Chen Tao, Zeng Dongyang, Zhou Guang, Qin Linghui, Qian Xiaoyuan
Department of Urology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, China.
Medicine (Baltimore). 2025 Jul 25;104(30):e42831. doi: 10.1097/MD.0000000000042831.
Adrenal cortical carcinoma (ACC) is rare in clinical practice, and its prognosis and treatment have not been systematically studied. This study aimed to investigate the prognostic factors and impact of treatment strategies on overall survival (OS) and cancer-specific survival (CSS) in patients with ACC, using Surveillance, Epidemiology, and End Results registry data. Patient's data for ACC pathologically diagnosed between 2000 and 2021 were identified from Surveillance, Epidemiology, and End Results database. The Kaplan-Meier method was used to assess OS and CSS. While Cox proportional hazards regression analysis was used to evaluate the risk predictors of OS and CSS, the effects of surgery, chemotherapy, and radiotherapy on OS and CSS were also assessed using directed acyclic graphs-guided multivariate Cox regression model. A total of 444 patients with ACC were enrolled. The median OS and CSS in this cohort were 25 and 30 months, respectively. The OS at 1, 2, and 5 years were 62.7%, 50.2%, and 31.5%, respectively, while the CSS at 1, 2, and 5 years were 66.6%, 54.8%, and 37.2%, respectively. Patients with ≥ 53 years old, pathological grade Ⅲ/Ⅳ, clinical stage Ⅲ/Ⅳ, T3/4, N1, M1, and none receiving the therapy of surgery or radiation had worse survival. Old age, worse clinical stages, poor pathological grade, distant metastasis, no surgical treatment, and no radiation therapy were risk predictors of OS and CSS. In addition, receiving surgery or radiation therapy improved OS and CSS in the directed acyclic graph-guided multivariate Cox regression model. ACC has malignant behavior and a relatively poor prognosis. Old age, poor pathological grades, late clinical stages, and advanced tumor node metastasis classification indicate poor survival. While surgical resection of tumor lesions is one of the effective treatments, which can improve the outcome of patients with ACC, radiation therapy may be a palliative and beneficial treatment for patients with advanced disease.
肾上腺皮质癌(ACC)在临床实践中较为罕见,其预后和治疗尚未得到系统研究。本研究旨在利用监测、流行病学和最终结果登记数据,调查ACC患者的预后因素以及治疗策略对总生存期(OS)和癌症特异性生存期(CSS)的影响。从监测、流行病学和最终结果数据库中识别出2000年至2021年间病理诊断为ACC的患者数据。采用Kaplan-Meier方法评估OS和CSS。同时,使用Cox比例风险回归分析评估OS和CSS的风险预测因素,并使用有向无环图引导的多变量Cox回归模型评估手术、化疗和放疗对OS和CSS的影响。共纳入444例ACC患者。该队列的中位OS和CSS分别为25个月和30个月。1年、2年和5年的OS分别为62.7%、50.2%和31.5%,而1年、2年和5年的CSS分别为66.6%、54.8%和37.2%。年龄≥53岁、病理分级Ⅲ/Ⅳ级、临床分期Ⅲ/Ⅳ期、T3/4、N1、M1且未接受手术或放疗治疗的患者生存期较差。高龄、临床分期较差、病理分级差、远处转移、未接受手术治疗和未接受放疗是OS和CSS的风险预测因素。此外,在有向无环图引导的多变量Cox回归模型中,接受手术或放疗可改善OS和CSS。ACC具有恶性行为且预后相对较差。高龄、病理分级差、临床分期晚和肿瘤淋巴结转移分类晚期提示生存期较差。虽然手术切除肿瘤病灶是有效的治疗方法之一,可改善ACC患者的预后,但放疗可能是晚期疾病患者的一种姑息性有益治疗。