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乳头状甲状腺癌:医学管理与随访

Papillary thyroid cancer: medical management and follow-up.

作者信息

Kloos Richard T

机构信息

The Ohio State University, 446 McCampbell Hall, 1581 Dodd Drive, Columbus, OH 43210-1296, USA.

出版信息

Curr Treat Options Oncol. 2005 Jul;6(4):323-38. doi: 10.1007/s11864-005-0036-8.

Abstract

The incidence of epithelial derived thyroid cancer (papillary thyroid cancer and follicular thyroid cancer, known collectively as differentiated thyroid cancer) is rising. About 80% of patients with thyroid cancer have PTC and are best treated with thyroidectomy and functional lymph node dissection, followed by radioiodine ablation or therapy and performance of a posttreatment whole-body scan, followed by thyroid stimulating hormone (TSH) suppression. One year after radioiodine administration, the use of sensitive thyroglobulin (Tg) assays can separate the vast majority of patients with persistent disease from those who are free of disease and unlikely to have recurrent disease all without the need for repeat whole-body radioiodine imaging. Patients with detectable serum Tg during TSH suppression (Tg-on) or Tg that rises above 2 ng/mL after TSH stimulation (TSH-Tg) are highly likely to harbor residual tumor. TSH stimulation can be achieved using either thyroid hormone withdrawal or recombinant human TSH (rhTSH). Highly skilled screening neck ultrasonography can identify a few additional patients with subcentimeter residual neck lymph node metastases not detected by TSH-Tg. However, ultrasonography and chest computed tomography (CT) are most critical for tumor localization in those patients with Tg values that suggest residual disease or in those patients with persistent antithyroglobulin antibodies (TgAb) that falsely lower Tg measurement. TgAb quantitative titers typically resolve steadily over just a few years in patients free of disease after initial therapy. Another paradigm shift is the recognition that most patients who eventually achieve freedom from disease do so by surgery with fewer patients cured by repetitive radioiodine treatments, and even fewer cured with external beam radiation. Patients who appear to be free of disease require a lifetime of follow-up to optimize levothyroxine treatment, and they will undergo periodic stimulation testing because some will still manifest recurrent disease. Patients with persistent disease despite negative ultrasonography, chest CT, and whole-body radioiodine imaging may have a tumor identified by fluorodeoxyglucose positron emission tomography, optimally performed with combined TSH stimulation and image fusion with CT or magnetic resonance imaging. Patients with metastatic disease who are unresponsive to conventional treatment are encouraged to participate in increasingly available thyroid cancer-specific clinical trials using targeted experimental oral or intravenous chemotherapeutic agents to address this tumor that has historically proven resistant to conventional chemotherapeutic agents.

摘要

上皮源性甲状腺癌(乳头状甲状腺癌和滤泡状甲状腺癌,统称为分化型甲状腺癌)的发病率正在上升。约80%的甲状腺癌患者患有乳头状甲状腺癌,最佳治疗方法是甲状腺切除术和功能性淋巴结清扫,随后进行放射性碘消融或治疗,并进行治疗后全身扫描,接着进行促甲状腺激素(TSH)抑制。放射性碘给药一年后,使用敏感的甲状腺球蛋白(Tg)检测可将绝大多数患有持续性疾病的患者与无疾病且不太可能复发的患者区分开来,而无需重复进行全身放射性碘成像。在TSH抑制期间可检测到血清Tg(Tg-on)或TSH刺激后Tg升高至2 ng/mL以上(TSH-Tg)的患者极有可能存在残留肿瘤。TSH刺激可通过停用甲状腺激素或使用重组人TSH(rhTSH)来实现。技术娴熟的筛查颈部超声检查可识别出一些通过TSH-Tg未检测到的亚厘米级残留颈部淋巴结转移的额外患者。然而,超声检查和胸部计算机断层扫描(CT)对于那些Tg值提示存在残留疾病的患者或那些存在持续抗甲状腺球蛋白抗体(TgAb)从而错误降低Tg测量值的患者的肿瘤定位最为关键。在初始治疗后无疾病的患者中,TgAb定量滴度通常在短短几年内会稳步消退。另一个范式转变是认识到大多数最终实现无病状态的患者是通过手术做到的,通过重复放射性碘治疗治愈的患者较少,而通过外照射治愈的患者更少。看似无病的患者需要终身随访以优化左甲状腺素治疗,并且他们将接受定期刺激测试,因为有些患者仍会出现疾病复发。尽管超声检查、胸部CT和全身放射性碘成像均为阴性,但仍患有持续性疾病的患者可能通过氟脱氧葡萄糖正电子发射断层扫描发现肿瘤,最佳做法是联合TSH刺激以及与CT或磁共振成像的图像融合。鼓励对传统治疗无反应的转移性疾病患者参与越来越多的甲状腺癌特异性临床试验,这些试验使用靶向实验性口服或静脉化疗药物来治疗这种历来对传统化疗药物耐药的肿瘤。

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