Khan Saqib Raza, Breadner Daniel
Division of Medical Oncology, Department of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 3K7, Canada.
Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.
Curr Oncol. 2025 Mar 31;32(4):206. doi: 10.3390/curroncol32040206.
Lung cancer remains the leading cause of cancer-related mortality worldwide, with non-small-cell lung cancer (NSCLC) accounting for the majority of the cases. Despite advancements in targeted therapies and immunotherapies, many patients still rely on chemotherapy, highlighting the need for innovative treatment strategies. Bispecific antibodies (bsAbs), which feature two distinct binding sites capable of targeting different antigens, have emerged as a promising therapeutic approach, particularly in combination with chemotherapy. This review explores the scientific evolution and clinical application of bsAbs in NSCLC, focusing on their synergistic potential with chemotherapy. BsAbs, such as amivantamab, which targets EGFR and MET, have demonstrated significant efficacy in clinical trials, particularly in patients with EGFR mutations. The combination of bsAbs with chemotherapy enhances immune-mediated tumor destruction by modulating the tumor microenvironment and overcoming resistance mechanisms. Recent clinical trials have shown improved progression-free survival and overall survival when bsAbs such as amivantamab are combined with chemotherapy, underscoring their potential to transform NSCLC treatment. Many other clinical trials are underway that are evaluating newer bsAbs, such as ivonescimab, which targets PD1 and VEGF. This review also discusses ongoing clinical trials investigating various bsAbs targeting EGFR, PD-1, PD-L1, HER2, and other pathways, highlighting the future directions of bsAb-based therapies. As the field evolves, bsAbs are poised to become a cornerstone of multimodal NSCLC treatment, offering more effective and personalized therapeutic options for patients with advanced disease.
肺癌仍然是全球癌症相关死亡的主要原因,其中非小细胞肺癌(NSCLC)占大多数病例。尽管靶向治疗和免疫治疗取得了进展,但许多患者仍依赖化疗,这凸显了创新治疗策略的必要性。双特异性抗体(bsAbs)具有两个能够靶向不同抗原的独特结合位点,已成为一种有前景的治疗方法,特别是与化疗联合使用时。本综述探讨了bsAbs在NSCLC中的科学发展和临床应用,重点关注它们与化疗的协同潜力。BsAbs,如靶向EGFR和MET的阿米万他单抗,在临床试验中已显示出显著疗效,特别是在EGFR突变患者中。BsAbs与化疗联合使用可通过调节肿瘤微环境和克服耐药机制增强免疫介导的肿瘤破坏。最近的临床试验表明,当阿米万他单抗等bsAbs与化疗联合使用时,无进展生存期和总生存期得到改善,突出了它们改变NSCLC治疗的潜力。许多其他临床试验正在进行中,评估更新的bsAbs,如靶向PD1和VEGF的伊沃西单抗。本综述还讨论了正在进行的针对靶向EGFR、PD-1、PD-L1、HER2和其他通路的各种bsAbs的临床试验,突出了基于bsAb疗法的未来方向。随着该领域的发展,bsAbs有望成为多模式NSCLC治疗的基石,为晚期疾病患者提供更有效和个性化的治疗选择。