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Pediatric adrenocortical carcinoma.
Ilanchezhian, Maran; Varghese, Diana Grace; Glod, John W; Reilly, Karlyne M; Widemann, Brigitte C; Pommier, Yves; Kaplan, Rosandra N; Del Rivero, Jaydira.
Affiliation
  • Ilanchezhian M; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Varghese DG; Developmental Therapeutics Branch, Rare Tumor Initiative, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Glod JW; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Reilly KM; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Widemann BC; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Pommier Y; Developmental Therapeutics Branch, Rare Tumor Initiative, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Kaplan RN; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
  • Del Rivero J; Developmental Therapeutics Branch, Rare Tumor Initiative, Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
Front Endocrinol (Lausanne) ; 13: 961650, 2022.
Article in En | MEDLINE | ID: mdl-36387865
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy of the adrenal gland with an unfavorable prognosis. It is rare in the pediatric population, with an incidence of 0.2-0.3 patients per million in patients under 20 years old. It is primarily associated with Li-Fraumeni and Beckwith-Wiedemann tumor predisposition syndromes in children. The incidence of pediatric ACC is 10-15fold higher in southern Brazil due to a higher prevalence of TP53 mutation associated with Li-Fraumeni syndrome in that population. Current treatment protocols are derived from adult ACC and consist of surgery and/or chemotherapy with etoposide, doxorubicin, and cisplatin (EDP) with mitotane. Limited research has been reported on other treatment modalities for pediatric ACC, including mitotane, pembrolizumab, cabozantinib, and chimeric antigen receptor autologous cell (CAR-T) therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Li-Fraumeni Syndrome / Adrenal Cortex Neoplasms / Adrenocortical Carcinoma Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Adult / Child / Humans Language: En Journal: Front Endocrinol (Lausanne) Year: 2022 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Li-Fraumeni Syndrome / Adrenal Cortex Neoplasms / Adrenocortical Carcinoma Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Adult / Child / Humans Language: En Journal: Front Endocrinol (Lausanne) Year: 2022 Document type: Article Affiliation country: Country of publication: