Pancreatic Ductal Adenocarcinoma with Medullary Features and a Complete Pathological Response After Neoadjuvant FOLFIRINOX: A Case Report and Literature Review.

IF 1.6 Q4 ONCOLOGY Journal of Gastrointestinal Cancer Pub Date : 2025-01-13 DOI:10.1007/s12029-024-01140-5
Rodrigo Gomes Taboada, Maria Fernanda Arruda Almeida, Karina Miranda Santiago, Dirce Maria Carraro, Warley Abreu Nunes, Alessandro Landskron Diniz, Tiago Cordeiro Felismino, Victor Hugo Fonseca de Jesus
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引用次数: 0

Abstract

Purpose: Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with poor response to chemotherapy. High-frequency microsatellite instability (MSI-H) is a rare biological phenomenon in conventional PDAC, being more frequently described in tumors with medullary or mucinous features.

Methods and results: In this manuscript, we report the case of a patient with an MSI-H pancreatic carcinoma with medullary features (medullary carcinoma of the pancreas-MCP) that achieved a complete pathological response after neoadjuvant modified FOLFIRINOX. Additionally, we summarize the available evidence on the clinical, pathological, and molecular features of patients with MCP, along with survival outcomes.

Conclusions: MCPs present significant sensitivity not only to immune checkpoint inhibitors, but also to systemic chemotherapy and that the latter treatment modality should not be overlooked. They also present different pathological and molecular features compared with conventional PDAC, meaning they should be considered a separate pathological entity.

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具有髓样特征的胰腺导管腺癌和新辅助FOLFIRINOX后的完全病理反应:1例报告和文献回顾。
目的:胰腺导管腺癌(Pancreatic ductal adencarcinoma, PDAC)是一种对化疗反应差的侵袭性恶性肿瘤。高频微卫星不稳定性(MSI-H)在传统PDAC中是一种罕见的生物学现象,更常见于具有髓质或粘液特征的肿瘤。方法和结果:在这篇文章中,我们报告了一例具有髓质特征的MSI-H胰腺癌(胰腺髓质癌- mcp)患者在新辅助改良的FOLFIRINOX治疗后获得了完全的病理反应。此外,我们总结了MCP患者的临床、病理和分子特征以及生存结果的现有证据。结论:MCPs不仅对免疫检查点抑制剂有明显的敏感性,而且对全身化疗也有明显的敏感性,后者的治疗方式不应被忽视。与传统PDAC相比,它们也表现出不同的病理和分子特征,这意味着它们应被视为单独的病理实体。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
121
期刊介绍: The Journal of Gastrointestinal Cancer is a multidisciplinary medium for the publication of novel research pertaining to cancers arising from the gastrointestinal tract.The journal is dedicated to the most rapid publication possible.The journal publishes papers in all relevant fields, emphasizing those studies that are helpful in understanding and treating cancers affecting the esophagus, stomach, liver, gallbladder and biliary tree, pancreas, small bowel, large bowel, rectum, and anus. In addition, the Journal of Gastrointestinal Cancer publishes basic and translational scientific information from studies providing insight into the etiology and progression of cancers affecting these organs. New insights are provided from diverse areas of research such as studies exploring pre-neoplastic states, risk factors, epidemiology, genetics, preclinical therapeutics, surgery, radiation therapy, novel medical therapeutics, clinical trials, and outcome studies.In addition to reports of original clinical and experimental studies, the journal also publishes: case reports, state-of-the-art reviews on topics of immediate interest or importance; invited articles analyzing particular areas of pancreatic research and knowledge; perspectives in which critical evaluation and conflicting opinions about current topics may be expressed; meeting highlights that summarize important points presented at recent meetings; abstracts of symposia and conferences; book reviews; hypotheses; Letters to the Editors; and other items of special interest, including:Complex Cases in GI Oncology:  This is a new initiative to provide a forum to review and discuss the history and management of complex and involved gastrointestinal oncology cases. The format will be similar to a teaching case conference where a case vignette is presented and is followed by a series of questions and discussion points. A brief reference list supporting the points made in discussion would be expected.
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