Pancreatic ductal adenocarcinoma: the latest on diagnosis, molecular profiling, and systemic treatments.

computed tomography (CT) magnetic resonance imaging (MRI) molecular profiling pancreatic cancer novel therapy pancreatic cancer treatments pancreatic ductal adenocarcinoma pancreatic neoplasm

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2024
Historique:
received: 16 02 2024
accepted: 30 05 2024
medline: 16 7 2024
pubmed: 16 7 2024
entrez: 16 7 2024
Statut: epublish

Résumé

Pancreatic ductal adenocarcinoma (PDAC) is currently the fourth leading cause of death in the United States and is expected to be ranked second in the next 10 years due to poor prognosis and a rising incidence. Distant metastatic PDAC is associated with the worst prognosis among the different phases of PDAC. The diagnostic options for PDAC are convenient and available for staging, tumor response evaluation, and management of resectable or borderline resectable PDAC. However, imaging is crucial in PDAC diagnosis, monitoring, resectability appraisal, and response evaluation. The advancement of medical technologies is evolving, hence the use of imaging in PDAC treatment options has grown as well as the utilization of ctDNA as a tumor marker. Treatment options for metastatic PDAC are minimal with the primary goal of therapy limited to symptom relief or palliation, especially in patients with low functional capacity at the point of diagnosis. Molecular profiling has shown promising potential solutions that would push the treatment boundaries for patients with PDAC. In this review, we will discuss the latest updates from evidence-based guidelines regarding diagnosis, therapy response evaluation, prognosis, and surveillance, as well as illustrating novel therapies that have been recently investigated for PDAC, in addition to discussing the molecular profiling advances in PDAC.

Identifiants

pubmed: 39011469
doi: 10.3389/fonc.2024.1386699
pmc: PMC11247645
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1386699

Informations de copyright

Copyright © 2024 Bugazia, Al-Najjar, Esmail, Abdelrahim, Abboud, Abdelrahim, Umoru, Rayyan, Abudayyeh, Al Moustafa and Abdelrahim.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Doaa Bugazia (D)

Department of Medicine, Massachusetts General Hospital, Boston, MA, United States.

Ebtesam Al-Najjar (E)

Section of GI Oncology, Department of Medical Oncology, Houston Methodist Cancer Center, Houston, TX, United States.

Abdullah Esmail (A)

Section of GI Oncology, Department of Medical Oncology, Houston Methodist Cancer Center, Houston, TX, United States.

Saifudeen Abdelrahim (S)

Challenge Early College HS, Houston Community College, Houston, TX, United States.

Karen Abboud (K)

Department of Pharmacy, Houston Methodist Hospital, Houston, TX, United States.

Adham Abdelrahim (A)

Endoprothic Center, Hochwald Hospital, Frankfurt, Germany.

Godsfavour Umoru (G)

Department of Pharmacy, Houston Methodist Hospital, Houston, TX, United States.

Hashem A Rayyan (HA)

Department of Medicine, Faculty of Medicine, The University of Jordan, Amman, Jordan.

Ala Abudayyeh (A)

Section of Nephrology, Division of Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Ala-Eddin Al Moustafa (AE)

College of Medicine, Qatar University, Doha, Qatar.

Maen Abdelrahim (M)

Section of GI Oncology, Department of Medical Oncology, Houston Methodist Cancer Center, Houston, TX, United States.
Department of Medicine, Weill Cornell Medical College, New York, NY, United States.

Classifications MeSH