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Melanoma Stage IvMINI-MDNCT06236360

Metastatic Melanoma Patients on Immunotherapy With Nutritive Intervention Based on Mediterranean Diet

A study testing Mediterranean Diet Intervention in people with Melanoma Stage Iv and Metastatic Melanoma, run by University Hospital Rijeka at 1 site in Croatia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This research will study the effect of Mediterranean diet intervention in patients undergoing immunotherapy treatment for metastatic melanoma and its relationship with gut microbiome and quality of life. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Melanoma Stage Iv, Metastatic Melanoma
What is being tested?
Mediterranean Diet Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteCroatia
Study dates
21 Dec 2023to 1 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • age ≥18 years
  • pathophysiologically confirmed cutaneous melanoma stage IV or inoperable stage IIIC,
  • radiologically measurable disease on computerized tomography (CT) or positron emission tomography (PET)/CT,
  • The multidisciplinary team recommended initiation of treatment with dual immunotherapy with anti-PD-1 + anti-CTLA4 immunotherapy
  • written informed consent prior to participation
  • willingness to monitor and adjust the dietary regimen if necessary
  • Eastern Cooperative Oncology Group (ECOG) status 0-1.

Who cannot join

  • lifetime history of psychiatric disorders
  • active brain metastases
  • active autoimmune disease
  • systemic use of equal or more than 10 mg of prednisone or an appropriate corticosteroid equivalent during screening
  • exposure to antibiotics and probiotics or other supplements that can affect the study outcome during screening within the last 3 weeks,
  • uncontrolled diabetes
Show all 9Show fewer
  • history of clinically significant drug or alcohol abuse within the last 6 months
  • specific dietary habits that are not inclined or able to change or the existence of food allergy or intolerance to certain food
  • inability or refusal to participate in all research procedures

Trial locations and contacts

1 site in 1 country.

Marin Golčić, MD, PhD contact

385-658-431

marin.golcic@gmail.com

Luka Simetić, MD contact

385-0124-20005

luka.doc@gmail.com

Croatia1 site, 1 recruiting
  • University Hospital Zagreb-Rebro

    Zagreb, City of Zagreb, 10000

    Luka Simetić, MD, 0919117494, luka.doc@gmail.com

    Luka Simetić, MD

    Recruiting

Other trials in Croatia

About this study

Official title: The Effect of Individualized Nutritive Intervention Based on the Mediterranean Diet on the Changes in the Gut Microbiome, Quality of Life, and Radiological and Biochemical Response to Immunotherapy in Metastatic Melanoma Patients

This research will study the effect of Mediterranean diet intervention in patients undergoing immunotherapy treatment for metastatic melanoma and its relationship with gut microbiome and quality of life. One group of patients will continue with their regular diet, while the other will receive dietary tele-intervention with trained nutritionist during the 12-week period. Gut microbiome, quality of life questionnaires, blood parameters and radiological examination will be evaluated before and 12-weeks after the start of the intervention.

Read the detailed description

Metastatic melanoma is a malignant tumor of melanocyte origin that has spread to other organs. The basis of treatment is systemic therapy, most commonly anti-programmed death-1 (PD-1) and anti- cytotoxic T-lymphocyte-associated protein 4 (CTLA- 4) immunotherapy, although for some patients, thyrosine kinase inhibition is also a treatment option. Survival of metastatic melanoma patients has been significantly extended over the last decade, and the use of immunotherapy has led to a median overall survival of 72 months and a response rate of up to 60%. However, not all cancer patients respond equally to immunotherapy, and the variation in response may be attributed to the individual's microbiome, which is heavily influenced by dietary habits. Over 2/3 of patients will progress during the 6.5 years of follow-up and currently there is a limited number prognostic and predictive parameters to assess the response to immunotherapy. However, understanding and manipulating the microbiome through dietary interventions offers a potential avenue for enhancing immunotherapy outcomes in cancer patients and, consequently, may serve as a complementary therapeutic strategy. Due to previous data, as well as investigators' previous publication on the importance of gut microbiome as a co-denominator for immunotherapy response, and aiming towards constructing a protocol on dietary intervention for enhancing immunotherapy response in metastatic melanoma patients, the investigators evaluated a systematic search for the data showing association with an improved immunotherapy response.

A diet with moderately elevated sodium use (2.3-4 g daily), diet rich in fiber (20-25 g daily), fruits and vegetables (≥5 servings daily), vitamin D, 23 omega-3 fatty acids and whole grains (≥3 servings daily) has been associated with a more diverse and beneficial microbiome, which in turn promotes the production of short-chain fatty acids (SCFA). All the listed foods belong to the Mediterranean diet (MD), which is based on fresh fruits and vegetables, legumes, olive oil, and unrefined fiber. MD also includes a lower intake of meat, eggs, processed foods, sugars, and saturated fatty acids, which may all lead to a less diverse and potentially less favorable microbiome and health outcomes. Various clinical studies already demonstrated the beneficial effect of MD in non-oncology patients. As for oncology patients, the benefit of the MD in reducing the incidence of cancer has been known for many years, especially for breast cancer patients. Furthermore, a published cohort study with 52 patients receiving immune checkpoint blockade (ICB) treatment for various solid tumors revealed that higher fecal SCFA concentrations were associated with longer progression-free survival. Another cohort study comprising patients with advanced melanoma in the UK and the Netherlands, demonstrated that a stronger adherence to the MD principles was linked to a higher likelihood of responding positively to ICB treatment. However, there is a scarcity of randomized trials evaluating the effect of the nutritional intervention based on the MD in cancer patients undergoing treatment. As far as the investigators are aware, there are no current clinical trials applying a nutritional intervention based on the MD in patients with metastatic melanoma; however, there is an ongoing randomized DIET study - NCT04645680 (with expected ending in 2024), aiming to evaluate effectiveness of fiber-enriched diet within the melanoma setting. The potential effect of the MD based nutritional intervention could result in a greater benefit compared to trials focusing only on one nutrient. Considering the issues learned from COVID-19 pandemic, the main goal of the trial is to determine the effectiveness and applicability of a remote personalized nutritional intervention based on the MD to increase the intake of micronutrients (flavones, anthocyanins, omega-3 fatty acids, vitamin D and fiber) previously associated with a positive response to immunotherapy.

