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Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations
PURPOSE: Li-Fraumeni syndrome (LFS) is a rare autosomal cancer syndrome caused by a germline mutation in the TP53 gene. Breast cancer in LFS patients is of various subtypes; however, limited data are available on the clinicopathological features of these subtypes and their appropriate treatments. Th...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Breast Cancer Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090805/ https://www.ncbi.nlm.nih.gov/pubmed/33818021 http://dx.doi.org/10.4048/jbc.2021.24.e16 |
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author | Alyami, Hassan Yoo, Tae-Kyung Cheun, Jong-Ho Lee, Han-Byoel Jung, Sung Mi Ryu, Jai Min Bae, Soong June Jeong, Joon Yoon, Chang Ik Ahn, Juneyoung Paik, Pill Sun Cho, Min Kyung Park, Woo-Chan |
author_facet | Alyami, Hassan Yoo, Tae-Kyung Cheun, Jong-Ho Lee, Han-Byoel Jung, Sung Mi Ryu, Jai Min Bae, Soong June Jeong, Joon Yoon, Chang Ik Ahn, Juneyoung Paik, Pill Sun Cho, Min Kyung Park, Woo-Chan |
author_sort | Alyami, Hassan |
collection | PubMed |
description | PURPOSE: Li-Fraumeni syndrome (LFS) is a rare autosomal cancer syndrome caused by a germline mutation in the TP53 gene. Breast cancer in LFS patients is of various subtypes; however, limited data are available on the clinicopathological features of these subtypes and their appropriate treatments. This study aimed to review the clinical features and treatments for breast cancer in South Korean patients with germline TP53 mutations. METHODS: Data on the clinicopathological features and treatment of all breast cancer patients with LFS were collected retrospectively from the available database of 4 tertiary hospitals in the Republic of Korea. RESULTS: Twenty-one breast cancer cases in 12 unrelated women with confirmed germline TP53 mutations were included in the study. The median age at diagnosis was 33.5 years. The histopathological diagnosis included invasive ductal carcinoma (n = 16), ductal carcinoma in situ (n = 3), and malignant phyllodes tumor (n = 2). While 42% and 31% of the cases were positive for estrogen and progesterone receptors, respectively, 52.6% were human epidermal growth factor receptor 2 (HER2) positive, and 21% were triple-negative. The treatments included mastectomy (52%) and breast-conserving surgery (38%). Five patients underwent radiotherapy (RT). The median follow-up period was 87.5 (8–222) months. There were 3 ipsilateral and 4 contralateral breast recurrences during the follow-up, and 8 patients developed new primary cancers. In the post-RT subgroup, there were 2 ipsilateral and 2 contralateral breast recurrences in 1 patient, and 4 patients had a new primary cancer. CONCLUSION: As reported in other countries, breast cancer in LFS patients in South Korea had an early onset and were predominantly but not exclusively positive for HER2. A multidisciplinary approach with adherence to the treatment guidelines, considering mastectomy, and avoiding RT is encouraged to prevent RT-associated sequelae in LFS patients. |
format | Online Article Text |
id | pubmed-8090805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Breast Cancer Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80908052021-05-11 Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations Alyami, Hassan Yoo, Tae-Kyung Cheun, Jong-Ho Lee, Han-Byoel Jung, Sung Mi Ryu, Jai Min Bae, Soong June Jeong, Joon Yoon, Chang Ik Ahn, Juneyoung Paik, Pill Sun Cho, Min Kyung Park, Woo-Chan J Breast Cancer Original Article PURPOSE: Li-Fraumeni syndrome (LFS) is a rare autosomal cancer syndrome caused by a germline mutation in the TP53 gene. Breast cancer in LFS patients is of various subtypes; however, limited data are available on the clinicopathological features of these subtypes and their appropriate treatments. This study aimed to review the clinical features and treatments for breast cancer in South Korean patients with germline TP53 mutations. METHODS: Data on the clinicopathological features and treatment of all breast cancer patients with LFS were collected retrospectively from the available database of 4 tertiary hospitals in the Republic of Korea. RESULTS: Twenty-one breast cancer cases in 12 unrelated women with confirmed germline TP53 mutations were included in the study. The median age at diagnosis was 33.5 years. The histopathological diagnosis included invasive ductal carcinoma (n = 16), ductal carcinoma in situ (n = 3), and malignant phyllodes tumor (n = 2). While 42% and 31% of the cases were positive for estrogen and progesterone receptors, respectively, 52.6% were human epidermal growth factor receptor 2 (HER2) positive, and 21% were triple-negative. The treatments included mastectomy (52%) and breast-conserving surgery (38%). Five patients underwent radiotherapy (RT). The median follow-up period was 87.5 (8–222) months. There were 3 ipsilateral and 4 contralateral breast recurrences during the follow-up, and 8 patients developed new primary cancers. In the post-RT subgroup, there were 2 ipsilateral and 2 contralateral breast recurrences in 1 patient, and 4 patients had a new primary cancer. CONCLUSION: As reported in other countries, breast cancer in LFS patients in South Korea had an early onset and were predominantly but not exclusively positive for HER2. A multidisciplinary approach with adherence to the treatment guidelines, considering mastectomy, and avoiding RT is encouraged to prevent RT-associated sequelae in LFS patients. Korean Breast Cancer Society 2021-03-12 /pmc/articles/PMC8090805/ /pubmed/33818021 http://dx.doi.org/10.4048/jbc.2021.24.e16 Text en © 2021 Korean Breast Cancer Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Alyami, Hassan Yoo, Tae-Kyung Cheun, Jong-Ho Lee, Han-Byoel Jung, Sung Mi Ryu, Jai Min Bae, Soong June Jeong, Joon Yoon, Chang Ik Ahn, Juneyoung Paik, Pill Sun Cho, Min Kyung Park, Woo-Chan Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations |
title | Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations |
title_full | Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations |
title_fullStr | Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations |
title_full_unstemmed | Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations |
title_short | Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations |
title_sort | clinical features of breast cancer in south korean patients with germline tp53 gene mutations |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090805/ https://www.ncbi.nlm.nih.gov/pubmed/33818021 http://dx.doi.org/10.4048/jbc.2021.24.e16 |
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