Holm L E, Wiklund K E, Lundell G E, Bergman N A, Bjelkengren G, Ericsson U B, Cederquist E S, Lidberg M E, Lindberg R S, Wicklund H V
Department of Cancer Prevention, Karolinska Hospital, Stockholm, Sweden.
J Natl Cancer Inst. 1989 Feb 15;81(4):302-6. doi: 10.1093/jnci/81.4.302.
Previously, we conducted a study of 35,074 patients receiving diagnostic doses of 131I for suspected thyroid disorders between 1951 and 1969. We reported that, between 1958 and 1984, the incidence of thyroid cancers in these patients was insignificantly greater than the incidence expected in the general population. This increase was attributed to the underlying condition that prompted the examination and not to the administration of 131I. The purpose of the present study was to analyze the total cancer risk in the same cohort of patients examined with diagnostic doses of 131I. To further evaluate the underlying risk of disease in these patients, we compared the incidence of all cancers with that expected in the general population. The average radiation dose was approximately 500 mGy to the thyroid and less than 10 mGy to other organs. In the 35,074 patients, 3,746 cancers occurred following the first 5 years after examination, and the resulting standardized incidence rate (SIR) was 1.01 (95% confidence interval = 0.98-1.04). SIRs were significantly increased for endocrine tumors other than thyroid cancer (1.93) and for lymphomas (1.24), leukemias (1.34), and nervous system tumors (1.19). The risk of leukemia was similar for chronic lymphocytic leukemia (CLL) (SIR = 1.30) and non-CLL (SIR = 1.34). SIR was significantly decreased for cancers of the female genital organs (0.86). The risk for cancer of all sites and types combined was highest 5-9 years after examination (SIR = 1.07) and did not differ from unity thereafter. With greater than or equal to 10 years of follow-up, risk was not statistically associated with the dose of 131I. Overall, the data exclude cancer risk increments greater than 5% (SIR = 1.05) with 95% confidence. The significant increase in the risk of non-CLL, a prominent radiogenic malignancy, however, warrants special attention. We are continuing our study to determine the possible factors involved in the significant increase in the risk of leukemia.
此前,我们对1951年至1969年间接受诊断剂量131I治疗疑似甲状腺疾病的35074例患者进行了一项研究。我们报告称,1958年至1984年间,这些患者中甲状腺癌的发病率略高于普通人群预期的发病率。这种增加归因于促使进行检查的潜在疾病,而非131I的给药。本研究的目的是分析同一组接受诊断剂量131I检查的患者的总体癌症风险。为了进一步评估这些患者潜在的疾病风险,我们将所有癌症的发病率与普通人群预期的发病率进行了比较。平均辐射剂量甲状腺约为500 mGy,其他器官小于10 mGy。在35074例患者中,检查后的前5年发生了3746例癌症,由此得出的标准化发病率(SIR)为1.01(95%置信区间=0.98 - 1.04)。除甲状腺癌外的内分泌肿瘤(1.93)、淋巴瘤(1.24)、白血病(1.34)和神经系统肿瘤(1.19)的SIR显著升高。慢性淋巴细胞白血病(CLL)(SIR = 1.30)和非CLL(SIR = 1.34)的白血病风险相似。女性生殖器官癌症的SIR显著降低(0.86)。所有部位和类型的癌症综合风险在检查后5 - 9年最高(SIR = 1.07),此后与1无差异。随访时间大于或等于10年时,风险与131I剂量无统计学关联。总体而言,数据以95%的置信度排除了癌症风险增加超过5%(SIR = 1.05)的情况。然而,非CLL风险的显著增加,一种突出的放射性恶性肿瘤,值得特别关注。我们正在继续我们的研究,以确定白血病风险显著增加可能涉及的因素。