为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:When immunotherapy meets liver transplantation for hepatocellular carcinoma: A bumpy but promising road.
When immunotherapy meets liver transplantation for hepatocellular carcinoma: A bumpy but promising road.
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肝移植(LT)是肝细胞癌(HCC)患者的一种高度治愈性疗法。然而,由于供体肝脏短缺和HCC快速进展,大多数患者从等待名单中脱落。近年来,免疫治疗在晚期HCC治疗中显示出巨大前景。
然而,免疫治疗在LT中的应用受到限制,主要原因是可能增加的移植物排斥风险。研究人员面临的主要挑战之一是保护供体移植物免受宿主免疫治疗增强的免疫反应。
此外,免疫治疗的安全性、可及性和成本是其他需要解决的挑战。在此,我们回顾了有关在移植前接受免疫治疗以避免等待名单脱落以及在移植后接受免疫治疗以防止肿瘤复发和转移进展的患者的文献。统计学上,排斥反应的发生率在移植前为25.0%,移植后为18.5%。基于对这些临床研究的回顾,我们可以得出结论:对当前可用的免疫治疗药物的安全性和有效性开展临床试验,并通过广泛研究确定新的免疫治疗靶点,可能对不符合LT选择标准以及移植后复发的患者具有前景。迄今为止,关于LT前或后使用免疫治疗的临床经验来自个别病例研究。尽管一些报告的结果令人鼓舞,但不足以支持免疫治疗在临床实践中的标准化使用。
Liver transplantation (LT) is a highly curative therapy for patients with hepatocellular carcinoma (HCC).
However, due to the shortage of donor livers and rapid progression of HCC, a majority of patients are dropped out from the waitlist. Recently, immunotherapy has shown great promise in the treatment of advanced HCC.
However, the use of immunotherapy is limited in LT mainly due to the potentially increasing risk of graft rejection. One of the main challenges for researchers is the protection of donor graft from an immunotherapy-boosted immune response mounted by the host. Besides, the safety, availability, and costs of immunotherapy are other challenges that need to be addressed.
Here, we reviewed the literature involving patients who received immunotherapy prior to transplant to avoid waitlist dropouts and following transplantation to prevent the progression of tumor recurrence and metastasis. Statistically, the incidence of rejection was 25. 0% pre-transplant and 18. 5% post-transplant.
Based on the review of these clinical studies, we can conclude that conducting clinical trials on the safety and efficacy of currently available immunotherapy drugs and identifying novel immunotherapy targets through extensive research may be promising for patients who do not meet the selection criteria for LT and who experience post-transplant recurrence.
To date, the clinical experience on the use of immunotherapy before or after LT comes from individual case studies. Although some of the reported results are promising, they are not sufficient to support the standardized use of immunotherapy in clinical practice.
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