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.
英文原题:CLDN18.2: a potential nanotherapeutic target for cholangiocarcinoma.
CLDN18.2: a potential nanotherapeutic target for cholangiocarcinoma.
胆管癌(CCA)是一种极度恶性且具有侵袭性的原发性肝脏肿瘤,近年来其发病率不断上升。
胆管癌(CCA)是一种高度恶性、侵袭性强的原发性肝脏肿瘤,近年来发病日益增多,患者预后仍极差。目前主要治疗方式为手术和化疗,但术后化疗疗效有限,缓解持续时间短,复发和转移率高,患者生存获益甚微。因此,亟需开发更安全有效的新治疗策略。近年来,随着肿瘤学研究进展,靶向Claudin 18.2(CLDN18.2)的治疗开始显现,为改善CLDN18.2阳性肿瘤患者生存带来希望。研究提示,在CLDN18.2阳性实体瘤中,将靶向CLDN18.2的新药与标准细胞毒性治疗联合可显著改善生存,预期可为晚期胆管癌患者提供更有效的治疗选择。尽管现有免疫检查点或治疗靶点存在阳性率低、患者绝对生存获益有限等局限,靶向FGFR、IDH和HER2的药物及抗血管生成药物已为晚期胆道恶性肿瘤患者显示出希望。探索这些新型治疗策略有望为胆管癌精准治疗提供新思路。本综述聚焦CLDN18.2在实体瘤、尤其胆管癌治疗中的潜在应用,系统总结该靶点研究进展,并全面探讨其在胆管癌诊断、治疗和预后评估中的价值。
Cholangiocarcinoma (CCA) is an extremely malignant and aggressive primary liver tumor that has become increasingly prevalent in recent years. Unfortunately, the prognosis for patients diagnosed with CCA remains exceptionally poor. Currently, the primary treatment options include surgery and chemotherapy. However, the effectiveness of postoperative chemotherapy is limited, characterized by a brief duration of remission and high rates of recurrence and metastasis, resulting in minimal survival benefits for patients. Therefore, there is an urgent need to develop new therapeutic strategies that are both safer and more effective. In recent years, as oncology research has progressed, Claudin 18.2 (CLDN18.2)-targeted therapy has emerged, showing promise for improving the survival of patients with CLDN18.2-positive cancers. Studies suggest that combining new agents targeting CLDN18.2 with standard cytotoxic therapies offers significant survival benefits in CLDN18.2-positive solid tumors, which is expected to provide a more effective treatment option for patients with advanced cholangiocarcinoma. While existing immune checkpoints or therapeutic targets have limitations, such as low positivity rates and minimal absolute improvement in patient survival time, drugs that target FGFR, IDH, and Her-2, along with antiangiogenic agents, have shown promise for patients with advanced malignancies affecting the bile ducts. Therefore, exploring these novel therapeutic strategies may yield new insights for precision treatment of cholangiocarcinoma in the future. This review aims to focus on the potential application of CLDN18.2 in treating solid tumors, particularly cholangiocarcinoma, to systematically summarize research progress related to this target and thoroughly examine its value in diagnosing, treating, and assessing the prognosis of cholangiocarcinoma.
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