更正:B7-H3 CAR-T 细胞清除肝内胆管癌并诱导持久应答
Correction: B7-H3 CAR T cells eradicate intrahepatic cholangiocarcinoma and induce durable response.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Evolving Role of Immunotherapy in Advanced Biliary Tract Cancers.
Evolving Role of Immunotherapy in Advanced Biliary Tract Cancers.
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胆道癌(BTC)包括一组罕见且异质性强的恶性肿瘤,累及胆囊和胆道系统。由于这些癌症具有侵袭性,且患者在疾病早期通常无症状,因此往往在晚期才被发现。
此外,BTC通常对细胞毒性化疗耐药,这进一步导致了其相关的不良生存结局。显然需要新的治疗方法。基于我们对BTC潜在基因突变认识的不断扩展,分子靶向药物已被开发出来,在经分子筛选的患者亚组中代表了一种有前景的治疗策略。
此外,近年来免疫疗法的出现极大地改变了黑色素瘤等恶性肿瘤所观察到的黯淡结局。我们对BTC复杂肿瘤微环境日益深入的理解,已识别出可能通过免疫疗法加以靶向的肿瘤免疫逃逸机制。
因此,包括免疫检查点抑制剂、癌症疫苗和过继细胞疗法在内的不同免疫治疗策略已被研究。目前,基于微卫星不稳定性(MSI)状态和肿瘤突变负荷(TMB),免疫治疗药物仅被批准用于一小部分治疗难治性BTC,但随着TOPAZ-1试验结果可能推动免疫治疗联合化疗的获批,这一局面可能会发生改变。
Biliary tract cancers (BTC) comprise a rare and diverse group of malignancies that involve the gallbladder and biliary tree. These cancers typically present in later stages because they are aggressive in nature and affected patients are often asymptomatic in earlier stages of disease.
Moreover, BTCs are generally refractory to cytotoxic chemotherapy, which further contributes to their associated poor survival outcomes. Novel therapy approaches are clearly needed. Molecular targeted agents have been developed based on our expanding knowledge of the genetic mutations underlying BTCs and represent a promising treatment strategy in molecularly selected subgroups of patients.
In addition, the advent of immunotherapy over recent years has dramatically changed the bleak outcomes observed in malignancies such as melanoma.
Our growing understanding of the complex tumor microenvironment in BTC has identified mechanisms of tumor immune evasion that could potentially be targeted with immunotherapy. As a result, different immunotherapeutic approaches including immune checkpoint inhibitors, cancer vaccines, and adoptive cell therapy, have been investigated.
The use of immunotherapeutic agents is currently only approved for a small subset of treatment-refractory BTCs based on microsatellite instability (MSI) status and tumor mutational burden (TMB), but this will likely change with the potential approval of immunotherapy plus chemotherapy as a result of the TOPAZ-1 trial.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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