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吉西他滨和顺铂联合纳武利尤单抗作为肌层浸润性膀胱癌的保器官治疗:一项 2 期试验。

Gemcitabine and cisplatin plus nivolumab as organ-sparing treatment for muscle-invasive bladder cancer: a phase 2 trial.

机构信息

Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Nat Med. 2023 Nov;29(11):2825-2834. doi: 10.1038/s41591-023-02568-1. Epub 2023 Oct 2.

Abstract

Cystectomy is a standard treatment for muscle-invasive bladder cancer (MIBC), but it is life-altering. We initiated a phase 2 study in which patients with MIBC received four cycles of gemcitabine, cisplatin, plus nivolumab followed by clinical restaging. Patients achieving a clinical complete response (cCR) could proceed without cystectomy. The co-primary objectives were to assess the cCR rate and the positive predictive value of cCR for a composite outcome: 2-year metastasis-free survival in patients forgoing immediate cystectomy or <ypT1N0 in patients electing immediate cystectomy. Seventy-six patients were enrolled; of these, 33 achieved a cCR (43%, 95% confidence interval (CI): 32%, 55%), and 32 of 33 who achieved a cCR opted to forgo immediate cystectomy. The positive predictive value of cCR was 0.97 (95% CI: 0.91, 1), meeting the co-primary objective. The most common adverse events were fatigue, anemia, neutropenia and nausea. Somatic alterations in pre-specified genes (ATM, RB1, FANCC and ERCC2) or increased tumor mutational burden did not improve the positive predictive value of cCR. Exploratory analyses of peripheral blood mass cytometry and soluble protein analytes demonstrated an association between the baseline and on-treatment immune contexture with clinical outcomes. Stringently defined cCR after gemcitabine, cisplatin, plus nivolumab facilitated bladder sparing and warrants further study. ClinicalTrials.gov identifier: NCT03451331 .

摘要

膀胱切除术是肌层浸润性膀胱癌(MIBC)的标准治疗方法,但会改变患者的生活。我们启动了一项 2 期研究,入组 MIBC 患者接受吉西他滨、顺铂联合纳武利尤单抗治疗 4 个周期,然后进行临床重新分期。达到临床完全缓解(cCR)的患者可以不进行膀胱切除术。主要共同终点是评估 cCR 率和 cCR 对复合终点的阳性预测值:不立即进行膀胱切除术的患者 2 年无转移生存率,或立即进行膀胱切除术的患者<ypT1N0。共入组 76 例患者,其中 33 例达到 cCR(43%,95%置信区间[CI]:32%,55%),33 例达到 cCR 的患者中有 32 例选择不立即进行膀胱切除术。cCR 的阳性预测值为 0.97(95%CI:0.91,1),达到了主要共同终点。最常见的不良反应是疲劳、贫血、中性粒细胞减少和恶心。预先指定基因(ATM、RB1、FANCC 和 ERCC2)的体细胞改变或肿瘤突变负担增加并不能提高 cCR 的阳性预测值。对外周血液质谱流式细胞术和可溶性蛋白分析物的探索性分析表明,基线和治疗期间的免疫结构与临床结局之间存在关联。吉西他滨、顺铂联合纳武利尤单抗后严格定义的 cCR 有助于保留膀胱并值得进一步研究。临床试验注册:NCT03451331。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34db/10667093/3e44dffdd5e5/41591_2023_2568_Fig1_HTML.jpg

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