Ignite Creation Date:
2024-05-06 @ 7:19 AM
Last Modification Date:
2024-10-26 @ 11:47 AM
Study NCT ID:
NCT02515513
Status:
WITHDRAWN
Last Update Posted:
2023-06-28
First Post:
2015-06-03
Brief Title:
The Role of Muscle Cachexia in Pancreatic Cancer
Sponsor:
University of Florida
Organization:
University of Florida
Study Overview
Official Title:
The Role of Muscle Cachexia in Pancreatic Cancer
Status:
WITHDRAWN
Status Verified Date:
2023-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Original PI left the institution No subjects enrolled
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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 andor 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
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 andor 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
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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 2R01AR060209-06A1 | NIH | None | httpsreporternihgovquickSearch2R01AR060209-06A1 |