MelanomaAPiTOXMMNCT06627595
Impact of Physical Activity on Immunotherapy-induced Toxicities in Melanoma Management
An observational study of Melanoma and Immunotoxicity, run by University Hospital, Montpellier at 2 sites in France.
Trial summary
Management of melanoma is based on primary excision of the tumor. In cases of melanoma with poor prognosis criteria, or when it is locally advanced or metastatic, there is an indication for the implementation of adjuvant therapy, which may, in this context, be immunotherapy. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Melanoma, Immunotoxicity
- What is being tested?
- Immunotherapy
- How many people
- 160 participants
- Where
- 2 sitesFrance
- Study dates
- 5 Nov 2024to 5 May 2028
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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
Study population: Subjects aged 18 years or older, newly diagnosed with melanoma with an indication for treatment initiation by immunotherapy (anti-PD1 or anti-PD1 + anti-CTLA4), in an adjuvant or metastatic setting. Only incident cases will be included. Patients treated at Montpellier University Hospital (CHU) or the Montpellier Cancer Institute (ICM)
Who may be able to join
- age 18 years or above
- ECOG performance status inferior or equal to 3
- patient with a melanoma confirmed histologically/pathologically
- indication for initiating treatment with anti-PD1 immunotherapy or anti-PD1 + anti-CTLA4
Who cannot join
- patient unable to read and/or write
- inability to follow up with the patient during the study period
- refusal to participate after a reflection period
- medical contraindication to initiating immunotherapy (active autoimmune disease requiring systemic treatment in the past 2 years, active infection, etc.)
- not affiliated with a social security system
- patient under legal protection, guardianship, or curatorship
- person participating in another study that includes an ongoing exclusion period
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
France2 sites, 2 recruiting
- Recruiting
CHU de Montpellier
Montpellier
Alexandre Maria, MD, PhD, 00330665849253, a-maria@chu-montpellier.fr
- Not yet recruiting
Institut du Cancer de Montpellier (ICM)
Montpellier
Anouck Lamoureux, MD, 00330467336906, a-lamoureux@chu-montpellier.fr
About this study
Management of melanoma is based on primary excision of the tumor. In cases of melanoma with poor prognosis criteria, or when it is locally advanced or metastatic, there is an indication for the implementation of adjuvant therapy, which may, in this context, be immunotherapy.
Immunotherapies are treatments that have revolutionized the prognosis of patients with melanoma. These are therapies that work by stimulating the immune system to enhance the anti-tumor response. Their toxicities are represented by immune-mediated toxicities, similar to true autoimmune diseases.
Read more
Adapted physical activity as supportive care in oncology is expanding. From a pathophysiological perspective, physical activity is thought to modulate the immune system (by reducing inflammation, restoring immune surveillance, stimulating anti-tumor responses through the induction of T cell proliferation, modulating the gut microbiota, and influencing tumor microenvironment cells, etc.).
The modulation of the immune system by physical activity may also allow us to hypothesize a modulation of the toxicities induced by immune checkpoint inhibitors. We wish to study this hypothesis in patients with advanced melanoma who are candidates for immunotherapy.
Originality and Innovative Aspects:
Physical activity as supportive care in oncology has developed significantly in recent years. However, adapted physical activity (APA) is currently only offered at one center in France (CHU de Lille).
In addition to the probable impact on patients\' quality of life, if we find evidence supporting a reduction in treatment-related toxicities for melanoma through physical activity, it would be even more interesting to introduce APA at the CHU of Montpellier.
Primary and Secondary Objectives:
Primary Objective: To analyze the association between the level of physical activity (estimated by the IPAQ questionnaire) at the initiation of immunotherapy and the occurrence of adverse effects at 6 months after starting treatment in adult patients with melanoma.
Secondary Objectives:
Analyze the association between physical activity level and treatment efficacy of immunotherapy in adult melanoma patients.
Describe the quarterly evolution of patients\' general condition through measurement of WHO status and BMI.
Assess the evolution of patients\' general condition: WHO status and BMI at treatment introduction, after 3 months, and at 6 months of treatment.
Study the evolution of patients\' quality of life during their treatment based on their physical activity level, using the QLQ-C30 questionnaire.
Preliminary study:
We aim to evaluate the correlation between self-reported physical activity by patients and their actual physical activity. To obtain an objective measurement of patients\' physical activity level, we plan to work with the CARTIGEN platform and offer a small number of included patients (maximum of 50) to wear wrist actimeters for one week before treatment initiation. We will then analyze these data to determine patients\' baseline physical activity levels and compare them with the data collected via questionnaires.
This is a prospective cohort study within the context of analytical epidemiological research. It is a bicentric study: CHRU Montpellier - Saint-Eloi Hospital and ICM Val d\'Aurelle.
