Extended spectrum of cancers in PTEN hamartoma tumor syndrome

PTEN hamartoma tumor syndrome (PHTS) is associated with increased lifetime risks of breast, thyroid, kidney, endometrial, and colorectal cancers, as well as melanoma (collectively, component cancers). We sought to characterize non-component cancers (NCC) in PHTS. Of 701 research participants with PHTS, 340 (49%) had cancer, with 101 (30%) having at least one NCC. Interestingly, 71 (70%) of those with NCC had at least one other PHTS component malignancy. Patients with pathogenic PTEN variants showed higher risks for prostate cancer and soft tissue sarcomas at younger ages than the general population. A literature survey showed independent cases of NCC in PHTS, with PTEN-related molecular changes including second-hit somatic PTEN alterations in a subset of various specimens. We recommend increased awareness regarding NCC in individuals with PHTS, particularly increased risks for prostate cancer and sarcoma. Further studies are needed to define age-related penetrance and accordingly, the appropriate strategies for cancer risk management.

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Publication Details

Journal
npj Precision Oncology
Published
2025-03-06
DOI
https://doi.org/10.1038/s41698-025-00847-3
Citations
9
Primary Topic
PI3K/AKT/mTOR signaling in cancer
Type
article
Field-Weighted Citation Impact
7.25

Funders

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article

Extended spectrum of cancers in PTEN hamartoma tumor syndrome

Julia H. Joo, Lamis Yehia, Charis Eng, Sujata Patil et al.
9 citations
npj Precision Oncology
PI3K/AKT/mTOR signaling in cancer
7.25
article

Extended spectrum of cancers in PTEN hamartoma tumor syndrome

Julia H. Joo, Lamis Yehia, Charis Eng, Sujata Patil, Gilman Plitt, Darren Liu, Ann M. Tushar, Ying Ni
article en
9 citations

Abstract

PTEN hamartoma tumor syndrome (PHTS) is associated with increased lifetime risks of breast, thyroid, kidney, endometrial, and colorectal cancers, as well as melanoma (collectively, component cancers). We sought to characterize non-component cancers (NCC) in PHTS. Of 701 research participants with PHTS, 340 (49%) had cancer, with 101 (30%) having at least one NCC. Interestingly, 71 (70%) of those with NCC had at least one other PHTS component malignancy. Patients with pathogenic PTEN variants showed higher risks for prostate cancer and soft tissue sarcomas at younger ages than the general population. A literature survey showed independent cases of NCC in PHTS, with PTEN-related molecular changes including second-hit somatic PTEN alterations in a subset of various specimens. We recommend increased awareness regarding NCC in individuals with PHTS, particularly increased risks for prostate cancer and sarcoma. Further studies are needed to define age-related penetrance and accordingly, the appropriate strategies for cancer risk management.

npj Precision OncologyVol. 9(1)
Cleveland Clinic (US), Cleveland Clinic Lerner College of Medicine (US), Community Care (US), University School (US), Case Western Reserve University (US)
American Cancer Society, Breast Cancer Research Foundation, Ambrose Monell Foundation, PTEN Research, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Good health and well-being
Openalex Percentile: Top 3%
PI3K/AKT/mTOR signaling in cancer
7.25
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