Wang Fei, Yu Xiaolong, Shen Xiaopei, Zhu Guangwu, Huang Yueye, Liu Rengyun, Viola David, Elisei Rossella, Puxeddu Efisio, Fugazzola Laura, Colombo Carla, Jarzab Barbara, Czarniecka Agnieszka, Lam Alfred K, Mian Caterina, Vianello Federica, Yip Linwah, Riesco-Eizaguirre Garcilaso, Santisteban Pilar, O'Neill Christine J, Sywak Mark S, Clifton-Bligh Roderick, Bendlova Bela, Sýkorová Vlasta, Wang Yangang, Liu Shiguo, Zhao Jiajun, Zhao Shihua, Xing Mingzhao
Laboratory for Cellular and Molecular Thyroid Research, Division of Endocrinology, Diabetes & Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287.
Department of Endocrinology and Metabolism, The Affiliated Hospital of Qingdao University, Qingdao 266003, China.
J Clin Endocrinol Metab. 2017 Sep 1;102(9):3241-3250. doi: 10.1210/jc.2017-00277.
Multifocality is often treated as a risk factor for papillary thyroid cancer (PTC), prompting aggressive treatments, but its prognostic value remains unestablished.
To investigate the role of tumor multifocality in clinical outcomes of PTC.
Multicenter study of the relationship between multifocality and clinical outcomes of PTC in 2638 patients (623 men and 2015 women) with median [interquartile range (IQR)] age of 46 (35 to 58) years and median (IQR) follow-up time of 58 (26 to 107) months at 11 medical centers in six countries. Surveillance, Epidemiology and End Results (SEER) data were used for validation.
Disease recurrence in multifocal and unifocal PTC was 198 of 1000 (19.8%) and 221 of 1624 (13.6%) (P < 0.001), with a hazard ratio of 1.55 [95% confidence interval (CI), 1.28 to 1.88], which became insignificant at 1.13 (95% CI, 0.93 to 1.37) on multivariate adjustment. Similar results were obtained in PTC variants: conventional PTC, follicular-variant PTC, tall-cell PTC, and papillary thyroid microcarcinoma. There was no association between multifocality and mortality in any of these PTC settings, whereas there was a strong association between classic risk factors and cancer recurrence or mortality, which remained significant after multivariate adjustment. In 1423 patients with intrathyroidal PTC, disease recurrence was 20 of 455 (4.4%) and 41 of 967 (4.2%) (P = 0.892) and mortality was 0 of 455 (0.0%) and 3 of 967 (0.3%) (P = 0.556) in multifocal and unifocal PTC, respectively. The results were reproduced in 89,680 patients with PTC in the SEER database.
Tumor multifocality has no independent risk prognostic value in clinical outcomes of PTC; its indiscriminate use as an independent risk factor, prompting overtreatments of patients, should be avoided.
多灶性常被视为甲状腺乳头状癌(PTC)的一个危险因素,从而促使采取积极的治疗措施,但其预后价值仍未明确。
探讨肿瘤多灶性在PTC临床结局中的作用。
对来自六个国家11个医疗中心的2638例患者(623例男性和2015例女性)进行多中心研究,这些患者的年龄中位数[四分位间距(IQR)]为46(35至58)岁,中位(IQR)随访时间为58(26至107)个月,研究PTC多灶性与临床结局之间的关系。采用监测、流行病学和最终结果(SEER)数据进行验证。
多灶性PTC和单灶性PTC的疾病复发率分别为1000例中的198例(19.8%)和1624例中的221例(13.6%)(P<0.001),风险比为1.55[95%置信区间(CI),1.28至1.88],多因素调整后变为1.13(95%CI,0.93至1.37),无统计学意义。在PTC的不同亚型中也得到了类似结果:经典型PTC、滤泡亚型PTC、高细胞型PTC和甲状腺微小乳头状癌。在这些PTC类型中,多灶性与死亡率之间均无关联,而经典危险因素与癌症复发或死亡率之间存在强关联,多因素调整后仍具有统计学意义。在1423例甲状腺内PTC患者中,多灶性PTC和单灶性PTC的疾病复发率分别为455例中的20例(4.4%)和967例中的41例(4.2%)(P=0.892),死亡率分别为455例中的0例(0.0%)和967例中的3例(0.3%)(P=0.556)。SEER数据库中89680例PTC患者的结果也再现了这一情况。
肿瘤多灶性在PTC临床结局中没有独立的风险预后价值;应避免将其不加区分地用作独立危险因素,以免导致对患者的过度治疗。