Department of Medicine, Hematology and Medical Oncology, Oregon Health & Science University (OHSU), OR 97239, Portland.
Brenden-Colson Center for Pancreatic Care, Knight Cancer Institute (OHSU), OR, Portland.
Future Oncol. 2024;20(37):2915-2925. doi: 10.1080/14796694.2024.2395235. Epub 2024 Oct 8.
Asparagine synthetase (ASNS) catalyzes the biosynthesis of asparagine from aspartate and glutamine. Cells lacking ASNS, however, are auxotrophic for asparagine. Use of L-asparaginase to promote asparagine starvation in solid tumors with low ASNS levels, such as pancreatic ductal adenocarcinoma (PDAC), is a rationale treatment strategy. However, tumor cell resistance to L-asparaginase has limited its clinical utility. Our preclinical studies show that RAS/MAPK signaling circumvents L-asparaginase-induced tumor killing, but L-asparaginase and MEK inhibition potentiated tumor killing; suggesting that this combination may provide meaningful clinical benefit to patients with PDAC. This Phase I trial (NCT05034627) will evaluate the safety and tolerability of the MEK inhibitor, cobimetinib, in combination with pegylated L-asparaginase, L calaspargase pegol-mknl, in patients with locally-advanced or metastatic PDAC.
天冬酰胺合成酶 (ASNS) 催化天冬氨酸和谷氨酰胺合成天冬酰胺。然而,缺乏 ASNS 的细胞对天冬酰胺是营养缺陷型的。使用 L-天冬酰胺酶促进低 ASNS 水平的实体瘤(如胰腺导管腺癌 (PDAC))中的天冬酰胺饥饿是一种合理的治疗策略。然而,肿瘤细胞对 L-天冬酰胺酶的耐药性限制了其临床应用。我们的临床前研究表明,RAS/MAPK 信号通路规避了 L-天冬酰胺酶诱导的肿瘤杀伤,但 L-天冬酰胺酶和 MEK 抑制增强了肿瘤杀伤;表明这种联合治疗可能为 PDAC 患者提供有意义的临床获益。这项 I 期临床试验 (NCT05034627) 将评估 MEK 抑制剂 cobimetinib 与聚乙二醇化 L-天冬酰胺酶、L-卡培天冬酰胺酶 pegol-mknl 联合用于局部晚期或转移性 PDAC 患者的安全性和耐受性。