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纳武单抗用于肌肉浸润性膀胱癌的溶瘤免疫疗法:一项1b期试验。

Oncolytic immunotherapy with nivolumab in muscle-invasive bladder cancer: a phase 1b trial.

作者信息

Li Roger, Villa Nancy Y, Yu Xiaoqing, Johnson Joseph O, Borjas Gustavo, Dhillon Jasreman, Moran-Segura Carlos M, Kim Youngchul, Francis Natasha, Dorman Denise, Powers John J, Sexton Wade J, Spiess Philippe E, Poch Michael A, Zemp Logan, Gilbert Scott M, Zhang Jingsong, Pow-Sang Julio M, Anderson Alexander R A, Li Tingyi, Wang Xuefeng, Grass G Daniel, Burke James M, Dinney Colin P N, Rodriguez Paulo C, Jain Rohit K, Mulé James J, Conejo-Garcia Jose R

机构信息

Department of Genitourinary Oncology, H. Lee Moffitt Cancer Center, Tampa, FL, USA.

Department of Immunology, H. Lee Moffitt Cancer Center, Tampa, FL, USA.

出版信息

Nat Med. 2025 Jan;31(1):176-188. doi: 10.1038/s41591-024-03324-9. Epub 2024 Nov 9.

Abstract

There is a critical unmet need for safe and efficacious neoadjuvant treatment for cisplatin-ineligible patients with muscle-invasive bladder cancer. Here we launched a phase 1b study using the combination of intravesical cretostimogene grenadenorepvec (oncolytic serotype 5 adenovirus encoding granulocyte-macrophage colony-stimulating factor) with systemic nivolumab in cisplatin-ineligible patients with cT2-4aN0-1M0 muscle-invasive bladder cancer. The primary objective was to measure safety, and the secondary objective was to assess the anti-tumor efficacy as measured by pathologic complete response along with 1-year recurrence-free survival. No dose-limiting toxicity was encountered in 21 patients enrolled and treated. Combination treatment achieved a pathologic complete response rate of 42.1% and a 1-year recurrence-free survival rate of 70.4%. Pathologic response was associated with baseline free E2F activity and tumor mutational burden but not PD-L1 status. Although T cell infiltration was broadly induced after intravesical oncolytic immunotherapy, the formation, enlargement and maturation of tertiary lymphoid structures was specifically associated with complete response, supporting the importance of coordinated humoral and cellular immune responses. Together, these results highlight the potential of this combination regimen to enhance therapeutic efficacy in cisplatin-ineligible patients with muscle-invasive bladder cancer, warranting additional study as a neoadjuvant therapeutic option. ClinicalTrials.gov identifier: NCT04610671 .

摘要

对于不符合顺铂治疗条件的肌层浸润性膀胱癌患者,迫切需要安全有效的新辅助治疗。在此,我们开展了一项1b期研究,在不符合顺铂治疗条件的cT2-4aN0-1M0肌层浸润性膀胱癌患者中,将膀胱内注射cretostimogene grenadenorepvec(编码粒细胞-巨噬细胞集落刺激因子的5型溶瘤腺病毒)与全身使用纳武单抗联合应用。主要目标是评估安全性,次要目标是通过病理完全缓解率以及1年无复发生存率来评估抗肿瘤疗效。入组并接受治疗的21例患者均未出现剂量限制性毒性。联合治疗的病理完全缓解率为42.1%,1年无复发生存率为70.4%。病理反应与基线游离E2F活性和肿瘤突变负荷相关,但与PD-L1状态无关。尽管膀胱内溶瘤免疫治疗后广泛诱导了T细胞浸润,但三级淋巴结构的形成、扩大和成熟与完全缓解特别相关,这支持了协调的体液免疫和细胞免疫反应的重要性。总之,这些结果突出了这种联合方案在不符合顺铂治疗条件的肌层浸润性膀胱癌患者中提高治疗效果的潜力,有必要作为新辅助治疗选择进行进一步研究。ClinicalTrials.gov标识符:NCT04610671 。

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