Cancer Division, Garvan Institute of Medical Research, Sydney, Australia
Biostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
JAMA Oncol. 2017 Dec 1;3(12):1634-1639. doi: 10.1001/jamaoncol.2017.1968.
Guidelines for clinical management in Li-Fraumeni syndrome, a multiple-organ cancer predisposition condition, are limited. Whole-body magnetic resonance imaging (WBMRI) may play a role in surveillance of this high-risk population.
To assess the clinical utility of WBMRI in germline TP53 mutation carriers at baseline.
Clinical and research surveillance cohorts were identified through the Li-Fraumeni Exploration Research Consortium.
Cohorts that incorporated WBMRI for individuals with germline TP53 mutations from January 1, 2004, through October 1, 2016, were included.
Data were extracted by investigators from each cohort independently and synthesized by 2 investigators. Random-effects meta-analysis methods were used to estimate proportions.
The proportions of participants at baseline in whom a lesion was detected that required follow-up and in whom a new primary malignant neoplasm was detected.
A total of 578 participants (376 female [65.1%] and 202 male [34.9%]; mean [SD] age, 33.2 [17.1] years) from 13 cohorts in 6 countries were included in the analysis. Two hundred twenty-five lesions requiring clinical follow-up were detected by WBMRI in 173 participants. Sixty-one lesions were diagnosed in 54 individuals as benign or malignant neoplasms. Overall, 42 cancers were identified in 39 individuals, with 35 new localized cancers treated with curative intent. The overall estimated detection rate for new, localized primary cancers was 7% (95% CI, 5%-9%).
These data suggest clinical utility of baseline WBMRI in TP53 germline mutation carriers and may form an integral part of baseline clinical risk management in this high-risk population.
Li-Fraumeni 综合征是一种多器官癌症易感性疾病,其临床管理指南有限。全身磁共振成像(WBMRI)可能在监测这种高危人群方面发挥作用。
评估 WBMRI 在胚系 TP53 突变携带者基线时的临床应用价值。
通过 Li-Fraumeni 探索研究联盟确定了临床和研究监测队列。
纳入了 2004 年 1 月 1 日至 2016 年 10 月 1 日期间纳入了携带胚系 TP53 突变个体的 WBMRI 队列。
由两名研究人员分别从每个队列中提取数据,并由两名研究人员进行综合。采用随机效应荟萃分析方法估计比例。
基线时发现需要随访的病变和新原发性恶性肿瘤的参与者比例。
共纳入来自 6 个国家的 13 个队列的 578 名参与者(376 名女性[65.1%]和 202 名男性[34.9%];平均[SD]年龄为 33.2[17.1]岁)。在 173 名参与者中,WBMRI 检测到 225 个需要临床随访的病变。在 54 名个体中,61 个病变被诊断为良性或恶性肿瘤。总体而言,39 名个体中有 42 名癌症被确诊,其中 35 名新的局限性癌症接受了治愈性治疗。新局限性原发性癌症的总体估计检出率为 7%(95%CI,5%-9%)。
这些数据表明 WBMRI 在 TP53 胚系突变携带者中的基线临床应用价值,并可能成为该高危人群基线临床风险管理的重要组成部分。