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AzTrials

Solid TumorNCT05626764

QUALITOP - Monitoring Multidimensional Aspects of QUAlity of Life After Cancer ImmunoTherapy, an Open Smart Digital Platform for Personalized Prevention and Patient Management

An observational study of Solid Tumor and Hematologic Cancer, run by Hospices Civils de Lyon at 5 sites in 4 countries.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

An increasing number of cancer patients are eligible to receive immunotherapy. Efficacy and tolerance have been demonstrated in multicentre randomized clinical trials with positive results. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Solid Tumor, Hematologic Cancer
What is being tested?
QoL & irAEs determinants
How many people
3,000 participants
Where
5 sitesin 4 countries
Study dates
27 Jan 2020to Dec 2024
Phase
Observational
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

Study population: to define

Who may be able to join

  • - Age > 18
  • Patients starting an immunotherapy treatment by immune checkpoint inhibitor or CAR-T cells
  • Patients receiving the QUALITOP informational note
  • Patients receiving an immunotherapy treatment within a clinical trial could be eligible according to the promotor of the clinical trial' indications
  • Patients in clinical trial which includes a combination of therapy with one of the drug administered in a blind manner vs placebo, can be eligible to QUALITOP provided that (i) the treatment administered in a blind manner is not the immunotherapy and (ii) the clinical trial allows concomitant participation of patients in non-interventional study
  • Patients treated with immunotherapy by immune checkpoint inhibitors or CAR-T cells and recruited in the consortium clinical trials
  • Patients in existing databases with a data sharing consent

Who cannot join

  • Patients under 18
  • Patients who received an immunotherapy treatment within 6 months before entering QUALITOP
  • Pregnant women
  • Patient refusal to participate

Trial locations and contacts

5 sites in 4 countries.

Delphine MAUCORT-BOULCH, PhD contact

+33 4 78 86 57 64

delphine.maucort-boulch@chu-lyon.fr

Aurore FOUDA ESONGUE, PhD contact

+33 4 78 86 41 14

aurore.fouda@chu-lyon.fr

5 sites in 4 countries

Netherlands2 sites, 2 recruiting
  • Academic Medical Center Amsterdam

    Amsterdam

    MJ KERSTEN, MD

    Recruiting
  • University Medical Center Groningen

    Amsterdam

    GH DE BOCK

    Recruiting

Other trials in Netherlands

France1 site, 1 recruiting
  • Medical Clinical Research Platform, Cancer Institute of the Hospices Civils de Lyon

    Pierre-Bénite, 69310

    Stephane DALLE, MD, stephane.dalle@chu-lyon.fr

    Recruiting

Other trials in France

Portugal1 site, 1 recruiting
  • Instituto Português de Oncologia

    Lisbon

    M Gomes da Silva, MD

    Recruiting

Other trials in Portugal

Spain1 site, 1 recruiting
  • Hospital Clinic de Barcelona - Consorci Institut d'Investigacions Biomediques August Pi i Sunyer

    Barcelona

    S Puig, MD

    Recruiting

Other trials in Spain

About this study

Official title: Monitoring Multidimensional Aspects of QUAlity of Life After Cancer ImmunoTherapy, an Open Smart Digital Platform for Personalized Prevention and Patient Management - QUALITOP -

An increasing number of cancer patients are eligible to receive immunotherapy. Efficacy and tolerance have been demonstrated in multicentre randomized clinical trials with positive results. However, real-life experience differs from clinical trial results, especially regarding the management of potential adverse events. HR-QoL (Health Related Quality of Life) is one of the components of QoL (Quality of Life) in its broad acceptation and is certainly the only one usually collected in trials while little is known about QoL in cancer patients treated in the 'real-world'. QUALITOP partners intend to bring together all relevant longitudinal information present in large heterogeneous data (big data) to estimate patient QoL and find surrogate markers of QoL and its evolution. Within the QUALITOP consortium, 5 countries will collect prospective clinical and QoL data and also retrospective clinical data, and share it. This project will enable collecting, managing, sharing, modelling, processing, and exploiting big data on QoL. Furthermore, beyond the description of QoL, analytical tools (including causal inference methods and machine learning) are needed to understand the determinants of QoL and their complex relationships with irAEs (immune related Adverse Events) in a big-data context where standard statistical techniques would be limited. Artificial intelligence and causal models may be applied and developed to empower the patient, prevent adverse medical conditions, and promote QoL. The created knowledge will enable proposing guidelines for promoting better QoL.

QUALITOP aims at identifying the determinants of health status regarding immunotherapy-related adverse events (IR-AEs, such as toxicities) depending on the patient's profile in a real-world context.

