Identify microRNAs in Cachexia in Pancreatic Carcinoma

Sponsor
University of Oklahoma (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05275075
Collaborator
(none)
100
1
55
1.8

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the proportion of pancreatic patients who experience weight loss and cachexia, and to identify any differences in the genes between patient groups.

Condition or Disease Intervention/Treatment Phase
  • Other: Pancreatic cancer microRNA and messenger RNA expression.

Detailed Description

This research study will retrospectively examine 1395 patients from the University of Alabama and the University of Oklahoma Stephenson Cancer Center (OU-SCC) pancreatic cancer cohorts. The prospective arm, will enroll a total of 100 eligible volunteers at the OU-SCC. The demographic and medical data from the retrospective and prospective arms will be combined (1495 patients) to ascertain any racial disparities in pancreatic cancer patients with cachexia. Perspective volunteers at the OU-SCC will undergo routine tests to determine if their cancer is operable. Pancreatic tumors will be removed from the eligible patients, as part of their normal standard of care and will be examined for genes that may be related to unexplained muscle loss and compared to tumor tissue from other patients with pancreatic cancer. An optional hand strength exam, and standing on a scale that measures weight, muscle, and body fat will be available to OU-SCC patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
Pilot Trial to Identify microRNAs in Cachexia in Patients With Pancreatic Carcinoma
Anticipated Study Start Date :
Nov 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2026
Anticipated Study Completion Date :
Jun 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Pancreatic Cancer Cohort

All eligible adenocarcinoma pancreatic cancer patients with operable cancer.

Other: Pancreatic cancer microRNA and messenger RNA expression.
Tumor specimens from pancreatic patients will be analyzed for markers associated with muscle loss.

Outcome Measures

Primary Outcome Measures

  1. Proportion of African American pancreatic cancer patients with weight loss and cachexia. [1 - 12 months]

    Evaluate weight loss and the markers of cachexia, albumin and psoas cross-sectional area, to see if African Americans with pancreatic cancer patients experience Grade I-IV cachexia at a higher frequency than other racial groups.

Secondary Outcome Measures

  1. Differences in microRNA and messenger RNA tumor expression profiles in all cancer patients undergoing pancreatic surgery. [1 - 12 months]

    Assess fold-change expression differences in microRNA and messenger RNA tumor expression profiles in all cancer patients undergoing pancreatic surgery.

  2. Differences in cachexia-associated RNA signatures in African American pancreatic cancer patients, and other racial groups. [1 - 12 months]

    Assess fold-change expression differences in cachexia-associated RNA signatures in African American pancreatic cancer patients, and other racial groups.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Male or female patient, who is ≥ 18 years old at the time of informed consent.

  2. Patients with operable pancreatic tumors diagnosed in the last 12 months prior to consent with clinical discretion or pathology confirmed as adenocarcinoma.

  3. Patient has stage I or higher disease who is considered a candidate for surgical resection of pancreatic cancer, with or without neoadjuvant chemotherapy.

  4. Ability to provide written informed consent and HIPAA authorization.

Exclusion Criteria:
  1. Patients with pancreatic adenocarcinoma who do not meet the criteria for surgical resection.

  2. Patient has cancer diagnosis other than primary pancreatic adenocarcinoma.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stephenson Cancer Center Oklahoma City Oklahoma United States 73117

Sponsors and Collaborators

  • University of Oklahoma

Investigators

  • Principal Investigator: Ajay Jain, MD, University of Oklahoma Stephenson Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Oklahoma
ClinicalTrials.gov Identifier:
NCT05275075
Other Study ID Numbers:
  • OU-SCC-miRPanCa
First Posted:
Mar 11, 2022
Last Update Posted:
Aug 11, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Oklahoma
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 11, 2022