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[肾细胞癌的免疫疗法——现状]

[Immunotherapy for renal cell carcinoma - current status].

作者信息

Grimm Marc-Oliver, Foller Susan

机构信息

Universitätsklinikum Jena, Urologische Klinik und Poliklinik, Jena.

出版信息

Aktuelle Urol. 2018 Apr;49(2):187-191. doi: 10.1055/a-0581-4451. Epub 2018 Mar 27.

Abstract

Systemic treatment of metastatic renal cell carcinoma (mRCC) has substantially changed during the last 2 years due to approval of the immune-checkpoint inhibitor Nivolumab (Opdivo) and new multikinase inhibitors (Cabozantinib, Lenvatinib, Tivozanib). The german kidney tumor guideline strongly recommends Nivolumab and Cabozantinib as 2nd line treatments after prior VEGF targeted therapy. CheckMate 025, the prospective randomized trial which led to approval of Nivolumab demonstrated improved overall survival (26 month vs. 19.7 month; hazard ratio 0.73; p = 0.0006) and response rate (26 % vs. 5 %) as well as a favorable toxicity profile compared with Everolimus. Currently, numerous combinations with PD-1/PD-L1 inhibitors are compared to Sunitinib as first line treatment of mRCC. Out of these CheckMate 214, a randomized phase-3 trial is the first to demonstrate a significant higher objective response rate (42 % vs. 27 %, p < 0.0001) and overall survival (Sunitinib 26.0 month, median for Nivo + Ipi has been not yet reached (28.2 - NR); Hazard ratio 0.63) for the combination of Nivolumab and the CTLA-4 antibody Ipilimumab in IMDC intermediate and high risk patients. Furthermore, CheckMate 214 shows better side effect profile and quality of life in patients receiving Nivolumab and Ipilimumab compared with Sunitinib. However, a considerable increase of immune related adverse events is associated with the immune combination therapy. Another randomized trial demonstrates improved progression-free survival for the combination of the PD-L1 inhibitor Atezolizumab and the VEGF antibody Bevacizumab in patients with PD-L1 positive tumors; this was found in all IMDC risk groups. Further phase-3 trials with "new" VEGFR-TKIs (Axitinib, Cabozantinib, Lenvatinib) and PD-1/PD-L1 inhibitor combinations are ongoing.In conclusion, the PD-1 immune checkpoint inhibitor Nivolumab will remain a standard treatment for patients with metastatic renal cell carcinoma after prior VEGF targeted therapy. Nivolumab in combination with Ipilimumab will become a standard 1st line option for patients with intermediate and high risk profile according to IMDC. Further data are required regarding PD-1/PD-L1 inhibitors in combination with Bevacizumab and VEGFR-TKIs, respectively, including overall survival and side effect profile.

摘要

在过去两年中,由于免疫检查点抑制剂纳武单抗(欧狄沃)和新型多激酶抑制剂(卡博替尼、乐伐替尼、替沃扎尼)的获批,转移性肾细胞癌(mRCC)的全身治疗发生了重大变化。德国肾脏肿瘤指南强烈推荐纳武单抗和卡博替尼作为先前VEGF靶向治疗后的二线治疗方案。CheckMate 025这一前瞻性随机试验促使纳武单抗获批,该试验表明,与依维莫司相比,纳武单抗可提高总生存期(26个月对19.7个月;风险比0.73;p = 0.0006)、缓解率(26%对5%),且毒性特征良好。目前,多种PD-1/PD-L1抑制剂联合方案正与舒尼替尼对比,用于mRCC的一线治疗。其中,随机3期试验CheckMate 214首次表明,对于IMDC中高危患者,纳武单抗与CTLA-4抗体伊匹单抗联合使用具有显著更高的客观缓解率(42%对27%,p < 0.0001)和总生存期(舒尼替尼为26.0个月,纳武单抗+伊匹单抗的中位数尚未达到(28.2 - 未达到);风险比0.63)。此外,CheckMate 214显示,与舒尼替尼相比,接受纳武单抗和伊匹单抗治疗的患者副作用更小,生活质量更高。然而,免疫联合治疗会使免疫相关不良事件显著增加。另一项随机试验表明,PD-L1抑制剂阿特珠单抗与VEGF抗体贝伐单抗联合使用,可改善PD-L1阳性肿瘤患者的无进展生存期;在所有IMDC风险组中均发现了这一结果。关于“新型”VEGFR-TKI(阿昔替尼、卡博替尼、乐伐替尼)与PD-1/PD-L1抑制剂联合使用的进一步3期试验正在进行。总之,PD-1免疫检查点抑制剂纳武单抗仍将是先前接受VEGF靶向治疗的转移性肾细胞癌患者的标准治疗方案。根据IMDC标准,纳武单抗与伊匹单抗联合使用将成为中高危患者的标准一线治疗选择。关于PD-1/PD-L1抑制剂分别与贝伐单抗和VEGFR-TKI联合使用的数据,包括总生存期和副作用特征,仍需进一步研究。

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