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This trial investigates the impact of netrin1 blockade on chemotherapy resistance in locally advanced pancreatic cancer.

April 24, 2026Open Access

Netrin1 blockade alleviates resistance to chemotherapy in pancreatic cancer

GRGaël RothInserm PAPascal ArtruHôpital Privé Jean Mermo OBO BOUCHECentre Hospitalier Universitaire de Reims

Key Points

This trial investigates the impact of netrin1 blockade on chemotherapy resistance in locally advanced pancreatic cancer.
Forty-three patients received mFOLFIRINOX plus NP137 every other week for up to 12 cycles.
Progression-free and overall survival were measured alongside patient tolerability.
Microbulk RNA sequencing assessed the down-regulation of tumor EMT pathways.
Median progression-free survival was 10.85 months, while median overall survival was 16.43 months.
Post-therapy conversion surgery was successful in 23% of participants.
Higher neogenin levels correlated with improved survival outcomes.

Abstract

Netrin1, a developmental cue, is a master regulator of tumour epithelial-to-mesenchymal transition (EMT)1, a mechanism that is known to drive resistance to chemotherapy2. A netrin1 antibody (NP137)3 has been shown to inhibit tumour EMT in preclinical1 and clinical4 settings. In animal models of pancreatic cancer, netrin1 and its receptor neogenin have been shown to promote tumour progression5, EMT5 and metastasis6. Here we report the results of a phase 1b study that assesses the combination of NP137 with modified FOLFIRINOX (mFOLFIRINOX) in first line patients with locally advanced pancreatic cancer (ClinicalTrials.gov: NCT05546853 ). Forty-three patients were enrolled and received mFOLFIRINOX plus NP137 every other week for up to 12 cycles. NP137 was well tolerated. Median progression-free survival (PFS) was 10.85 months (95% confidence interval, 10.03–15.61) and median overall survival was 16.43 months (95% confidence interval, 12.75–non-reached), with 21 patients remaining alive at the time of data cut-off. Post-therapy conversion surgery occurred in 23% of patients. Laser capture microdissection was performed on pre-therapeutic biopsies and surgical specimens. Microbulk RNA sequencing confirmed that the main pathway that was down-regulated with the combination of mFOLFIRINOX plus NP137 was EMT. Moreover, survival outcomes were extended for patients with tumour cells that expressed high levels of the netrin1 receptor neogenin—median PFS 15.65 months in neogenin-high versus 10.22 months in neogenin low. Our results support the idea that netrin1 blockade alleviates resistance to chemotherapy by inhibiting EMT, particularly in neogenin-high pancreatic cancer. The Lap-NET1 phase 1b trial reports that combined netrin1 antibody (NP137) plus modified FOLFIRINOX therapy on patients with locally advanced pancreatic cancer was well tolerated and improved progression-free survival and overall survival via inhibition of epithelial–mesenchymal transition.

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