Cancers (Jan 2023)

Outcomes of Patients Treated for Hepatoblastoma with Low Alpha-Fetoprotein and/or Small Cell Undifferentiated Histology: A Report from the Children’s Hepatic Tumors International Collaboration (CHIC)

  • Angela D. Trobaugh-Lotrario,
  • Rudolf Maibach,
  • Daniel C. Aronson,
  • Arun Rangaswami,
  • Beate Häberle,
  • Allison F. O’Neill,
  • Irene Schmid,
  • Marc Ansari,
  • Tomoro Hishiki,
  • Sarangarajan Ranganathan,
  • Rita Alaggio,
  • Ronald R. de Krijger,
  • Yukichi Tanaka,
  • Soo-Jin Cho,
  • Christian Vokuhl,
  • Rebecca Maxwell,
  • Mark Krailo,
  • Eiso Hiyama,
  • Piotr Czauderna,
  • Milton Finegold,
  • James H. Feusner,
  • Marcio H. Malogolowkin,
  • Rebecka L. Meyers,
  • Dolores Lopez-Terrada

DOI
https://doi.org/10.3390/cancers15020467
Journal volume & issue
Vol. 15, no. 2
p. 467

Abstract

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Small cell undifferentiated (SCU) histology and alpha-fetoprotein (AFP) levels below 100 ng/mL have been reported as poor prognostic factors in hepatoblastoma (HB); subsequent studies reported SMARCB1 mutations in some SCU HBs confirming the diagnosis of rhabdoid tumor. The Children’s Hepatic tumors International Collaboration (CHIC) database was queried for patients with HB who had AFP levels less than 100 ng/mL at diagnosis or were historically diagnosed as SCU HBs. Seventy-three of 1605 patients in the CHIC database were originally identified as SCU HB, HB with SCU component, or HB with low AFP levels. Upon retrospective review, they were re-classified as rhabdoid tumors (n = 11), HB with SCU component (n = 41), and HB with low AFP (n = 14). Seven were excluded for erroneously low AFP levels. Overall survival was 0% for patients with rhabdoid tumors, 76% for patients with HB with SCU component, and 64% for patients with HB with AFP less than 100 ng/mL. Patients with HB with SCU component or low AFP should be assessed for SMARCB1 mutations and, if confirmed, treated as rhabdoid tumors. When rhabdoid tumors are excluded, the presence of SCU component and low AFP at diagnosis were not associated with poor prognosis in patients diagnosed with HB.

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