Diagnosis and Management of Adrenocortical Carcinoma
Mitotane, the only Food and Drug Administration-approved drug for ACC, is combined with etoposide, doxorubicin, and cisplatin as the standard treatment for patients with recurrent disease.
Adrenocortical carcinoma (ACC) is a rare, aggressive malignancy with symptoms arising from mass effect or hormonal excess, particularly hypercortisolism. Accurate diagnosis requires comprehensive clinical, hormonal, radiologic, and histopathologic evaluation. Surgical resection is the only curative treatment. Treatment decisions are guided by risk stratification based on stage, Ki67 index, and resection margin status. Mitotane, the only Food and Drug Administration-approved drug for ACC, is combined with etoposide, doxorubicin, and cisplatin as the standard treatment for patients with recurrent disease. Investigational therapies include tyrosine kinase inhibitors, immune checkpoint inhibitors, image‑guided locoregional therapies, radiation therapy, and cell‑based therapies.
Standard therapy for recurrent adrenocortical carcinoma combines mitotane with cytotoxic agents to improve patient outcomes.
Bizonyítékszint: Sejtvonalas. Laboratóriumi sejtekben vizsgálták.
Kapcsolódó jelek
- Adrenocortical Carcinoma
- Oncological Management of Adrenocortical Carcinoma: An Update and Critical Review
- Targeting pediatric adrenocortical carcinoma: Molecular insights and emerging therapeutic strategies
- Phase II Trial of Pembrolizumab Plus Lenvatinib in Advanced Adrenal Cortical Carcinoma
- Novel Targeted Therapies in Adrenocortical Carcinoma