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Adrenocortical carcinoma: a practical guide for clinicians.
Martin Fassnacht1, Soraya Puglisi2, Otilia Kimpel3
1Department of Medicine, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany; Comprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany; National Center for Tumor Diseases WERA, Würzburg, Germany.
Adrenocortical carcinoma (ACC) management is complex due to its rarity and aggressive nature. This review addresses key clinical questions for ACC patients, drawing on extensive experience.
Area of Science:
- Endocrinology
- Oncology
Background:
- Adrenocortical carcinoma (ACC) is a rare and aggressive endocrine malignancy.
- Patient management is complicated by hormonal excess, limited evidence, and few specialized centers.
Purpose of the Study:
- To address critical clinical management questions in adult adrenocortical carcinoma.
- To provide expert perspectives based on extensive clinical experience and published data.
Main Methods:
- A review of 25 frequently asked questions regarding adrenocortical carcinoma management.
- Synthesis of published evidence and over 60 years of collective clinical experience from two major European centers.
Main Results:
- The review consolidates expert answers to complex clinical scenarios in ACC.
- It highlights the challenges and nuances in diagnosing and treating this rare cancer.
Conclusions:
- This expert-driven review offers practical guidance for managing adrenocortical carcinoma.
- It aims to improve patient care by addressing knowledge gaps and sharing clinical insights.
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