Comprehensive evaluation of adrenal cortical cancer: Single-center 22-year experience

Basem Al Achras , Joud Zakhour , Aditya Chauhan , James Bena , Divya Yogi-Morren , Kevin M. Pantalone , Pratibha Rao
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Abstract

Background

Adrenocortical carcinoma (ACC) is a rare malignancy with a reported incidence of 0.5–2 cases per million population per year. Literature is scarce on this malignancy with poor prognosis and limited treatment options. The objective of this report was to report a single-center experience of this rare malignancy.

Methods

A retrospective chart review (1997–2019) was performed on patients diagnosed with ACC via surgical pathology. Data were subsequently split into two time periods defined by the date of initial presentation: 1996–2007 and 2008–2019.

Results

52 patients were identified, 55.8 % were female, and the mean age at the time of surgery was 53 years. Most common presentations (25 % each) were: incidentalomas, abdominal pain, or hormonal hypersecretion. Laboratory evidence of hormonal hypersecretion was identified in 40.4 %. Among those patients, elevated 24-hour urinary free cortisol was the most common finding in both time periods.

The overall 5-year survival rate was 53.1 % and showed significant improvement in recent years when compared between the two time periods, 85.7 % vs 40.0 %. P = 0.004.

Conclusion

Overall, the most common presentation of ACC was found to be equally distributed among incidentaloma, hormonal hypersecretion, and abdominal pain. Hypercortisolism, a recognized poor prognosticator, was the most frequent form of hormonal hypersecretion. The 5-year survival rate for ACC was noted to be poor in general; however, it was observed to be substantially higher in more recent years. More research is necessary to further understand this malignancy in order to optimize management and improve outcomes.

Clinical relevance

This report provides a valuable contribution and expands the knowledge base for this important yet rare malignancy. The objective of this study was to report a single-center experience of ACC by characterizing patients diagnosed with this rare disease and managed at our institution and assessing their outcomes.

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肾上腺皮质癌症的综合评价:22年单中心经验
背景肾上腺皮质癌(ACC)是一种罕见的恶性肿瘤,据报道其发病率为每年每百万人口0.5-2例。关于这种预后不良、治疗选择有限的恶性肿瘤的文献很少。本报告的目的是报告这种罕见恶性肿瘤的单中心经验。方法对1997~2019年经手术病理诊断为ACC的患者进行回顾性分析。随后,数据被分为两个时间段,根据首次就诊日期确定:1996-2007年和2008-2019年。结果共确定52名患者,55.8%为女性,手术时的平均年龄为53岁。最常见的表现(各占25%)是:偶发性牙瘤、腹痛或激素分泌过多。40.4%的患者有激素分泌过多的实验室证据。在这些患者中,24小时尿游离皮质醇升高是这两个时期最常见的发现。总的5年生存率为53.1%,与这两个时间段相比,近年来有显著改善,分别为85.7%和40.0%。P=0.004。结论总体而言,ACC最常见的表现在偶发性牙瘤、激素分泌过多和腹痛中平均分布。皮质醇增多症是公认的预后不佳的疾病,是激素分泌过多的最常见形式。ACC的5年生存率普遍较差;然而,据观察,近年来这一数字明显更高。需要更多的研究来进一步了解这种恶性肿瘤,以优化管理并改善结果。临床相关性本报告为这种重要但罕见的恶性肿瘤提供了宝贵的贡献,并扩大了知识库。本研究的目的是通过描述在我们机构诊断和治疗的ACC患者的特征,并评估他们的结果,报告ACC的单中心经验。
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来源期刊
Endocrine and Metabolic Science
Endocrine and Metabolic Science Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.80
自引率
0.00%
发文量
4
审稿时长
84 days
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