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混合亚型比其他组织学亚型预后更差:217 例化生性乳腺癌患者的回顾性分析。

The mixed subtype has a worse prognosis than other histological subtypes: a retrospective analysis of 217 patients with metaplastic breast cancer.

机构信息

Department of Breast Oncology, National Clinical Research Center of Cancer, Key Laboratory of Cancer Prevention and Therapy, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.

Department of Breast Pathology and Lab, Department of Breast Oncology, National Clinical Research Center of Cancer, Key Laboratory of Breast Cancer of Breast Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.

出版信息

Breast Cancer Res Treat. 2023 Jul;200(1):23-36. doi: 10.1007/s10549-023-06945-9. Epub 2023 May 9.


DOI:10.1007/s10549-023-06945-9
PMID:37160814
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10224839/
Abstract

OBJECTIVE: Metaplastic breast cancer (MpBC) is an aggressive subtype of all breast cancer. We aimed to investigate the clinicopathological features, treatments and prognoses of MpBC patients. METHODS: We collected the data from MpBC patients diagnosed at Tianjin Medical University Cancer Hospital from 2010 to 2017. Kaplan Meier curves and Cox regression model were used to evaluating clinical outcomes and prognostic factors. After removing baseline differences by propensity score matching (PSM), we analyzed the prognosis between MpBC patients and invasive ductal carcinomas of no special type (IDC-NST) patients. RESULTS: A total of 217 MpBC patients were subsumed. Of all histological subtypes, 45.1% were mixed subtypes, followed by with mesenchymal differentiation (27.2%), pure squamous (15.2%) and pure spindle (12.4%) subtypes. 69.6% of MpBC were triple-negative, 25.3% and 6.5% were HR-positive and HER2-positive. MpBC patients had worse survival compared to IDC-NST patients, with 5-year RFS of 73.8 and 83.6% (HR = 1.177 95%CI (1.171-2.676) P = 0.0068), and 5-year BCSS of 79.0% and 89.7% (HR = 2.187 95%CI (1.357-3.523) P = 0.0013). In the multivariate COX model, AJCC stage, mixed subtype and chemotherapy were independent prognostic factors. Mixed MpBC is more aggressive than pure and with heterologous mesenchymal differentiation subtypes. And whether squamous or spindle MpBC, mixed forms have shorter outcomes than pure forms. CONCLUSIONS: MpBCs are associated with poorer prognoses than IDC-NSTs. They are heterogeneous with different clinicopathological features and clinical outcomes between histological subtypes. Pure and with heterologous mesenchymal differentiation subtypes have more survival benefits than the mixed subtype.

摘要

目的:化生性乳腺癌(MpBC)是所有乳腺癌的一种侵袭性亚型。本研究旨在探讨 MpBC 患者的临床病理特征、治疗方法和预后。

方法:回顾性分析 2010 年至 2017 年在天津医科大学肿瘤医院诊断为 MpBC 的患者临床资料,采用 Kaplan-Meier 曲线和 Cox 回归模型评估临床结局和预后因素。通过倾向评分匹配(PSM)消除基线差异后,分析 MpBC 患者与非特殊型浸润性导管癌(IDC-NST)患者的预后差异。

结果:共纳入 217 例 MpBC 患者,其中 45.1%为混合亚型,其次为伴间叶分化(27.2%)、单纯鳞癌(15.2%)和单纯梭形细胞癌(12.4%)。69.6%的 MpBC 为三阴性,25.3%和 6.5%为 HR 阳性和 HER2 阳性。与 IDC-NST 患者相比,MpBC 患者的生存情况更差,5 年 RFS 分别为 73.8%和 83.6%(HR=1.177,95%CI:1.1712.676,P=0.0068),5 年 BCSS 分别为 79.0%和 89.7%(HR=2.187,95%CI:1.3573.523,P=0.0013)。多因素 COX 模型分析显示,AJCC 分期、混合亚型和化疗是独立的预后因素。混合亚型的 MpBC 比单纯和伴异源间叶分化的亚型更具侵袭性。无论是鳞癌还是梭形细胞癌,混合亚型的结局均短于单纯亚型。

结论:MpBC 与 IDC-NST 相比,预后较差。MpBC 具有不同的组织病理学特征和不同组织学亚型之间的临床结局,具有异质性。单纯和伴异源间叶分化的亚型比混合亚型具有更好的生存获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/48e2ace39b03/10549_2023_6945_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/48835712ddb8/10549_2023_6945_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/689c1d4cefa8/10549_2023_6945_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/e291d8bdbce3/10549_2023_6945_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/ec1bf81ea821/10549_2023_6945_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/d4a692a947e3/10549_2023_6945_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/48e2ace39b03/10549_2023_6945_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/48835712ddb8/10549_2023_6945_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/689c1d4cefa8/10549_2023_6945_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/e291d8bdbce3/10549_2023_6945_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/ec1bf81ea821/10549_2023_6945_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/d4a692a947e3/10549_2023_6945_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b27e/10224839/48e2ace39b03/10549_2023_6945_Fig6_HTML.jpg

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TNMpBC-NeoBCSS model: a breast cancer specific survival prediction model for triple-negative metaplastic breast carcinoma patients with neoadjuvant therapy.

Sci Rep. 2025-3-11

[2]
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[3]
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[4]
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[5]
Complete Response of Triple-Negative Metaplastic Carcinoma of the Breast Using Pembrolizumab.

Case Rep Oncol. 2023-10-16

本文引用的文献

[1]
Metaplastic breast cancer: A review.

Crit Rev Oncol Hematol. 2023-2

[2]
Prognostic relevance of mixed histological subtypes in invasive breast carcinoma: a retrospective analysis.

J Cancer Res Clin Oncol. 2023-7

[3]
Prognostic Factor Analysis and Model Construction of Triple-Negative Metaplastic Breast Carcinoma After Surgery.

Front Oncol. 2022-6-23

[4]
Molecular Characterization and Prospective Evaluation of Pathologic Response and Outcomes with Neoadjuvant Therapy in Metaplastic Triple-Negative Breast Cancer.

Clin Cancer Res. 2022-7-1

[5]
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Mod Pathol. 2022-8

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Am J Transl Res. 2021-10-15

[7]
A Multicenter Phase II Trial of Ipilimumab and Nivolumab in Unresectable or Metastatic Metaplastic Breast Cancer: Cohort 36 of Dual Anti-CTLA-4 and Anti-PD-1 Blockade in Rare Tumors (DART, SWOG S1609).

Clin Cancer Res. 2022-1-15

[8]
Presentation and survival by hormonal receptor status in metaplastic breast cancer: A propensity score-matched analysis.

Breast. 2021-12

[9]
Epithelial Mesenchymal Transition and Immune Response in Metaplastic Breast Carcinoma.

Int J Mol Sci. 2021-7-9

[10]
MicroRNA-495/TGF-β/FOXC1 axis regulates multidrug resistance in metaplastic breast cancer cells.

Biochem Pharmacol. 2021-10

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