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ESMO 2026

2026 年 10 月 23–27 日 · Madrid · 共 4873 条

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TALENT

★★★

22 人 · 25 条

本事件热度走势

当前热度 0·可比范围峰值 1(10月26日 00:00)·近 24 小时可比范围变化 –·当前参与者 1

参与者计数1
00.250.50.751
热度走势
00.250.50.75110月26日00:0010月26日06:0010月26日11:0010月26日17:00
深度解读

在HER2-low、HR+乳腺癌领域,HER2靶向ADC的随机III期证据目前集中在晚期阶段:HORIZON-Breast06评估trastuzumab rezetecan(SHR-A1811)用于HER2-low晚期乳腺癌[1],APEX-Breast01比较TQB2102与化疗用于HER2-low复发或转移性乳腺癌[5],PANKU-Breast01检验izalontamab brengitecan用于既往治疗的HR+/HER2-局部晚期或转移性乳腺癌[6]。至于T-DXd在转移性场景的成功,仅见于现场帖的表述,本批已发表文献中没有其III期全文可引。

本届会议报告的是TALENT最终结果(LBA23),讲者Sara Hurvitz,设计为新辅助T-DXd(6–8周期)单药、联合anastrozole或序贯化疗(T-DXd×4后接TC×4),人群为HER2-low、HR+早期乳腺癌。pCR读数只能照抄现场帖:T-DXd单药7%,联合anastrozole为3%,序贯化疗为9%;RCB 0/I在单药与序贯组分别约16%与17%;尽管ORR约66%,pCR仍低,且有帖提示未满8周期者无pCR。作者结论称获益“modest”,有专家直言“disappointing”;联合内分泌未改善、序贯化疗仅带来边际提升,另有帖提到基线HER2蛋白水平较高者pCR可能更高,并提及潜在安全性顾虑。有现场帖称这“probably first negative trial for Trastuzumab deruxtecan”。

本次收录的主站新闻(N1–N8)均为就业市场、企业收购、连接组学等其他主题,未对TALENT作独立报道,因此没有新闻侧补充数字,以上读数与定性判断均以现场帖为准。

就推进而言,TALENT把“HER2-low晚期获益能否平移到治愈意图的早期治疗”这一疑问具体化了:dr_yakupergun认为结果不支持T-DXd作为标准新辅助化疗的替代,并强调HER2-low的异质性以及pCR在HR+疾病中作为替代终点的局限;Barbara Pistilli在讨论中将TALENT与另外两个靶点、连接子与载荷类别相同的ADC试验并列,指出其低pCR与NACT及其他ADC在HR+/HER2-早期乳腺癌中的水平相当。局限在于:无事件生存与总生存等长期终点未披露,样本量、随机化细节与安全性数据亦未在帖中给出;不同现场帖对anastrozole组RCB读数的记录不一致(9%与17%),完整数据待确认。

参考来源
  1. 1.LBA13 Trastuzumab rezetecan (SHR-A1811) in HER2-low advanced breast cancer (BC): A randomized, phase 3 study (HORIZON-Breast06) · ESMO 2026 2026
  2. 2.LBA23 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 · ESMO 2026 2026
  3. 3.LBA24 Final analysis of NRG oncology/NSABP B-42, a randomized, double-blinded, placebo-controlled trial of extended letrozole in postmenopausal women with hormone-receptor positive breast cancer who have completed previous adj… · ESMO 2026 2026
  4. 4.LBA25 Adjuvant ribociclib (RIB) + nonsteroidal aromatase inhibitor (NSAI) in patients (pts) with HR+/HER2− early breast cancer (EBC): NATALEE 6-y overall survival (OS) and efficacy outcomes · ESMO 2026 2026
  5. 5.LBA27 APEX-Breast01: TQB2102 versus chemotherapy in HER2-low recurrent or metastatic breast cancer (r/m BC) - Results from a randomized phase 3 study · ESMO 2026 2026
  6. 6.LBA50 PANKU-Breast01: Randomized phase III study of izalontamab brengitecan (iza-bren) in previously treated unresectable locally advanced or metastatic (LA/M) hormone receptor-positive/HER2-negative (HR+/HER2-) breast cancer… · ESMO 2026 2026
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  8. 8.Development and validation of a TP53-associated immune prognostic model for hepatocellular carcinoma · EBioMedicine 2019
  9. 9.Global, regional, and national lifetime risks of developing and dying from gastrointestinal cancers in 185 countries: a population-based systematic analysis of GLOBOCAN · Lancet Gastroenterol Hepatol 2024
  10. 10.Biomechanics and tennis · Br J Sports Med 2006
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  12. 12.Predictive and prognostic impact of ferroptosis-related genes ACSL4 and GPX4 on breast cancer treated with neoadjuvant chemotherapy · EBioMedicine 2021
现场
  1. Yakup Ergün

