Evidence mapPaperPMID 39518005Full record

ReviewCancers2024

Unveiling the Promise: Navigating Clinical Trials 1978-2024 for PDAC.

Angel A Dominguez, Matthew T Perz, Yi Xu, Leonor G Cedillo, Orry D Huang, Caitlin A McIntyre, Vignesh Vudatha, Jose G Trevino, Jun Liu, Pei Wang

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Angel A DominguezDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Matthew T PerzDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Yi XuDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Leonor G CedilloDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.ORCID 0009-0005-4005-5596
Orry D HuangDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Caitlin A McIntyreDivision of Surgical Oncology and Endocrine Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Vignesh VudathaDepartment of Surgery, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.ORCID 0000-0002-3624-3771
Jose G TrevinoDepartment of Surgery, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.
Jun LiuDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Pei WangDepartment of Cell Systems & Anatomy; University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0003-2373-7315

Funding

IMSD at UT Health San AntonioT32GM148752 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Ann Venables Griffith, BABATUNDE OLUKAYODE OYAJOBI · 2024 to 2024
$433k
Cancer Biology Training ProgramT32CA148724 · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · 2025 to 2025
$224k
Mechanisms of pancreatic cancer initiation and progression from normal human pancreatic tissueR01CA237159 · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · 2025 to 2025
$202k
NCI NIH HHS R01 CA237159NCI NIH HHS R21 CA245437NCI NIH HHS T32 CA148724NIDDK NIH HHS R01 DK110361NIGMS NIH HHS T32 GM148752
6 · The paper itself

Abstract

Despite many decades of research, pancreatic ductal adenocarcinoma (PDAC) remains one of the most difficult cancers to diagnose and treat effectively. Although there have been improvements in the 5-year overall survival rate, it is still very low at 12.5%. The limited efficacy of current therapies, even when PDAC is detected early, underscores the aggressive nature of the disease and the urgent need for more effective treatments. Clinical management of PDAC still relies heavily on a limited repertoire of therapeutic interventions, highlighting a significant gap between research efforts and available treatments. Over 4300 clinical trials have been or are currently investigating different treatment modalities and diagnostic strategies for PDAC, including targeted therapies, immunotherapies, and precision medicine approaches. These trials aim to develop more effective treatments and improve early detection methods through advanced imaging techniques and blood-based biomarkers. This review seeks to categorize and analyze PDAC-related clinical trials across various dimensions to understand why so few chemotherapeutic options are available to patients despite the numerous trials being conducted. This review aims to provide a comprehensive and nuanced understanding of the landscape of PDAC-related clinical trials, with the overarching goal of identifying opportunities to accelerate progress in drug development and improve patient outcomes in the fight against this devastating disease.

Indexed as

clinical trialsPDACtreatment

Identifiers

PMID39518005
PMCPMC11544830

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.