TY - JOUR
T1 - Predicting post-recurrence survival for patients with pancreatic cancer recurrence after primary resection
T2 - A Bi-institutional validated risk classification
AU - van Oosten, A. Floortje
AU - Daamen, Lois A.
AU - Groot, Vincent P.
AU - Biesma, Nanske C.
AU - Habib, Joseph R.
AU - van Goor, Iris W.J.M.
AU - Kinny-Köster, Benedict
AU - Burkhart, Richard A.
AU - Wolfgang, Christopher L.
AU - van Santvoort, Hjalmar C.
AU - He, Jin
AU - Molenaar, I. Quintus
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/9
Y1 - 2023/9
N2 - Background: Over 80% of patients will develop disease recurrence after radical resection of pancreatic ductal adenocarcinoma (PDAC). This study aims to develop and validate a clinical risk score predicting post-recurrence survival (PRS) at time of recurrence. Methods: All patients who had recurrence after undergoing pancreatectomy for PDAC at the Johns Hopkins Hospital or at the Regional Academic Cancer Center Utrecht during the study period were included. Cox proportional hazard model was used to develop the risk model. Performance of the final model was assessed in a test set after internal validation. Results: Of 718 resected PDAC patients, 72% had recurrence after a median follow-up of 32 months. The median overall survival was 21 months and the median PRS was 9 months. Prognostic factors associated with shorter PRS were age (hazard ratio [HR] 1.02; 95% confidence interval [95%CI] 1.00–1.04), multiple-site recurrence (HR 1.57; 95%CI 1.08–2.28), and symptoms at time of recurrence (HR 2.33; 95%CI 1.59–3.41). Recurrence-free survival longer than 12 months (HR 0.55; 95%CI 0.36–0.83), FOLFIRINOX and gemcitabine-based adjuvant chemotherapy (HR 0.45; 95%CI 0.25–0.81; HR 0.58; 95%CI 0.26–0.93, respectively) were associated with a longer PRS. The resulting risk score had a good predictive accuracy (C-index: 0.73). Conclusion: This study developed a clinical risk score based on an international cohort that predicts PRS in patients who underwent surgical resection for PDAC. This risk score will become available on www.evidencio.com and can help clinicians with patient counseling on prognosis.
AB - Background: Over 80% of patients will develop disease recurrence after radical resection of pancreatic ductal adenocarcinoma (PDAC). This study aims to develop and validate a clinical risk score predicting post-recurrence survival (PRS) at time of recurrence. Methods: All patients who had recurrence after undergoing pancreatectomy for PDAC at the Johns Hopkins Hospital or at the Regional Academic Cancer Center Utrecht during the study period were included. Cox proportional hazard model was used to develop the risk model. Performance of the final model was assessed in a test set after internal validation. Results: Of 718 resected PDAC patients, 72% had recurrence after a median follow-up of 32 months. The median overall survival was 21 months and the median PRS was 9 months. Prognostic factors associated with shorter PRS were age (hazard ratio [HR] 1.02; 95% confidence interval [95%CI] 1.00–1.04), multiple-site recurrence (HR 1.57; 95%CI 1.08–2.28), and symptoms at time of recurrence (HR 2.33; 95%CI 1.59–3.41). Recurrence-free survival longer than 12 months (HR 0.55; 95%CI 0.36–0.83), FOLFIRINOX and gemcitabine-based adjuvant chemotherapy (HR 0.45; 95%CI 0.25–0.81; HR 0.58; 95%CI 0.26–0.93, respectively) were associated with a longer PRS. The resulting risk score had a good predictive accuracy (C-index: 0.73). Conclusion: This study developed a clinical risk score based on an international cohort that predicts PRS in patients who underwent surgical resection for PDAC. This risk score will become available on www.evidencio.com and can help clinicians with patient counseling on prognosis.
KW - Pancreatic ductal adenocarcinoma
KW - Post-recurrence survival
KW - Recurrence
KW - Risk score
KW - Survival after recurrence
UR - http://www.scopus.com/inward/record.url?scp=85158916478&partnerID=8YFLogxK
U2 - 10.1016/j.ejso.2023.04.009
DO - 10.1016/j.ejso.2023.04.009
M3 - Article
C2 - 37173152
AN - SCOPUS:85158916478
SN - 0748-7983
VL - 49
SP - 1
EP - 9
JO - European Journal of Surgical Oncology
JF - European Journal of Surgical Oncology
IS - 9
M1 - 106910
ER -