TY - JOUR
T1 - Guidelines of the French National ENDOCAN-COMETE, Association of Endocrine Surgery, Society of Urology for the management of adrenocortical carcinoma
AU - Libé, Rossella
AU - Haissaguerre, Magalie
AU - Renaudin, Karine
AU - Faron, Matthieu
AU - Decaussin-Petrucci, Myriam
AU - Deschamps, Fréderic
AU - Gimenez-Roqueplo, Anne Paule
AU - Mirallie, Eric
AU - Murez, Thibaut
AU - Pattou, François
AU - Rocher, Laurence
AU - Taïeb, David
AU - Savoie, Pierre Henri
AU - Tabarin, Antoine
AU - Bertherat, Jérôme
AU - Baudin, Eric
AU - de la Fouchardière, Christelle
N1 - Publisher Copyright:
© 2023 Société Française du Cancer
PY - 2023/6/1
Y1 - 2023/6/1
N2 - The adrenocortical carcinoma (ACC) is a primary malignant tumor developed from the adrenal cortex, defined by a Weiss score ≥ 3. Its prognosis is poor and depends mainly on the stage of the disease at diagnosis. Care is organized in France by the multidisciplinary expert centers of the national ENDOCAN-COMETE “Adrenal Cancers” network, certified by the National Cancer Institute. This document updates the guidelines for the management of ACC in adults based on the most robust data in the literature. It's divided into 11 chapters: (1) circumstances of discovery; (2) pre-therapeutic assessment; (3) diagnosis of ACC; (4) oncogenetics; (5) prognostic classifications; (6) treatment of hormonal hypersecretion; (7) treatment of localized forms; (8) treatment of relapses; (9) treatment of advanced forms; (10) follow-up; (11) the particular case of ACC and pregnancy. R0 resection of all localized ACC remains an unmet need and it must be performed in expert centers. Flow-charts for the therapeutic management of localized ACC, relapse or advanced ACC are provided. It was written by the experts from the national ENDOCAN-COMETE network and validated by all French Societies involved in the management of these patients (endocrinology, medical oncology, endocrine surgery, urology, pathology, genetics, nuclear medicine, radiology, interventional radiology).
AB - The adrenocortical carcinoma (ACC) is a primary malignant tumor developed from the adrenal cortex, defined by a Weiss score ≥ 3. Its prognosis is poor and depends mainly on the stage of the disease at diagnosis. Care is organized in France by the multidisciplinary expert centers of the national ENDOCAN-COMETE “Adrenal Cancers” network, certified by the National Cancer Institute. This document updates the guidelines for the management of ACC in adults based on the most robust data in the literature. It's divided into 11 chapters: (1) circumstances of discovery; (2) pre-therapeutic assessment; (3) diagnosis of ACC; (4) oncogenetics; (5) prognostic classifications; (6) treatment of hormonal hypersecretion; (7) treatment of localized forms; (8) treatment of relapses; (9) treatment of advanced forms; (10) follow-up; (11) the particular case of ACC and pregnancy. R0 resection of all localized ACC remains an unmet need and it must be performed in expert centers. Flow-charts for the therapeutic management of localized ACC, relapse or advanced ACC are provided. It was written by the experts from the national ENDOCAN-COMETE network and validated by all French Societies involved in the management of these patients (endocrinology, medical oncology, endocrine surgery, urology, pathology, genetics, nuclear medicine, radiology, interventional radiology).
KW - Adrenocortical carcinoma
KW - Diagnosis
KW - Follow-up
KW - Guidelines
KW - Treatment
UR - http://www.scopus.com/inward/record.url?scp=85152400673&partnerID=8YFLogxK
U2 - 10.1016/j.bulcan.2023.03.015
DO - 10.1016/j.bulcan.2023.03.015
M3 - Article
C2 - 37061367
AN - SCOPUS:85152400673
SN - 0007-4551
VL - 110
SP - 707
EP - 730
JO - Bulletin du Cancer
JF - Bulletin du Cancer
IS - 6
ER -