Final results of TALENT: A neoadjuvant trial of T-DXd with or without anastrozole, or in sequence with chemotherapy for HER2-low, HR+ early-stage breast cancer
https://esmocongress.esmo.org
ESMO 2026
2026 年 10 月 23–27 日 · Madrid · 共 2722 条
TALENT
★★★晚破33 人 · 36 条 · 1 篇摘要
本事件热度走势
当前热度 2·可比范围峰值 4(10月24日 03:00)·近 24 小时可比范围变化 –·当前参与者 6
T-DXd(trastuzumab deruxtecan)属于抗HER2抗体偶联药物(ADC)类别。就这一资产已经站住的证据而言,本次材料中可用的信息来自现场讨论者的表述:多位专家以T-DXd在转移性乳腺癌中的成功作为参照背景,并由此讨论其获益能否外推到早期疾病。至于同类ADC已发表的关键III期试验,本次提供的背景文献均属心理学、统计学方法学、运动科学等其他领域,未包含任何抗HER2 ADC或乳腺癌试验数据,相关既往证据在本材料中待确认,故此处不作展开。
在本届ESMO26上,Sara Hurvitz汇报了TALENT试验(LBA23)的最终结果:在HR+/HER2-low早期乳腺癌新辅助治疗中比较三种策略——T-DXd单药(6-8周期)、T-DXd联合阿那曲唑、以及T-DXd×4个周期后序贯TC化疗×4。核心数字方面,pCR分别为7%、3%和9%;RCB 0/1分别为16%、17%和17%。尽管总体缓解率(ORR)约66%,pCR依然很低,且据现场帖,未满8个周期治疗者没有pCR。作者的结论是获益"modest",有评论者则直接用"disappointing"来形容。另有一帖提到,基线HER2蛋白水平较高可能与更高的pCR相关。
相对已有认识,TALENT推进的一步在于回答了三个问题:其一,在T-DXd基础上加用内分泌治疗(阿那曲唑)并未改善pCR(3%对单药7%);其二,序贯TC化疗仅带来边缘性改善(9%);其三,高ORR与低pCR的反差再次印证pCR在HR+疾病中是受限的替代终点,这一点被多位讨论者强调。讨论环节中,Barbara Pistilli将TALENT置于三个同靶点、同linker与payload类别ADC试验的背景下,指出其低pCR率与HR+/HER2-早期乳腺癌中新辅助化疗及其他ADC的水平相当。现场还有评论称这可能是T-DXd的"首个阴性试验"(probably first negative trial),但样本量与统计学设计细节现场帖未披露,该判断有待确认。
局限方面,本次材料仅为会议现场帖,未披露样本量、研究设计与生存随访数据;安全性上,有讨论者明确提出应权衡疗效、ILD风险与早期治疗定位,但具体安全性数字帖中未给出。结合HER2-low疾病本身的异质性,与会者的总体判断是:这些结果不支持将T-DXd作为HR+/HER2-low早期乳腺癌标准新辅助化疗的替代方案,其能否从转移性获益走向治愈意图的早期治疗,仍需更多证据。
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Yakup Ergün@dr_yakupergun Dr Amol Akhade@SuyogCancer 可能是 Trastuzumab deruxtecan 的首个阴性试验。Talent 试验。适用于早期 HR 阳性、Her2 低表达 EBC @myESMO #esmo26 @OncoAlert
Sara Tolaney@stolaney1 Matteo Lambertini, MD PhD@matteolambe Stephanie Graff, MD, FACP, FASCO@DrSGraff Mustafa Özdoğan, MD@ozdogan_md Erika Hamilton, MD, FASCO@ErikaHamilton9 ESMO - Eur. Oncology@myESMO Gaia Griguolo@GaiaGriguolo Yakup Ergün@dr_yakupergun 引用@#ESMO26 | TALENT Neoadjuvant T-DXd showed very low pCR rates in HR+/HER2-low early breast cancer: - T-DXd: 7% - T-DXd + anastrozole: 3% - T-DXd → chemotherapy: 9% We should remember that pCR is a limited surrogate endpoint in HR+ disease. However, these results do not support T-DXd as an alternative to standard neoadjuvant chemotherapy. Moreover, given the heterogeneity of HER2-low disease, I find it unsurprising that the success of T-DXd in the metastatic setting does not translate into similar outcomes in early-stage disease, despite the lower tumor burden.
Philippe Aftimos, MD @aftimosp Kazuki Nozawa, MD@kazuki_nozawa TALENT 试验 #ESMO26 新辅助 T-DXd 显示出有限疗效(pCR 3–9%),追加治疗的获益有限,并存在潜在安全性问题。
Ahmed Alanazi | أحمد العنزي@alanazi002 🚨#ESMO26 | #Talent 加用激素治疗未能改善 CR 而序贯加用 CEHMO 可略微改善 CR @OncoAlert @myESMO
Carmen Criscitiello@CarmenCriscit Armando Orlandi@ArmandOrlandi Mitsuo Terada, MD, PhD@乳腺科医@MamMa_mimumemo TALENT試験。HR+/HER2-low早期乳がんに術前T-DXd±アナストロゾール、T-DXd→TCを検討。ORR約65%だがRCB0は3〜9%。ILDは稀。
Kristina Jankovic, MD@JankovicK Yakup Ergün@dr_yakupergun 引用@#ESMO26 | TALENT Neoadjuvant T-DXd showed very low pCR rates in HR+/HER2-low early breast cancer: - T-DXd: 7% - T-DXd + anastrozole: 3% - T-DXd → chemotherapy: 9% We should remember that pCR is a limited surrogate endpoint in HR+ disease. However, these results do not support T-DXd as an alternative to standard neoadjuvant chemotherapy. Moreover, given the heterogeneity of HER2-low disease, I find it unsurprising that the success of T-DXd in the metastatic setting does not translate into similar outcomes in early-stage disease, despite the lower tumor burden.
