2019
DOI: 10.1007/s12672-019-00367-0
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Metastatic Adrenocortical Carcinoma: a Single Institutional Experience

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Cited by 15 publications
(25 citation statements)
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“…Koh et al (21) documented partial remission after embolization of a solitary liver lesion but no survival benefit. Owen et al (22) suggested from data of 6 patients that TACE or SIRT for liver metastases may contribute to better survival of their patients. Cazejust (23) et al achieved stabilization or radiological regression in the majority of their patients in a larger series of 26 cases, but complete response was not achieved.…”
Section: Discussionmentioning
confidence: 99%
“…Koh et al (21) documented partial remission after embolization of a solitary liver lesion but no survival benefit. Owen et al (22) suggested from data of 6 patients that TACE or SIRT for liver metastases may contribute to better survival of their patients. Cazejust (23) et al achieved stabilization or radiological regression in the majority of their patients in a larger series of 26 cases, but complete response was not achieved.…”
Section: Discussionmentioning
confidence: 99%
“…These 6 cases had significantly longer median OS at 32 months, compared with 10 months in those patients with liver metastases who did not receive liver-directed therapies (p = 0.011). Although the results of this analysis are favorable and suggest a possible role for incorporating liver-directed therapies for patients with hepatic metastases, the sample number was small and bias in case selection may have contributed to perceived better outcomes [52]. Beyond this, only single case reports are available, which often describe extremely prolonged PFS or OS following TACE and SIRT [53,54].…”
Section: Local Therapiesmentioning
confidence: 96%
“…Adrenocortical carcinoma (ACC) is an uncommon, aggressive malignant tumor with an incidence of 0.5-2.0 cases per million inhabitants per year [1][2][3]. ACC has a bimodal age distribution, with small peaks in the first decades and a larger peak in the fourth to fifth decades of life [2,3].…”
Section: Introductionmentioning
confidence: 99%
“…Adrenocortical carcinoma (ACC) is an uncommon, aggressive malignant tumor with an incidence of 0.5-2.0 cases per million inhabitants per year [1][2][3]. ACC has a bimodal age distribution, with small peaks in the first decades and a larger peak in the fourth to fifth decades of life [2,3]. Patients with functional ACC may present with excess steroid hormone production resulting in Cushing syndrome with or without virilization [2,3], while non-functional ACC patients may present with either symptoms related to tumor mass, such as abdominal discomfort, nausea, vomiting, and back pain, or discovered incidentally during radiological procedures [2,3].…”
Section: Introductionmentioning
confidence: 99%