Read more

The richness of QUALITOP is in the diversity of the experts who will collaborate in it. Clinicians involved in the care (thus the health status of the patients) will collaborate with psychologists and sociologists to understand and integrate complementary dimensions of QoL related to immunotherapy. Experts in pharmacovigilance and pharmacists will investigate the IR-AEs and their associations with patient behaviour and non-drug consumption. Epidemiologists, data scientists (including bioinformaticians and biostatisticians) and economists will extract information from the data and develop simulation models to produce knowledge. The project will take place in close relation with patient associations that will interact with experts to design the analyses, interpret their results, and proceed to their dissemination.

The main objective is to collect data of patients receiving immunotherapy in order to describe its impact in their quality of life.

  • Create the first real-life cohort of cancer patients treated with immunotherapy within a context of multidimensional management (with data on clinical information, health-related QoL (HR-QoL), IR-AEs, drug consumption, lifestyle, and administrative data).
  • Accelerate knowledge directed to different stakeholders (patients, relatives, clinicians, pharmacists, health authorities, and the general public) for a better understanding of the determinants of QoL and its optimization after immunotherapy through the development of innovative analytic tools (artificial intelligence and causal models).
  • Produce policies and recommendations to improve patients QoL and participate in the implementation of the SDGs (Sustainable Development Goals) for 4P medicine (Predictive, Preventive, Personalized, Participative) in immunotherapy for cancer patients.
Being tested
QoL & irAEs determinants
Keywords
hematologic tumor, immunotherapy, immune checkpoint inhibitor, CAR-T cell, cancer, QoL, HR-QoL, irAEs
Medical subject headings
Hematologic Neoplasms, Neoplasms

What participants receive

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

  • QoL & irAEs determinantsOther

    Assesment of the QoL \& irAEs determinants in patients diagnosed with solid tumor and treated in France, Netherlands, Portugal, Spain, with immunotherapy by immune checkpoint inhibitors.

  • QoL & irAEs determinantsOther

    Assesment of the QoL \& irAEs determinants in patients diagnosed with hematologic cancer and treated in France, Netherlands, Portugal, Spain, by CAR-T cells.

Study groups in NCT05626764
Study groupRoleWhat they receive
Immune checkpoint inhibitorsAny immunotherapy by immune checkpoint inhibitor molecule in combination or monotherapy, associated or no with any other cancer treatment such as chemotherapy, targeted therapy, radiotherapy, etc.
Receives: Other: QoL & irAEs determinants
CAR-T cellsTransplantation of recombined autologous immune T-cells
Receives: Other: QoL & irAEs determinants

What is being measured

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

  1. Assesment of the QoL& irAEs determinants in patients diagnosed with solid or hematologic cancer and treated in France, Netherlands, Portugal, Spain, with immunotherapy by immune checkpoint inhibitors or CAR-T cells.

    Descriptive analysis of QoL determinants (which are there ? what are their impacts ? etc) based on collected data from the beginning of the treatment to 2 years.

    Measured: Clinical data will be collected during 18 months starting from treatment initiation, or until the last patient reaches the 18 months follow-up. Clinical and biological changes occurring during the treatment will be assessed and compared to baseline. QoL

Timeline

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

  1. First posted25 Nov 2022
  2. Study start27 Jan 2020
  3. Primary completionDec 2023 (estimated)
  4. Study completionDec 2024 (estimated)

Resources

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
Other
Time perspective
Other
Enrolment
3,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05626764
Sponsor's protocol ID
346
Status last verified
Nov 2022
First submitted
25 Oct 2022
Last updated
25 Nov 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Vinke PC, Combalia M, de Bock GH, Leyrat C, Spanjaart AM, Dalle S, Gomes da Silva M, Fouda Essongue A, Rabier A, Pannard M, Jalali MS, Elgammal A, Papazoglou M, Hacid MS, Rioufol C, Kersten MJ, van Oijen MG, Suazo-Zepeda E, Malhotra A, Coquery E, Anota A, Preau M, Fauvernier M, Coz E, Puig S, Maucort-Boulch D. Monitoring multidimensional aspects of quality of life after cancer immunotherapy: protocol for the international multicentre, observational QUALITOP cohort study. BMJ Open. 2023 Apr 27;13(4):e069090. doi: 10.1136/bmjopen-2022-069090.

    PubMed 37105689

Questions about this trial

What is this clinical trial studying?

An observational study of Solid Tumor and Hematologic Cancer, run by Hospices Civils de Lyon at 5 sites in 4 countries.

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 4 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 25 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Netherlands, France, Portugal, Spain. 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 Delphine MAUCORT-BOULCH, PhD (+33 4 78 86 57 64, delphine.maucort-boulch@chu-lyon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assesment of the QoL& irAEs determinants in patients diagnosed with solid or hematologic cancer and treated in France, Netherlands, Portugal, Spain, with immunotherapy by immune checkpoint inhibitors or CAR-T cells. (time frame: Clinical data will be collected during 18 months starting from treatment initiation, or until the last patient reaches the 18 months follow-up. Clinical and biological changes occurring during the treatment will be assessed and compared to baseline. QoL). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05626764, which also lists 1 linked publication.

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 25 Nov 2022.

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