Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging

Mandy L. Ballinger(Garvan Institute of Medical Research), Ana F. Best(National Institutes of Health), Phuong L. Mai(National Institutes of Health), Payal P. Khincha(National Institutes of Health), Jennifer T. Loud(National Institutes of Health), June A. Peters(National Institutes of Health), Maria Isabel Achatz(National Institutes of Health), Rubens Chojniak(AC Camargo Hospital), Alexandre André Balieiro Anastácio da Costa(AC Camargo Hospital), Karina Miranda Santiago(AC Camargo Hospital), Judy E. Garber(Dana-Farber Cancer Institute), Allison F. O’Neill(Dana-Farber Cancer Institute), Rosalind A. Eeles(National Health Service), D. Gareth Evans(St. Mary’s Hospital), Eveline M. A. Bleiker(The Netherlands Cancer Institute), Gabe S. Sonke(The Netherlands Cancer Institute), Mariëlle Ruijs(The Netherlands Cancer Institute), Claudette E. Loo(The Netherlands Cancer Institute), Joshua D. Schiffman(University of Utah), Anne Naumer(University of Utah), Wendy Kohlmann(University of Utah), Louise C. Strong(The University of Texas MD Anderson Cancer Center), Jasmina Bojadzieva(The University of Texas MD Anderson Cancer Center), David Malkin(University of Toronto), Surya P. Rednam(Baylor College of Medicine), Elena M. Stoffel(University of Michigan), Erika Koeppe(University of Michigan), Jeffrey N. Weitzel(City of Hope), Thomas P. Slavin(City of Hope), Bita Nehoray(City of Hope), Mark E. Robson(Memorial Sloan Kettering Cancer Center), Michael F. Walsh(Memorial Sloan Kettering Cancer Center), Lorenzo Manelli(Memorial Sloan Kettering Cancer Center), Anita Villani(Hospital for Sick Children), David M. Thomas(Garvan Institute of Medical Research), Sharon A. Savage(National Institutes of Health)
JAMA Oncology
August 3, 2017
Cited by 192Open Access
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Abstract

Importance: 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. Objective: To assess the clinical utility of WBMRI in germline TP53 mutation carriers at baseline. Data Sources: Clinical and research surveillance cohorts were identified through the Li-Fraumeni Exploration Research Consortium. Study Selection: Cohorts that incorporated WBMRI for individuals with germline TP53 mutations from January 1, 2004, through October 1, 2016, were included. Data Extraction and Synthesis: Data were extracted by investigators from each cohort independently and synthesized by 2 investigators. Random-effects meta-analysis methods were used to estimate proportions. Main Outcomes and Measures: 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. Results: 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%). Conclusions and Relevance: 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.


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