Using the collected data on patients\' physical activity levels (IPAQ questionnaire), we will compare two groups: patients who experienced immuno-toxicities without physical activity versus those with moderate or high physical activity.
We will also analyze treatment efficacy in these two groups, patients\' quality of life, and the evolution of their general condition.
Procedure:
Inclusion is planned at day 0 (D0), with physical activity (IPAQ3) and quality of life (QLQ-C30) questionnaires, along with clinical and oncological evaluation.
A follow-up visit at month 3 (M3) will include reassessment of clinical and oncological status, followed by another visit at month 6 (M6) for further clinical, oncological, physical activity, and quality of life reassessment.
The inclusion period is expected to last 18 months.
Outcomes / Perspectives:
If we consider that physical exercise may help mitigate the toxic effects of treatments-an aspect we wish to explore through this project-it would be relevant to introduce adapted physical activity (APA) sessions supervised by a specialized instructor within the Dermatology Day Hospital at the CHU of Montpellier.
Implementing APA in the context of onco-dermatology will strengthen the multidisciplinary approach of the CHU.
Collaboration between healthcare professionals, including specialized APA instructors, will foster effective care coordination.
This initiative is part of a holistic approach to patient care, integrating complementary interventions to address physical, psychological, and social needs.
- Conditions
- Melanoma, Immunotoxicity
- Being tested
- Immunotherapy
- Keywords
- physical activity, melanoma, immunotherapy, anti-PD-1, anti-CTLA4, immunotoxicity
- Medical subject headings
- Melanoma, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ImmunotherapyDrug
Also called pembrolizumab, nivolumab, ipilimumab
Patients will be treated in accordance with the guidelines for melanoma treatment.
| Study group | Role | What they receive |
|---|---|---|
| Patients with no physical activity / low physical activity | Patients with low score according to the IPAQ questionnaire at baseline. This is the lowest level of physical activity. Receives: Drug: Immunotherapy | |
| Patients with moderate to high physical activity | Patients with moderate or high score according to the IPAQ questionnaire at baseline. Receives: Drug: Immunotherapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Immunotoxicity
Occurrence of immune-induced side effects
Measured: From the time of enrollment until 6 months following the initiation of treatment
Secondary outcomes (1)
Efficacy of immunotherapy
Tumoral response to immunotherapy
Measured: From the time of enrollment until 6 months following the initiation of treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Oct 2024
- Study start5 Nov 2024
- Primary completion5 Nov 2027 (estimated)
- Study completion5 May 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for MelanomaStudies of the same condition, open and under way.
- More trials run by University Hospital, MontpellierThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 160 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Montpellier
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06627595
- Sponsor's protocol ID
- RECHMPL24_0195
- Acronym
- APiTOXMM
- Status last verified
- Jul 2026
- First submitted
- 2 Oct 2024
- Last updated
- 28 Jul 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Physical Activity on Immunotherapy-induced Toxicities in Melanoma Management
- ClinicalTrials.gov ID
- NCT06627595
- Acronym / sponsor ID
- APiTOXMM / RECHMPL24_0195
- Conditions
- Melanoma, Immunotoxicity
- Keywords
- physical activity, melanoma, immunotherapy, anti-PD-1, anti-CTLA4, immunotoxicity
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 160 participants (estimated)
- Lead sponsor
- University Hospital, MontpellierUniversity, hospital or other
- Study start
- 5 Nov 2024 (actual)
- Primary completion
- 5 Nov 2027 (estimated)
- Study completion
- 5 May 2028 (estimated)
- First posted
- 4 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Management of melanoma is based on primary excision of the tumor. In cases of melanoma with poor prognosis criteria, or when it is locally advanced or metastatic, there is an indication for the implementation of adjuvant therapy, which may, in this context, be immunotherapy.
Immunotherapies are treatments that have revolutionized the prognosis of patients with melanoma. These are therapies that work by stimulating the immune system to enhance the anti-tumor response. Their toxicities are represented by immune-mediated toxicities, similar to true autoimmune diseases.
Adapted physical activity as supportive care in oncology is expanding. From a pathophysiological perspective, physical activity is thought to modulate the immune system (by reducing inflammation, restoring immune surveillance, stimulating anti-tumor responses through the induction of T cell proliferation, modulating the gut microbiota, and influencing tumor microenvironment cells, etc.).
The modulation of the immune system by physical activity may also allow us to hypothesize a modulation of the toxicities induced by immune checkpoint inhibitors. We wish to study this hypothesis in patients with advanced melanoma who are candidates for immunotherapy.
Originality and Innovative Aspects:
Physical activity as supportive care in oncology has developed significantly in recent years. However, adapted physical activity (APA) is currently only offered at one center in France (CHU de Lille).
