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首页> 外文期刊>Ecancermedicalscience >Highlights from the 15th St Gallen International Breast Cancer Conference 15–18 March, 2017, Vienna: tailored treatments for patients with early breast cancer
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Highlights from the 15th St Gallen International Breast Cancer Conference 15–18 March, 2017, Vienna: tailored treatments for patients with early breast cancer

机译:2017年3月15日至18日在维也纳举行的第15届圣加仑国际乳腺癌会议的要点:针对早期乳腺癌患者的量身定制的治疗方法

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The 15th St Gallen International Breast Cancer Conference was held in Vienna for the second time, from 15th–18th March 2017. 4000people from 105 countries all over the world were invited to take part in the event. The real highlight of the conference was the last day withthe International Consensus Session which was chaired by around 50 experts on breast cancer worldwide. With reference to data fromscientific research, the consensus panel tried to offer guidelines for the management of breast cancer with the aim of providing patientswith optimal treatment. The topics covered focused on the treatment of breast cancer, consideration of surgery, radiotherapy, neo-adjuvant,and adjuvant systemic therapy for breast cancer, as well as genetics and prevention of breast cancer.In particular, in terms of precision medicine, an important topic of the conference was ‘is it possible to think that it could become routine inclinical practice to use immunotherapy and targeted therapy based on genetic signatures?’In view of personalised therapy, it is important to take into consideration women’s treatment preferences. It is also important not only tooffer guidelines which help breast cancer experts all over the world to choose the proper treatment for women with breast cancer but alsoto discuss the pros and cons of the therapy with the patient. This allows for a better understanding of the disease.‘From the maximum tolerable to the minimum effective treatment: it is essential to escalate treatment when necessary and to de-escalatewhen unnecessary’. These few words could summarise the meaning of the 15th St Gallen International Breast Cancer Conference.Prof Martine Piccart-Gebhart was awarded with the St Gallen International Breast Cancer Award 2017 for her fundamental clinical researchcontribution and Prof Giuseppe Curigliano with the Umberto Veronesi Memorial Award which aims to recognise a physician’s leading rolein advancing the science and care of breast cancer patients. Curigliano, in his lecture, spoke about the revolutionary immunotherapy in the clinical management of breast cancer (BC). For the development of these therapies, it is necessary to identify the genetic determinants of BC immune phenotypes in which The Cancer Genome Atlas (TCGA) has contributed towards this. For example, the T helper (Th-1) phenotype (ICR4), which also exhibits upregulation of immune-regulatory transcripts (eg. PDL1, PD1, FOXP3, IDO1, and CTLA4), was associated with prolonged patients’ survival. Chromosome segment 4q21, which includes genes encoding the Th-1 chemokines CXCL9-11, was significantly amplified only in the immune favourable phenotype (ICR4). The mutation and neoantigen load progressively decreased from ICR4 to ICR1 but could not explain immune phenotypic differences. Mutations of TP53 were enriched in the immune favourable phenotype (ICR4). Instead, the presence of MAP3K1 and MAP2K4 mutations were closely associated with an immune unfavourable phenotype (ICR1). Using both the TCGA and the validation dataset, the degree of MAPK deregulation segregates BC according to their immune disposition. These findings suggest that mutational-driven deregulation of MAPK pathways is linked to the negative regulation of intratumoural immune response in BC. The main themes of this congress were: 1) Surgery of the primary tumour and margins; 2) Surgery of the axilla; 3) Radiotherapy: hypofractionated, ‘boost’ to tumour bed, partial breast, regional node, after mastectomy, advanced technology; 4) Pathology: subtypes, TILs; 5) Multi-gene signatures and therapy; 6) Endocrine therapy: pre- and post-menopausal and duration; 7) Chemotherapy: subtypes, stages; 8) Anti-HER-2 therapy; 9) Neo-adjuvant therapy; 10) Adjuvant bisphosponates; 11) Adjuvant diet and exercise.
机译:第15届圣加仑国际乳腺癌大会于2017年3月15日至18日第二次在维也纳举行。来自全球105个国家的4000人应邀参加了该活动。会议的真正亮点是国际共识会议的最后一天,该会议由全球约50位乳腺癌专家主持。参照科学研究的数据,共识小组试图为乳腺癌的治疗提供指导,以期为患者提供最佳治疗。主题涵盖乳腺癌的治疗,对乳腺癌的手术,放疗,新辅助和辅助全身治疗以及遗传学和乳腺癌的预防等方面的考虑,特别是在精准医学方面,重要的是会议的主题是“是否有可能认为使用基于基因特征的免疫疗法和靶向疗法成为常规的临床实践?”鉴于个性化疗法,重要的是要考虑女性的治疗偏好。同样重要的是,太妃指南不仅可以帮助全世界的乳腺癌专家为乳腺癌女性选择合适的治疗方法,而且还可以与患者讨论该疗法的利弊。这样可以更好地了解该疾病。“从最大的耐受性到最小的有效治疗:在必要时升级治疗,在不必要时降低治疗至关重要”。这几句话可以概括第15届圣加仑国际乳腺癌大会的意义。马丁·皮卡特-格巴特教授因其基本的临床研究贡献而荣获2017年圣加仑国际乳腺癌奖,朱塞佩·库里利亚诺教授获得了翁贝托·韦罗内西纪念奖,旨在表彰他的基本临床研究成果。认识到医师在促进乳腺癌患者的科学和护理方面的领导作用。 Curigliano在演讲中谈到了乳腺癌临床治疗中的革命性免疫疗法。为了开发这些疗法,有必要确定癌症基因组图谱(TCGA)促成的BC免疫表型的遗传决定因素。例如,T辅助(Th-1)表型(ICR4)也表现出免疫调节转录本(例如PDL1,PD1,FOXP3,IDO1和CTLA4)的上调,与延长患者的生存率有关。包括编码Th-1趋化因子CXCL9-11的基因的染色体区段4q21仅在免疫有利表型(ICR4)中被显着扩增。突变和新抗原负荷从ICR4逐渐降低到ICR1,但不能解释免疫表型的差异。 TP53突变丰富了免疫有利表型(ICR4)。而是,MAP3K1和MAP2K4突变的存在与免疫不良表型(ICR1)密切相关。使用TCGA和验证数据集,MAPK失调的程度会根据BC的免疫状况将其隔离。这些发现表明,突变驱动的MAPK通路失调与BC中肿瘤内免疫反应的负调控有关。本次大会的主题是:1)原发肿瘤和切缘的手术; 2)腋窝手术; 3)放疗:超分割,“助推”到肿瘤床,部分乳房,局部淋巴结,乳房切除术后,先进技术; 4)病理学:亚型,TIL; 5)多基因签名和治疗; 6)内分泌治疗:绝经前后及持续时间; 7)化学疗法:亚型,阶段; 8)抗HER-2疗法; 9)新辅助治疗; 10)辅助双膦酸盐; 11)辅助饮食和运动。

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