COffee and Metabolites Modulating the Gut MicrobiomE in Colorectal caNCER

Last updated: May 5, 2025
Sponsor: Massachusetts General Hospital
Overall Status: Active - Recruiting

Phase

1/2

Condition

Colon Cancer; Rectal Cancer

Colon Cancer

Colorectal Cancer

Treatment

Nestlé NESCAFÉ® TASTER'S CHOICE® House Blend capsule.

Placebo

Clinical Study ID

NCT05692024
23-061
R01CA263776
  • Ages > 18
  • All Genders

Study Summary

This is research study is assessing the effects of 6-g daily use of freeze-dried instant coffee on liver fat and fibrosis and the gut microbiome and metabolome in patients who have completed routine treatment (including surgery, chemotherapy and radiotherapy) for stage I-III colorectal cancer.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Participants must meet the following criteria on screening examination to be eligible to participate in the study:

  • Participants must have histologically confirmed stage I, II, or III colon or rectaladenocarcinoma and have completed standard treatment (including surgery,chemotherapy and radiotherapy) at least 2 months ago.

  • Age 18 years or older.

  • This study will only include adult participants because colorectal carcinogenesis inchildren is more likely to be related to a cancer predisposition syndrome withdistinct biological mechanisms compared with sporadic colorectal cancer in adults.

  • The effects of coffee on the developing human fetus are unknown. For this reason,women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry andfor the duration of study participation. Should a woman become pregnant or suspectshe is pregnant while participating in this study, she should inform her treatingphysician immediately.

  • Subjects must be able and willing to follow study procedures and instructions.

  • Ability to understand and the willingness to sign a written informed consentdocument.

Exclusion

Exclusion Criteria:

Participants who exhibit any of the following conditions at screening will not be eligible for admission into the study.

  • Participants who are receiving any other investigational agents.

  • Concurrent use of other anti-cancer therapy, including chemotherapy agents, targetedagents, biological agents, immunotherapy, or investigational agents not otherwisespecified in this protocol.

  • Regularly consuming more than 2 cups of coffee ( 8 oz) per day for at least 3 days aweek in the past month.

  • Current or recent use (within 1 month) of any coffee supplements (e.g., green coffeeextracts).

  • History of diagnosed conditions that may be worsen by coffee, including arrhythmias,insomnia, tremors, tics, generalized anxiety disorder, bipolar disease, panicattacks, Tourette's, epilepsy or overactive bladder.

  • History of adverse reactions to coffee or intolerance of coffee consumption.

  • Inability or unwillingness to swallow capsules.

  • History of malabsorption or uncontrolled vomiting or diarrhea, or any other diseasethat could interfere with absorption of oral medications.

  • Any uncontrolled intercurrent illness including, but not limited to, ongoing oractive infection, symptomatic congestive heart failure, unstable angina pectoris, orpsychiatric illness/social situations that, in the opinion of the investigator, mayincrease the risks associated with study participation or study treatment, limitcompliance with study requirements, or interfere with the interpretation of studyresults.

  • Pregnant or breastfeeding. The effects of coffee on the developing human fetus areunknown. For this reason, women of child-bearing potential must agree to useadequate contraception (hormonal or barrier method of birth control; abstinence)prior to study entry and for the duration of study participation.

Should a woman become pregnant or suspect she is pregnant while she is participating in this study, she should inform her treating physician immediately. Similarly, lactating women are excluded from this study because there is an unknown but potential risk of adverse events in nursing infants secondary to treatment of the mother with coffee. Consequently, breastfeeding should be discontinued if the mother is enrolled on the study.

  • Presence of synchronous (at the same time) malignancy for which the patient iscurrently receiving active treatment.

  • Known positive test for human immunodeficiency virus (HIV), hepatitis C virus, oracute or chronic hepatitis B infection.

Study Design

Total Participants: 80
Treatment Group(s): 2
Primary Treatment: Nestlé NESCAFÉ® TASTER'S CHOICE® House Blend capsule.
Phase: 1/2
Study Start date:
March 21, 2024
Estimated Completion Date:
December 01, 2027

Study Description

This research study is a chemoprevention clinical trial, designed to test the safety and effectiveness of an investigational intervention to learn whether the intervention works in treating a specific disease. "Investigational" means that the drug is being studied. The investigators plan to recruit 80 participants.

  • Coffee is a complex mixture of hundreds of bioactive compounds, including caffeine, chlorogenic acids, and other polyphenols. Increasing data suggest the anti-cancer benefit of coffee. Observational data have linked coffee drinking to better survival among patients with colorectal cancer. However, there remains uncertainty surrounding the mode of action.

  • The U.S. Food and Drug Administration (FDA) has not approved coffee as a treatment for any disease.

  • The research study procedures include:

  • Screening for eligibility.

  • Two study visits

  • Proton magnetic resonance spectroscopy.

  • Magnetic resonance imaging

  • Ultrasound elastography.

  • Urine, blood, and stool samples collected.

  • Diet and lifestyle questionnaires

  • Collection of archival tumor biopsy tissue.

  • Treatment: Coffee or placebo administered daily, orally for 8-12 weeks.

Connect with a study center

  • Massachusetts General Hospital

    Boston, Massachusetts 02115
    United States

    Active - Recruiting

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