Surgical Oncology Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.
Front Endocrinol (Lausanne). 2021 Mar 1;12:613248. doi: 10.3389/fendo.2021.613248. eCollection 2021.
Adrenocortical carcinoma (ACC) is a rare malignancy with a poor prognosis. The current treatment standards include complete surgical resection for localized resectable disease and systemic therapy with mitotane alone or in combination with etoposide, doxorubicin, and cisplatin in patients with advanced ACC. However, the efficacy of systemic therapy in ACC is very limited, with high rates of toxicities. The understanding of altered molecular pathways is critically important to identify effective treatment options that currently do not exist. In this review, we discuss the results of recent advanced in molecular profiling of ACC with the focus on dysregulated pathways from various genomic and epigenetic dysregulation. We discuss the potential translational therapeutic implication of molecular alterations. In addition, we review and summarize the results of recent clinical trials and ongoing trials.
肾上腺皮质癌 (ACC) 是一种罕见的恶性肿瘤,预后不良。目前的治疗标准包括对局限性可切除疾病进行完全手术切除,以及对晚期 ACC 患者使用米托坦单独或联合依托泊苷、多柔比星和顺铂进行全身治疗。然而,全身治疗在 ACC 中的疗效非常有限,毒性反应发生率很高。了解改变的分子途径对于确定目前尚不存在的有效治疗选择至关重要。在这篇综述中,我们讨论了最近在 ACC 的分子谱分析方面的进展,重点是讨论各种基因组和表观遗传失调导致的失调途径。我们讨论了分子改变的潜在转化治疗意义。此外,我们还回顾和总结了最近的临床试验和正在进行的试验的结果。