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术前伊匹单抗联合纳武利尤单抗治疗局部晚期尿路上皮癌:NABUCCO 试验。

Preoperative ipilimumab plus nivolumab in locoregionally advanced urothelial cancer: the NABUCCO trial.

机构信息

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Department of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, the Netherlands.

出版信息

Nat Med. 2020 Dec;26(12):1839-1844. doi: 10.1038/s41591-020-1085-z. Epub 2020 Oct 12.

Abstract

Preoperative immunotherapy with anti-PD1 plus anti-CTLA4 antibodies has shown remarkable pathological responses in melanoma and colorectal cancer. In NABUCCO (ClinicalTrials.gov: NCT03387761 ), a single-arm feasibility trial, 24 patients with stage III urothelial cancer (UC) received two doses of ipilimumab and two doses of nivolumab, followed by resection. The primary endpoint was feasibility to resect within 12 weeks from treatment start. All patients were evaluable for the study endpoints and underwent resection, 23 (96%) within 12 weeks. Grade 3-4 immune-related adverse events occurred in 55% of patients and in 41% of patients when excluding clinically insignificant laboratory abnormalities. Eleven patients (46%) had a pathological complete response (pCR), meeting the secondary efficacy endpoint. Fourteen patients (58%) had no remaining invasive disease (pCR or pTisN0/pTaN0). In contrast to studies with anti-PD1/PD-L1 monotherapy, complete response to ipilimumab plus nivolumab was independent of baseline CD8 presence or T-effector signatures. Induction of tertiary lymphoid structures upon treatment was observed in responding patients. Our data indicate that combined CTLA-4 plus PD-1 blockade might provide an effective preoperative treatment strategy in locoregionally advanced UC, irrespective of pre-existing CD8 T cell activity.

摘要

术前免疫治疗联合抗 PD-1 和抗 CTLA-4 抗体在黑色素瘤和结直肠癌中显示出显著的病理反应。在 NABUCCO(ClinicalTrials.gov:NCT03387761),一项单臂可行性试验中,24 例 III 期尿路上皮癌(UC)患者接受了两剂伊匹单抗和两剂纳武单抗治疗,随后进行了切除术。主要终点是在治疗开始后 12 周内进行切除术的可行性。所有患者均符合研究终点评估标准,并接受了切除术,其中 23 例(96%)在 12 周内进行了切除术。3-4 级免疫相关不良事件发生在 55%的患者中,排除临床意义不大的实验室异常后,有 41%的患者发生。11 例(46%)患者出现病理完全缓解(pCR),达到次要疗效终点。14 例(58%)患者无残留浸润性疾病(pCR 或 pTisN0/pTaN0)。与抗 PD-1/PD-L1 单药治疗研究相比,伊匹单抗联合纳武单抗的完全缓解与基线 CD8 存在或 T 效应细胞特征无关。在应答患者中观察到治疗后三级淋巴结构的诱导。我们的数据表明,联合 CTLA-4 和 PD-1 阻断可能为局部晚期 UC 提供一种有效的术前治疗策略,而与预先存在的 CD8 T 细胞活性无关。

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