Sampson Elliot, Brierley James D, Le Lisa W, Rotstein Lorne, Tsang Richard W
Department of Radiation Oncology, Princess Margaret Hospital, University Health Network, University of Toronto, Toronto, Canada.
Cancer. 2007 Oct 1;110(7):1451-6. doi: 10.1002/cncr.22956.
Differentiated thyroid cancer has a good prognosis and only rarely presents with distant metastasis at diagnosis. The clinical outcome of this presentation was assessed with respect to survival and factors that may determine prognosis.
A retrospective review was undertaken of patients with stage M1 differentiated thyroid cancer at presentation (n = 49), referred from 1980-2000 at a single institution.
The median age was 68 (range, 17-90), with 69% females. The initial site(s) of metastasis were lung only, 45%, bone only, 39%, other single site, 4%, and multiple sites, 12%.
papillary, 51%, follicular, 49%. Initial treatment(s) included: thyroidectomy, 82%, radioactive iodine (RAI), 88%, excision of metastasis, 29%, radiotherapy, 47%, and chemotherapy, 6%. With a median follow-up time of 3.5 years, 25 patients are alive (51%) and 24 died (49%), with 3-year and 5-year actuarial survivals of 69% and 50%, respectively. Only a minority of patients (4/25, 16%) had no clinical evidence of disease at last follow-up. Most deaths (17/24, 71%) were due to progressive cancer. Prognosis was associated with age, site of metastasis, histology, and iodine avidity of the metastasis. Patients aged </=45 (n = 8) had a 3-year survival of 100%, versus 62% for those age > 45 years (P = .001). The 3-year survival for lung only versus bone only metastasis was 77% versus 56% (P = .02); for papillary versus follicular carcinoma, 75% versus 62% (P = .006); for iodine-avid disease (n = 29) versus not avid (n = 14), 82% versus 57% (P = .02), respectively. In multivariate analysis after adjusting for age, only histology and iodine avidity remained significant for survival. The hazard ratio for follicular histology was 3.7 (95% confidence interval [CI], 1.1-12.1, P = .03), and for tumors not avid for iodine, 3.4 (95% CI, 1.2-9.2, P = .02).
The data support the aggressive management of patients presenting with stage M1 thyroid cancer, with thyroidectomy and RAI. Complete clinical eradication of disease was rarely seen, and 50% of patients survived for more than 5 years. Young patients with papillary tumors and/or iodine-avid disease have an even better prognosis.
分化型甲状腺癌预后良好,诊断时很少出现远处转移。本文评估了该疾病的临床结局以及可能决定预后的因素。
对1980年至2000年间在单一机构就诊的M1期分化型甲状腺癌患者(n = 49)进行回顾性研究。
患者中位年龄为68岁(范围17 - 90岁),女性占69%。转移的初始部位仅为肺部的占45%,仅为骨骼的占39%,其他单一部位的占4%,多个部位的占12%。
乳头状癌占51%,滤泡状癌占49%。初始治疗包括:甲状腺切除术82%,放射性碘(RAI)治疗88%,转移灶切除术29%,放射治疗47%,化疗6%。中位随访时间为3.5年,25例患者存活(51%),24例死亡(49%),3年和5年精算生存率分别为69%和50%。最后一次随访时,只有少数患者(4/25,16%)没有疾病的临床证据。大多数死亡病例(17/24,71%)是由于癌症进展。预后与年龄、转移部位、组织学类型以及转移灶的碘摄取情况有关。年龄≤45岁的患者(n = 8)3年生存率为100%,而年龄>45岁的患者为62%(P = .001)。仅肺部转移与仅骨骼转移患者的3年生存率分别为77%和56%(P = .02);乳头状癌与滤泡状癌患者分别为75%和62%(P = .006);碘摄取阳性疾病患者(n = 29)与碘摄取阴性患者(n = 14)分别为82%和57%(P = .02)。多因素分析在调整年龄后,仅组织学类型和碘摄取情况对生存仍有显著意义。滤泡状组织学类型的风险比为3.7(95%置信区间[CI],1.1 - 12.1,P = .03),碘摄取阴性肿瘤的风险比为3.4(95%CI,1.2 - 9.2,P = .02)。
数据支持对M1期甲状腺癌患者采取积极的治疗措施,包括甲状腺切除术和RAI治疗。很少能实现疾病的完全临床根除,50%的患者存活超过5年。患有乳头状肿瘤和/或碘摄取阳性疾病的年轻患者预后甚至更好。