What this study is
The goal of this clinical trial is to test meal-timing as a novel and sustainable interventional approach during cancer treatment to improve therapeutic response and metabolic health in an understudied population. This clinical trial will enroll patients with rectal or breast cancer receiving neoadjuvant treatment at the Alaska Native Medical Center (ANMC), which is part of the Alaska Native Tribal Health Consortium (ANTHC).
A promising strategy for improving the efficacy of anticancer treatments and reducing associated toxicities involves combining treatment with fasting regimens. In pre-clinical and clinical studies, various forms of fasting have been shown to induce tumor regression and improve long-term survival. According to the differential stress sensitization theory, fasting is thought to sensitize tumor cells to the cytotoxic effects of chemotherapy and radiation, while protecting healthy cells by increasing stress resistance. While healthy cells slow their growth and become more stress resistant in response to fasting, cancer cells cannot survive in nutrient-deficient environments; although the underlying mechanisms are not fully understood. However, extended water-only fasting can be challenging for patients and poses undue health risks. Intermittent fasting, and specifically time-restricted eating (TRE), may offer a viable alternative. TRE involves eating within a shorter window (e.g., 8 hours) and fasting for the remainder of the day but involves no other dietary restrictions. Because of its simplicity, TRE may be more sustainable than other fasting regimens. TRE also improves several cardio-metabolic endpoints, including insulin sensitivity, which may also be beneficial during anticancer treatments.
What's being tested
- Time-restricted eating
Intervention · BEHAVIORAL
Participate in time-restricted eating plan
- Questionnaire Administration
Intervention · OTHER
Complete questionnaire
- Biospecimen Collection
Intervention · PROCEDURE
Undergo collection of blood and stool
- Health coaching
Intervention · BEHAVIORAL
Receive nutrition counseling
Study details
- Sponsor
- Fred Hutchinson Cancer Center
- Conditions
- Rectal Cancer Stage II · Rectal Cancer Stage III · Breast Cancer Stage I · Rectal Cancer Stage IV · Breast Cancer Stage II · Breast Cancer Stage III · Solid Tumor Cancer
- Enrolling
- 100 people
- Starts
- 2026-07-07
- Est. completion
- 2029-08-31
- Design
- Open-label, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 21 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Male or female
- Self-identify as Alaska Native or American Indian person and eligible for care at the ANMC
- Age≥21 years
- Histologically confirmed rectal cancer stage II, III, or IV (if curative) per AJCC criteria (neoadjuvant)
- Histologically confirmed HER2+ or triple negative breast cancer stage I, II, or III, per AJCC criteria (neoadjuvant)
- Histologically or cytologically confirmed solid tumor (adjuvant)
- BMI≥18.5 kg/m2
- Plan to receive neoadjuvant or adjuvant therapy
- Planned duration of neoadjuvant or systemic adjuvant therapy for >3 months to allow sufficient time to assess impact of intervention
- Must have capacity to give informed consent
- Willing and able to adhere to the assessments, visit schedules, prohibitions, and restrictions
- Has completed ≤ 4 weeks of neoadjuvant or adjuvant treatment prior to study enrollment
- Score of < 4 on U.S. Household Food Security Survey Module: Six-Item Short Form OR if score >5, have clearance from dietitian
You can't join if
- History of cytotoxic chemotherapy ≤12 months prior to rectal or breast cancer diagnosis (neoadjuvant)
- Allergic reaction to any of the treatment agents
- Any prior pelvic radiotherapy
- Active second malignancy (exceptions: non-melanoma skin cancers or cervical carcinoma in situ adequately treated) requiring systemic therapy
- History of GI perforation ≤12 months prior to enrollment
- History of predisposing colonic or small bowel disorders with severe or rapidly worsening symptoms (not related to current cancer symptoms)
- Receiving any parenteral nutrition or enteral (tube) feeding or using similar nutritional supplement during the study period
- History of uncontrolled CHF defined as NYHA Class III or greater
- Pre-existing grade ≥3 neuropathy
- Currently participating in or has participated in a study of an investigational agent or investigational device ≤4 weeks of the first dose of treatment
- Unstable psychiatric, sleep, or circadian conditions (common conditions such as sleep apnea and depression are acceptable as long as they are stabilized and not rapidly worsening)
- Pregnant or breastfeeding
- Currently perform overnight shift work >1 day/week
- Strictly adhering to a <10-hour eating window on most days
- Severe psychiatric, cognitive, or substance misuse disorders or social conditions that would interfere with adherence to study procedures.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openAlaska Native Medical Center (ANMC)
Anchorage, Alaska, United States
- Timothy Thomas, MD · Contact(907) 729-3095tkthomas@anthc.org
- Timothy Thomas, MD · Principal investigator
Recruiting
Study team
Sponsor
Fred Hutchinson Cancer Center
Study ID RG1124486
Principal investigator
Timothy Thomas, MD
Alaska Native Tribal Health Consortium (ANTHC)
Principal investigator
Jane Figueiredo, PhD, M.Sc.
Cedars-Sinai Medical Center
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.