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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
Smith, Jennifer Susan

Univ Of North Carolina Chapel Hill
United States

UNC CASCADE Network Research Base 5UG1CA275403-04 Maria Silvina Frech, Ph.D., M.S.
Smith, Ellen Mary Lavoie

University Of Alabama At Birmingham
United States

Duloxetine to Prevent Oxaliplatin-Induced Chemotherapy-Induced Peripheral Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Phase II to Phase III Study 5R01CA235726-07 Brennan Streck, Ph.D., RN, M.P.H.
Smith, Ellen Mary Lavoie

University Of Alabama At Birmingham
United States

Duloxetine to Prevent Oxaliplatin-Induced Chemotherapy-Induced Peripheral Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Phase II to Phase III Study 5R01CA235726-07 Brennan Streck, Ph.D., RN, M.P.H.
Sohl, Stephanie Jean

Wake Forest University Health Sciences
United States

REmotely-delivered Supportive Programs for Improving surgical pain and disTrEss (RESPITE) 5R01CA266995-04 Goli Samimi, Ph.D., M.P.H.
Sohl, Stephanie Jean

Wake Forest University Health Sciences
United States

REmotely-delivered Supportive Programs for Improving surgical pain and disTrEss (RESPITE) 5R01CA266995-04 Goli Samimi, Ph.D., M.P.H.
Somers, Tamara J

Duke University
United States

A Mobile Health Behavioral Pain Intervention Protocol for Breast Cancer Patients with Pain in Medically Underserved Communities: A Randomized Controlled Trial 5R01CA237892-05 Brennan Streck, Ph.D., RN, M.P.H.
Somers, Tamara J

Duke University
United States

A Mobile Health Behavioral Pain Intervention Protocol for Breast Cancer Patients with Pain in Medically Underserved Communities: A Randomized Controlled Trial 5R01CA237892-05 Brennan Streck, Ph.D., RN, M.P.H.
Song, Ming

University Of Louisville
United States

Dietary fructose and NASH/HCC progression 5R21CA290420-02 Amit Kumar, Ph.D.
Sorror, Mohamed

Fred Hutchinson Cancer Center
United States

Novel Intervention Approaches to Alleviate Allogeneic Transplant-Related Morbidity and Mortality 5R01CA227092-06 Marjorie Perloff, M.D.
Sorror, Mohamed

Fred Hutchinson Cancer Center
United States

Novel Intervention Approaches to Alleviate Allogeneic Transplant-Related Morbidity and Mortality 5R01CA227092-06 Marjorie Perloff, M.D.
Sorror, Mohamed

Fred Hutchinson Cancer Center
United States

Novel Intervention Approaches to Alleviate Allogeneic Transplant-Related Morbidity and Mortality 5R01CA227092-06 Marjorie Perloff, M.D.
Spector, Tim

King'S College London
United States

PROSPECT: Pathways, Risk factors, and mOleculeS to Prevent Early-onset Colorectal Tumors 1OT2CA297289-01 Asad Umar, D.V.M., Ph.D.
Spiegel, Brennan

Cedars-Sinai Medical Center
United States

Randomized Controlled Trial of Virtual Reality for GI Cancer Pain to Improve Patient Reported Outcomes 5R01CA252211-05 Rachel Altshuler, Ph.D.
Spiegel, Brennan

Cedars-Sinai Medical Center
United States

Randomized Controlled Trial of Virtual Reality for GI Cancer Pain to Improve Patient Reported Outcomes 5R01CA252211-05 Rachel Altshuler, Ph.D.
Stachler, Matthew D

University Of California, San Francisco
United States

Optimization and validation of a biomarker panel for risk stratification in Barrett's esophagus 3R37CA269649-03S1 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