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Adrenocortical Carcinoma

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Management of Adrenal Masses in Children and Adults

Abstract

Adrenocortical carcinoma (ACC) is a rare malignancy with a poor prognosis. Incidence rates of 0.7–2.0 cases per million per year are reported. Approximately 40–60 % of patients present with symptoms due to hormone excess, while the remaining present with symptoms as a result of local or distant tumor growth. A growing proportion of ACC is incidentally discovered. The prediction of malignancy and the decision on adrenalectomy is supported by specific characteristics on CT scan, of which tumor size is the most important feature. Also, several radionucleotides have been evaluated and show promising results regarding differential diagnosis of adrenocortical tumors. The Weiss score, consisting of nine histopathological parameters, is currently considered the “gold standard” for ACC diagnosis. Successful tumor-directed surgery, performed by an experienced surgeon, is the only curative therapy. In patients with high risk of recurrence after resection (Ki67 > 10 % and stage III tumors), adjuvant mitotane treatment is recommended. In case of progression of advanced disease, mitotane can be combined with etoposide, doxorubicin, and cisplatin. However, mitotane is only effective in a subset of patients, indicating the need for predictive markers like CYP2W1, RRM1, or SOAT1 expression. Recently, also targeted therapies have been investigated, however, to date with discouraging results. Initial close surveillance by imaging and measurement of tumor markers is mandatory every 3 months. The staging system proposed by the European Network of the Study of Adrenal Tumors (ENSAT), the resection status, and the Ki67 index are important for prognostication. Research is focusing on molecular markers for stratification of survival outcome and on possibilities to use tumor and patient characteristics for a more personalized approach of patients with ACC.

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Creemers, S.G., Hofland, L.J., Feelders, R.A. (2017). Adrenocortical Carcinoma. In: Kebebew, E. (eds) Management of Adrenal Masses in Children and Adults. Springer, Cham. https://doi.org/10.1007/978-3-319-44136-8_12

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