)50:5<821::AID-CNCR2820500502>3.0.CO;2-K
Curtis E, Quale C, Haggstrom D, Smith-Bindman R (2008) Racial and ethnic differences in breast cancer survival: how much is explained by screening, tumor severity, biology, treatment, comorbidities, and demographics? Cancer 112(1):171–180. doi:10.1002/cncr.23131
Pfeiffer RM, Mitani A, Matsuno RK, Anderson WF (2008) Racial differences in breast cancer trends in the United States (2000–2004). J Natl Cancer Inst 100(10):751–752. doi:10.1093/jnci/djn112
Kim J, Jang SN (2008) Socioeconomic disparities in breast cancer screening among US women: trends from 2000 to 2005. J Prev Med Pub Health 41(3):186–194
Morris LG, Sikora AG, Myssiorek D, DeLacure MD (2008) The basis of racial differences in the incidence of thyroid cancer. Ann Surg Oncol 15(4):1169–1176. doi:10.1245/s10434-008-9812-6
Gauthier F, Valayer J, Thai BL, Sinico M, Kalifa C (1986) Hepatoblastoma and hepatocarcinoma in children: analysis of a series of 29 cases. J Pediatr Surg 21(5):424–429. doi:10.1016/S0022-3468(86)80513-9
Park JR, Eggert A, Caron H (2008) Neuroblastoma: biology, prognosis, and treatment. Pediatr Clin North Am 55(1):97–120. doi:10.1016/j.pcl.2007.10.014
Yanagisawa T, Bartels U, Bouffet E (2008) Role of prognostic factors in the management of pediatric solid tumors. Ann N Y Acad Sci 1138:32–42
Nathan H, Pawlik TM, Wolfgang CL, Choti MA, Cameron JL, Schulick RD (2007) Trends in survival after surgery for cholangiocarcinoma: a 30-year population-based SEER database analysis. J Gastrointest Surg 11(11):1488–1496. doi:10.1007/s11605-007-0282-0 discussion 1496–1497
Strouse JJ, Fears TR, Tucker MA, Wayne AS (2005) Pediatric melanoma: risk factor and survival analysis of the surveillance, epidemiology and end results database. J Clin Oncol 23(21):4735–4741. doi:10.1200/JCO.2005.02.899
Wang X, Hershman DL, Abrams JA et al (2007) Predictors of survival after hepatic resection among patients with colorectal liver metastasis. Br J Cancer 97(12):1606–1612. doi:10.1038/sj.bjc.6604093
Shapiro NL, Bhattacharyya N (2005) Population-based outcomes for pediatric thyroid carcinoma. Laryngoscope 115(2):337–340. doi:10.1097/01.mlg.0000154743.71184.09
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The views expressed in this document are those of the author(s) and do not reflect the official policy of William Beaumont Army Medical Center, the Department of the Army, the Department of Defense, or the United States Government.
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Horton, J.D., Lee, S., Brown, S.R. et al. Survival trends in children with hepatoblastoma. Pediatr Surg Int 25, 407–412 (2009). https://doi.org/10.1007/s00383-009-2349-3
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DOI: https://doi.org/10.1007/s00383-009-2349-3