Bilen Mehmet A, Vo BaoHan T, Liu Yuan, Greenwald Rachel, Davarpanah Amir H, McGuire Donald, Shiradkar Rakesh, Li Liping, Nazha Bassel, Brown Jacqueline T, Williams Sierra, Session Wilena, Russler Greta, Caulfield Sarah, Joshi Shreyas S, Narayan Vikram M, Filson Christopher P, Ogan Kenneth, Kucuk Omer, Carthon Bradley Curtis, Del Balzo Luke, Cohen Athena, Boyanton Adriana, Prokhnevska Nataliya, Cardenas Maria Andrea, Sobierajska Ewelina, Jansen Caroline S, Patil Dattatraya H, Nicaise Edouard, Osunkoya Adeboye O, Kissick Haydn, Master Viraj A
Winship Cancer Institute, Emory University, Atlanta, GA, USA.
Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Res Sq. 2024 Aug 8:rs.3.rs-4849400. doi: 10.21203/rs.3.rs-4849400/v1.
Cabozantinib is an oral multikinase inhibitor approved for treatment in metastatic renal cell carcinoma (RCC). We hypothesized that neoadjuvant cabozantinib could downstage localized tumors, facilitating partial nephrectomy, and facilitating surgery in patients with locally advanced tumors that would require significant adjacent organ resection. We, therefore, conducted a phase 2, single-arm trial of cabozantinib treatment for 12 weeks in 17 patients with locally advanced biopsy-proven non-metastatic clear cell RCC before surgical resection. Six patients (35%) experienced a partial response, and 11 patients (65%) had stable disease. We identified that plasma cell-free DNA (cfDNA), VEGF, c-MET, Gas6, and AXL were significantly increased while VEGFR2 decreased during cabozantinib treatments. There was a trend towards CD8+ T cells becoming activated in the blood, expressing the proliferation marker Ki67 and activation markers HLA-DR and CD38. Cabozantinib treatment depleted myeloid populations acutely. Importantly, immune niches made up of the stem-like CD8+ T cells and antigen presenting cells were increased in every patient. These data suggest that cabozantinib treatment was clinically active and safe in the neoadjuvant setting in patients with locally advanced non-metastatic clear cell RCC and activated the anti-tumor CD8+ T cell response. The trial is registered at ClinicalTrials.gov under registration no. NCT04022343.
卡博替尼是一种口服多激酶抑制剂,已被批准用于治疗转移性肾细胞癌(RCC)。我们假设新辅助卡博替尼可以降低局部肿瘤的分期,促进部分肾切除术,并为需要进行大量相邻器官切除的局部晚期肿瘤患者的手术提供便利。因此,我们进行了一项2期单臂试验,对17例经活检证实为局部晚期非转移性透明细胞RCC的患者在手术切除前给予卡博替尼治疗12周。6例患者(35%)出现部分缓解,11例患者(65%)病情稳定。我们发现,在卡博替尼治疗期间,血浆游离DNA(cfDNA)、血管内皮生长因子(VEGF)、c-MET、生长停滞特异性蛋白6(Gas6)和AXL显著增加,而血管内皮生长因子受体2(VEGFR2)减少。血液中CD8 + T细胞有被激活趋势,表达增殖标志物Ki67以及激活标志物人类白细胞抗原-DR(HLA-DR)和CD38。卡博替尼治疗可迅速消耗髓系细胞群。重要的是,每位患者中由干细胞样CD8 + T细胞和抗原呈递细胞组成的免疫微环境均有所增加。这些数据表明,卡博替尼治疗在局部晚期非转移性透明细胞RCC患者的新辅助治疗中具有临床活性且安全,并激活了抗肿瘤CD8 + T细胞反应。该试验已在ClinicalTrials.gov上注册,注册号为NCT04022343。