Şişman Pınar, Şahin Ahmet Bilgehan, Peynirci Hande, Cander Soner, Gül Özen Öz, Ertürk Erdinç, Ersoy Canan
Clinic of Endocrinology and Metabolism, Harakani State Hospital, Kars, Turkey.
Department of Internal Medicine, Uludağ University School of Medicine, Bursa, Turkey.
Turk J Urol. 2017 Dec;43(4):462-469. doi: 10.5152/tud.2017.81598. Epub 2017 Dec 1.
Adrenocortical carcinoma is an aggressive endocrine malignancy with an annual incidence of 0.5-2 cases per million. The most important factors that determine prognosis are tumor stage at the time of diagnosis and the success of surgery. However, advanced age, large tumor size, hormone secretion, high Ki-67 index (>10%), tumor necrosis and high mitotic activity are other factors associated with poor prognosis. In the present study, we aimed to evaluate the contribution of the patient and treatment- related factors to the prognosis in adrenocortical carcinoma.
We included 15 adrenocortical carcinoma patients who were followed in our center between 2005 and 2015. The effects of age, gender, tumor size, type of operation, postoperative resection status and adjuvant treatment on disease-free survival and overall survival were analyzed.
Disease-free survival was 23.32±3.69 months and overall survival was 36.60±10.78 months. Gender, tumor size, tumor stage, type of operation, hormonal activity, presence of necrosis, recurrence and development of metastasis were not found to be associated with disease-free survival and overall survival (p>0.05). Postoperatively applied adjuvant treatments including mitotane, chemotherapy and radiotherapy did not significantly affect disease-free survival in our study, but statistically significant increase in overall survival was observed in patients getting adjuvant treatments (p=0.006).
Adrenocortical carcinoma has poor prognosis and short overall survival, and in its clinical course, recurrence and development of metastasis can be commonly observed even after complete resection of the tumor. Therefore, the patients should be evaluated carefully while determining the surgical procedure during the preoperative period, and the operation and post-operative follow-up should be performed in experienced centers. However, due to the positive effects of adjuvant treatments on survival, all patients should be evaluated postoperatively for the necessity of adjuvant treatments, especially mitotane.
肾上腺皮质癌是一种侵袭性内分泌恶性肿瘤,年发病率为每百万人口0.5 - 2例。决定预后的最重要因素是诊断时的肿瘤分期和手术成功率。然而,高龄、肿瘤体积大、激素分泌、高Ki-67指数(>10%)、肿瘤坏死和高有丝分裂活性是与预后不良相关的其他因素。在本研究中,我们旨在评估患者及治疗相关因素对肾上腺皮质癌预后的影响。
我们纳入了2005年至2015年在本中心随访的15例肾上腺皮质癌患者。分析了年龄、性别、肿瘤大小、手术类型、术后切除状态及辅助治疗对无病生存期和总生存期的影响。
无病生存期为23.32±3.69个月,总生存期为36.60±10.78个月。未发现性别、肿瘤大小、肿瘤分期、手术类型、激素活性、坏死情况、复发及转移的发生与无病生存期和总生存期相关(p>0.05)。在我们的研究中,包括米托坦、化疗和放疗在内的术后辅助治疗对无病生存期无显著影响,但接受辅助治疗的患者总生存期有统计学意义的增加(p = 0.006)。
肾上腺皮质癌预后较差,总生存期短,在其临床过程中,即使肿瘤完全切除后也常可观察到复发和转移的发生。因此,术前确定手术方案时应仔细评估患者,手术及术后随访应在有经验的中心进行。然而,由于辅助治疗对生存有积极作用,所有患者术后均应评估辅助治疗的必要性,尤其是米托坦。