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认知指南 - 早期乳腺癌患者的基因组学引导的新辅助治疗后靶向治疗:一项多中心、开放标签、伞形II期研究的研究设计

COGNITION-GUIDE - Genomics-Guided Targeted Post-Neoadjuvant Therapy in Patients with Early Breast Cancer: Study Design of a Multicenter, Open-Label, Umbrella Phase II Study.

作者信息

Pixberg Constantin, Maurer Christian, Smetanay Katharina, Straßl Luise, Hlevnjak Mario, Zapatka Marc, Wagner Celina V, Yazdanparast Haniyeh, Kurzawa Johanna, Erben Vanessa, Feng Fangyoumin, Hong Chen, Hübschmann Daniel, Buschhorn Lars, Suppelna Jan Philip, Michel Laura, Heublein Sabine, Fremd Carlo, Zivanovic Oliver, Sinn Peter, Stenzinger Albrecht, Haidinger Renate, Schumacher-Wulf Eva, Ditsch Nina, Loibl Sibylle, Fröhling Stefan, Link Theresa, Wimberger Pauline, Blohmer Jens-Uwe, Huebner Hanna, Fasching Peter A, Janni Wolfgang, Schlenk Richard F, Thewes Verena, Lichter Peter, Schneeweiss Andreas

机构信息

National Center for Tumor Diseases (NCT) Heidelberg (University Hospital and German Cancer Research Center), Heidelberg, Germany.

Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

出版信息

Geburtshilfe Frauenheilkd. 2025 Apr 10;85(6):611-619. doi: 10.1055/a-2557-1876. eCollection 2025 Jun.

Abstract

BACKGROUND

As part of the COGNITION diagnostic registry program, residual tumor material after neoadjuvant therapy (NAT) of patients with early breast cancer (eBC), who are still at high-risk for relapse after NAT, is analyzed by next generation sequencing to identify biomarkers and actionable alterations. This strategy aims to stratify patients for subsequent genomics-guided therapies to reduce the significant risk of metastatic dissemination and hence to improve disease-free survival.

PATIENTS AND METHODS

COGNITION-GUIDE is a multicenter umbrella phase-II-trial to translate molecular biomarker profiles generated in the COGNITION platform into six molecular-guided post-neoadjuvant therapeutic options in addition to standard-of-care treatment. Patients can be allocated toimmune checkpoint inhibition (PD-L1-antibody),PI3K inhibition,AKT inhibition,PARP inhibition,anti-Trop-2 antibody-drug-conjugate,HER2 inhibition or, in case of missing biomarkers, to observation for 12 months.The primary endpoint is invasive disease-free survival (IDFS) four years after surgery. Secondary endpoints include IDFS in each study arm separately, distant disease-free survival, overall survival and safety. 240 patients will be enrolled within four years.

CONCLUSIONS

The COGNITION-GUIDE trial, which was activated in June 2023 and will recruit in different centers in Germany, empowers a risk-adapted, biomarker-guided therapy escalation algorithm in eBC patients who are still at high risk of metastasis.

摘要

背景

作为COGNITION诊断注册项目的一部分,对新辅助治疗(NAT)后仍有高复发风险的早期乳腺癌(eBC)患者的残留肿瘤组织进行二代测序分析,以识别生物标志物和可靶向改变。该策略旨在对患者进行分层,以便后续进行基因组学指导的治疗,降低转移扩散的重大风险,从而提高无病生存期。

患者与方法

COGNITION-GUIDE是一项多中心伞形II期试验,旨在将COGNITION平台生成的分子生物标志物谱转化为除标准治疗外的六种分子指导的新辅助治疗选择。患者可被分配至免疫检查点抑制(PD-L1抗体)、PI3K抑制、AKT抑制、PARP抑制、抗Trop-2抗体药物偶联物、HER2抑制组,若生物标志物缺失则接受12个月的观察。主要终点是术后四年的无侵袭性疾病生存期(IDFS)。次要终点包括各研究组单独的IDFS、远处无病生存期、总生存期和安全性。四年内将招募240名患者。

结论

COGNITION-GUIDE试验于2023年6月启动,将在德国不同中心招募患者,为仍有高转移风险的eBC患者提供了一种风险适应性、生物标志物指导的治疗升级算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eadf/12158538/4fdd4497cfb9/10-1055-a-2557-1876-igf01ab.jpg

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