Yau Thomas, Lo C Y, Epstein R J, Lam A K Y, Wan K Y, Lang Brian H
Department of Medicine, University of Hong Kong Medical Centre, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong, China.
Ann Surg Oncol. 2008 Sep;15(9):2500-5. doi: 10.1245/s10434-008-0005-0. Epub 2008 Jun 26.
Anaplastic thyroid carcinoma (ATC) is a notoriously aggressive malignancy associated with a highly lethal clinical course despite therapeutic intervention. Our present study attempts to identify factors that could potentially improve therapeutic strategies by analyzing the clinicopathological features, treatment and outcome of ATC patients managed over the past four decades at our institution.
Fifty patients with biopsy-proven ATC during the period 1966 to 2006 were studied. All patients were managed with surgery, radiotherapy, chemotherapy and/or chemoradiation. Survival was calculated by the Kaplan-Meier method. Potential factors affecting survival were compared by the log rank test.
Most patients (88%) presented with a neck mass; 17 patients (34%) also had cervical lymphadenopathy. Distant metastases were clinically present in 9 (18%). Median survival was 97 days, whereas the 1- and 3-year survival was 14% and 8%, respectively. On univariate analysis, patients aged </=65 years (P = .04), absence of metastatic disease at presentation (P < .01), surgical resection (P < .01), and postoperative radiotherapy (P < .01) were associated with longer survival. The adoption of cytotoxic chemotherapy was not associated with better survival (P = .4). Moreover, there was no improvement in survival rate over the last four decades despite the adoption of multimodal treatment (P = .5).
ATC remains a deadly disease despite technical advances in surgical technique and adoption of multidisciplinary treatment strategies over the last four decades. However, younger patients with localized ATC might benefit from an aggressive multidisciplinary approach.
间变性甲状腺癌(ATC)是一种侵袭性极强的恶性肿瘤,尽管进行了治疗干预,其临床病程仍具有高度致死性。我们目前的研究旨在通过分析我院在过去四十年间诊治的ATC患者的临床病理特征、治疗方法及预后,来确定可能改善治疗策略的因素。
对1966年至2006年间经活检证实为ATC的50例患者进行研究。所有患者均接受了手术、放疗、化疗和/或放化疗。采用Kaplan-Meier法计算生存率。通过对数秩检验比较影响生存的潜在因素。
大多数患者(88%)表现为颈部肿块;17例患者(34%)还伴有颈部淋巴结肿大。9例(18%)临床出现远处转移。中位生存期为97天,1年和3年生存率分别为14%和8%。单因素分析显示,年龄≤65岁的患者(P = 0.04)、初诊时无转移性疾病(P < 0.01)、手术切除(P < 0.01)及术后放疗(P < 0.01)与较长生存期相关。采用细胞毒性化疗与更好的生存率无关(P = 0.4)。此外,尽管在过去四十年中采用了多模式治疗,但生存率并无改善(P = 0.5)。
尽管在过去四十年中手术技术取得了进步且采用了多学科治疗策略,但ATC仍然是一种致命疾病。然而,年轻的局限性ATC患者可能从积极的多学科治疗方法中获益。