Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study

Background: Malignant phyllodes tumors (MPTs) with sarcomatous components are often associated with substantial risks for local and distant recurrences. A more comprehensive characterization of their clinicopathological features and molecular profiles may offer significant potential innovative thera...

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Main Authors: Ting Lei, Yunjie Song, Zhiyi Shen, Yongqiang Shi, Cunyan Xia, Xu Deng, Wenyue Da, Yan Peng, Qing Li
Format: Article
Language:English
Published: Elsevier 2025-03-01
Series:Translational Oncology
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Online Access:http://www.sciencedirect.com/science/article/pii/S193652332500049X
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author Ting Lei
Yunjie Song
Zhiyi Shen
Yongqiang Shi
Cunyan Xia
Xu Deng
Wenyue Da
Yan Peng
Qing Li
author_facet Ting Lei
Yunjie Song
Zhiyi Shen
Yongqiang Shi
Cunyan Xia
Xu Deng
Wenyue Da
Yan Peng
Qing Li
author_sort Ting Lei
collection DOAJ
description Background: Malignant phyllodes tumors (MPTs) with sarcomatous components are often associated with substantial risks for local and distant recurrences. A more comprehensive characterization of their clinicopathological features and molecular profiles may offer significant potential innovative therapeutic strategies. Methods: A total of ten cases were collected with eight cases undergoing DNA next-generation sequencing (NGS). The clinicopathological characteristics, prognostic information, and genomic profiles were compared to those of MPTs without sarcomatous components. Results: Compared to MPT without sarcomatous components, no significant differences were found in age, tumor position, tumor size, menopausal status, or presence of fibroadenoma (p > 0.05). MPTs with osteosarcoma components had a poor prognosis either compared with other sarcomatous components (p = 0.027) or MPTs without sarcomatous components (p = 0.033). A notably high frequency of mutations was observed in several key genes within MPTs exhibiting sarcomatous components: TP53 (n = 6, 75.0 %), MUC16 (n = 4, 50.0 %), PTCH1 (n = 3, 37.5 %), and APC (n = 3, 37.5 %). In MPTs characterized by sarcomatous components, MCL1 (n = 6, 75.0 %) and MYC (n = 5, 62.5 %) demonstrated a notably high frequency of amplification. The NOTCH signaling pathway was significantly associated with MPTs characterized by sarcomatous components (13.6 % vs 75.0 %, p = 0.001). Conclusions: The presence of an osteosarcoma component may serve as an indicator for unfavorable prognosis. Activating mutations in TP53 have been identified in these tumors. Furthermore, it typically facilitates tumor formation and progression via the NOTCH signaling pathway. These findings may offer valuable insights for clinical prognosis and identify potential therapeutic targets.
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spelling doaj-art-d99a32362e85462c8aca27ed10dd89be2025-02-08T05:00:06ZengElsevierTranslational Oncology1936-52332025-03-0153102318Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular studyTing Lei0Yunjie Song1Zhiyi Shen2Yongqiang Shi3Cunyan Xia4Xu Deng5Wenyue Da6Yan Peng7Qing Li8Department of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaJiangsu Simcere Diagnostics Co., Ltd., Nanjing Simcere Medical Laboratory Science Co., Ltd., The State Key Laboratory of Neurology and Oncology Drug DevelopmentDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR ChinaDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR China; Corresponding author at: Department of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, PR China.Background: Malignant phyllodes tumors (MPTs) with sarcomatous components are often associated with substantial risks for local and distant recurrences. A more comprehensive characterization of their clinicopathological features and molecular profiles may offer significant potential innovative therapeutic strategies. Methods: A total of ten cases were collected with eight cases undergoing DNA next-generation sequencing (NGS). The clinicopathological characteristics, prognostic information, and genomic profiles were compared to those of MPTs without sarcomatous components. Results: Compared to MPT without sarcomatous components, no significant differences were found in age, tumor position, tumor size, menopausal status, or presence of fibroadenoma (p > 0.05). MPTs with osteosarcoma components had a poor prognosis either compared with other sarcomatous components (p = 0.027) or MPTs without sarcomatous components (p = 0.033). A notably high frequency of mutations was observed in several key genes within MPTs exhibiting sarcomatous components: TP53 (n = 6, 75.0 %), MUC16 (n = 4, 50.0 %), PTCH1 (n = 3, 37.5 %), and APC (n = 3, 37.5 %). In MPTs characterized by sarcomatous components, MCL1 (n = 6, 75.0 %) and MYC (n = 5, 62.5 %) demonstrated a notably high frequency of amplification. The NOTCH signaling pathway was significantly associated with MPTs characterized by sarcomatous components (13.6 % vs 75.0 %, p = 0.001). Conclusions: The presence of an osteosarcoma component may serve as an indicator for unfavorable prognosis. Activating mutations in TP53 have been identified in these tumors. Furthermore, it typically facilitates tumor formation and progression via the NOTCH signaling pathway. These findings may offer valuable insights for clinical prognosis and identify potential therapeutic targets.http://www.sciencedirect.com/science/article/pii/S193652332500049XMalignant phyllodes tumorSarcomatous componentOsteosarcoma componentsTP53NOTCH pathway
spellingShingle Ting Lei
Yunjie Song
Zhiyi Shen
Yongqiang Shi
Cunyan Xia
Xu Deng
Wenyue Da
Yan Peng
Qing Li
Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study
Translational Oncology
Malignant phyllodes tumor
Sarcomatous component
Osteosarcoma components
TP53
NOTCH pathway
title Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study
title_full Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study
title_fullStr Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study
title_full_unstemmed Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study
title_short Malignant phyllodes tumors with sarcomatous components: A histopathologic and molecular study
title_sort malignant phyllodes tumors with sarcomatous components a histopathologic and molecular study
topic Malignant phyllodes tumor
Sarcomatous component
Osteosarcoma components
TP53
NOTCH pathway
url http://www.sciencedirect.com/science/article/pii/S193652332500049X
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