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特瑞普利单抗联合阿昔替尼新辅助治疗伴下腔静脉瘤栓的肾透明细胞癌:NEOTAX,一项 2 期研究。

Neoadjuvant toripalimab plus axitinib for clear cell renal cell carcinoma with inferior vena cava tumor thrombus: NEOTAX, a phase 2 study.

机构信息

Department of Urology, Chinese PLA General Hospital, Beijing, China.

Chinese PLA Medical School, Beijing, China.

出版信息

Signal Transduct Target Ther. 2024 Oct 4;9(1):264. doi: 10.1038/s41392-024-01990-2.

Abstract

The potential benefit of neoadjuvant toripalimab plus axitinib in cases with clear cell renal cell carcinoma (ccRCC) and inferior vena cava tumor thrombus (IVC-TT) remains unclear. NEOTAX was a phase 2 study to investigate the efficacy and safety of neoadjuvant toripalimab plus axitinib in patients with ccRCC and IVC-TT (ChiCTR2000030405). The primary endpoint was the down-staging rate of IVC-TT level. Secondary endpoints included change in TT length, response rate, percentage change in surgical approach, surgical morbidity, progression-free survival (PFS), safety, and biomarker analyses. In all, 25 patients received study treatment, 44.0% (11/25) patients had a reduction in thrombus level, and none experienced an increase in Mayo level. The median change in tumor thrombus length was -2.3 cm (range: -7.1 to 1.1 cm). Overall, 61.9% (13/21) patients experienced changes in surgical strategy compared with planned surgery, three patients experienced major complications. The median PFS was 25.3 months (95% CI: 17.0-NE). The 1-year PFS was 89.1% (95% CI: 62.7-97.2). No any of grade 4 or 5 treatment-related adverse event was identified. Biopsy samples of non-responders exhibited increased T cytotoxic cell infiltration, but these cells were predominantly PD-1 positive. Biopsy samples of responders exhibited lower T helper cells, however, their subtype, regulatory T cells remained unchanged. In surgical samples of the TT, non-responders exhibited increased CD8T_01_GZMK_CXCR4 subset T cells. NEOTAX met preset endpoints proving that toripalimab in combination with axitinib downstages IVC-TT in a significant proportion of patients leading to simplification in the procedure of surgery.

摘要

新辅助特瑞普利单抗联合阿昔替尼治疗透明细胞肾细胞癌(ccRCC)合并下腔静脉瘤栓(IVC-TT)的潜在获益尚不清楚。NEOTAX 是一项评估新辅助特瑞普利单抗联合阿昔替尼治疗 ccRCC 合并 IVC-TT 患者的疗效和安全性的 II 期研究(ChiCTR2000030405)。主要终点是 IVC-TT 分级的降期率。次要终点包括 TT 长度的变化、反应率、手术方式改变的百分比、手术发病率、无进展生存期(PFS)、安全性和生物标志物分析。共 25 例患者接受了研究治疗,44.0%(11/25)患者血栓分级降低,无 Mayo 分级升高。肿瘤血栓长度的中位数变化为-2.3cm(范围:-7.1 至 1.1cm)。总体而言,61.9%(13/21)的患者与计划手术相比改变了手术策略,3 例患者发生了主要并发症。中位 PFS 为 25.3 个月(95%CI:17.0-NE)。1 年 PFS 为 89.1%(95%CI:62.7-97.2)。未观察到任何 4 级或 5 级治疗相关不良事件。无应答者活检样本中观察到 T 细胞毒性细胞浸润增加,但这些细胞主要为 PD-1 阳性。应答者活检样本中 T 辅助细胞减少,但辅助性 T 细胞亚群调节性 T 细胞保持不变。在 TT 的手术样本中,无应答者表现出增加的 CD8T_01_GZMK_CXCR4 亚群 T 细胞。NEOTAX 达到了预设终点,证明特瑞普利单抗联合阿昔替尼可使相当一部分患者的 IVC-TT 分级降低,从而简化手术程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc94/11450193/f74c14452b42/41392_2024_1990_Fig1_HTML.jpg

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