    #ESMO26 | TALENT 新辅助 T-DXd 在 HR+/HER2-low 早期乳腺癌中显示出非常低的 pCR 率: - T-DXd:7% - T-DXd + anastrozole:3% - T-DXd → 化疗:9% 我们应当记住,pCR 是 HR+ 疾病中有限的替代终点。然而,这些结果并不支持将 T-DXd 作为标准新辅助化疗的替代方案。 此外,鉴于 HER2-low 疾病的异质性,T-DXd 在转移性治疗中的成功未能在早期疾病中转化为相似的结果,这并不令人意外,尽管早期疾病的肿瘤负荷更低。

    ★★★同题 TALENT · 22 人HER24313 浏览43 赞19 转发1 回复
  2. Mustafa Özdoğan, MD

    ADC 能否从转移性乳腺癌中的获益迈向以治愈为目的的早期乳腺癌治疗? 在 #ESMO26 上,TALENT (LBA23) 将测试新辅助 trastuzumab deruxtecan 治疗 HER2-low / HR+ 早期乳腺癌——联合或不联合 anastrozole,或与化疗序贯使用。 真正的问题是:仅有活性还不够。 在早期疾病中,我们应如何权衡疗效、ILD 风险和治疗定位? 报告者:Sara Hurvitz #bcsm

    ★★★同题 TALENT · 22 人LBA23trastuzumabderuxtecanHER2388 浏览13 赞8 转发0 回复
  3. Yakup Ergün

    在 TALENT 中,加用 anastrozole 并未提高 pCR。 鉴于这些数据,在 DB-05/09 中同时使用 ET 与 T-DXd 时应采取何种策略?是否有按 ET 使用情况划分的亚组结果? 您怎么看? #ESMO26

    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.

    ★★★同题 TALENT · 22 人1140 浏览7 赞0 转发5 回复
  4. Yakup Ergün

    #ESMO26 | TALENT 在HR+/HER2-low早期乳腺癌中,新辅助T-DXd ± anastrozole或序贯化疗的pCR/接近pCR率仅为16–17%。 加用anastrozole或序贯化疗未显示出明确获益。

    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.

    同题 TALENT · 22 人HER2600 浏览5 赞2 转发0 回复
  5. Dr Rishabh Jain

    🚨 TALENT | #ESMO26 | LBA23 T-DXd 用于 HR+/HER2-low 早期乳腺癌:肿瘤缩小,但 pCR 仍然较低! 📊 pCR 率: • T-DXd 单药:7% • + Anastrozole:3% • → 化疗:9% ✅ ORR:各组均为 65–67% 🔍 结论:肿瘤缩小令人鼓舞,但病理缓解有限。加用内分泌治疗或序贯化疗均无明确获益。 不改变临床实践。 @ESMO_open @my_esmo @oncoalert #ESMO26 #BreastCancer

    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

    同题 TALENT · 22 人LBA23HER2#BREASTCANCER567 浏览3 赞1 转发0 回复
  6. Philippe Aftimos, MD 

    T-DXd 在 HER2-low 和 ultra-low HR+/HER2- MBC 中获批,此前其在关键性 ph3 试验中改善了治疗结局。 ❓T-DXd 在 HER2-low/HR+ 早期乳腺癌中的作用? TALENT 的最终结果于今天在 #ESMO26 上公布,@breastDoktor 对其进行了描述与点评。 #ESMOAmbassadors 👇

    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

    同题 TALENT · 22 人HER2183 浏览2 赞0 转发1 回复
  7. ScienceLink

    #ScienceLink #Madrid2026 #ESMO26 #TALENT #Trastuzumabderuxtecán 在 TALENT(II期;n=132)中,使用 trastuzumab deruxtecán(T-DXd)的新辅助方案在 HR+/HER2-low 早期乳腺癌中显示出较低的 RPC 率。 🎯 可评估患者中的 RPC(RCB 0): • T-DXd:7%(3/42) • T-DXd + anastrozol:3%(1/29) • T-DXd → docetaxel/ciclofosfamida:9%(5/55) 🔬 RCB 0/I:分别为 16%、17% 和 17%。 ⚠️ ≥3级不良事件(AE):13–28%,具体取决于方案。报告了3例间质性肺病(EPI),均为2级。 🔗 阅读/收听完整报道:https://buff.ly/usUzxqE

CBACBA Frontier Insights (CFI)美国华人生物医药科技协会(CBA)www.cba-usa.org

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