Suppr超能文献

急性淋巴细胞白血病幸存者中甲状腺功能障碍及后续甲状腺癌的风险:来自儿童癌症幸存者研究的报告

Risk of thyroid dysfunction and subsequent thyroid cancer among survivors of acute lymphoblastic leukemia: a report from the Childhood Cancer Survivor Study.

作者信息

Chow Eric J, Friedman Debra L, Stovall Marilyn, Yasui Yutaka, Whitton John A, Robison Leslie L, Sklar Charles A

机构信息

Department of Pediatrics, University of Washington, Seattle, Washington, USA.

出版信息

Pediatr Blood Cancer. 2009 Sep;53(3):432-7. doi: 10.1002/pbc.22082.

Abstract

BACKGROUND

To determine the risk of thyroid dysfunction and subsequent thyroid cancer among childhood acute lymphoblastic leukemia (ALL) survivors.

PROCEDURE

Rates of self-reported thyroid dysfunction and thyroid cancer were determined among 3,579 ALL survivors participating in the Childhood Cancer Survivor Study, a cohort of 5-year survivors of pediatric cancers diagnosed from 1970 to 1986, and compared with 3,846 siblings and population rates, respectively.

RESULTS

The cumulative incidence of hypo- and hyperthyroidism among survivors 15 years following leukemia diagnosis was 1.6% (95% CI 1.1, 2.1) and 0.6% (95% CI 0.3, 1.1), respectively, both significantly increased compared with siblings. In multivariate analysis, survivors who received >or=20 Gy cranial radiotherapy plus any spinal radiotherapy had the highest risk of subsequent hypothyroidism (HR 8.3, 95% CI 3.3, 20.5) compared with those treated with chemotherapy alone. Craniospinal radiotherapy also was associated with an increased risk of subsequent hyperthyroidism (HR 6.1, 95% CI 1.1, 34.2) compared with chemotherapy alone, as well as an increased risk of subsequent thyroid cancers (SIR 30.3, 95% CI 14.5, 55.7) compared with population rates. In radiation dosimetry analysis, pituitary doses >or=20 Gy combined with thyroid doses >or=10 Gy were associated with hypothyroidism, whereas pituitary doses >or=20 Gy combined with thyroid doses >or=15 Gy were associated with hyperthyroidism.

CONCLUSIONS

The risk of thyroid dysfunction and thyroid cancer was increased among childhood ALL survivors treated with craniospinal radiotherapy. In these individuals, long-term surveillance is warranted as no obvious plateau in risk was seen, even after 25 years of follow-up.

摘要

背景

确定儿童急性淋巴细胞白血病(ALL)幸存者发生甲状腺功能障碍及后续甲状腺癌的风险。

方法

在参与儿童癌症幸存者研究的3579名ALL幸存者中确定自我报告的甲状腺功能障碍和甲状腺癌发生率,该队列研究对象为1970年至1986年诊断的儿科癌症5年幸存者,分别与3846名同胞及总体发生率进行比较。

结果

白血病诊断后15年幸存者中甲状腺功能减退和亢进的累积发生率分别为1.6%(95%可信区间1.1, 2.1)和0.6%(95%可信区间0.3, 1.1),均显著高于同胞。多变量分析显示,接受≥20 Gy颅部放疗加任何脊髓放疗的幸存者后续发生甲状腺功能减退的风险最高(风险比8.3,95%可信区间3.3, 20.5),与仅接受化疗者相比。与仅接受化疗相比,颅脊髓放疗还与后续发生甲状腺功能亢进的风险增加(风险比6.1,95%可信区间1.1, 34.2)以及后续发生甲状腺癌的风险增加(标准化发病比30.3,95%可信区间14.5, 55.7)相关。在放射剂量分析中,垂体剂量≥20 Gy联合甲状腺剂量≥10 Gy与甲状腺功能减退相关,而垂体剂量≥20 Gy联合甲状腺剂量≥15 Gy与甲状腺功能亢进相关。

结论

接受颅脊髓放疗的儿童ALL幸存者发生甲状腺功能障碍和甲状腺癌的风险增加。对于这些个体,即使经过25年随访风险未见明显平台期,仍需进行长期监测。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验