Metastatic Melanoma Clinical Trial
— MINI-MDOfficial 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.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | December 1, 2025 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 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. Exclusion Criteria: - 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 - 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 |
Country | Name | City | State |
---|---|---|---|
Croatia | University Hospital Zagreb-Rebro | Zagreb | Grad Zagreb |
Lead Sponsor | Collaborator |
---|---|
University Hospital Rijeka |
Croatia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | A change of concentration of microbiome associated with a good immune response | evaluate the connection between changes in the intake of micronutrients and the microbiome | From enrollment to the end of treatment at 12 weeks | |
Other | A correlation between microbiome associated with a good immune response and response | To evaluate the association of the basic microbiome and the rate of biochemical and radiological response | From enrollment to the end of treatment at 12 weeks | |
Other | A correlation between microbiome associated with a good immune response and less adverse effects | To assess the association between the basic microbiome and the rate of immunotherapy side effects | From enrollment to the end of treatment at 12 weeks | |
Primary | 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) | From enrollment to the end of treatment at 12 weeks | |
Primary | 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) | From enrollment to the end of treatment at 12 weeks | |
Primary | 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) | From enrollment to the end of treatment at 12 weeks | |
Primary | 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) | From enrollment to the end of treatment at 12 weeks | |
Primary | 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) | From enrollment to the end of treatment at 12 weeks | |
Secondary | A change in radiological response rate (PET/CT or CT) | Assess the impact of INIMP on the radiological response rate (PET/CT or CT) | From enrollment to the end of treatment at 12 weeks | |
Secondary | A change in gut microbiome strains associated with an improved response to immunotherapy | Assess the impact of INIMP on changes in the microbiome | From enrollment to the end of treatment at 12 weeks | |
Secondary | 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 | From enrollment to the end of treatment at 12 weeks | |
Secondary | A change of biochemical biomarkers of melanoma (S100 and LDH) | Assess the impact of INIMP on biochemical biomarkers of melanoma (S100 and LDH) | From enrollment to the end of treatment at 12 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT02224781 -
Dabrafenib and Trametinib Followed by Ipilimumab and Nivolumab or Ipilimumab and Nivolumab Followed by Dabrafenib and Trametinib in Treating Patients With Stage III-IV BRAFV600 Melanoma
|
Phase 3 | |
Active, not recruiting |
NCT05470283 -
Phase I, Open-Label, Study of Tumor Infiltrating Lymphocytes Engineered With Membrane Bound IL15 Plus Acetazolamide in Adult Patients With Metastatic Melanoma
|
Phase 1 | |
Recruiting |
NCT05388877 -
E6201 and Dabrafenib for the Treatment of Central Nervous System Metastases From BRAF V600 Mutated Metastatic Melanoma
|
Phase 1 | |
Active, not recruiting |
NCT05103891 -
Relative Bioavailability of Binimetinib 3 x 15 mg and 45 mg Formulations
|
Phase 1 | |
Completed |
NCT00414765 -
Aldesleukin in Participants With Metastatic Renal Cell Carcinoma or Metastatic Melanoma
|
Phase 4 | |
Completed |
NCT02857270 -
A Study of LY3214996 Administered Alone or in Combination With Other Agents in Participants With Advanced/Metastatic Cancer
|
Phase 1 | |
Completed |
NCT01621490 -
PH 1 Biomarker Study of Nivolumab and Ipilimumab and Nivolumab in Combination With Ipilimumab in Advanced Melanoma
|
Phase 1 | |
Recruiting |
NCT05779423 -
Cryoablation+Ipilimumab+Nivolumab in Melanoma
|
Phase 2 | |
Active, not recruiting |
NCT04940299 -
Tocilizumab, Ipilimumab, and Nivolumab for the Treatment of Advanced Melanoma, Non-Small Cell Lung Cancer, or Urothelial Carcinoma
|
Phase 2 | |
Active, not recruiting |
NCT02278887 -
Study Comparing TIL to Standard Ipilimumab in Patients With Metastatic Melanoma
|
Phase 3 | |
Active, not recruiting |
NCT02360579 -
Study of Lifileucel (LN-144), Autologous Tumor Infiltrating Lymphocytes, in the Treatment of Patients With Metastatic Melanoma
|
Phase 2 | |
Terminated |
NCT02521870 -
A Trial of Intratumoral Injections of SD-101 in Combination With Pembrolizumab in Patients With Metastatic Melanoma or Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma
|
Phase 1/Phase 2 | |
Completed |
NCT02177110 -
A Translational Systems Medicine Approach to Provide Predictive Capacity for Therapy Response in Advanced or Metastatic Malignant Melanoma
|
||
Withdrawn |
NCT01340729 -
Open-Label Study of TPI 287 for Patients With Metastatic Melanoma
|
Phase 1/Phase 2 | |
Withdrawn |
NCT01416844 -
Study of Immune Responses in Patients With Metastatic Melanoma
|
Phase 2 | |
Terminated |
NCT01468818 -
Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Melanoma
|
Phase 2 | |
Completed |
NCT00984464 -
Study of REOLYSIN® in Combination With Paclitaxel and Carboplatin in Patients With Metastatic Melanoma
|
Phase 2 | |
Completed |
NCT00631618 -
Clinical Trial of Sutent to Treat Metastatic Melanoma
|
Phase 2 | |
Terminated |
NCT00571116 -
Disulfiram Plus Arsenic Trioxide In Patients With Metastatic Melanoma and at Least One Prior Systemic Therapy
|
Phase 1 | |
Recruiting |
NCT00226473 -
Standard Palliative Care Versus Standard Palliative Care Plus Polychemotherapy in Metastasized Malignant Melanoma
|
Phase 4 |