Atezolizumab monotherapy window preceding combined neoadjuvant chemo- and immune therapy in triple negative breast cancer (TNBC) - the neoMono trial.

IF 10.2 1区 医学 Q1 ONCOLOGY
Hans-Christian Kolberg,Johannes Schumacher,Ramona Erber,Michael Braun,Peter A Fasching,Eva-Maria Grischke,Christian Schem,Michael P Lux,Mustafa Deryal,Oliver Hoffmann,Bernhard Heinrich,Georg Kunz,Kristina Lübbe,Petra Krabisch,Arndt Hartmann,Philip Räth,Sabine Kasimir-Bauer,Cornelia Kolberg-Liedtke
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Abstract

INTRODUCTION Exploratory data suggest a benefit of an immune-checkpoint inhibitor (ICI) monotherapy window in early TNBC. The neoMono trial prospectively analyzed whether the addition of an atezolizumab monotherapy window prior to neoadjuvant atezolizumab and chemotherapy improves pCR rates in early TNBC. METHODS NeoMono is a phase 2 randomized multicenter trial that recruited patients with primary TNBC larger than 10 mm. Neoadjuvant treatment consisted of neoadjuvant atezolizumab and chemotherapy, in arm A preceded by atezolizumab monotherapy two weeks before combination therapy. This study used a Bayesian trial design. RESULTS A total of 359 patients were included. Overall, pCR rates in study arms A and B were similar (ITT population: 65.7% and 69.0%, respectively). In an exploratory analysis pCR rates in PD-L1-positive tumors were 91.5% in arm A and 82.2% in arm B. The corresponding pCR rates in the PD-L1-negative group were 56.1% in arm A and 64.5% in arm B. In patients with low-risk TNBC (cT1c AND cN0) pCR rates in the PD-L1-positive group were 100.0% in arm A and 90.0% in arm B, the corresponding pCR rates in the PD-L1 (IC)-negative group were 65.9% and 76.3 %, respectively. CONCLUSION The neoMono trial demonstrated the highest pCR rates reported in a phase II/III trial in TNBC, particularly in the case of PD-L1 positivity. While no significant impact of an ICI monotherapy window on the pCR rate in the unselected ITT population could be demonstrated, our data reinforce the use of combinations of neoadjuvant chemotherapy and ICI in this indication.CCR-25-2186R1.
三阴性乳腺癌(TNBC)的新辅助化疗和免疫联合治疗前的Atezolizumab单药治疗窗口- neoMono试验。
探索性数据表明,免疫检查点抑制剂(ICI)单药治疗窗口期对早期TNBC有益处。neoMono试验前瞻性地分析了在新辅助atezolizumab和化疗之前增加atezolizumab单药治疗窗口是否能提高早期TNBC的pCR率。sneomono是一项2期随机多中心试验,招募原发性TNBC大于10mm的患者。新辅助治疗包括新辅助atezolizumab和化疗,在A组中,在联合治疗前两周进行atezolizumab单药治疗。本研究采用贝叶斯试验设计。结果共纳入359例患者。总体而言,研究组A和B的pCR率相似(ITT人群分别为65.7%和69.0%)。探索性分析pCR利率PD-L1-positive肿瘤在手臂91.5%和82.2%臂B PD-L1-negative组对应的pCR率56.1%,胳膊手臂和64.5%低风险TNBC患者B (cT1c和cN0) pCR率在手臂PD-L1-positive组分别为100.0%和90.0%臂B,相应的pCR率PD-L1 (IC)负组分别为65.9%和76.3%,分别。结论neoMono试验在TNBC的II/III期试验中显示出最高的pCR率,特别是在PD-L1阳性的情况下。虽然在未选择的ITT人群中,ICI单药治疗窗口对pCR率没有显著影响,但我们的数据强化了新辅助化疗和ICI在该适应症中的联合使用。
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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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