Dr Rishabh Jain@DrRishabhOnco 引用@🚨 ESMO 2026 | TOP 15 BREAST CANCER TRIALS TO WATCH! 🎗️ Breast cancer takes center stage at #ESMO26! From selective CDK4 inhibition and next-generation ADCs to immunotherapy, treatment sequencing, and long-term survival updates, these are the 15 studies I’m watching most closely. 👇 🔴 HR+/HER2− BREAST CANCER 1️⃣ FOURLIGHT-1: Can selective CDK4 inhibition with atirmociclib + fulvestrant improve outcomes in second-line metastatic disease? 2️⃣ PANKU-Breast01: Can the EGFR×HER3 bispecific ADC izalontamab brengitecan outperform standard chemotherapy? 3️⃣ KEYNOTE-B49: Could pembrolizumab + chemotherapy establish a role for immunotherapy in PD-L1+ HR+/HER2− metastatic breast cancer? 4️⃣ NATALEE: Will the 6-year follow-up strengthen the case for adjuvant ribociclib in early breast cancer? 5️⃣ FINER / MA.40: Does ipatasertib + fulvestrant deliver an overall survival benefit after CDK4/6 inhibitor exposure? 6️⃣ NSABP B-42: What do the final long-term results tell us about extended adjuvant aromatase inhibitor therapy? 7️⃣ TALENT: Can neoadjuvant T-DXd sequencing with chemotherapy improve outcomes in HR+/HER2-low early breast cancer? 8️⃣ SWITCH: Can switching ADC targets while retaining a TOP1 inhibitor payload overcome resistance to prior ADC treatment? 🔵 HER2-POSITIVE / HER2-LOW BREAST CANCER 9️⃣ BRIDGET: Can tucatinib-based treatment improve disease control after isolated progression in HER2+ metastatic breast cancer? 🔟 DESTINY-Breast09: What do the CNS analyses reveal about first-line T-DXd + pertuzumab in HER2+ metastatic disease? 1️⃣1️⃣ HORIZON-Breast06: Can trastuzumab rezetecan establish a new treatment option in HER2-low metastatic breast cancer? 1️⃣2️⃣ APEX-Breast01: Could another novel TOP1 ADC challenge standard chemotherapy in HER2-low disease? 🟢 TRIPLE-NEGATIVE BREAST CANCER 1️⃣3️⃣ TROPION-Breast02: What do the CNS outcomes reveal about datopotamab deruxtecan in metastatic TNBC? 1️⃣4️⃣ POP-DURVA: Can short-course neoadjuvant durvalumab produce meaningful pathological responses in selected stage I TNBC? 1️⃣5️⃣ OptiTROP-Breast01: Will the final overall survival analysis strengthen the evidence for sacituzumab tirumotecan in metastatic TNBC? 🔬 ALSO ON MY RADAR VIKTORIA-1, postMONARCH, lidERA, DESTINY-Breast05, GIM3 FATA, MRD studies and CHARISMA. 🔥 THREE BIG QUESTIONS FOR ESMO 2026 🔹 Will next-generation ADCs redefine treatment sequencing? 🔹 Can immunotherapy and selective CDK4 inhibition expand therapeutic options in HR-positive disease? 🔹 Will mature survival and CNS outcomes change clinical practice? 📌 This is a pre-congress watchlist ranked and grouped for clinical relevance, not a summary of established positive results. Which breast cancer trial are you most excited about, and which has the greatest potential to change your practice? 👇 @myesmo @ESMO_open @ASCO @oncoalert #ESMO26 #BreastCancer #Oncology #ClinicalTrials
Philippe Aftimos, MD @aftimosp 引用@#ESMO26: Final results from the TALENT #ClinicalTrial show low pathological complete response rates with the antibody–drug conjugate (#ADC) trastuzumab deruxtecan in HR-positive, HER2-low #EarlyBreastCancer, as discussed by @breastDoktor #InsightsbyESMO ➡️ https://ow.ly/ZBwi50ZZXLm
Oncoinfo@Oncoinfo_it KOL Pulse AI@KolPulseAI ScienceLink@sciencelinkonco 专家解读(YouTube) 电子显微镜连接组学揭示鸣禽成年期新生神经元“打隧道”穿越成熟脑回路
一项鸣禽连接组学研究发现,成年期新生神经元会直接挤过成熟脑组织,在成熟神经元胞体留下深压痕,并推移邻近树突与突触。团队以电子显微镜在纳米分辨率下重建大规模鸣禽脑连接组,并用机器学习分割和注释细胞与突触,从图像中移除迁移神经元后可见空腔,因而称为 tunneling。EM 仅记录冻结瞬间,这种重塑对记忆连接和脑可塑性的后果仍待研究。
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