Marta Eguía-Larrea , Carmen Parra-Pérez , Teresa Cabero-Morán , Raquel Jiménez Rosellón , Luis Muñoz-Bellvís
{"title":"三阴性乳腺癌、雄激素受体和其他标记物。治疗策略","authors":"Marta Eguía-Larrea , Carmen Parra-Pérez , Teresa Cabero-Morán , Raquel Jiménez Rosellón , Luis Muñoz-Bellvís","doi":"10.1016/j.senol.2024.100595","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Triple Negative Breast Cancer (TNBC) has dreadful prognosis. Surgery, radiotherapy and chemotherapy are the only effective therapies, since it has no target treatments. In TNBC, AR modulation has been demonstrated to inhibit cell development and increase apoptosis in vitro and in vivo.</p></div><div><h3>Objective</h3><p>To assess whether AR in TNBC is associated with a better prognosis.</p></div><div><h3>Material and methods</h3><p>This study is a retrospective description of a cohort of 163 TNBC patients, who underwent treatment from 2003 to 2017. Immunohistochemical determinations were examined in the surgical specimen for AR, E-cadherina and GATA3.</p></div><div><h3>Results</h3><p>AR positive TNBC are more differentiated and less proliferative tumors than AR negative (p < 0.05). However, this fact has not been significantly associated with better overall survival nor disease free survival. Loss of expression of GATA3 and E-cadherina has not been related to worse overall survival in our paper.</p></div><div><h3>Conclusions</h3><p>Although no difference in TNBC survival related to AR expression has been observed, determination of AR may be useful in TNBC due to possibility of modulating AR as a target therapy. Future treatment options in TNBC may be the combined use of selective androgen receptor and other drugs such as Pi3K inhibitors or immunomodulators, due to the frequent pi3K mutations of AR positive TNBC and the usefulness of immunotherapy in TNBC.</p></div>","PeriodicalId":38058,"journal":{"name":"Revista de Senologia y Patologia Mamaria","volume":"37 3","pages":"Article 100595"},"PeriodicalIF":0.2000,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cáncer de mama triple negativo, receptor de andrógeno y otros marcadores. Estrategias terapéuticas\",\"authors\":\"Marta Eguía-Larrea , Carmen Parra-Pérez , Teresa Cabero-Morán , Raquel Jiménez Rosellón , Luis Muñoz-Bellvís\",\"doi\":\"10.1016/j.senol.2024.100595\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>Triple Negative Breast Cancer (TNBC) has dreadful prognosis. Surgery, radiotherapy and chemotherapy are the only effective therapies, since it has no target treatments. In TNBC, AR modulation has been demonstrated to inhibit cell development and increase apoptosis in vitro and in vivo.</p></div><div><h3>Objective</h3><p>To assess whether AR in TNBC is associated with a better prognosis.</p></div><div><h3>Material and methods</h3><p>This study is a retrospective description of a cohort of 163 TNBC patients, who underwent treatment from 2003 to 2017. Immunohistochemical determinations were examined in the surgical specimen for AR, E-cadherina and GATA3.</p></div><div><h3>Results</h3><p>AR positive TNBC are more differentiated and less proliferative tumors than AR negative (p < 0.05). However, this fact has not been significantly associated with better overall survival nor disease free survival. Loss of expression of GATA3 and E-cadherina has not been related to worse overall survival in our paper.</p></div><div><h3>Conclusions</h3><p>Although no difference in TNBC survival related to AR expression has been observed, determination of AR may be useful in TNBC due to possibility of modulating AR as a target therapy. Future treatment options in TNBC may be the combined use of selective androgen receptor and other drugs such as Pi3K inhibitors or immunomodulators, due to the frequent pi3K mutations of AR positive TNBC and the usefulness of immunotherapy in TNBC.</p></div>\",\"PeriodicalId\":38058,\"journal\":{\"name\":\"Revista de Senologia y Patologia Mamaria\",\"volume\":\"37 3\",\"pages\":\"Article 100595\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2024-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista de Senologia y Patologia Mamaria\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0214158224000239\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"OBSTETRICS & GYNECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista de Senologia y Patologia Mamaria","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0214158224000239","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
导言三阴性乳腺癌(TNBC)的预后非常糟糕。由于没有靶向治疗,手术、放疗和化疗是唯一有效的治疗方法。在 TNBC 中,AR 调节已被证实可在体外和体内抑制细胞发育并增加细胞凋亡。目的 评估 TNBC 中的 AR 是否与更好的预后相关。对手术标本中的AR、E-cadherina和GATA3进行了免疫组化检测。结果AR阳性的TNBC比AR阴性的肿瘤分化程度更高、增殖更少(p <0.05)。然而,这一事实与更好的总生存率和无病生存率并无明显关联。结论虽然没有观察到与AR表达有关的TNBC生存率差异,但由于有可能将调节AR作为靶向治疗,因此测定AR可能对TNBC有用。由于AR阳性TNBC的Pi3K突变频繁以及免疫疗法在TNBC中的作用,TNBC未来的治疗方案可能是联合使用选择性雄激素受体和其他药物,如Pi3K抑制剂或免疫调节剂。
Cáncer de mama triple negativo, receptor de andrógeno y otros marcadores. Estrategias terapéuticas
Introduction
Triple Negative Breast Cancer (TNBC) has dreadful prognosis. Surgery, radiotherapy and chemotherapy are the only effective therapies, since it has no target treatments. In TNBC, AR modulation has been demonstrated to inhibit cell development and increase apoptosis in vitro and in vivo.
Objective
To assess whether AR in TNBC is associated with a better prognosis.
Material and methods
This study is a retrospective description of a cohort of 163 TNBC patients, who underwent treatment from 2003 to 2017. Immunohistochemical determinations were examined in the surgical specimen for AR, E-cadherina and GATA3.
Results
AR positive TNBC are more differentiated and less proliferative tumors than AR negative (p < 0.05). However, this fact has not been significantly associated with better overall survival nor disease free survival. Loss of expression of GATA3 and E-cadherina has not been related to worse overall survival in our paper.
Conclusions
Although no difference in TNBC survival related to AR expression has been observed, determination of AR may be useful in TNBC due to possibility of modulating AR as a target therapy. Future treatment options in TNBC may be the combined use of selective androgen receptor and other drugs such as Pi3K inhibitors or immunomodulators, due to the frequent pi3K mutations of AR positive TNBC and the usefulness of immunotherapy in TNBC.