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肿瘤长期生存患者 CT 随访后第二癌症诱发风险评估。

Evaluation of second cancer induction risk by CT follow-up in oncological long-surviving patients.

机构信息

Medical Physics Department, San Raffaele Scientific Institute, Via Olgettina 60, Milano, Italy.

出版信息

Health Phys. 2013 Jan;104(1):1-8. doi: 10.1097/HP.0b013e3182690c8e.

Abstract

The goal of establishing prompt localization of the malignant spread or recurrence of a tumor has found a powerful solution in the definition of follow-up protocols, which include the indication for CT scans on an annual or semiannual basis. In the case of long-surviving patients, however, this approach will lead to a considerable integrated dose level over a period of several years after recovery from the illness. Pathologies treated primarily by surgery and/or chemotherapy have been considered, not taking into account cancers treated with adjuvant or radical radiotherapy. Given that the most likely protocols for these cancers often call for total body scans, an estimation of the consequent effective and organ doses can be performed with acceptable accuracy. The data acquired from five centers have been collected and the related effective and organ doses calculated by means of IMPACT software. Use of the effective dose concept, however, has lately become the subject of criticism, and the recently proposed Effective Risk Model has therefore also been applied. The evaluated absolute additional risk of second tumor induction ranges between 0.1% and 10%, depending primarily on age and pathology. These results depict this additional risk as an issue of significant importance for clinical practice. A revision of follow-up and scan parameter protocols, as well as the introduction of new algorithms for dose reduction, could significantly improve the risk-benefit ratio for all the pathologies studied.

摘要

建立肿瘤恶性播散或复发的快速定位目标,在随访方案的定义中找到了一个强有力的解决方案,其中包括每年或每半年进行 CT 扫描的指征。然而,对于长期存活的患者,这种方法将导致在疾病康复后的几年内产生相当大的综合剂量水平。已经考虑了主要通过手术和/或化疗治疗的病理,而没有考虑辅助或根治性放疗治疗的癌症。鉴于这些癌症最有可能的方案通常需要全身扫描,可以使用 IMPACT 软件以可接受的准确度估算相应的有效和器官剂量。已经收集了来自五个中心的数据,并通过 IMPACT 软件计算了相关的有效和器官剂量。然而,有效剂量概念的使用最近受到了批评,因此最近提出的有效风险模型也得到了应用。评估的继发第二肿瘤诱导的绝对附加风险在 0.1%到 10%之间,主要取决于年龄和病理。这些结果表明,这种额外风险是临床实践中一个非常重要的问题。对随访和扫描参数方案进行修订,并引入新的剂量降低算法,可以显著提高所有研究病理的风险效益比。

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