Evaluation of Overall Survival in Patients With Anaplastic Thyroid Carcinoma, 2000-2019

医学 总体生存率 回顾性队列研究 内科学 甲状腺 队列 肿瘤科 比例危险模型 阶段(地层学) 队列研究 外科 生存分析 存活率 甲状腺间变性癌 危险系数 真实世界的证据 甲状腺癌 靶向治疗 甲状腺癌 倾向得分匹配 年轻人 无进展生存期 癌症
作者
Anastasios Maniakas,Ramona Dadu,Naifa L. Busaidy,Jennifer Wang,Renata Ferrarotto,Charles Lu,Michelle D. Williams,G. Brandon Gunn,Marie‐Claude Hofmann,Gilbert J. Cote,Jared Sperling,Neil D. Gross,Erich M. Sturgis,Ryan P. Goepfert,Stephen Y. Lai,Maria E. Cabanillas,Mark Zafereo
出处
期刊:JAMA Oncology [American Medical Association]
卷期号:6 (9): 1397-1397 被引量:350
标识
DOI:10.1001/jamaoncol.2020.3362
摘要

IMPORTANCE: Anaplastic thyroid carcinoma (ATC) historically has a 4-month median overall survival (OS) from time of diagnosis, with disease-specific mortality approaching 100%. The association between recent major advancements in treatment and OS has yet to be evaluated. OBJECTIVE: To evaluate rates of OS in patients with ATC over the last 2 decades. DESIGN, SETTING, AND PARTICIPANTS: Retrospective cohort study in a single tertiary care institution. Patients with histopathological confirmation of ATC from January 2000 to October 2019 were included and divided into 3 groups according to date of presentation: 2000-2013, 2014-2016, and 2017-2019. MAIN OUTCOMES AND MEASURES: Overall survival compared among different treatment eras and differing therapies, including targeted therapy, immunotherapy, and surgery. RESULTS: Of 479 patients (246 men [51%]; median age, 65.0 [range, 21.1-92.6] years) with ATC evaluated, 52 (11%) were stage IVA, 172 (36%) stage IVB, and 255 (53%) stage IVC at presentation. The median OS of the entire cohort was 0.79 years (9.5 months), ranging from 0.01 to 16.63. The OS at 1 and 2 years was 35% (95% CI, 29%-42%) and 18% (95% CI, 13%-23%) in the 2000-2013 group (n = 227), 47% (95% CI, 36%-56%) and 25% (95% CI, 17%-34%) in the 2014-2016 group (n = 100), and 59% (95% CI, 49%-67%) and 42% (95% CI, 30%-53%) in the 2017-2019 group (n = 152), respectively (P < .001). The hazard ratio was 0.50 (95% CI, 0.38-0.67) for the 2017-2019 group compared with the 2000-2013 patients (P < .001). Factors associated with improved OS included targeted therapy (hazard ratio, 0.49; 95% CI, 0.39-0.63; P < .001), the addition of immunotherapy to targeted therapy (hazard ratio, 0.58; 95% CI, 0.36-0.94; P = .03), and surgery following neoadjuvant BRAF-directed therapy (hazard ratio, 0.29; 95% CI, 0.10-0.78; P = .02). Patients undergoing surgery following neoadjuvant BRAF-directed therapy (n = 20) had a 94% 1-year survival with a median follow-up of 1.21 years. CONCLUSION AND RELEVANCE: In this large single-institution cohort study spanning nearly 20 years, changes in patient management appear to be associated with significant increase in survival. The era of untreatable ATC is progressively being replaced by molecular-based personalized therapies, with integration of multidisciplinary therapies including surgery and radiation therapy.
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