Robbins J, Merino M J, Boice J D, Ron E, Ain K B, Alexander H R, Norton J A, Reynolds J
Ann Intern Med. 1991 Jul 15;115(2):133-47. doi: 10.7326/0003-4819-115-2-133.
This conference focuses on the controversies about managing thyroid cancer, emphasizing the possibility that the treatment of patients with potentially fatal thyroid cancer may be improved. Although the mortality rate from thyroid cancer is low, it is the highest among cancers affecting the endocrine glands (excluding the ovary). Exposure to radiation during childhood in the 1930s and 1940s increased the incidence of but not the mortality from thyroid cancer, because these tumors are mainly papillary cancers developing in young adults. These rates may change as the exposed cohort ages. Risk factors that increase mortality include older patient age and the growth characteristics of the tumor at diagnosis, the presence of distant metastases, and cell type (for example, the tall-cell variants of papillary cancer, follicular cancer [to be distinguished from the more benign follicular variant of papillary cancer], medullary cancer, and anaplastic cancer). Local metastases in lymph nodes do not seem to increase the risk for death from papillary cancer, but they do increase the risk for death from follicular and medullary cancer. In the latter, mortality is decreased by the early detection and treatment of patients with the familial multiple endocrine neoplasia syndrome 2a. There are excellent tumor markers for differentiated cancer of the parafollicular and of the follicular cells (serum calcitonin and serum thyroglobulin levels, respectively). Measuring the calcitonin level allows early diagnosis of familial medullary cancer, whereas measuring the thyroglobulin level, although useful only after total thyroidectomy, allows early recognition of recurrence or metastases of papillary or follicular cancer. Initial surgery, protocols for follow-up, and the use of radioiodine for the ablation of any residual thyroid and the treatment of metastatic cancer are discussed. Because these tumors resist currently available chemotherapy regimens, possible ways to increase the effectiveness of radioiodine therapy are considered as are new approaches to treatment.
本次会议聚焦于甲状腺癌治疗方面的争议,强调改善潜在致命性甲状腺癌患者治疗效果的可能性。尽管甲状腺癌的死亡率较低,但在影响内分泌腺的癌症(不包括卵巢癌)中却是最高的。20世纪30年代和40年代儿童期接受辐射增加了甲状腺癌的发病率,但并未增加死亡率,因为这些肿瘤主要是发生在年轻成年人中的乳头状癌。随着受辐射人群年龄的增长,这些发病率可能会发生变化。增加死亡率的危险因素包括患者年龄较大、诊断时肿瘤的生长特征、远处转移的存在以及细胞类型(例如,乳头状癌的高细胞变体、滤泡状癌[需与乳头状癌中更良性的滤泡状变体区分开来]、髓样癌和未分化癌)。淋巴结局部转移似乎不会增加乳头状癌的死亡风险,但会增加滤泡状癌和髓样癌的死亡风险。对于后者,通过对患有家族性多发性内分泌肿瘤综合征2a的患者进行早期检测和治疗可降低死亡率。对于滤泡旁细胞和滤泡细胞的分化癌有出色的肿瘤标志物(分别为血清降钙素和血清甲状腺球蛋白水平)。测量降钙素水平可早期诊断家族性髓样癌,而测量甲状腺球蛋白水平虽然仅在全甲状腺切除术后有用,但可早期识别乳头状癌或滤泡状癌的复发或转移。讨论了初始手术、随访方案以及使用放射性碘消融任何残留甲状腺和治疗转移性癌的问题。由于这些肿瘤对目前可用的化疗方案有抗性,因此考虑了提高放射性碘治疗效果的可能方法以及新的治疗方法。