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Pancreatic Cancer Detection Consortium (PCDC)

The Pancreatic Cancer Detection Consortium (PCDC) develops and tests new molecular and imaging biomarkers to detect early stage pancreatic ductal adenocarcinoma (PDAC) and its precursor lesions. These biomarkers would be used to identify individuals who are at high risk of developing PDAC and are candidates for early intervention.

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The Recalcitrant Cancer Research Act of 2012 called on the National Cancer Institute (NCI) to develop scientific frameworks for research on recalcitrant cancers that have a 5-year relative survival rate of less than 20% and are estimated to cause the death of at least 30,000 individuals in the United States per year.

About PCDC

Pancreatic cancer is a recalcitrant cancer with a 5-year relative survival rate of less than 13% and resulting in nearly 52,000 deaths each year (Source: SEER Stat Fact Sheets: Pancreatic Cancer). NCI’s 2014 Scientific Framework for Pancreatic Ductal Adenocarcinoma identified four research priorities. These priorities were in part based on the recommendations of an expert panel of extramural scientists convened by the NCI in October 2012. One of the specific initiatives recommended by this panel was "evaluating longitudinal screening protocols concomitant with development of new molecular and imaging biomarkers for patients at high risk for PDAC (because of genetic factors or the presence of mucinous pancreatic cysts) who could be candidates for early surgical intervention."

Objectives of the Consortium

The main objective of the consortium is to develop and test new molecular and imaging biomarkers to improve the detection of early stage pancreatic ductal adenocarcinoma (PDAC) and its precursor lesions and identify individuals who are at high risk of developing PDAC and are candidates for early intervention.

The scope of the studies include, but are not limited to:

  • Development of more accurate and sensitive imaging methods to detect early stage PDAC and PanIN-3s that could be used to select patients for surgical intervention (imaging modalities can be anatomical, functional, or molecular);
  • Development and validation of biomarkers to detect early stage PDAC and precursor lesions that could be used to select patients for surgical intervention;
  • Development and integration of imaging approaches and multiplexed biomarker panels;
  • Development of imageable biomarkers yielding 3D localization of PDAC and high-grade precursor lesions;
  • Evaluation of longitudinal screening protocols using patients at high risk of developing pancreatic cancer;
  • Evaluation of longitudinal screening protocols of patients with resected PDAC with subsequent follow-ups using imagining modalities;
  • Longitudinal collection of samples and images from patients with pancreatic cysts to determine those lesions that are likely to progress to adenocarcinoma within a defined period (e.g., 3 years), and determination of cysts with high malignant potential that are resectable;
  • Development of novel methods to obtain and interrogate pancreatic tissues containing preneoplastic lesions.

Grantee Details

The participating institutions include U01 grants to Research Units (PAR-21-334) and a U24 grant to the Management and Data Coordination Unit (PAR-21-335).

PI Name Sort descending PI Organization Title Grant Number Program Official
Zarrinpar, Amir

University Of California, San Diego
United States

Engineering Native E. coli to Detect, Report, and Treat Colorectal Cancer 5U01CA265719-05 Guillermo Marquez, Ph.D.
Zeng, Melody Yue

Weill Medical Coll Of Cornell Univ
United States

Dissecting the interplay between immunoglobulin G and the gut microbiome in cancer progression and metastasis 5R21CA270998-02 Young Kim, Ph.D.
Zhang, Zhen

Johns Hopkins University
United States

A multidisciplinary BCC for ovarian cancer early detection: translating discoveries to clinical use with a by-design approach 5U2CCA271891-04 Christos Patriotis, Ph.D., M.Sc.
Zhao, Yingqi

Fred Hutchinson Cancer Center
United States

Developing methods for advancing the early detection of pancreatic ductal adenocarcinoma leveraging electronic medical records data 1R01CA289668-01A1 Matthew Young, Ph.D.
Zhao, Hua

University Of Virginia
United States

Homologous recombination repair capacity in peripheral blood lymphocytes as a breast cancer risk factor 4U01CA260731-04 Claire Zhu, Ph.D.
Zheng, Qin

