Racu Marie-Lucie, Bernardi Dana, Chaouche Aniss, Zindy Egor, Navez Julie, Loi Patrizia, Maris Calliope, Closset Jean, Van Laethem Jean-Luc, Decaestecker Christine, Salmon Isabelle, D'Haene Nicky
Departement of Pathology, CUB Hôpital Erasme, Hôpital Universitaire de Bruxelles (H.U.B), Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070 Brussels, Belgium.
Digital Image Analysis in Pathology (DIAPath), Center for Microscopy and Molecular Imaging (CMMI), Université Libre de Bruxelles (ULB), 6041 Gosselies, Belgium.
Cancers (Basel). 2023 Jul 25;15(15):3765. doi: 10.3390/cancers15153765.
SMAD4 is inactivated in 50-55% of pancreatic ductal adenocarcinomas (PDACs). SMAD4 loss of expression has been described as a negative prognostic factor in PDAC associated with an increased rate of metastasis and resistance to therapy. However, the impact of SMAD4 inactivation in patients receiving neoadjuvant therapy (NAT) is not well characterized. The aim of our study was to investigate whether SMAD4 status is a prognostic and predictive factor in patients receiving NAT.
We retrospectively analyzed 59 patients from a single center who underwent surgical resection for primary PDAC after NAT. SMAD4 nuclear expression was assessed by immunohistochemistry, and its relationship to clinicopathologic variables and survival parameters was evaluated. Interaction testing was performed between SMAD4 status and the type of NAT.
49.15% of patients presented loss of SMAD4. SMAD4 loss was associated with a higher positive lymph node ratio ( = 0.03), shorter progression-free survival (PFS) ( = 0.02), and metastasis-free survival (MFS) ( = 0.02), but it was not an independent prognostic biomarker in multivariate analysis. Interaction tests demonstrated that patients with SMAD4-positive tumors receiving FOLFIRINOX-based NAT showed the best outcome.
This study highlights the potential prognostic and predictive role of SMAD4 status in PDAC patients receiving FOLFIRINOX-based NAT.
在50%-55%的胰腺导管腺癌(PDAC)中,SMAD4基因失活。SMAD4表达缺失被认为是PDAC的一个不良预后因素,与转移率增加和治疗耐药相关。然而,SMAD4失活对接受新辅助治疗(NAT)的患者的影响尚未得到充分描述。我们研究的目的是调查SMAD4状态是否是接受NAT患者的预后和预测因素。
我们回顾性分析了来自单一中心的59例接受NAT后因原发性PDAC接受手术切除的患者。通过免疫组织化学评估SMAD4核表达,并评估其与临床病理变量和生存参数的关系。对SMAD4状态与NAT类型进行交互测试。
49.15%的患者出现SMAD4缺失。SMAD4缺失与较高的阳性淋巴结比率(P=0.03)、较短的无进展生存期(PFS)(P=0.02)和无转移生存期(MFS)(P=0.02)相关,但在多变量分析中它不是一个独立的预后生物标志物。交互测试表明,接受基于FOLFIRINOX方案新辅助化疗的SMAD4阳性肿瘤患者预后最佳。
本研究强调了SMAD4状态在接受基于FOLFIRINOX方案新辅助化疗的PDAC患者中的潜在预后和预测作用。