Phase Ib study of anti-PD-L1 monoclonal antibody socazolimab in combination with nab-paclitaxel as first-line therapy for advanced urothelial carcinoma.

IF 4.8 2区 医学 Q1 ONCOLOGY
Oncologist Pub Date : 2025-02-06 DOI:10.1093/oncolo/oyae260
Bixia Tang, Jun Xiao, Zhihong Chi, Rong Duan, Chuanliang Cui, Lu Si, Yixun Liu, Xuechun Hu, Zhi Liu, Ping Xiang, Siming Li, Xieqiao Yan, Li Zhou, Juan Li, Yujie Li, Xiaohui Yu, Xiangrong Dai, Xiaoyi Li, Jun Guo, Xinan Sheng
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引用次数: 0

Abstract

Background: PD-1/PD-L1 immune checkpoint inhibitors (ICIs) have demonstrated activity in the post-platinum and platinum-ineligible settings for advanced urothelial carcinoma (aUC). As only around 50% of patients with aUC can tolerate platinum-containing treatment, treatments combining first-line ICIs with non-platinum drugs are urgently needed. Therefore, we assessed the safety and efficacy of the anti-PD-L1 monoclonal antibody Socazolimab in combination with nab-paclitaxel as first-line therapy in aUC (NCT04603846).

Methods: This was a multi-center, single-arm, phase Ib study that enrolled patients with treatment-naive aUC. Patients received Socazolimab (5 mg/kg) and nab-paclitaxel (260 mg/m2) Q3w. The primary endpoint was safety and tolerability of the combination regimen. Second endpoints were the objective response rate (ORR) and progression-free survival.

Results: Between September, 2020 and September, 2021, 20 patients with urothelial carcinoma were enrolled, arising from renal pelvis (5), bladder (8), and ureter (7). After a median follow-up of 17 months, the median number of treatment cycles was 12. No patients had dose limiting toxicity. All patients had treatment-related adverse events (TRAEs), most of which were grade 1 or 2. The common TRAEs (≥20%) were peripheral neurotoxicity, alopecia, rash, increased ALT, weight loss, weakness, pruritus, increased AST, increased γGT, increased ALP, neutropenia, emesis, and anorexia. Nine patients (45%) developed grade 3 TRAEs including peripheral neurotoxicity (30.0%), increased ALT (10.0%), and increased γGT (5.0%). Two patients (10%) discontinued treatment because of grade 3 mouth ulcer (n = 1) and grade 2 lung fibrosis (n = 1). No grade 4-5 TRAEs were observed. Among the 17 patients who had received at least one tumor assessment, ORR was 58.8% (95% CI, 32.9%-81.6%) and the median progression-free survival was 8.3 months (95% CI, 5.2-19.5). The median duration of response was 13.3 months (95% CI, 2.0-20.1), and the overall survival was 19.5 months (95% CI, 11.2-not reached).

Conclusion: Socazolimab combined with nab-paclitaxel has shown good safety and promising antitumor activity as first-line therapy in patients with advanced urothelial carcinoma.

抗PD-L1单克隆抗体索卡唑单抗联合纳布-紫杉醇作为晚期尿路上皮癌一线疗法的Ib期研究。
背景:PD-1/PD-L1免疫检查点抑制剂(ICIs)在晚期尿路上皮癌(aUC)的铂后治疗和不符合铂治疗条件的治疗中已显示出活性。由于只有约50%的晚期尿路癌患者可以耐受含铂治疗,因此迫切需要将一线ICIs与非铂类药物相结合的治疗方法。因此,我们评估了抗PD-L1单克隆抗体Socazolimab联合纳布-紫杉醇作为aUC一线疗法的安全性和有效性(NCT04603846):这是一项多中心、单臂、Ib期研究,招募了未经治疗的aUC患者。患者接受索卡唑单抗(5 毫克/千克)和纳布-紫杉醇(260 毫克/平方米)Q3w 治疗。主要终点是联合疗法的安全性和耐受性。第二终点是客观反应率(ORR)和无进展生存期:2020 年 9 月至 2021 年 9 月,20 名尿路上皮癌患者入组,分别来自肾盂(5 例)、膀胱(8 例)和输尿管(7 例)。中位随访时间为 17 个月,中位治疗周期数为 12 个周期。没有患者出现剂量限制性毒性。所有患者都出现了治疗相关不良事件(TRAEs),其中大多数为 1 级或 2 级。常见的不良反应(≥20%)有周围神经毒性、脱发、皮疹、ALT升高、体重下降、虚弱、瘙痒、AST升高、γGT升高、ALP升高、中性粒细胞减少、呕吐和厌食。9名患者(45%)出现了3级TRAE,包括外周神经毒性(30.0%)、谷丙转氨酶升高(10.0%)和γ-谷草转氨酶升高(5.0%)。两名患者(10%)因出现 3 级口腔溃疡(1 例)和 2 级肺纤维化(1 例)而中断治疗。未观察到 4-5 级 TRAE。在至少接受过一次肿瘤评估的17名患者中,ORR为58.8%(95% CI,32.9%-81.6%),中位无进展生存期为8.3个月(95% CI,5.2-19.5)。中位应答持续时间为13.3个月(95% CI,2.0-20.1),总生存期为19.5个月(95% CI,11.2-未达到):结论:索卡唑单抗联合纳布-紫杉醇作为晚期尿路上皮癌患者的一线疗法具有良好的安全性和抗肿瘤活性。
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来源期刊
Oncologist
Oncologist 医学-肿瘤学
CiteScore
10.40
自引率
3.40%
发文量
309
审稿时长
3-8 weeks
期刊介绍: The Oncologist® is dedicated to translating the latest research developments into the best multidimensional care for cancer patients. Thus, The Oncologist is committed to helping physicians excel in this ever-expanding environment through the publication of timely reviews, original studies, and commentaries on important developments. We believe that the practice of oncology requires both an understanding of a range of disciplines encompassing basic science related to cancer, translational research, and clinical practice, but also the socioeconomic and psychosocial factors that determine access to care and quality of life and function following cancer treatment.
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