STCube to present BTN1A1-targeted lung cancer data at WCLC 2025

2025-08-18     Lee Han-soo

STCube said it will present new preclinical and clinical data on its BTN1A1-targeted therapeutic strategy for non-small cell lung cancer (NSCLC) at the 2025 World Conference on Lung Cancer (WCLC), scheduled for Sept. 6–9 in Barcelona, Spain.

STCube will present data at WCLC 2025 showing its BTN1A1-targeted antibody nelmastobart could offer new treatment options for refractory lung cancer patients. (Screen captured from STCube homepage)

Two abstracts related to STCube’s anti-BTN1A1 antibody, nelmastobart, have been accepted for presentation. The studies include results from patient-derived organoid (PDO)-based preclinical research and retrospective analyses of phase 1 clinical trial data.

The first abstract, titled “Targeting BTN1A1 in PD-L1-Negative NSCLC: A Clinically Actionable Immune Checkpoint for Docetaxel-Based Combination Therapy,” reported that BTN1A1 expression increases following chemotherapy with docetaxel, thereby enhancing response to nelmastobart.

Using patient-derived organoid models, STCube researchers found that BTN1A1 and PD-L1 are differentially expressed in NSCLC, and that docetaxel treatment specifically upregulated BTN1A1.

This increase led to greater responsiveness to anti-BTN1A1 therapy compared with anti-PD-L1 therapy.

“Chemotherapy-induced upregulation of BTN1A1 shows that targeting BTN1A1 could be a promising strategy for PD-L1-negative NSCLC patients who fail to respond to or develop resistance against current immunotherapies,” STCube CSO Yoo Sung-han said. “These findings highlight the clinical potential of BTN1A1-based combination strategies in treating refractory NSCLC.”

The second abstract, “BTN1A1 and Nuclear YAP1 Co-Expression as Predictive Biomarkers for Nelmastobart Efficacy in Lung Cancer: Findings from a Phase 1 Trial,” demonstrated that co-expression of BTN1A1 and nuclear YAP1 correlates with improved outcomes.

In an analysis of tissue samples from four lung cancer patients enrolled in the phase 1 trial (three with small cell lung cancer and one with NSCLC), patients positive for BTN1A1 and with high nuclear YAP1 expression showed longer progression-free survival (PFS).

“BTN1A1-high tumors also displayed a greater proportion of YAP1-positive cells, and patients with both biomarkers tended to show prolonged disease control and PFS,” Yoo said “This supports STCube’s biomarker-driven clinical strategy and strengthens the therapeutic rationale for nelmastobart.”

By validating BTN1A1 as a prognostic biomarker in colorectal and lung cancers, the company is advancing nelmastobart as a potential global first-in-class therapy.”

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