References
- Valdez JM, Nichols KE, Kesserwan C. Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition. Br J Haematol 2017;176:539-552 https://doi.org/10.1111/bjh.14461
- Mai PL, Best AF, Peters JA, DeCastro RM, Khincha PP, Loud JT, et al. Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort. Cancer 2016;122:3673-3681 https://doi.org/10.1002/cncr.30248
- Hyder Z, Harkness EF, Woodward ER, Bowers NL, Pereira M, Wallace AJ, et al. Risk of contralateral breast cancer in women with and without pathogenic variants in BRCA1, BRCA2, and tp53 genes in women with very early-onset (< 36 Years) breast cancer. Cancers (Basel) 2020;12:378
- Shimatani A, Aono M, Hoshi M, Oebisu N, Iwai T, Takada N, et al. Secondary osteosarcoma in patients previously treated for childhood cancer: three case reports. Mol Clin Oncol 2019;10:153-158
- Ji M, Wang L, Shao Y, Cao W, Xu T, Chen S, et al. A novel dysfunctional germline P53 mutation identified in a family with Li-Fraumeni syndrome. Am J Cancer Res 2018;8:165-169
- Lee DS, Yoon SY, Looi LM, Kang P, Kang IN, Sivanandan K, et al. Comparable frequency of BRCA1, BRCA2 and TP53 germline mutations in a multi-ethnic Asian cohort suggests TP53 screening should be offered together with BRCA1/2 screening to early-onset breast cancer patients. Breast Cancer Res 2012;14:R66
- Heymann S, Delaloge S, Rahal A, Caron O, Frebourg T, Barreau L, et al, Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome. Radiat Oncol 2010;5:104
- Hendrickson PG, Luo Y, Kohlmann W, Schiffman J, Maese L, Bishop AJ, et al. Radiation therapy and secondary malignancy in Li-Fraumeni syndrome: a hereditary cancer registry study. Cancer Med 2020;9:7954-7963 https://doi.org/10.1002/cam4.3427
- Boyle JM, Spreadborough A, Greaves MJ, Birch JM, Varley JM, Scott D. The relationship between radiation-induced G1arrest and chromosome aberrations in Li-Fraumeni fibroblasts with or without germline TP53 mutations. Br J Cancer 2001;85:293-296 https://doi.org/10.1054/bjoc.2001.1896
- Daly MB, Pilarski R, Yurgelun MB, Berry MP, Buys SS, Dickson P, et al. NCCN guidelines insights: genetic/familial high-risk assessment: breast, ovarian, and pancreatic, version 1.2020: featured updates to the NCCN guidelines. J Natl Compr Canc Netw 2020;18:380-391 https://doi.org/10.6004/jnccn.2020.0017