一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
肿瘤细胞治疗研究
英文原题:Current and emerging therapies targeting cell surface antigens and epigenetics in extensive stage small cell lung cancer: primer for clinicians.
Current and emerging therapies targeting cell surface antigens and epigenetics in extensive stage small cell lung cancer: primer for clinicians.
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广泛期小细胞肺癌(ES-SCLC)预后极差,一直是密集研究的重点。靶向细胞表面分子的治疗已取得进展。除免疫检查点抑制剂(ICI)外,在既往接受治疗的ES-SCLC中靶向DLL3的tarlatamab取得了前所未有的应答。血管内皮生长因子(VEGF)/PD-1/PD-L1抗体联合化疗似乎比ICI联合化疗更有效。靶向PD-1/PD-L1/VEGF的双特异性抗体联合化疗正在一线治疗中接受研究。B7H3和SEZ6抗体药物偶联物在早期研究中取得了令人鼓舞的结果。研究者也正在探索调节表观遗传过程,通过重编程癌细胞使其不利于生长和免疫逃逸。鉴于肿瘤异质性和可塑性,未来可能需要针对更广泛癌细胞脆弱点的合理联合方案,以预防复发。亟需更好的疗效监测工具来评估治疗进展。
广泛期小细胞肺癌的当前及新兴靶向治疗:转移性/广泛期小细胞肺癌(ES-SCLC)预后极差,一直是临床研究的重点。靶向细胞表面分子的治疗已取得进展。除阿替利珠单抗等免疫检查点抑制剂(ICI)外,在既往接受治疗的ES-SCLC中靶向DLL3的tarlatamab取得了前所未有的应答。VEGF/PD-1/PD-L1抗体联合化疗似乎有效,正在一线治疗中与ICI联合化疗进行比较。B7H3和SEZ6抗体药物偶联物在早期研究中取得了非常令人鼓舞的结果。研究者正在探索调节表观遗传过程,以重编程癌细胞,使其不利于生长和免疫逃逸。由于肿瘤具有异质性和可塑性,未来可能需要针对更广泛癌细胞脆弱点的合理联合方案,以预防初始治疗后复发。亟需更好的疗效监测工具来评估疾病进展和状态。
Extensive stage small cell lung cancer (ES-SCLC) carries a very poor prognosis and has been the focus of intensive research. Targeting cell surface molecules is paying off. Moving beyond immune checkpoint inhibitors (ICI), targeting DLL3 with tarlatamab in previously treated ES-SCLC generated an unprecedented response. Use of a combination of vascular endothelial growth factor (VEGF)/PD-1/PD-L1 antibody and chemotherapy seemed more effective than ICI plus chemotherapy. Bispecific antibodies targeting PD-1/PD-L1/VEGF in combination with chemotherapy are being tested in the first-line setting. B7H3 and SEZ6 antibody-drug conjugates yielded encouraging results in the early phase. Modulation of epigenetic processes is being pursued for its potential to reprogram cancer cells to a disadvantage for growth and immune evasion. Due to tumor heterogeneity and plasticity, rational combinations pursuing broader cancer cell vulnerabilities are likely necessary in the future to prevent relapse. Better tools for response monitoring are urgently needed to gauge progress.
Current and emerging targeted therapies for extensive stage small cell lung cancer Metastatic/extensive stage small cell lung cancer (ES-SCLC) carries a very poor prognosis and has been the focus of intensive clinical research. Targeting cell surface molecules is paying off. Moving beyond immune checkpoint inhibitors (ICI) such as atezolizumab, targeting DLL3 with tarlatamab in previously treated ES-SCLC generated unprecedented response. Use of combination VEGF/PD-1/PD-L1 antibody and chemotherapy seems to be effective and is being compared to ICI plus chemotherapy in first line.
B7H3 and SEZ6 antibody drug conjugates yielded very encouraging results in early phase. Modulation of epigenetic process is being pursued for its potential to reprogram cancer cells to a disadvantage for growth and immune evasion. Due to tumor heterogeneity and plasticity, rational combinations pursuing broader cancer cell vulnerabilities are likely necessary in the future to prevent relapse after initial treatment. Better tools for response monitoring are urgently needed to gauge progress and disease status.
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