Intermittent Fasting for Pancreatic Cancer Risk

FM
Overseen ByFlorencia McAllister, MD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: M.D. Anderson Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether individuals at high risk for pancreatic cancer can adhere to an eating pattern called intermittent fasting (IF) and how it affects their health. Participants will fast for 16 hours daily and eat during an 8-hour window. The study aims to determine if this eating style alters biological markers related to metabolism, inflammation, gut health, and more. Suitable candidates may have a family history of pancreatic cancer, certain genetic conditions, pancreatic cysts, or new-onset diabetes considered suspicious for cancer. Participants should be willing to adjust their eating schedule and track fasting times with an app. As an unphased trial, this study offers a unique opportunity to contribute to groundbreaking research on dietary patterns and cancer risk.

Do I have to stop taking my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that intermittent fasting is safe for individuals at high risk of pancreatic cancer?

Research has shown that intermittent fasting (IF) is generally safe for most people, including those with cancer. Studies have found that individuals can follow this eating pattern with few side effects. For instance, participants report adhering well to fasting without suffering from malnutrition and experiencing only minor negative effects. Additionally, fasting might improve health measures like insulin sensitivity and blood sugar levels, which benefit overall health.

In some cases, intermittent fasting has been linked to reduced inflammation and a lower risk of cancer recurrence. While more research is needed to confirm these benefits, early results are encouraging. Overall, IF appears to be a safe choice for many, though individual experiences can vary.12345

Why are researchers excited about this trial?

Unlike the standard treatments for reducing pancreatic cancer risk, which often involve medications or surgery, intermittent fasting is a lifestyle change that focuses on when you eat, not what you eat. Researchers are excited about intermittent fasting because it taps into the body's natural metabolic processes, potentially lowering cancer risk without the need for drugs or invasive procedures. This approach is non-invasive, easy to implement, and may offer a new way to help manage cancer risk by leveraging the body's own biology.

What evidence suggests that intermittent fasting might be an effective approach for reducing pancreatic cancer risk?

Studies have shown that intermittent fasting (IF) might help reduce cancer risk. Research suggests that fasting can lower blood sugar levels and improve insulin use, which links to a reduced chance of developing cancer. Some studies also indicate that IF can lessen chemotherapy side effects and slow tumor growth. Early findings suggest that fasting may be safe for cancer patients and could help prevent cancer recurrence. While more research is needed, these initial insights suggest potential benefits of intermittent fasting for those at risk of pancreatic cancer. Participants in this trial will follow an intermittent fasting regimen, fasting for 16 consecutive hours each day with an 8-hour eating window, to evaluate its effects on pancreatic cancer risk.13678

Who Is on the Research Team?

FM

Florencia McAllister, MD

Principal Investigator

M.D. Anderson Cancer Center

Are You a Good Fit for This Trial?

This trial is for adults (18+) who are at high risk for pancreatic cancer due to family history, genetic factors, certain pancreatic cysts or lesions, new-onset diabetes, or chronic pancreatitis. Participants must be able to understand and consent to the study.

Inclusion Criteria

* Eligibility and surveillance risk assessment must be consistent with NCCN (National Comprehensive Cancer Network) Guidelines for Pancreatic Cancer Screening in High- Risk Individuals.
I have a genetic mutation or syndrome that increases my risk for pancreatic cancer.
I have a family history of pancreatic cancer.
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants follow an intermittent fasting regimen, fasting for 16 consecutive hours each day with an 8-hour eating window

12 months

Follow-up

Participants are monitored for safety and effectiveness after treatment, including changes in biological markers

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Intermittent Fasting

Trial Overview

The study tests whether intermittent fasting is practical and tolerable in people at high risk of pancreatic cancer. It also looks at how this eating pattern affects various health markers related to metabolism, inflammation, gut bacteria, and imaging results.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Intermittent fastingExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

M.D. Anderson Cancer Center

Lead Sponsor

Trials
3,107
Recruited
1,813,000+

Citations

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