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VIDEO: iTeos and GSK’s TIGIT Combination Therapy Shows Significant Promise at ESMO 2024

iTeos and GSK TIGIT combo therapy showing significant tumor shrinkage in non-small cell lung cancer (NSCLC)

The iTeos-GSK combination therapy demonstrates a 30% improvement in tumor shrinkage in PD-L1-high NSCLC, offering promising new treatment options for patients.

TIGIT Combo Delivers Significant Improvement in Lung Cancer Treatment at ESMO 2024

iTeos Therapeutics and GSK revealed promising results from their phase 2 TIGIT trial at the 2024 European Society for Medical Oncology (ESMO) conference in Barcelona. The mid-stage trial, known as GALAXIES Lung-201, evaluated the combination of belrestotug, an anti-TIGIT antibody, and dostarlimab (Jemperli), GSK’s anti-PD-1 treatment, in patients with previously untreated, unresectable, or metastatic PD-L1-high non-small cell lung cancer (NSCLC).

The results demonstrated a 30% improvement in tumor shrinkage with the combination therapy compared to dostarlimab monotherapy. The overall response rate (ORR) was impressive across all dosing cohorts:

These results stand in contrast to the 37.5% ORR for patients who received dostarlimab alone.

Confirmed Response and Follow-Up

In terms of confirmed overall response rate (cORR), the combination therapy showed approximately 60% cORR across all doses, compared to 28.1% with monotherapy. Median follow-up times varied, with 8.5 months for Groups A and B, 6.7 months for Group C, and 7 months for the monotherapy group.

Safety Profile

While the combination therapy was linked to a higher incidence of immune-related adverse events, these were manageable and consistent with the known profile of checkpoint inhibitor treatments. The most common side effects included skin and subcutaneous tissue disorders.

Moving Forward: Phase 3 Trial

Following these strong results, iTeos and GSK have already initiated a phase 3 trial, GALAXIES Lung-301, which will enroll around 1,000 patients and compare the combination therapy against a placebo-Keytruda arm. The study is expected to be completed by 2028.

Dr. Michel Detheux, President and CEO of iTeos, noted the significance of these findings: “The improvement in depth of response in tumor measurement in patients treated with the doublet compared to those treated with PD-1 alone holds promising therapeutic potential for a patient population with limited options.”

This promising data positions iTeos and GSK as key players in the TIGIT-therapy space, especially in light of Roche’s recent setbacks with its TIGIT program.

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External Links:

iTeos Therapeutics: https://www.iteostherapeutics.comGSK: https://www.gsk.com

ESMO 2024 Conference: https://www.esmo.org/meetings/esmo-congress-2024J

emperli (Dostarlimab) Information: https://www.gsk.com/en-gb/media/press-releases/gsk-receives-us-fda-approval-for-jemperli-in-endometrial-cancer/

Clinical Trials: GALAXIES Lung-301: https://clinicaltrials.gov/ct2/show/NCT05246590

Checkpoint Inhibitors Overview: https://www.cancer.gov/about-cancer/treatment/types/immunotherapy/checkpoint-inhibitors

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