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Second Malignant Neoplasms Following Treatment for Hepatoblastoma: An International Report and Review of the Literature.
Trobaugh-Lotrario, Angela; Watanabe, Kenichiro; O'Neill, Allison F; Dembowska-Baginska, Bozenna; Häberle, Beate; Murphy, Andrew; Hiyama, Eiso; Czauderna, Piotr; Meyers, Rebecka L; Langham, Max; Feusner, James.
Affiliation
  • Trobaugh-Lotrario A; Providence Sacred Heart Children's Hospital, Spokane, WA.
  • Watanabe K; Kyoto University, Kyoto.
  • O'Neill AF; Dana-Farber Cancer Institute, Boston Children's Hospital and Harvard Medical School, Boston, MA.
  • Dembowska-Baginska B; The Children's Memorial Health Institute, Warsaw.
  • Häberle B; University of Munich, Munich, Germany.
  • Murphy A; St Jude Children's Research Hospital.
  • Hiyama E; Hiroshima University, Hiroshima, Japan.
  • Czauderna P; Medical University of Gdansk, Gdansk, Poland.
  • Meyers RL; Primary Children's Hospital, Salt Lake City, UT.
  • Langham M; University of Tennessee Health Science Center, Memphis, TN.
  • Feusner J; Benioff Children's Hospital Oakland, Oakland, CA.
J Pediatr Hematol Oncol ; 46(2): 80-87, 2024 03 01.
Article in En | MEDLINE | ID: mdl-38316145
ABSTRACT
Treatment intensification has improved survival in patients with hepatoblastoma (HB); however, these treatments are associated with an increased risk of late effects, including second malignant neoplasms (SMNs). Data is limited regarding SMNs following HB treatment. Cases of SMNs following treatment for HB reported in the literature and from personal communication were analyzed to further assess this late effect. Thirty-eight patients were identified. The median age at diagnosis of HB was 16 months (range 3 to 168 mo). All patients had received a platinum agent, and almost all had anthracycline exposure. The SMNs reported were hematopoietic malignancies (n=19), solid tumors (n=12), and post-transplant lymphoproliferative disorder (n=7). Of the 36 patients with outcome data, 19 survived. SMNs following HB treatment were primarily seen in patients with chemotherapy exposure, a history of liver transplantation, hereditary tumor predisposition syndromes, and/or a history of radiation treatment. Hematopoietic malignancies were the most common SMN reported in this cohort and were diagnosed earlier than other SMNs. Prospective collection of data through a companion late effects study or international registry could be used to further evaluate the rates and risks of SMNs as well as tumor predisposition syndromes in patients treated for HB.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neoplasms, Second Primary / Hepatoblastoma / Hematologic Neoplasms / Liver Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neoplasms, Second Primary / Hepatoblastoma / Hematologic Neoplasms / Liver Neoplasms Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2024 Type: Article