In addition to the probable impact on patients\' quality of life, if we find evidence supporting a reduction in treatment-related toxicities for melanoma through physical activity, it would be even more interesting to introduce APA at the CHU of Montpellier.
Primary and Secondary Objectives:
Primary Objective: To analyze the association between the level of physical activity (estimated by the IPAQ questionnaire) at the initiation of immunotherapy and the occurrence of adverse effects at 6 months after starting treatment in adult patients with melanoma.
Secondary Objectives:
Analyze the association between physical activity level and treatment efficacy of immunotherapy in adult melanoma patients.
Describe the quarterly evolution of patients\' general condition through measurement of WHO status and BMI.
Assess the evolution of patients\' general condition: WHO status and BMI at treatment introduction, after 3 months, and at 6 months of treatment.
Study the evolution of patients\' quality of life during their treatment based on their physical activity level, using the QLQ-C30 questionnaire.
Preliminary study:
We aim to evaluate the correlation between self-reported physical activity by patients and their actual physical activity. To obtain an objective measurement of patients\' physical activity level, we plan to work with the CARTIGEN platform and offer a small number of included patients (maximum of 50) to wear wrist actimeters for one week before treatment initiation. We will then analyze these data to determine patients\' baseline physical activity levels and compare them with the data collected via questionnaires.
This is a prospective cohort study within the context of analytical epidemiological research. It is a bicentric study: CHRU Montpellier - Saint-Eloi Hospital and ICM Val d\'Aurelle.
Using the collected data on patients\' physical activity levels (IPAQ questionnaire), we will compare two groups: patients who experienced immuno-toxicities without physical activity versus those with moderate or high physical activity.
We will also analyze treatment efficacy in these two groups, patients\' quality of life, and the evolution of their general condition.
Procedure:
Inclusion is planned at day 0 (D0), with physical activity (IPAQ3) and quality of life (QLQ-C30) questionnaires, along with clinical and oncological evaluation.
A follow-up visit at month 3 (M3) will include reassessment of clinical and oncological status, followed by another visit at month 6 (M6) for further clinical, oncological, physical activity, and quality of life reassessment.
The inclusion period is expected to last 18 months.
Outcomes / Perspectives:
If we consider that physical exercise may help mitigate the toxic effects of treatments-an aspect we wish to explore through this project-it would be relevant to introduce adapted physical activity (APA) sessions supervised by a specialized instructor within the Dermatology Day Hospital at the CHU of Montpellier.
Implementing APA in the context of onco-dermatology will strengthen the multidisciplinary approach of the CHU.
Collaboration between healthcare professionals, including specialized APA instructors, will foster effective care coordination.
This initiative is part of a holistic approach to patient care, integrating complementary interventions to address physical, psychological, and social needs.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Patients with no physical activity / low physical activity | – | Drug: ImmunotherapyPatients with low score according to the IPAQ questionnaire at baseline. This is the lowest level of physical activity. |
| Patients with moderate to high physical activity | – | Drug: ImmunotherapyPatients with moderate or high score according to the IPAQ questionnaire at baseline. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Subjects aged 18 years or older, newly diagnosed with melanoma with an indication for treatment initiation by immunotherapy (anti-PD1 or anti-PD1 + anti-CTLA4), in an adjuvant or metastatic setting. Only incident cases will be included. Patients treated at Montpellier University Hospital (CHU) or the Montpellier Cancer Institute (ICM)
Key inclusion criteria (4 listed)
- age 18 years or above
- ECOG performance status inferior or equal to 3
- patient with a melanoma confirmed histologically/pathologically
- indication for initiating treatment with anti-PD1 immunotherapy or anti-PD1 + anti-CTLA4
Key exclusion criteria (7 listed)
- patient unable to read and/or write
- inability to follow up with the patient during the study period
- refusal to participate after a reflection period
- medical contraindication to initiating immunotherapy (active autoimmune disease requiring systemic treatment in the past 2 years, active infection, etc.)
- not affiliated with a social security system
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ImmunotherapyAlso: pembrolizumab, nivolumab, ipilimumabPatients will be treated in accordance with the guidelines for melanoma treatment. | Drug | Patients with moderate to high physical activity, Patients with no physical activity / low physical activity |
Primary outcome
Immunotoxicity
Time frame: From the time of enrollment until 6 months following the initiation of treatment
Occurrence of immune-induced side effects
1 secondary outcome
Efficacy of immunotherapy
Time frame: From the time of enrollment until 6 months following the initiation of treatment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Melanoma and Immunotoxicity, run by University Hospital, Montpellier at 2 sites in France.
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 4 inclusion and 7 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: looking for participants now, as of the sponsor's last update on 28 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in France. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Alexandre Maria, MD, PhD (00330665849253, a-maria@chu-montpellier.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Immunotoxicity (time frame: From the time of enrollment until 6 months following the initiation of treatment). 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 28 Jul 2026.