Literature DB >> 28772291

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis.

Mandy L Ballinger1, Ana Best2, Phuong L Mai3, Payal P Khincha3, Jennifer T Loud3, June A Peters3, Maria Isabel Achatz3,4, Rubens Chojniak4, Alexandre Balieiro da Costa5, Karina Miranda Santiago6, Judy Garber7, Allison F O'Neill8, Rosalind A Eeles9, D Gareth Evans10, Eveline Bleiker11, Gabe S Sonke12, Marielle Ruijs13, Claudette Loo14, Joshua Schiffman15, Anne Naumer15, Wendy Kohlmann15, Louise C Strong16, Jasmina Bojadzieva16, David Malkin17,18, Surya P Rednam19, Elena M Stoffel20, Erika Koeppe20, Jeffrey N Weitzel21, Thomas P Slavin21, Bita Nehoray21, Mark Robson22, Michael Walsh23, Lorenzo Manelli24, Anita Villani17, David M Thomas1, Sharon A Savage2.   

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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Year:  2017        PMID: 28772291      PMCID: PMC5824277          DOI: 10.1001/jamaoncol.2017.1968

Source DB:  PubMed          Journal:  JAMA Oncol        ISSN: 2374-2437            Impact factor:   31.777


  25 in total

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Journal:  Breast Cancer Res Treat       Date:  2006-06-22       Impact factor: 4.872

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Journal:  J Clin Oncol       Date:  2005-11-20       Impact factor: 44.544

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Journal:  Ann Intern Med       Date:  1969-10       Impact factor: 25.391

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Authors:  M O Leach; C R M Boggis; A K Dixon; D F Easton; R A Eeles; D G R Evans; F J Gilbert; I Griebsch; R J C Hoff; P Kessar; S R Lakhani; S M Moss; A Nerurkar; A R Padhani; L J Pointon; D Thompson; R M L Warren
Journal:  Lancet       Date:  2005 May 21-27       Impact factor: 79.321

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Authors:  J M Varley
Journal:  Hum Mutat       Date:  2003-03       Impact factor: 4.878

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Authors:  Gaëlle Bougeard; Mariette Renaux-Petel; Jean-Michel Flaman; Camille Charbonnier; Pierre Fermey; Muriel Belotti; Marion Gauthier-Villars; Dominique Stoppa-Lyonnet; Emilie Consolino; Laurence Brugières; Olivier Caron; Patrick R Benusiglio; Brigitte Bressac-de Paillerets; Valérie Bonadona; Catherine Bonaïti-Pellié; Julie Tinat; Stéphanie Baert-Desurmont; Thierry Frebourg
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9.  Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.

Authors:  Anita Villani; Ari Shore; Jonathan D Wasserman; Derek Stephens; Raymond H Kim; Harriet Druker; Bailey Gallinger; Anne Naumer; Wendy Kohlmann; Ana Novokmet; Uri Tabori; Marta Tijerin; Mary-Louise C Greer; Jonathan L Finlay; Joshua D Schiffman; David Malkin
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10.  Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.

Authors:  D Malkin; F P Li; L C Strong; J F Fraumeni; C E Nelson; D H Kim; J Kassel; M A Gryka; F Z Bischoff; M A Tainsky
Journal:  Science       Date:  1990-11-30       Impact factor: 47.728

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2.  Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.

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Review 3.  Recommendations for Long-Term Follow-up of Adults with Heritable Retinoblastoma.

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4.  Germ Cell Mosaicism: A Rare Cause of Li-Fraumeni Recurrence Among Siblings.

Authors:  Lauren N Donovan; Wendy Kohlmann; Angela K Snow; Deborah W Neklason; Joshua D Schiffman; Luke Maese
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5.  Incorrect Spelling in Byline.

Authors: 
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7.  TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

Authors:  J J Bakhuizen; F B Hogervorst; M E Velthuizen; M W Ruijs; K van Engelen; T A van Os; J J Gille; M Collée; A M van den Ouweland; C J van Asperen; C M Kets; A R Mensenkamp; E M Leter; M J Blok; M M de Jong; M G Ausems
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