Perioperative pancreatic ductal adenocarcinoma care in 2025: who needs neoadjuvant?-who needs radiation?

IF 1.9 3区 医学 Q3 SURGERY
Gland surgery Pub Date : 2026-07-31 Epub Date: 2026-06-29 DOI:10.21037/gs-2026-0177
Runan Sheng, Qiong Wu, Kejia Lan
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引用次数: 0

Abstract

Despite advances in multimodal therapy, pancreatic ductal adenocarcinoma (PDAC) remains a highly fatal tumor. For surgically resectable and borderline-resectable PDAC (BR-PDAC), the optimal integration of neoadjuvant chemotherapy and radiotherapy has yet to be established. Recent randomized studies (e.g., ESPAC-5F, NORPACT-1, Alliance A021501, and PREOPANC) and updated guidelines [of the National Comprehensive Cancer Network (NCCN), European Society for Medical Oncology (ESMO), and Japanese Society of Hepato‑Biliary‑Pancreatic Surgery (JASPAC)] now identify which patients are likely to benefit from treatment before surgery. For resectable PDAC, upfront surgery followed by adjuvant chemotherapy (typically modified FOLFIRINOX) remains the standard of care. However, new research (e.g., Prep-02/JSAP05) suggests that some high-risk patients may benefit from neoadjuvant therapy. For BR-PDAC, neoadjuvant multiagent chemotherapy (typically FOLFIRINOX) is widely accepted as the standard approach for increasing the likelihood of margin-negative resection and improving survival. Induction chemotherapy (with or without ablative radiotherapy) is commonly employed to downstage tumors in locally advanced PDAC. Debate continues as to the role of radiotherapy [either conventional chemoradiotherapy or stereotactic body radiotherapy (SBRT)]. PREOPANC reported a slight survival benefit for preoperative gemcitabine-based chemoradiotherapy in resectable PDAC and BR-PDAC, while Alliance A021501 reported no additional benefit from SBRT following FOLFIRINOX in BR-PDAC. Advanced imaging [multiphasic computed tomography/magnetic resonance imaging (CT/MRI) and positron emission tomography/computed tomography (PET/CT)] enhances the precision of staging and response evaluation. Molecular diagnostics, particularly germline/somatic BRCA and KRAS status and circulating tumor DNA (ctDNA) monitoring, are currently informing perioperative decisions and innovative therapeutics. As of 2025, personalized perioperative care guided by resectability status, tumor biology, and patient-specific characteristics has emerged as the key strategy for optimizing the selection of patients for neoadjuvant chemotherapy and/or radiotherapy. This review sought to synthesize the most recent evidence and guidelines on the treatment of resectable, BR, and locally advanced PDAC.

2025年胰管腺癌围手术期护理:谁需要新辅助?-谁需要辐射?
尽管多模式治疗取得了进展,胰腺导管腺癌(PDAC)仍然是一种高度致命的肿瘤。对于手术可切除和边缘可切除的PDAC (BR-PDAC),新辅助化疗和放疗的最佳结合尚未确定。最近的随机研究(如ESPAC-5F、NORPACT-1、Alliance A021501和PREOPANC)和更新的指南[国家综合癌症网络(NCCN)、欧洲医学肿瘤学会(ESMO)和日本肝胆胰外科学会(JASPAC)]现在确定了哪些患者可能从术前治疗中受益。对于可切除的PDAC,术前手术后辅助化疗(通常改良的FOLFIRINOX)仍然是标准的治疗方法。然而,新的研究(如Prep-02/JSAP05)表明,一些高危患者可能受益于新辅助治疗。对于BR-PDAC,新辅助多药化疗(通常为FOLFIRINOX)被广泛接受为增加边缘阴性切除可能性和提高生存率的标准方法。诱导化疗(伴或不伴消融放疗)通常用于局部晚期PDAC的肿瘤降期。关于放射治疗的作用(无论是常规放化疗还是立体定向体放射治疗)的争论仍在继续。PREOPANC报告了术前基于吉西他滨的放化疗在可切除的PDAC和BR-PDAC中的轻微生存获益,而Alliance A021501报告了FOLFIRINOX在BR-PDAC中的SBRT没有额外的获益。先进的成像[多相计算机断层扫描/磁共振成像(CT/MRI)和正电子发射断层扫描/计算机断层扫描(PET/CT)]提高了分期和反应评估的准确性。分子诊断,特别是生殖系/体细胞BRCA和KRAS状态和循环肿瘤DNA (ctDNA)监测,目前正在为围手术期决策和创新治疗提供信息。截至2025年,以可切除状态、肿瘤生物学和患者特异性特征为指导的个性化围手术期护理已成为优化新辅助化疗和/或放疗患者选择的关键策略。本综述旨在综合可切除、BR和局部晚期PDAC治疗的最新证据和指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gland surgery
Gland surgery Medicine-Surgery
CiteScore
3.60
自引率
0.00%
发文量
113
期刊介绍: Gland Surgery (Gland Surg; GS, Print ISSN 2227-684X; Online ISSN 2227-8575) being indexed by PubMed/PubMed Central, is an open access, peer-review journal launched at May of 2012, published bio-monthly since February 2015.
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