Experience of mitotane successful in the treatment of metastatic adrenocortical cancer

D. P. Yashina, Z. Afanasieva
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Abstract

Background. Adrenocortical cancer (ACC) is a rare malignant endocrine tumor endowed with an aggressive biological potential and a poor prognosis. Surgical adrenalectomy remains the only radical treatment for local ACC. The overall 5-year survival rate of stages with local ACC varies from 56% to 96% and depends on the level of surgical training of a specialized center and the use of adjuvant therapy. Mitotan is the only approved chemotherapeutic agent for the adjuvant treatment of both the primary tumor and relapse and metastases.Aim. To evaluate the experience of mitotane successful use in a young patient with recurrent ACC using the experience of a large medical institution.Clinical observation. Patient R., 31 years old, is under dispensary observation for recurrent adrenocortical cancer of the left adrenal gland T1N0M0 stage 1, class 3. Progression from 2015, 2017, February 2019, April 2019, September 2020 (in the bed, MTS to the left kidney, MTS to the retroperitoneal tissue, MTS to the soft tissues of the lumbar region on the left, MTS to the lungs). Eradication of the tumor tissue was performed surgically, followed by morphological confirmation of the removed foci. For the first time, the diagnosis was established at the age of 23 during an examination for Itsenko-Cushing’s syndrome. Morphologically, the diagnosis of ACC was established after a histological examination of the tumor biopsy obtained by left-sided adrenalectomy (adrenocortical cancer, ki67 up to 20%).During a scheduled dispensary examination in September 2020, according to CT scan of the chest with contrast, two foci were identified in the right lung: in C1 — 10 * 15 mm, in C2 — 30 * 21 mm. By decision of the council (consisting of an oncologist-endocrinologist, a thoracic surgeon and a chemotherapist), a decision was made to prescribe mitotane with dose titration under the control of the level of mitotane in the blood until it reaches 14–20 ng/l, without morphological examination of the foci. Hypocorticism was corrected by the simultaneous use of hydrocortisone with mitotane at a dose of 20 mg per day under the control of ACTH levels. In X-ray evaluation by CT of the chest with a frequency of 3 months, the therapeutic effect in the form of a decrease in the size of the foci (RESIST1.1) occurred in the first 3 months. Mitotan was canceled in November 2021 after complete regression of tumor foci according to CT scan of the chest (pneumosclerosis areas 10*4 mm). Currently, the patient is receiving hormone replacement therapy with hydrocortisone 25 mg per day and is under dispensary observation.Conclusion. Clinical observation has demonstrated the successful use of mitotane in the treatment of metastatic adrenocortical cancer.
米托坦治疗转移性肾上腺皮质癌的成功经验
背景肾上腺皮质癌症(ACC)是一种罕见的恶性内分泌肿瘤,具有侵袭性和预后不良的生物学潜力。手术肾上腺切除术仍然是局部ACC的唯一根治性治疗方法。局部ACC分期的总5年生存率从56%到96%不等,这取决于专业中心的手术训练水平和辅助治疗的使用。米托坦是唯一被批准用于辅助治疗原发性肿瘤和复发转移的化疗药物。目标利用大型医疗机构的经验,评估米托坦在复发性ACC的年轻患者中的成功使用经验。临床观察。患者R,31岁,因左肾上腺复发性癌症T1N0M0 1期3级,正在接受药房观察。2015年、2017年、2019年2月、2019年4月、2020年9月的进展情况(在床上,MTS至左肾,MTS至腹膜后组织,MTS至左侧腰部软组织,MTS为肺部)。手术切除肿瘤组织,然后对切除的病灶进行形态学确认。23岁时,在对伊森科-库欣综合征进行检查时,首次确定了诊断。形态学上,ACC的诊断是在左侧肾上腺切除术(癌症,ki67高达20%)获得的肿瘤活检的组织学检查后确定的。在2020年9月的一次预定的药房检查中,根据胸部CT扫描和对比,在右肺中发现了两个病灶:C1-10*15 mm和C2-30*21 mm。根据委员会(由一名肿瘤学家、内分泌学家、一名胸外科医生和一名化疗医生组成)的决定,决定在不进行病灶形态学检查的情况下,在控制血液中的米托坦水平的情况下开米托坦,并进行剂量滴定,直到达到14-20 ng/ml。在控制促肾上腺皮质激素水平的情况下,通过同时使用氢化可的松和米托坦,每天20毫克的剂量来纠正皮质醇不足。在3个月频率的胸部CT X射线评估中,前3个月出现了病灶大小减小(RESIST1.1)的治疗效果。根据胸部CT扫描,肿瘤病灶完全消退后,Mitotan于2021年11月取消(肺硬化区10*4 mm)。目前,患者正在接受每天25毫克氢化可的松的激素替代治疗,并接受药房观察。结论临床观察表明米托坦治疗转移性癌症是成功的。
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