Being tested
Mediterranean Diet Intervention
Keywords
melanoma, immunotherapy, metastasis, mediterranean diet
Medical subject headings
Melanoma, Neoplasm Metastasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mediterranean Diet InterventionBehavioural

    The primary goal is to evaluate whether tele-intervention can elevate the level of flavonoids, anthocyanins, proteins, omega-3 fatty acids, short fatty acids, fruits and vegetables, and fibers (all previously associated with a better response to immunotherapy) and limit foods with added sugars.

Study groups in NCT06236360
Study groupRoleWhat they receive
Mediterranean diet interventionExperimentalThe intervention study will involve scheduled communications (via phone, video call, and/or email) with a trained nutritionist based on protocol-determined parameters and recommendations, organized weekly in the first month, every other week in the second month, and once a month in the third month. Each patient will receive general guidance and information about the MD. Additionally, a personalized nutritional plan based on the MD will be prepared for each patient, considering their initial dietary habits, preferences, food accessibility, and financial constraints. Throughout the 12-week period, patients will be motivated to adhere to the prescribed dietary regimen.
Receives: Behavioral: Mediterranean Diet Intervention
Continuing with previous dietNo interventionThe control group will continue with their usual/current diet, with the exception of supplementation of those in whom low serum vitamin D level (in accordance with current medical recommendations)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in the level of ingested flavones

    To evaluate the effectiveness and applicability of a tele-individualized nutritional intervention based on the Mediterranean diet (INIMP) to increase the intake of micronutrients (flavones)

    Measured: From enrollment to the end of treatment at 12 weeks

  2. Change in the level of ingested anthocyanins

    To evaluate the effectiveness and applicability of a tele-individualized nutritional intervention based on the Mediterranean diet (INIMP) to increase the intake of micronutrients (anthocyanin)

    Measured: From enrollment to the end of treatment at 12 weeks

  3. Change in the level of ingested omega-3 fatty acids

    To evaluate the effectiveness and applicability of a tele-individualized nutritional intervention based on the Mediterranean diet (INIMP) to increase the intake of micronutrients (omega-3 fatty acids)

    Measured: From enrollment to the end of treatment at 12 weeks

  4. Change in the level of ingested vitamin D

    To evaluate the effectiveness and applicability of a tele-individualized nutritional intervention based on the Mediterranean diet (INIMP) to increase the intake of micronutrients (vitamin D)

    Measured: From enrollment to the end of treatment at 12 weeks

  5. Change in the level of ingested fibre

    To evaluate the effectiveness and applicability of a tele-individualized nutritional intervention based on the Mediterranean diet (INIMP) to increase the intake of micronutrients (fibre)

    Measured: From enrollment to the end of treatment at 12 weeks

Secondary outcomes (4)
  1. A change in radiological response rate (PET/CT or CT)

    Assess the impact of INIMP on the radiological response rate (PET/CT or CT)

    Measured: From enrollment to the end of treatment at 12 weeks

  2. A change in gut microbiome strains associated with an improved response to immunotherapy

    Assess the impact of INIMP on changes in the microbiome

    Measured: From enrollment to the end of treatment at 12 weeks

  3. A change in the quality of life assessed by EORTC QLQ C15-PAL

    Assess the impact of INIMP on the quality of life measured by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 15 Palliative scores (EORTC QLQ-C15-PAL), which is a 'core questionnaire' for palliative care, measuring symptom burden and quality of life

    Measured: From enrollment to the end of treatment at 12 weeks

  4. A change of biochemical biomarkers of melanoma (S100 and LDH)

    Assess the impact of INIMP on biochemical biomarkers of melanoma (S100 and LDH)

    Measured: From enrollment to the end of treatment at 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Feb 2024
  2. Study start21 Dec 2023
  3. Primary completion1 Dec 2024 (estimated)
  4. Study completion1 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Care provider, Investigator, Outcomes assessor
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06236360
Sponsor's protocol ID
8.1-23/262-6
Acronym
MINI-MD
Status last verified
Jan 2024
First submitted
21 Dec 2023
Last updated
1 Feb 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Anonymous data regarding the basic information and microbiome.

Questions about this trial

What is this clinical trial studying?

A study testing Mediterranean Diet Intervention in people with Melanoma Stage Iv and Metastatic Melanoma, run by University Hospital Rijeka at 1 site in Croatia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 1 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Croatia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Marin Golčić, MD, PhD (385-658-431, marin.golcic@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in the level of ingested flavones (time frame: From enrollment to the end of treatment at 12 weeks). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Feb 2024.

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