Johns Hopkins University
United States

Determining the function of medium to large diameter sensory neurons in paclitaxel-induced pain via large-scale in vivo DRG imaging 1R01CA291906-01A1 Rachel Altshuler, Ph.D.
Zheng, Yingye

Fred Hutchinson Cancer Center
United States

Precompetitive Collaboration on Liquid Biopsy for Early Cancer Assessment: Data Management and Coordinating Unit 5U24CA288185-03 Guillermo Marquez, Ph.D.
Zheng, Qin

Johns Hopkins University
United States

Determining the function of medium to large diameter sensory neurons in paclitaxel-induced pain via large-scale in vivo DRG imaging 1R01CA291906-01A1 Rachel Altshuler, Ph.D.
Zheng, Qin

Johns Hopkins University
United States

Determining the function of medium to large diameter sensory neurons in paclitaxel-induced pain via large-scale in vivo DRG imaging 1R01CA291906-01A1 Rachel Altshuler, Ph.D.
Zheng, Yingye

Fred Hutchinson Cancer Center
United States

The Early Detection Research Network: Data Management and Coordinating Center 5U24CA086368-25 Guillermo Marquez, Ph.D.
Zheng, Yingye

Fred Hutchinson Cancer Center
United States

The Early Detection Research Network: Data Management and Coordinating Center 5U24CA086368-25 Guillermo Marquez, Ph.D.
Zhou, Xianghong Jasmine

University Of California Los Angeles
United States

Detecting and locating cancer for patients with CT-detected lung nodules 4R01CA264864-04 Guillermo Marquez, Ph.D.
Zhou, Xianghong Jasmine

University Of California Los Angeles
United States

The UCLA Center in Early Detection of Liver Cancer 5U01CA230705-08 Sidney Fu, M.D.
Zhou, Xianghong Jasmine

University Of California Los Angeles
United States

Multi-cancer early detection using cell-free DNA methylome analysis 5U01CA285010-03 Nicholas Hodges, Ph.D.
Zhu, Yazhen

University Of California Los Angeles
United States

Click Chemistry-Mediated Surface Protein Assay for Quantifying Subpopulations of Hepatocellular Carcinoma-associated Extracellular Vesicles 5R01CA277530-03 Matthew Young, Ph.D.

The Alliance of Pancreatic Cancer Consortia for Biomarkers for Early Detection Workshop

In order to bring together investigators funded through NCI-supported programs on pancreatic cancer detection and stakeholders that are supporting biomarker research on pancreatic cancer to discuss and debate existing or newly developed biomarkers that are likely to change the clinical management of pancreatic cancer in the coming years, the NCI, the Kenner Family Research Fund and the Pancreatic Cancer Action Network organized a “Data Jamboree on Biomarkers” workshop in December 2016. The expected outcome of this meeting was to identify a set of biomarkers/imaging or combined modalities that could be further tested and validated through the PCDC and the Early Detection Research Network (EDRN).

Representatives from four NCI-supported consortia on pancreatic cancer detection were invited to participate in this workshop. Other invited participants included representatives from the Kenner Family Research Fund- and the Pancreatic Cancer Action Network-supported researchers and from industry.

A synopsis of this workshop has been published in 2018.

Citation: Young MR, Wagner PD, Ghosh S, Rinaudo JA, Baker SG, Zaret KS, Goggins M, Srivastava S. Validation of Biomarkers for Early Detection of Pancreatic Cancer: Summary of The Alliance of Pancreatic Cancer Consortia for Biomarkers for Early Detection Workshop. Pancreas. 2018 Feb;47(2):135-141. doi: 10.1097/MPA.0000000000000973. PMID: 29346214; PMCID: PMC5777224.

Program Contact(s)

Sudhir Srivastava, Ph.D., M.P.H.
Email: sudhir.srivastava@nih.gov

Matthew Young, Ph.D.
Co-lead Program Director
Email: matthew.young@nih.gov

Guillermo Marquez, Ph.D.
Program Director
Email: guillermo.marquez@nih.gov