AI Article Synopsis

  • Gastric cancer is the most prevalent gastrointestinal cancer in China, with approximately 80% of patients diagnosed at an advanced stage, leading to a high recurrence rate after surgery.
  • Current neoadjuvant therapies, especially PD-1 inhibitors, show improved disease-free survival but only achieve complete tumor response in less than 35% of patients, highlighting the need for new treatment strategies.
  • A novel combination of gastric artery chemoembolization and the PD-1 inhibitor tislelizumab resulted in a pathologic complete response for a patient with locally advanced gastric cancer, demonstrating promising outcomes and potential for better prognosis in this patient population.

Article Abstract

Gastric cancer is the most common type of gastrointestinal cancer in China which about 80% of patients are locally advanced or advanced when diagnosed. Surgery along brings high recurrence rate for locally advanced gastric cancer (LAGC), and neoadjuvant therapies are needed. The use of programmed cell death-1 (PD-1)/programmed death-ligand 1 inhibitor nowadays improved the disease-free survival for LAGC, however, only <35% of patients achieved pathologic complete response (pCR) after neoadjuvant therapy nowadays. Therefore, new regimens are needed to be investigated. Gastric artery chemoembolization is applied to metastasis gastric cancer and researches showed interventional therapy can enhance the antitumor effect of PD-1 inhibitor. Here, for the first time, we combined gastric artery chemoembolization with tislelizumab (a PD-1 inhibitor) for neoadjuvant therapy of a patient with LAGC. The patient achieved pCR after a D2 resection and tumor regression grade score was 1. After surgery, the patient received tislelizumab 200 mg per 3 weeks, and showed no sign of recurrence after 6 months of follow-up. The study indicated the use of tislelizumab and gastric artery chemoembolization for neoadjuvant therapy may bring a better pCR rate and prognosis of LAGC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10913855PMC
http://dx.doi.org/10.1097/CJI.0000000000000488DOI Listing

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