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肿瘤-基质类型和肿瘤-基质比率可预测乳腺癌新辅助化疗反应。

Tumor-stroma type and tumor-stroma ratio predict neoadjuvant chemotherapy response in breast cancer.

作者信息

Okcu Oğuzhan, Öztürk Çiğdem, Yalçın Anıl Can, Şen Bayram, Yalçın Nazlıcan, Hacıhasanoğlu Ezgi, Aydın Esra

机构信息

Recep Tayyip Erdoğan University, Faculty of Medicine, Department of Pathology - Rize, Türkiye.

Recep Tayyip Erdoğan University Training and Research Hospital, Department of Pathology - Rize, Türkiye.

出版信息

Rev Assoc Med Bras (1992). 2025 Mar 31;71(2):e20241225. doi: 10.1590/1806-9282.20241225. eCollection 2025.

DOI:10.1590/1806-9282.20241225
PMID:40172391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11964313/
Abstract

OBJECTIVE

Breast cancer is the most common cancer type among women. One of the most important parameters in the prognosis of patients is the response to neoadjuvant chemotherapy. The most important parameter for neoadjuvant chemotherapy success is appropriate patient selection. We investigated the effect of tumor-stroma type and tumor-stroma ratio on neoadjuvant chemotherapy response, using the Residual Cancer Burden scoring systems.

METHODS

Patients diagnosed with breast carcinoma in core needle biopsy materials between 2010 and 2023 and whose neoadjuvant treatments and surgeries were performed in our institution were scanned from the database. A total of 158 patients who met the study criteria were included in the study.

RESULTS

Tumor-stroma ratio and collagen-dominant tumor-stroma type were associated with neoadjuvant chemotherapy resistance, and tumor-stroma ratio was found to be an independent risk factor in treatment response. The probability of response to neoadjuvant chemotherapy treatment was higher in luminal molecular subtype breast cancer patients with low tumor stroma.

CONCLUSION

An effective risk analysis for neoadjuvant chemotherapy treatment is not always possible with current clinicopathological parameters. Tumor-stroma ratio and tumor-stroma type seem useful in predicting neoadjuvant chemotherapy response as a reproducible practical marker and do not require additional cost and time.

摘要

目的

乳腺癌是女性中最常见的癌症类型。患者预后的最重要参数之一是对新辅助化疗的反应。新辅助化疗成功的最重要参数是合适的患者选择。我们使用残余癌负担评分系统研究了肿瘤-基质类型和肿瘤-基质比率对新辅助化疗反应的影响。

方法

从数据库中扫描2010年至2023年期间在粗针活检材料中被诊断为乳腺癌且在我们机构接受新辅助治疗和手术的患者。共有158名符合研究标准的患者纳入研究。

结果

肿瘤-基质比率和以胶原为主的肿瘤-基质类型与新辅助化疗耐药相关,且肿瘤-基质比率被发现是治疗反应的独立危险因素。肿瘤基质低的管腔分子亚型乳腺癌患者对新辅助化疗治疗有反应的概率更高。

结论

使用当前的临床病理参数并不总是能够对新辅助化疗治疗进行有效的风险分析。肿瘤-基质比率和肿瘤-基质类型作为一种可重复的实用标志物,在预测新辅助化疗反应方面似乎很有用,且不需要额外的成本和时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7952/11964313/fa7557bbb834/1806-9282-ramb-71-02-e20241225-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7952/11964313/fa7557bbb834/1806-9282-ramb-71-02-e20241225-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7952/11964313/fa7557bbb834/1806-9282-ramb-71-02-e20241225-gf01.jpg

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本文引用的文献

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Front Oncol. 2023 Nov 6;13:1293288. doi: 10.3389/fonc.2023.1293288. eCollection 2023.
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Investigating the role of core needle biopsy in evaluating tumor-stroma ratio (TSR) of invasive breast cancer: a retrospective study.探讨粗针活检在评估浸润性乳腺癌肿瘤间质比(TSR)中的作用:一项回顾性研究。
Breast Cancer Res Treat. 2023 Jan;197(1):113-121. doi: 10.1007/s10549-022-06768-0. Epub 2022 Nov 6.
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Standardization of the tumor-stroma ratio scoring method for breast cancer research.
乳腺癌研究中肿瘤间质比评分方法的标准化。
Breast Cancer Res Treat. 2022 Jun;193(3):545-553. doi: 10.1007/s10549-022-06587-3. Epub 2022 Apr 16.
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Adjuvant and neoadjuvant breast cancer treatments: A systematic review of their effects on mortality.辅助和新辅助乳腺癌治疗:对其死亡率影响的系统评价。
Cancer Treat Rev. 2022 Apr;105:102375. doi: 10.1016/j.ctrv.2022.102375. Epub 2022 Mar 4.
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An easy and practical prognostic parameter: tumor-stroma ratio in Luminal, Her2, and triple-negative breast cancers.一个简单实用的预后参数:Luminal、Her2 和三阴性乳腺癌中的肿瘤间质比。
Rev Assoc Med Bras (1992). 2022 Feb;68(2):227-233. doi: 10.1590/1806-9282.20210979.
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Residual cancer burden after neoadjuvant chemotherapy and long-term survival outcomes in breast cancer: a multicentre pooled analysis of 5161 patients.新辅助化疗后残余肿瘤负担与乳腺癌长期生存结局:5161 例患者的多中心汇总分析。
Lancet Oncol. 2022 Jan;23(1):149-160. doi: 10.1016/S1470-2045(21)00589-1. Epub 2021 Dec 11.
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