TY - JOUR
T1 - Patient survival outcomes in brain metastases of pancreatic ductal adenocarcinoma
T2 - A comprehensive analysis
AU - Ma, Yuanchi
AU - Li, Boyang
AU - Gao, Zhenchao
AU - Wang, Zheng
AU - Han, Liang
AU - Wei, Kongyuan
AU - He, Hairong
N1 - Publisher Copyright:
© 2026 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0/
PY - 2026
Y1 - 2026
N2 - Background: Pancreatic ductal adenocarcinoma (PDAC) often presents with metastases. Brain metastases are rare, necessitating a thorough analysis of patient profiles and management. Methods: Patients with PDAC and brain metastases (2010–2021) were identified from the SEER database. PDAC-specific survival (PSS) was the primary outcome. Survival differences were assessed via Kaplan–Meier analysis, and prognostic factors via Cox regression. Results: This study included 113 patients with PDAC brain metastasis, and survival analysis was conducted on 78 eligible patients. The median PSS times were 6 months for brain metastases combined with lung metastases, 5 months for brain-only metastases, 3 months for brain metastases combined with bone metastases, 2 months for brain metastases combined with multiple metastases, and 1.5 months for brain metastases combined with liver metastases. Patients who received both radiotherapy and chemotherapy had better prognoses than those who had received radiotherapy only (P < 0.001, hazard ratio (HR) = 0.110). Other risk factors were combined with liver metastases (compared with only brain metastasis: P < 0.001, HR = 4.57) and a separated, divorced, or widowed marital status (compared with a married status: P = 0.038, HR = 2.029). Conclusions: Patients with PDAC brain metastases combined with liver metastases showed a significantly shorter median PSS time than those with brain metastases only. Patients who had received both chemotherapy and radiotherapy had longer median PSS time than those who had received radiotherapy only. A study with a large sample size is still required.
AB - Background: Pancreatic ductal adenocarcinoma (PDAC) often presents with metastases. Brain metastases are rare, necessitating a thorough analysis of patient profiles and management. Methods: Patients with PDAC and brain metastases (2010–2021) were identified from the SEER database. PDAC-specific survival (PSS) was the primary outcome. Survival differences were assessed via Kaplan–Meier analysis, and prognostic factors via Cox regression. Results: This study included 113 patients with PDAC brain metastasis, and survival analysis was conducted on 78 eligible patients. The median PSS times were 6 months for brain metastases combined with lung metastases, 5 months for brain-only metastases, 3 months for brain metastases combined with bone metastases, 2 months for brain metastases combined with multiple metastases, and 1.5 months for brain metastases combined with liver metastases. Patients who received both radiotherapy and chemotherapy had better prognoses than those who had received radiotherapy only (P < 0.001, hazard ratio (HR) = 0.110). Other risk factors were combined with liver metastases (compared with only brain metastasis: P < 0.001, HR = 4.57) and a separated, divorced, or widowed marital status (compared with a married status: P = 0.038, HR = 2.029). Conclusions: Patients with PDAC brain metastases combined with liver metastases showed a significantly shorter median PSS time than those with brain metastases only. Patients who had received both chemotherapy and radiotherapy had longer median PSS time than those who had received radiotherapy only. A study with a large sample size is still required.
KW - Metastatic sites
KW - Pancreatic ductal adenocarcinoma
KW - SEER database
KW - Survival analysis
KW - Treatment
UR - https://www.scopus.com/pages/publications/105040746073
U2 - 10.1016/j.ctarc.2026.101266
DO - 10.1016/j.ctarc.2026.101266
M3 - 文献综述
AN - SCOPUS:105040746073
SN - 2468-2942
VL - 48
JO - Cancer Treatment and Research Communications
JF - Cancer Treatment and Research Communications
M1 - 101266
ER -