Department of Endocrinology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Centre for Endocrinology, William Harvey Research Institute, Queen Marry University of London, London, United Kingdom.
Front Endocrinol (Lausanne). 2024 Jan 8;14:1226348. doi: 10.3389/fendo.2023.1226348. eCollection 2023.
Medullary thyroid carcinoma (MTC) is a rare thyroid malignancy originating from parafollicular C cells. It accounts for 5%-10% of all thyroid malignancies.
An ambispective analysis of pathologically proven MTC presented in a tertiary care hospital in northwest India was performed after considering demography, clinical manifestation, mutation status, management, and outcome as denominators.
Among 2,735 thyroid malignancy cases who presented to our institute in the last 10 years (2012-2022), 78 (3%) had MTC with a mean age of presentation of 43 ± 11 years; 60% of them were female. The median duration of symptoms was 23 months (IQR 12-36 months). The most common presenting complaint was goiter with lymphadenopathy (80.8%). Among the atypical presentations, one each had ectopic Cushing's syndrome, hypertensive crisis in pregnancy due to pheochromocytoma, synchronous chondrosarcoma, and Von Hippel-Lindau disease spectrum. Median calcitonin and carcinoembryonic antigen (CEA) levels at presentation were 1,274 pg/mL ( = 64) and 149 ng/mL ( = 39), respectively. Twenty-two patients were germline mutation-positive, and they presented at a younger age. Majority of the patients presented with stage IV disease. Surgery was the primary modality of therapy. Twenty-nine patients received radiotherapy and 25 patients received tyrosine kinase inhibitors (TKIs). Nine patients received peptide receptor radiotherapy (PRRT) with Lu-177 with neoadjuvant capecitabine. Median progression-free survival (PFS) was 60 months. Patients without structurally and biochemically residual disease and stable disease after the first modality of therapy (Log-rank 11.4; = 0.004) had a better PFS. Female patients (Log-rank: 9.5; = 0.002) had a better PFS than male patients.
This study showed that MTC comprises 3% of thyroid malignancies with a female preponderance. mutation-positive patients had a younger age at presentation. Surgery was the first-line therapy. Radiotherapy, TKI, and PRRT were given as a part of second-line or third-line therapy due to persistent disease and/or disease recurrence. The median PFS was better in female patients and in patients who had no residual lesions and stable disease after the primary modality of therapy.
甲状腺髓样癌(MTC)是一种起源于滤泡旁 C 细胞的罕见甲状腺恶性肿瘤。它占所有甲状腺恶性肿瘤的 5%-10%。
对在印度西北部一家三级保健医院就诊的经病理证实的 MTC 患者进行前瞻性和回顾性分析,以患者的人口统计学、临床表现、突变状态、治疗方法和结局为计算基数。
在过去 10 年(2012-2022 年)我院就诊的 2735 例甲状腺恶性肿瘤患者中,78 例(3%)患有 MTC,平均发病年龄为 43±11 岁;其中 60%为女性。症状持续时间中位数为 23 个月(IQR 12-36 个月)。最常见的首发症状是伴有淋巴结病的甲状腺肿(80.8%)。在非典型表现中,各有 1 例患者表现为异位库欣综合征、妊娠嗜铬细胞瘤性高血压危象、同期软骨肉瘤和 von Hippel-Lindau 疾病谱。首发时降钙素和癌胚抗原(CEA)的中位数水平分别为 1274 pg/ml( = 64)和 149 ng/ml( = 39)。22 例患者为胚系突变阳性,且发病年龄较轻。大多数患者就诊时已处于 IV 期疾病。手术是主要的治疗方法。29 例患者接受了放疗,25 例患者接受了酪氨酸激酶抑制剂(TKI)治疗。9 例患者接受了 Lu-177 标记的肽受体放射性核素治疗(PRRT)联合卡培他滨新辅助治疗。中位无进展生存期(PFS)为 60 个月。在首次治疗后无结构性和生化残留疾病且病情稳定的患者(对数秩检验:11.4; = 0.004)具有更好的 PFS。女性患者(对数秩检验:9.5; = 0.002)的 PFS 优于男性患者。
本研究表明,MTC 占甲状腺恶性肿瘤的 3%,女性发病率较高。胚系突变阳性患者的发病年龄较轻。手术是一线治疗方法。由于持续性疾病和/或疾病复发,放疗、TKI 和 PRRT 作为二线或三线治疗方法。女性患者和首次治疗后无残留病变和病情稳定的患者中位 PFS 更好。