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CAR T-Cell Therapy: Gastric Cancer PFS Improvement

CAR T-Cell Therapy: Gastric Cancer PFS Improvement

May 31, 2025 Health

satri-cel CAR T-cell therapy significantly extends progression-free survival for advanced gastric cancer patients. ‍This groundbreaking treatment, targeting the CLDN18.2 protein,marks ⁢a crucial step ​forward⁤ in battling this challenging disease,presenting a meaningful reduction in the risk of disease progression or death. The phase 2 trial results, published in The Lancet, highlight satri-cel’s effectiveness, offering renewed hope for individuals facing advanced gastric or gastroesophageal junction cancers. Compared to treatment of physician’s choice, satri-cel demonstrates a notably improved median progression-free survival. Furthermore, this therapy shows promise in ‌demonstrating a better objective response rate. with manageable‍ safety profiles, researchers are optimistic about its long-term impact. News Directory 3 is following ​the story closely. Discover ‌what’s next for satri-cel and its future role in cancer care.

Key Points

Table of Contents

    • Key Points
  • Satri-cel ​CAR T-Cell Therapy Extends Survival in⁤ Gastric Cancer
    • What’s⁤ next
    • Further reading
  • Satri-cel CAR T-cell therapy extends progression-free survival in advanced gastric‍ cancer.
  • The therapy targets CLDN18.2, a protein overexpressed in gastric cancers.
  • Phase 2 trial ⁣shows a meaningful reduction ⁤in the risk of disease progression or ⁤death.

Satri-cel ​CAR T-Cell Therapy Extends Survival in⁤ Gastric Cancer

⁣ Updated May 31, ⁣2025

Satri-cel chimeric antigen receptor (CAR) T-cell therapy substantially ⁣improved progression-free survival (PFS) in‌ patients with advanced gastric or gastroesophageal junction cancers that⁣ tested positive for Claudin-18 ⁤isoform⁣ 2 ​(CLDN18.2), compared to treatment⁤ of physician’s choice (TPC), according to a new study.

The phase 2 randomized controlled trial, led by Dr. Changsong Qi at Peking​ University Cancer Hospital & Institute‍ in Beijing, china, involved 156 patients with advanced gastric or GEJ cancer refractory to two or more prior treatments. The ‌findings were published⁢ in The Lancet.

CLDN18.2, a tight-junction protein, is frequently enough​ overexpressed in thes ‍cancers. Satri-cel, an autologous CAR T-cell therapy targeting CLDN18.2, ‌had previously shown promise, prompting this further ‍investigation.

The ​study,conducted across ‌multiple centers ⁣in ​China,randomly assigned participants to receive ​either satri-cel ⁣(n=104) or TPC (n=52),wich could⁣ include nivolumab,paclitaxel,docetaxel,irinotecan,or rivoceranib. The median age of participants was ⁣52 years.

Results showed a median⁤ PFS‌ of 3.25 months in the satri-cel group versus 1.77 months in the⁤ TPC group. Satri-cel ‌reduced the risk of progression⁣ or death by 63%.

​ “Satri-cel was associated⁣ with a statistically significant ⁣increase in progression-free survival and clinically meaningful increase in overall survival compared​ with TPC, along with ​a ​manageable safety profile in patients with previously treated, advanced, CLDN18.2-positive ‌gastric or gastroesophageal junction‌ cancer,” the⁣ authors wrote.
‌⁢

The objective response rate ⁣was also higher in the satri-cel group‍ (22%) compared to the TPC group ‌(4%).While median overall survival (OS)‍ improved with ‍satri-cel (7.92 months vs 5.49 months), this difference did not reach statistical significance.

All patients in the satri-cel group experienced treatment-emergent adverse events, compared to 92% in the TPC group. Grade 3 or⁢ higher adverse events ⁣were more frequent in the satri-cel⁢ group ​(99%) than ‍in the TPC group (63%), with decreased​ lymphocyte count, ⁢decreased⁤ white blood cell count, and cytokine release‍ syndrome being the most ⁣common.

What’s⁤ next

Further research is ⁣needed to validate these⁤ findings and to optimize the use of satri-cel ⁤CAR ⁣T-cell ⁤therapy in treating advanced gastric‌ and gastroesophageal junction cancers. Studies ⁣addressing the limitations of this ‌trial,⁣ such as the time between apheresis and CAR T-cell infusion, are⁢ also warranted.

Further reading

  • Full study in The Lancet

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Related

artificial T-cell receptors, biologic therapy, biologics, CAR T; chimaeric antigen receptor T-cell therapy; chimaeric antigen receptors; chimaeric immunoreceptors; chimaeric T-cell receptors, chimeric antigen receptor T-cell therapy, chimeric antigen receptors, chimeric immunoreceptors, chimeric T-cell receptors, noncolorectal gastrointestinal cancer, noncolorectal gi cancer

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