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What You Can Learn from 7 Theme Fusion Success Stories

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Radiotherapy results in decreased time to second cancer in children with Li Fraumeni syndrome

By |March 3rd, 2025|Categories: LFS News, Papers & Research Literature, Reference|

UK researchers conducted a retrospective case-series study of four children diagnosed with solid cancers at age 16 or younger, aiming to assess

Clustering of TP53 variants into functional classes correlates with cancer risk and identifies different phenotypes of Li-Fraumeni syndrome

By |February 20th, 2025|Categories: LFS News, Papers & Research Literature, Press Release|

High resolution clustering of TP53 variants into functional classes  correlates with cancer risk among germline variant  carriers and identifies different phenotypes of

Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome (“Toronto Protocol”)

By |January 31st, 2025|Categories: Papers & Research Literature, Reference|

In October 2016, the American Association for Cancer Research organized a meeting with international experts on Li-Fraumeni Syndrome (LFS) to review the

New survey – vaccines for primary cancer prevention in adolescents & young adults

By |January 30th, 2024|Categories: LFS News|

The Huntsman Cancer Institute in Utah is studying attitudes pertaining to vaccines for primary cancer prevention in adolescents and young adults with cancer predisposition syndromes.

Congratulations to NCI’s Dr. Payal Kincha, co-chair of LFSA – India!

By |November 8th, 2023|Categories: LFS News|

Dr. Payal Khincha, M.B.B.S., M.S.H.S., the inaugural Lasker Clinical Research Scholar in DCEG's Clinical Genetics Branch (CGB), whose expertise in diagnosing and managing Li-Fraumeni Syndrome

A qualitative study to assess the psychological experiences and coping strategies of families affected with Li-Fraumeni syndrome in the Indian population

By |June 23rd, 2023|Categories: Papers & Research Literature, Psychosocial Issues, Reference|

Culture Matters:  Individuals affected by LFS reported a wide range of experiences with this rare and poorly understood condition. Limited availability of information often

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