TWIST1 is a prognostic factor for neoadjuvant chemotherapy for patients with resectable pancreatic cancer: a preliminary study.
Sho FujiwaraYuriko SaikiShinichi FukushigeMie YamanakaMasaharu IshidaFuyuhiko MotoiMichiaki UnnoAkira HoriiPublished in: Surgery today (2023)
Recent advances in the development of chemotherapies have helped improve the prognosis of pancreatic ductal adenocarcinoma (PDAC). However, predicting factors for the outcomes of chemotherapies (either gemcitabine or S-1) have not yet been established. We analyzed the expression of 4 major epithelial-to-mesenchymal transition-inducing transcription factors in 38 PDAC patients who received adjuvant chemotherapy after radical resection to examine the association with patients' prognoses. The TWIST1-positive group showed a significantly poorer prognosis than the TWIST1-negative group for both the relapse-free survival (median survival time [MST] of 8.9 vs. 18.5 months, P = 0.016) and the overall survival (MST of 15.2 vs. 33.4 months, P = 0.023). A multivariate analysis revealed that TWIST1 positivity was an independent prognostic factor for a poor response to adjuvant chemotherapies (hazard ratio 2.61; 95% confidence interval 1.10-6.79; P = 0.029). These results suggest that TWIST1 can be utilized as an important poor prognostic factor for radically resected PDAC patients with adjuvant chemotherapy, potentially including neoadjuvant therapy using these agents.
Keyphrases
- prognostic factors
- free survival
- locally advanced
- neoadjuvant chemotherapy
- epithelial mesenchymal transition
- rectal cancer
- lymph node
- transcription factor
- squamous cell carcinoma
- radiation therapy
- sentinel lymph node
- poor prognosis
- early stage
- stem cells
- single cell
- newly diagnosed
- dna binding
- ejection fraction
- type diabetes
- binding protein
- chronic kidney disease
- patient reported outcomes
- peritoneal dialysis
- metabolic syndrome