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临床Ⅰ期睾丸精原细胞瘤外照射放疗后第二恶性肿瘤的发生率。

Incidence of second malignancies after external beam radiotherapy for clinical stage I testicular seminoma.

机构信息

Virginia Mason Medical Center - Urology and Renal Transplantation, Fred Hutchinson Cancer Research Center - Human Biology, Seattle, WA, USA.

出版信息

BJU Int. 2012 Mar;109(5):706-12. doi: 10.1111/j.1464-410X.2011.10424.x. Epub 2011 Aug 22.

Abstract

OBJECTIVES

• To determine the use of adjuvant external beam radiotherapy (EBRT) for patients with clinical stage I testicular seminoma in the USA. • To quantify the risk of specific second primary malignancies (SPMs) associated with radiation exposure in these patients.

PATIENTS AND METHODS

• We used the Surveillance, Epidemiology and End Results database to identify patients diagnosed with clinical stage I testicular seminoma between 1973 and 2000. • We evaluated the use of EBRT in these patients. • We calculated standardized incidence ratios of specific SPMs in these patients. • We stratified the incidence of SPMs based on age at seminoma diagnosis and time to SPM from initial seminoma diagnosis.

RESULTS

• Adjuvant EBRT use declined from the first decade of the study period to the last decade of the study period (80.6% vs 70.2%). • Overall, there was a 19% increase in SPMs in patients exposed to EBRT (observed/expected, O/E, 1.51; 95% CI, 1.08-1.31) compared to the general population. • Specifically, significantly increased risks were observed for thyroid cancer (O/E, 2.32; 95% CI, 1.16-4.16), pancreatic cancer (O/E, 2.38; 95% CI, 1.43-3.72), non-bladder urothelial malignancies (O/E, 4.27; 95% CI, 1.57-9.29), bladder cancer (O/E, 1.47; 95% CI, 1.01-2.28), all haematological malignancies (O/E, 1.44; 95% CI, 1.08-1.89) and non-Hodgkin's lymphoma (O/E, 1.77; 95% CI, 1.22-2.48). • Patients had a persistently elevated risk of SPMs 15 years from the time of initial clinical stage I testicular seminoma diagnosis (O/E, 1.29; 95% CI, 1.10-1.49).

CONCLUSIONS

• We confirmed the increased risk of SPMs after EBRT for seminoma, and we identified the specific types of SPMs that develop. • The risk of EBRT-associated SPM persists for years after the initial seminoma diagnosis, and patients should be informed about these long-term risks.

摘要

目的

  • 确定美国临床 I 期睾丸精原细胞瘤患者使用辅助外照射放疗(EBRT)的情况。

  • 量化这些患者因辐射暴露而发生特定第二原发恶性肿瘤(SPM)的风险。

患者和方法

  • 我们使用监测、流行病学和最终结果数据库,确定了 1973 年至 2000 年间被诊断为临床 I 期睾丸精原细胞瘤的患者。

  • 我们评估了这些患者中 EBRT 的使用情况。

  • 我们计算了这些患者中特定 SPM 的标准化发病比。

  • 我们根据精原细胞瘤诊断时的年龄和从初始精原细胞瘤诊断到 SPM 的时间对 SPM 的发生进行了分层。

结果

  • 辅助 EBRT 的使用从研究期的第一个十年下降到最后一个十年(80.6%对 70.2%)。

  • 与一般人群相比,接受 EBRT 照射的患者 SPM 增加了 19%(观察到/预期到,O/E,1.51;95%置信区间,1.08-1.31)。

  • 具体而言,甲状腺癌(O/E,2.32;95%置信区间,1.16-4.16)、胰腺癌(O/E,2.38;95%置信区间,1.43-3.72)、非膀胱癌尿路上皮恶性肿瘤(O/E,4.27;95%置信区间,1.57-9.29)、膀胱癌(O/E,1.47;95%置信区间,1.01-2.28)、所有血液恶性肿瘤(O/E,1.44;95%置信区间,1.08-1.89)和非霍奇金淋巴瘤(O/E,1.77;95%置信区间,1.22-2.48)的风险显著增加。

  • 从初始临床 I 期睾丸精原细胞瘤诊断开始 15 年后,患者仍存在 SPM 风险增加(O/E,1.29;95%置信区间,1.10-1.49)。

结论

  • 我们证实了 EBRT 治疗精原细胞瘤后 SPM 风险增加,并确定了发生的特定 SPM 类型。

  • EBRT 相关 SPM 的风险在初始精原细胞瘤诊断后多年持续存在,患者应被告知这些长期风险。

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