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Adjuvant and Neoadjuvant Therapy, Treatment for Advanced Disease, and Genetic Considerations for Adrenocortical Carcinoma: An Update from the SSO Endocrine and Head and Neck Disease Site Working Group.
Dickson, Paxton V; Kim, Lawrence; Yen, Tina W F; Yang, Anthony; Grubbs, Elizabeth G; Patel, Dhavel; Solórzano, Carmen C.
Afiliação
  • Dickson PV; Division of Surgical Oncology, Department of Surgery, University of Tennessee Health Science Center, Memphis, TN, 38163, USA. pdickso1@uthsc.edu.
  • Kim L; Division of Surgical Oncology and Endocrine Surgery, University of North Carolina, Chapel Hill, NC, USA.
  • Yen TWF; Division of Surgical Oncology, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Yang A; Department of Surgery, Division of Surgical Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Grubbs EG; University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Patel D; Endocrine Oncology Branch, National Institutes of Health, Bethesda, MD, USA.
  • Solórzano CC; Division of Surgical Oncology and Endocrine Surgery, Vanderbilt University, Nashville, TN, USA.
Ann Surg Oncol ; 25(12): 3453-3459, 2018 Nov.
Article em En | MEDLINE | ID: mdl-30218246
ABSTRACT
This is the second of a two-part review on adrenocortical carcinoma (ACC) management. While margin-negative resection provides the only potential cure for ACC, recurrence rates remain high. Furthermore, many patients present with locally advanced, unresectable tumors and/or diffuse metastases. As a result, selecting patients for adjuvant therapy and understanding systemic therapy options for advanced ACC is important. Herein, we detail the current literature supporting the use of adjuvant mitotane therapy, consideration of adjuvant radiation therapy, and utility of cytotoxic chemotherapy in patients with advanced disease. Ongoing investigation into molecular targeted agents, immunotherapy, and inhibitors of steroidogenesis for the treatment of ACC are also highlighted. Lastly, the importance of genetic counseling in patients with ACC is addressed as up to 10% of patients will have an identifiable hereditary syndrome.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Suprarrenais / Carcinoma Adrenocortical / Aconselhamento Genético Limite: Humans Idioma: En Revista: Ann Surg Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Suprarrenais / Carcinoma Adrenocortical / Aconselhamento Genético Limite: Humans Idioma: En Revista: Ann Surg Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos