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:Current and emerging immunotherapeutic approaches for biliary tract cancers.
Current and emerging immunotherapeutic approaches for biliary tract cancers.
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免疫治疗在 BTCs 中的作用目前正在研究中,正在进行的研究结果备受期待。多项研究已证明 ICIs 联合化疗在初治患者中的安全性和有效性,例如 III 期 TOPAZ-1 试验,该试验将改变晚期 BTCs 一线化疗的标准治疗。然而,仍需进一步研究以了解与免疫治疗的最佳联合方案,并发现更多预测性生物标志物以指导临床实践。
胆道癌(BTCs)是一组异质性强的侵袭性恶性肿瘤,预后不佳。化疗的获益似乎已达到瓶颈,因此,晚期BTCs需要新的有效治疗策略。在特定患者中,分子靶向治疗正在迅速改变这一局面。然而,BTCs中特定驱动基因改变的发生频率较低,限制了其广泛应用。近年来,免疫治疗方法也在BTCs中受到积极研究,但免疫治疗在BTCs中的作用仍存在争议。
检索了PubMed、Web of Science和会议资源,以寻找2017年1月至2022年5月期间发表的相关文章。此次检索旨在确定BTCs当前和新兴的免疫治疗方法。临床试验信息来源于https://ClinicalTrials.gov/ 和http://www.chictr.org.cn/。
BTC患者的免疫治疗目前正在研究中,大多数研究集中在免疫检查点抑制剂(ICIs)的应用。然而,只有MSI-H/dMMR或TMB-H的BTC亚组能从ICIs单药治疗中获益,且在二线或后续治疗中观察到有限的活性。尽管如此,ICIs与其他治疗方法(包括化疗)联合应用于晚期BTC的研究带来了有希望的结果,且毒性特征适中。近期研究表明,与单独GEMCIS相比,durvalumab联合GEMCIS显著改善了患者生存(TOPAZ-1试验),且无论TMB和MMR/MSI状态如何,ICIs联合化学免疫治疗有望成为新的前线治疗选择。过继细胞治疗以及基于肽或树突状细胞的癌症疫苗是正在BTC中研究的其他免疫治疗选择。已对众多生物标志物进行了研究,以确定其在预测ICIs应答中的作用,但除MSI-H/dMMR外,尚无预测性生物标志物得到验证。
Biliary tract cancers (BTCs) comprise a heterogeneous group of aggressive malignancies with unfavorable prognoses. The benefit of chemotherapy seems to have reached a bottleneck and, therefore, new effective therapeutic strategies for advanced BTCs are needed. Molecularly targeted therapies in selected patients are rapidly changing the situation. However, the low frequency of specific driver alterations in BTCs limits their wide application. Recently, immunotherapeutic approaches are also under active investigation in BTCs, but the role of immunotherapy in BTCs remains controversial. DATA SOURCES: PubMed, Web of Science, and meeting resources were searched for relevant articles published from January 2017 to May 2022. The search aimed to identify current and emerging immunotherapeutic approaches for BTCs. Information on clinical trials was obtained from https://clinicaltrials.gov/ and http://www.chictr.org.cn/.
Immunotherapy in BTC patients is currently under investigation, and most of the investigations focused on the application of immune checkpoint inhibitors (ICIs). However, only a subgroup of BTCs with microsatellite-instability high (MSI-H)/DNA mismatch repair-deficient (dMMR) or tumor mutational burden-high (TMB-H) benefit from monotherapy of ICIs, and limited activity was observed in the second or subsequent settings. Nevertheless, promising results come from studies of ICIs in combination with other therapeutic approaches, including chemotherapy, in advanced BTCs, with a moderate toxicity profile. Recent studies demonstrated that compared to GEMCIS alone, durvalumab plus GEMCIS significantly improved patient survival (TOPAZ-1 trial) and that ICIs-combined chemoimmunotherapy is poised to become a new frontline therapy option, regardless of TMB and MMR/MSI status. Adoptive cell therapy and peptide- or dendritic-based cancer vaccines are other immunotherapeutic options that are being studied in BTCs. Numerous biomarkers have been investigated to define their predictive role in response to ICIs, but no predictive biomarker has been validated, except MSI-H/dMMR.
The role of immunotherapy in BTCs is currently under investigation and the results of ongoing studies are eagerly anticipated. Several studies have demonstrated the safety and efficacy of ICIs in combination with chemotherapy in treatment-naive patients, such as the phase III TOPAZ-1 trial, which will change the standard care of first-line chemotherapy for advanced BTCs. However, further research is needed to understand the best combination with immunotherapy and to discover more predictive biomarkers to guide clinical practice.
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