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抗IL1RAP抗体Nadunolimab(CAN04)联合吉西他滨和纳米白蛋白结合型紫杉醇治疗晚期/转移性胰腺癌患者的疗效和安全性

Efficacy and Safety of the Anti-IL1RAP Antibody Nadunolimab (CAN04) in Combination with Gemcitabine and Nab-Paclitaxel in Patients with Advanced/Metastatic Pancreatic Cancer.

作者信息

Van Cutsem Eric, Collignon Joelle, Eefsen Rikke L, Ochsenreither Sebastian, Zvirbule Zanete, Ivanauskas Audrius, Arnold Dirk, Baltruskeviciene Edita, Pfeiffer Per, Yachnin Jeffrey, Magnusson Susanne, Rydberg Millrud Camilla, Sanfridson Annika, Losic Nedjad, Garcia-Ribas Ignacio, Tersago Dominique, Awada Ahmad

机构信息

University Hospitals Gasthuisberg, Leuven and KU Leuven, Leuven, Belgium.

Centre Hospitalier Universitaire (CHU) de Liège, Liège, Belgium.

出版信息

Clin Cancer Res. 2024 Dec 2;30(23):5293-5303. doi: 10.1158/1078-0432.CCR-24-0645.

Abstract

PURPOSE

IL1 pathway upregulation is implicated in pancreatic ductal adenocarcinoma (PDAC) progression, therapy resistance, and survival. Nadunolimab is an IL1 receptor accessory protein (IL1RAP)-targeting antibody with enhanced antibody-dependent cellular cytotoxicity that blocks IL1α/IL1β signaling. We investigated efficacy and safety of nadunolimab in PDAC, in combination with gemcitabine/nab-paclitaxel (GN).

PATIENTS AND METHODS

Patients with previously untreated locally advanced/metastatic PDAC received nadunolimab (1.0-7.5 mg/kg) every 2 weeks with standard GN. The primary objective was safety; secondary objectives were antitumor response, progression-free survival, and overall survival (OS). Correlations between serum and tumor biomarkers and clinical response were explored.

RESULTS

Seventy-six patients were enrolled; the median age was 63 years (range, 43-89), 42% were female, 97% had metastatic disease, and 9% had received adjuvant chemotherapy. The most frequent grade ≥3 adverse event was neutropenia (66%), typically during cycle 1. Infusion-related reactions occurred in 29% (grade 3, 3%). Only 1 of the 76 patients had grade 3 or above peripheral neuropathy. No marked dose-dependent differences in safety or efficacy were observed among the four dose groups. The median OS was 13.2 months (95% confidence interval, 11.0-15.6), and the 1-year survival rate was 58%. The median immune PFS (immune Response Evaluation Criteria in Solid Tumours) was 7.1 months (95% confidence interval, 5.2-7.4). Treatment efficacy was higher in patients with high versus low tumor baseline IL1RAP expression (OS 14.2 vs. 10.6 months; P = 0.012). A reduction in serum IL8 on treatment correlated with prolonged OS.

CONCLUSIONS

Nadunolimab combined with GN shows promising efficacy and manageable safety in locally advanced/metastatic PDAC. Higher tumor baseline IL1RAP expression correlated with better outcome.

摘要

目的

白细胞介素1(IL1)信号通路的上调与胰腺导管腺癌(PDAC)的进展、治疗耐药性及生存情况有关。纳度诺单抗是一种靶向白细胞介素1受体辅助蛋白(IL1RAP)的抗体,具有增强的抗体依赖性细胞毒性,可阻断IL1α/IL1β信号传导。我们研究了纳度诺单抗联合吉西他滨/纳米白蛋白结合型紫杉醇(GN)治疗PDAC的疗效和安全性。

患者与方法

既往未接受过治疗的局部晚期/转移性PDAC患者每2周接受一次纳度诺单抗(1.0 - 7.5 mg/kg)治疗,并联合标准剂量的GN。主要目标是安全性;次要目标是抗肿瘤反应、无进展生存期和总生存期(OS)。探索了血清和肿瘤生物标志物与临床反应之间的相关性。

结果

共纳入76例患者;中位年龄为63岁(范围43 - 89岁),42%为女性,97%患有转移性疾病,9%接受过辅助化疗。最常见的≥3级不良事件是中性粒细胞减少(66%),通常发生在第1周期。29%的患者发生了输液相关反应(3级,3%)。76例患者中只有1例发生3级或以上周围神经病变。四个剂量组在安全性或疗效方面未观察到明显的剂量依赖性差异。中位OS为13.2个月(95%置信区间,11.0 - 15.6),1年生存率为58%。中位免疫无进展生存期(实体瘤免疫反应评估标准)为7.1个月(95%置信区间,5.2 - 7.4)。肿瘤基线IL1RAP表达高的患者治疗疗效高于低表达患者(OS分别为14.2个月和10.6个月;P = 0.012)。治疗期间血清IL8降低与OS延长相关。

结论

纳度诺单抗联合GN在局部晚期/转移性PDAC中显示出有前景的疗效和可管理的安全性。较高的肿瘤基线IL1RAP表达与更好的预后相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbd8/11609625/df85f8db725b/ccr-24-0645_f1.jpg

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