Final Results From a Phase I Trial and Expansion Cohorts of Cabozantinib and Nivolumab Alone or With Ipilimumab for Advanced/Metastatic Genitourinary Tumors.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-09-01 Epub Date: 2024-07-02 DOI:10.1200/JCO.23.02233
Andrea B Apolo, Daniel M Girardi, Scot A Niglio, Rosa Nadal, Andre R Kydd, Nicholas Simon, Lisa Ley, Lisa M Cordes, Elias Chandran, Seth M Steinberg, Sunmin Lee, Min-Jung Lee, Shraddha Rastogi, Nahoko Sato, Liang Cao, A Rouf Banday, Salah Boudjadi, Maria J Merino, Antoun Toubaji, Dilara Akbulut, Bernadette Redd, Hadi Bagheri, Rene Costello, Sandeep Gurram, Piyush K Agarwal, Heather J Chalfin, Vladimir Valera, Howard Streicher, John Joseph Wright, Elad Sharon, William D Figg, Howard L Parnes, James L Gulley, Biren Saraiya, Sumanta K Pal, David Quinn, Mark N Stein, Primo N Lara, Donald P Bottaro, Amir Mortazavi
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Abstract

Purpose: Cabozantinib and nivolumab (CaboNivo) alone or with ipilimumab (CaboNivoIpi) have shown promising efficacy and safety in patients with metastatic urothelial carcinoma (mUC), metastatic renal cell carcinoma (mRCC), and rare genitourinary (GU) tumors in a dose-escalation phase I study. We report the final data analysis of the safety, overall response rate (ORR), progression-free survival (PFS), and overall survival (OS) of the phase I patients and seven expansion cohorts.

Methods: This is an investigator-initiated, multicenter, phase I trial. CaboNivo doublet expansion cohorts included (1) mUC, (2) mRCC, and (3) adenocarcinoma of the bladder/urachal; CaboNivoIpi triplet expansion cohorts included (1) mUC, (2) mRCC, (3) penile cancer, and (4) squamous cell carcinoma of the bladder and other rare GU tumors (ClinicalTrials.gov identifier: NCT02496208).

Results: The study enrolled 120 patients treated with CaboNivo (n = 64) or CaboNivoIpi (n = 56), with a median follow-up of 49.2 months. In 108 evaluable patients (CaboNivo n = 59; CaboNivoIpi n = 49), the ORR was 38% (complete response rate 11%) and the median duration of response was 20 months. The ORR was 42.4% for mUC, 62.5% for mRCC (n = 16), 85.7% for squamous cell carcinoma of the bladder (n = 7), 44.4% for penile cancer (n = 9), and 50.0% for renal medullary carcinoma (n = 2). Grade ≥ 3 treatment-related adverse events occurred in 84% of CaboNivo patients and 80% of CaboNivoIpi patients.

Conclusion: CaboNivo and CaboNivoIpi demonstrated clinical activity and safety in patients with multiple GU malignancies, especially clear cell RCC, urothelial carcinoma, and rare GU tumors such as squamous cell carcinoma of the bladder, small cell carcinoma of the bladder, adenocarcinoma of the bladder, renal medullary carcinoma, and penile cancer.

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Cabozantinib和Nivolumab单独或联合Ipilimumab治疗晚期/转移性泌尿生殖系统肿瘤的I期试验和扩增组的最终结果。
目的:在一项剂量递增I期研究中,卡博替尼(Cabozantinib)和尼韦单抗(nivolumab,CaboNivo)单独或与伊匹单抗(ipilimumab,CaboNivoIpi)联合治疗转移性尿路上皮癌(mUC)、转移性肾细胞癌(mRCC)和罕见泌尿生殖系统肿瘤(GU)患者显示出良好的疗效和安全性。我们报告了 I 期患者和 7 个扩展队列的安全性、总反应率 (ORR)、无进展生存期 (PFS) 和总生存期 (OS) 的最终数据分析:这是一项由研究者发起的多中心 I 期试验。CaboNivo双组扩展队列包括(1)mUC、(2)mRCC和(3)膀胱/泌尿道腺癌;CaboNivoIpi三组扩展队列包括(1)mUC、(2)mRCC、(3)阴茎癌和(4)膀胱鳞状细胞癌及其他罕见GU肿瘤(ClinicalTrials.gov标识符:NCT02496208):该研究共招募了120名接受CaboNivo(64人)或CaboNivoIpi(56人)治疗的患者,中位随访时间为49.2个月。在 108 例可评估的患者中(CaboNivo n = 59;CaboNivoIpi n = 49),ORR 为 38%(完全应答率为 11%),中位应答持续时间为 20 个月。mUC的ORR为42.4%,mRCC为62.5%(n=16),膀胱鳞状细胞癌为85.7%(n=7),阴茎癌为44.4%(n=9),肾髓样癌为50.0%(n=2)。84%的CaboNivo患者和80%的CaboNivoIpi患者发生了≥3级的治疗相关不良事件:结论:CaboNivo和CaboNivoIpi对多种GU恶性肿瘤患者具有临床活性和安全性,尤其是透明细胞RCC、尿路上皮癌和罕见GU肿瘤,如膀胱鳞状细胞癌、膀胱小细胞癌、膀胱腺癌、肾髓样癌和阴茎癌。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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