RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report.
Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report.
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免疫检查点抑制剂/酪氨酸激酶抑制剂(ICI/TKI)联合治疗目前是转移性肾细胞癌(mRCC)的一线治疗。然而,其在三线及以上治疗中的疗效预计相对较差,且既往多药暴露可导致高级别毒性,使患者体能状态相对较差。确定最佳治疗方案和顺序仍然困难,需要在mRCC患者中进一步研究。
本研究描述了2例mRCC患者,在多种TKI和nivolumab治疗失败后,重新使用axitinib后表现出良好的抗癌效果。两例患者达到最佳缓解的时间均较既往治疗更快,无进展生存期(PFS)也更好。
此外,axitinib与nivolumab联合使用时,剂量可降至每日2.5 mg,同时仍能发挥令人印象深刻的抗癌效果。为确定细胞毒性效应,我们进行了淋巴细胞活化试验,发现axitinib与nivolumab联合时,细胞毒性T淋巴细胞和NK 细胞释放的颗粒酶B水平更高。为评估这一结果,采用生物信息学方法分析了PRISM数据库。
总之,基于淋巴细胞活化试验和PD-1表达的结果,我们的发现表明,在nivolumab耐药后重新使用axitinib的序贯治疗对于mRCC的治疗是合理的。
The immune checkpoint inhibitor/tyrosine kinase inhibitor (ICI/TKI) combination treatment is currently the first-line treatment for metastatic renal cell carcinoma (mRCC).
However, its efficacy beyond the third-line setting is expected to be relatively poor, and high-grade toxicities can develop by prior exposure to multiple drugs, resulting in a relatively poor performance in patients. Determining the best treatment regimen and sequence remains difficult and requires further investigation in patients with mRCC.
In this study, two cases of mRCC, who failed several lines of TKI and nivolumab but exhibited a good anticancer effect after rechallenging with axitinib, are described. Both patients had a faster time to best response and better progression-free survival (PFS) than during previous treatments.
Moreover, the axitinib dose could be reduced to 2. 5 mg daily when used in combination with nivolumab while continuing to exert an impressive anticancer effect. To determine the cytotoxic effect, we performed a lymphocyte activation test and found that the level of granzyme B released by cytotoxic T lymphocytes and natural killer cells was higher when axitinib was combined with nivolumab. To evaluate this result, a bioinformatics approach was used to analyze the PRISM database.
In conclusion, based on the results of a lymphocyte activation test and PD-1 expression, our findings indicate that sequential therapy with axitinib rechallenge after nivolumab resistance is reasonable for the treatment of mRCC.
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