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复旦大学附属肿瘤医院大内科,复旦大学附属肿瘤医院Ⅰ期临床试验病房,复旦大学上海医学院肿瘤学系,上海 200032
[ "周腾(ORCID: 0009-0004-8350-864X),硕士在读。" ]
[ "张剑,复旦大学附属肿瘤医院大内科主任医师。医疗特长:常见肿瘤(实体瘤)的诊断和治疗,乳腺癌和泌尿系统肿瘤的化疗/靶向治疗,抗肿瘤新药临床研究。担任上海市抗癌协会肿瘤药物临床研究专业委员会候任主任委员、中国抗癌协会乳腺癌专业委员会常委、中国抗癌协会乳腺癌专业委员会青委会副召集人、国家抗肿瘤药物临床应用监测青年专家委员会副主任委员。以第一作者、共同第一作者和通信作者在SCI收录期刊上发表论文70余篇。主持国家自然科学基金面上项目、上海市自然科学基金等10余项课题。曾荣获“全国首届妇幼健康科技奖科技成果奖”一等奖两次、“上海医学科技奖”一等奖、“江苏省科学技术奖”一等奖、“上海市抗癌协会科技奖”一等奖等。" ]
收稿:2023-11-10,
修回:2023-11-17,
纸质出版:2023-11-30
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周腾, 张剑. 2023年ESMO乳腺癌治疗最新进展[J]. 中国癌症杂志, 2023,33(11):981-988.
Teng ZHOU, Jian ZHANG. The latest progress of breast cancer treatment at 2023 ESMO[J]. China Oncology, 2023, 33(11): 981-988.
周腾, 张剑. 2023年ESMO乳腺癌治疗最新进展[J]. 中国癌症杂志, 2023,33(11):981-988. DOI: 10.19401/j.cnki.1007-3639.2023.11.002.
Teng ZHOU, Jian ZHANG. The latest progress of breast cancer treatment at 2023 ESMO[J]. China Oncology, 2023, 33(11): 981-988. DOI: 10.19401/j.cnki.1007-3639.2023.11.002.
在2023年欧洲肿瘤内科学会(European Society of Medical Oncology,ESMO)年会上,多项乳腺癌领域的最新研究成果公布。在早期乳腺癌方面,免疫检查点抑制剂不仅持续证实了在三阴性乳腺癌新辅助治疗中的价值(KEYNOTE-522和NeoTRIP),也显示出其在激素受体+/人表皮生长因子受体2(human epidermal growth factor receptor 2,HER2)-乳腺癌新辅助治疗中的潜在获益(KEYNOTE-756和CheckMate 7FL);细胞周期蛋白依赖性激酶4/6(cyclin-dependent kinase 4/6,CDK4/6)抑制剂(如monarchE和NATALEE研究所示)也巩固了在激素受体+/HER2-乳腺癌辅助强化治疗中的重要地位。在晚期乳腺癌治疗方面,新的内分泌治疗选择及抗体药物偶联物(如T-DXd和Dato-DXd)为激素受体+/HER2-患者带来治疗新机遇;汇总分析提示T-DXd对HER2+乳腺癌脑转移疗效表现突出;Dato-DXd联合免疫治疗、新靶点抗体药物偶联物HS-20089分别在一线和后线三阴性乳腺癌治疗中产生可喜效果。
At 2023 Annual Meeting of European Society of Medical Oncology (ESMO)
Several latest research achievements in the field of breast cancer were announced. For early-stage breast cancer
immune checkpoint inhibitor has not only continued to prove their value in the neoadjuvant treatment of triple-negative breast cancer (KEYNOTE-522 and NeoTRIP)
but also shown their potential benefit in the neoadjuvant therapy of hormone receptor+/human epidermal growth factor receptor 2 (HER2)- breast cancer (KEYNOTE-756 and CheckMate 7FL). Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors (as shown in the MONARCHE and NATALEE studies) have also solidified an important position in the adjuvant intensive treatment of hormone receptor+/HER2- breast cancer. In advanced breast cancer treatment
new endocrine therapy options and antibody-drug conjugate (T-DXd and Dato-DXd) have opened up new therapeutic opportunities for hormone receptor+/HER2- patients. Pooled analyses suggest that T-DXd has demonstrated outstanding efficacy in brain metastases of HER2+ breast cancer. Dato-DXd in combination with immunization and the new targeted antibody-drug conjugate HS-20089 produced promising efficacy in first-line treatment of and post-line triple-negative breast cancer
respectively.
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