TY - JOUR
T1 - Outcomes of children with well-differentiated fetal hepatoblastoma treated with surgery only
T2 - Report from Children's Oncology Group Trial, AHEP0731
AU - Vasudevan, Sanjeev A.
AU - Meyers, Rebecka L.
AU - Finegold, Milton J.
AU - López-Terrada, Dolores
AU - Ranganathan, Sarangarajan
AU - Dunn, Stephen P.
AU - Langham, Max R.
AU - McGahren, Eugene D.
AU - Tiao, Greg M.
AU - Weldon, Christopher B.
AU - Malogolowkin, Marcio H.
AU - Krailo, Mark D.
AU - Piao, Jin
AU - Randazzo, Jessica
AU - Towbin, Alexander J.
AU - BethMcCarville, M.
AU - O'Neill, Allison F.
AU - Furman, Wayne L.
AU - Rodriguez-Galindo, Carlos
AU - Katzenstein, Howard M.
N1 - Publisher Copyright:
© 2022
PY - 2022/10
Y1 - 2022/10
N2 - Background: Hepatoblastoma (HB) requires surgical resection for cure, but only 20–30% of patients have resectable disease at diagnosis. Patients who undergo partial hepatectomy at diagnosis have historically received 4–6 cycles of adjuvant chemotherapy; however, those with 100% well-differentiated fetal histology (WDF) have been observed to have excellent outcomes when treated with surgery alone. Patients and methods: Patients on the Children's Oncology Group non randomized, multicenter phase III study, AHEP0731, were stratified based on Evan's stage, tumor histology, and serum alpha-fetoprotein level at diagnosis. Patients were eligible for the very low risk stratum of surgery and observation if they had a complete resection at diagnosis and rapid central histologic review demonstrated HB with 100% WDF histology. Results: A total of 8 eligible patients were enrolled on study between September 14, 2009 and May 28, 2014. Outcome current to 06/30/2020 was used in this analysis. The median age at enrollment was 22.5 months (range: 8–84 months) and the median AFP at enrollment was 714 ng/ml (range: 18–77,747 ng/mL). With a median follow-up of 6.6 years (range: 3.6–9.8 years), the 5-year event-free (EFS) and overall survival (OS) were both 100%. Conclusion: This report supports that HB with 100% WDF histology completely resected at diagnosis is curable with surgery only. The development of evidence-based surgical guidelines utilizing criteria based on PRETEXT group, vascular involvement (annotation factors), tumor-specific histology and corresponding biology will be crucial for optimizing which patients are candidates for resection at diagnosis followed by observation. Level of evidence: Prognosis study, Level I evidence.
AB - Background: Hepatoblastoma (HB) requires surgical resection for cure, but only 20–30% of patients have resectable disease at diagnosis. Patients who undergo partial hepatectomy at diagnosis have historically received 4–6 cycles of adjuvant chemotherapy; however, those with 100% well-differentiated fetal histology (WDF) have been observed to have excellent outcomes when treated with surgery alone. Patients and methods: Patients on the Children's Oncology Group non randomized, multicenter phase III study, AHEP0731, were stratified based on Evan's stage, tumor histology, and serum alpha-fetoprotein level at diagnosis. Patients were eligible for the very low risk stratum of surgery and observation if they had a complete resection at diagnosis and rapid central histologic review demonstrated HB with 100% WDF histology. Results: A total of 8 eligible patients were enrolled on study between September 14, 2009 and May 28, 2014. Outcome current to 06/30/2020 was used in this analysis. The median age at enrollment was 22.5 months (range: 8–84 months) and the median AFP at enrollment was 714 ng/ml (range: 18–77,747 ng/mL). With a median follow-up of 6.6 years (range: 3.6–9.8 years), the 5-year event-free (EFS) and overall survival (OS) were both 100%. Conclusion: This report supports that HB with 100% WDF histology completely resected at diagnosis is curable with surgery only. The development of evidence-based surgical guidelines utilizing criteria based on PRETEXT group, vascular involvement (annotation factors), tumor-specific histology and corresponding biology will be crucial for optimizing which patients are candidates for resection at diagnosis followed by observation. Level of evidence: Prognosis study, Level I evidence.
KW - Fetal
KW - Hepatoblastoma
KW - Resection
KW - Well-differentiated
UR - https://www.scopus.com/pages/publications/85133784114
U2 - 10.1016/j.jpedsurg.2022.05.022
DO - 10.1016/j.jpedsurg.2022.05.022
M3 - Article
C2 - 35810020
AN - SCOPUS:85133784114
SN - 0022-3468
VL - 57
SP - 251
EP - 256
JO - Journal of Pediatric Surgery
JF - Journal of Pediatric Surgery
IS - 10
ER -