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The Role of Muscle Cachexia in Pancreatic Cancer

Not Applicable
Withdrawn
Conditions
Pancreas Cancer
Interventions
Procedure: Muscle Tissue Biopsy Sample
Registration Number
NCT02515513
Lead Sponsor
University of Florida
Brief Summary

The relationship between myopenia, nutritional status, and long-term oncologic outcomes remains poorly characterized in patients with anatomically resectable pancreatic cancer (PC). The investigators want to look at muscle properties in pancreatic cancer patients to determine possible therapeutic options toward better nutritional status. Patients with benign right upper quadrant pathology will be utilized as controls for the study.

The researchers hypothesize that improving cancer cachexia in PC will improve the quality of life and ultimately increase overall survival. The long term goal of is to identify areas of intervention to prevent and/or improve cachectic events in PC in order to significantly improve clinical outcomes. The first step in this long term goal is to fully characterize cachexia in the condition of PC. This research is to understand and modify the local response within skeletal muscle leading to a clinically relevant persistent wasting and to understand and interrupt the systemic stimulus produced by the tumor local environment resulting in these muscle specific mechanisms.

Detailed Description

Cancer cachexia (CC) is a devastating condition affecting up to 80% of cancer patients, diminishing quality of life and contributing to increased mortality. Cancer cachexia is a complex metabolic syndrome characterized by the loss of skeletal muscle mass and weakness. The muscle pathology of cancer cachexia is not only related to muscle atrophy but also to disruptions to the contractile apparatus of the muscle. While physiologic disruptions in muscle sarcomere and myofiber membrane integrity have been observed despite the lack of injury, the totality of the muscle specific mechanisms contributing to these phenotypes have not been described, nor investigated in the context of pancreatic cancer (PC) where cachexia is a significant clinical problem. Therefore, delineating specific mechanisms of muscle catabolism in PC is critical to developing clinical therapies to control wasting and improve patient quality of life, clinical outcomes and long-term survival.

A variety of tumor promoting and inflammatory cell signaling pathways have been implicated in cancer cachexia, whereby pro-inflammatory cytokines have been implicated as a driving force. Remarkably, approximately half of all patients with PC demonstrate a measurable acute phase response, which is associated with poor clinical outcomes. Importantly, systemic elevations of these inflammatory mediators are due to a complex local interplay between the developing tumor and the immune system which subsequently leads to a systemic chronic inflammatory state. PC appears to manipulate the immune system to promote its survival at the expense of nutritional stores which results in cachexia. Therefore, understanding of the local and systemic inflammatory response in PC and its relation to muscle specific mechanisms is crucial to developing effective therapies for cancer cachexia.

PC associated cachexia results in a significant therapeutic dilemma. Local approaches such as surgery for curative intent encounter a high recurrence rate which is indicative of the systemic nature of even very early-stage disease. Therefore, systemic therapies are necessary for long-term survival. Unfortunately, effective chemotherapies are only offered to patients with good clinical parameters such as nutritional status. In other words, if the patient is too weak, they are not offered effective therapies for the risk of causing more harm than good.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Pancreatic Cancer Patients who are potentially surgically resectable.
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Exclusion Criteria
  • Patients who do not meet the criteria for surgical resection.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Pancreatic Cancer PatientsMuscle Tissue Biopsy SampleDuring the surgical resection for the pancreatic cancer a muscle tissue biopsy sample will be performed.
Surgical Patients with benign pathologyMuscle Tissue Biopsy SampleDuring surgical resection for patients with benign right upper quadrant pathology, a muscle tissue biopsy sample will be performed.
Primary Outcome Measures
NameTimeMethod
Identify gene networks within the skeletal muscle between the groupsday 1

RT-PCR of RNA from biopsied muscle tissues

Ultrastructural abnormalities in muscle tissue samples between the groupsday 1

To look at the extent of ultrastructural abnormalities in the skeletal muscle by histologic examination of muscle biopsies

Myofiber atrophy in muscle tissue samples between the groupsday 1

2) identify the growth and atrophy-related transcription factors associated with the muscle pathology and 3) identify the genome-wide gene networks and biological process associated with skeletal muscle pathology in surgically resected PC patients and healthy control patients by RT-PCR and histologic staining of tissues for transcriptional factors associated with cachexia.

Secondary Outcome Measures
NameTimeMethod
History of weight lostBaseline

Clinical assessment at treatment follow-up

Nutritional statusApproximately 2 years

Clinical assessment at treatment follow-up

Blood Chemistry compositeApproximately 2 years

Clinical assessment at treatment follow-up

Preoperative sarcopenia using a muscular indexApproximately 2 years

Clinical assessment at treatment follow-up and radiographic measurements of muscle groups on routine surveillance for cancer recurrence or advancement

Measurement of lymphatic metastasisApproximately 2 years

Pathologic specimen at time of resection to determine extent of pathologic stage which is routine

Tumor gradeApproximately 2 years

Noted at pathologic assessment and part of routine examination

Survival dataApproximately 2 years

Noted on routine follow-up

Trial Locations

Locations (1)

UF Health

🇺🇸

Gainesville, Florida, United States

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