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PANTAX:一项Ib期临床试验,评估外排泵抑制剂SCO-101联合吉西他滨和纳米白蛋白结合型紫杉醇治疗不可切除或转移性胰腺癌的疗效。

PANTAX: a phase Ib clinical trial of the efflux pump inhibitor SCO-101 in combination with gemcitabine and nab-paclitaxel in non-resectable or metastatic pancreatic cancer.

作者信息

Shim Susy, Reinacher-Schick Anke, Kraeft Anna-Lena, Tarpgaard Line Schmidt, Ettrich Thomas Jens, Kestler Angelika, Christensen Signe, Jandu Haatisha, Nawabi Mubeen, Roest Nicklas Lindland, Damstrup Lars, Vestlev Peter Michael, Brünner Nils, Stenvang Jan, Ladekarl Morten

机构信息

Department of Oncology, Clinical Cancer Research Center, Aalborg University Hospital, Hobrovej 18 - 22, 9000, Aalborg, Denmark.

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

出版信息

Invest New Drugs. 2025 Apr;43(2):337-347. doi: 10.1007/s10637-025-01526-7. Epub 2025 Apr 24.

Abstract

De novo or acquired resistance to chemotherapy is ubiquitous in pancreatic ductal adenocarcinoma (PDAC). SCO-101 is an oral compound that may counteract chemo-resistance by interacting with SRPK1, ABCG2 drug transporter, and liver enzyme UGT1A1. We first conducted preclinical experiments in paclitaxel-resistant PDAC cells to access the tumoricidal effects of SCO-101 or SRPK1-inhibitor alone or in combination with paclitaxel. Second, we enrolled 22 patients with non-resectable PDAC in a phase Ib trial to investigate safety and pharmaco-kinetics, and to establish maximum tolerated dose (MTD) by evaluation of dose-limiting toxicities (DLTs) during the first cycle of 80% dose gemcitabine (Gem) and nab-paclitaxel (Nab) together with increasing doses of SCO-101. In paclitaxel-resistant PDAC cells in vitro, a synergistic effect between SCO-101 and paclitaxel was demonstrated. In patients, daily doses for 6 days of SCO-101 resulted in a two- to threefold drug accumulation, and drug exposure was dose proportional. Treatment was well tolerated. Transiently increased blood bilirubin attributable to SCO-101 was observed in 12 cases (55%) and associated with jaundice in three patients. One and two DLTs, respectively, were observed at 150 and 250mg dosing-levels of SCO-101, and the MTD was determined to be 200 mg of SCO-101 daily for 6 days on a bi-weekly schedule together with 80% dose of Gem and Nab. Median progression-free and overall survival was 3.3 and 9.5 months, respectively. In PDAC, SCO-101 can be added to Gem and Nab with little and manageable toxicity. However, no clear added efficacy signal was observed of the combination. Trial registration number: NCT04652205 (Nov 29, 2020).

摘要

在胰腺导管腺癌(PDAC)中,对化疗的原发性或获得性耐药普遍存在。SCO-101是一种口服化合物,它可能通过与SRPK1、ABCG2药物转运蛋白和肝脏酶UGT1A1相互作用来对抗化疗耐药性。我们首先在耐紫杉醇的PDAC细胞中进行临床前实验,以评估SCO-101或SRPK1抑制剂单独使用或与紫杉醇联合使用的杀瘤效果。其次,我们在一项Ib期试验中招募了22例不可切除的PDAC患者,以研究安全性和药代动力学,并通过评估80%剂量的吉西他滨(Gem)和纳米紫杉醇(Nab)联合递增剂量的SCO-101在第一个周期中的剂量限制性毒性(DLT)来确定最大耐受剂量(MTD)。在体外耐紫杉醇的PDAC细胞中,SCO-101与紫杉醇之间显示出协同作用。在患者中,SCO-101连续6天的每日剂量导致药物蓄积两到三倍,且药物暴露与剂量成比例。治疗耐受性良好。12例(55%)患者观察到因SCO-101导致的血胆红素短暂升高,其中3例患者伴有黄疸。在SCO-101剂量为150和250mg时分别观察到1例和2例DLT,MTD确定为每两周一次,SCO-101每日200mg,连用6天,同时联合80%剂量的Gem和Nab。无进展生存期和总生存期的中位数分别为3.3个月和9.5个月。在PDAC中,SCO-101可添加到Gem和Nab中,毒性小且可控。然而,未观察到该联合用药有明确的增效信号。试验注册号:NCT04652205(2020年11月29日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b795/12048447/57c2f48f4a16/10637_2025_1526_Fig1_HTML.jpg

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