#ScienceLink #Madrid2026 #ESMO26 #HBI8000303 #HBI8000 #Nivolumab
在 HBI-8000-303(III 期;n=404)中,HBI-8000(口服 HDAC 抑制剂)联合 nivolumab 相比安慰剂联合 nivolumab,改善了非葡萄膜黑色素瘤不可切除或转移性且既往未接受过抗 PD-(L)1 治疗患者的 SLP。
⏰ 中位随访:37 个月
⏳ SLP:11.7 对 7.4 个月(HR 0.73;96% CI:0.56–0.95;p=0.0141)
🎯 TRO:41.4% 对 32.3%(p=0.0569;差异无统计学意义)
📊 SG 仍不成熟
⚠️ 与治疗相关的 3–4 级不良事件:54.8% 对 17.9%。因相关不良事件永久停药:14.1% 对 5.0%。
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Emotional distress (ED) upfront neoadjuvant ipilimumab + nivolumab (IPI+NIVO) is associated with lower pathological response and toxicity
https://esmocongress.esmo.orgResults from a phase 3 trial of neoadjuvant (neoadj) chemotherapy alone vs in combination with nivolumab followed by postsurgical adjuvant nivolumab in patients (pts) with muscle-invasive bladder cancer (MIBC)
https://esmocongress.esmo.orgFinal pathological and radiological outcomes and initial EFS from a blinded, exploratory phase 2 trial of nivolumab ± visugromab in MIBC (GDFather-NEO)
https://esmocongress.esmo.orgPrimary analysis of HBI-8000-303: A randomized phase 3 trial of nivolumab plus HBI-8000 or placebo in advanced melanoma
https://esmocongress.esmo.org- **标题 / Title:** Efficacy of Tedopi Plus Docetaxel or Tedopi Plus Nivolumab as Second-line Therapy in Metastatic Non-small-cell Lung Cancer Progressing After First-line Chemo-immunotherapy (Combi-TED)
https://esmocongress.esmo.org来源:ScienceLink · x.com
