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AzTrials

Myelodysplastic Syndromes (MDS)CDA-AML-MDSNCT06886425

Involvement of CDA and/or dCK Metabolizing Enzymes in the Response to Azacytidine Treatment of Patients With Hematologic Malignancies

A study testing genetic study, Pharmacokinetic study and Study of phenotypic activity of cytidine deaminase in people with Myelodysplastic Syndromes (MDS) and Leukemia Acute Myeloid - AML, run by Assistance Publique Hopitaux De Marseille at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Until now, the development of personalized medicine in oncology has relied on the use of somatic biomarkers to help therapists choose the right molecule(s) to administer, based on the genetic and molecular profile of each hematological disease. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
genetic study, Pharmacokinetic study and Study of phenotypic activity of cytidine deaminase
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
1 siteFrance
Study dates
14 Jun 2021to 14 Jun 2028
Phase
Interventional
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

Who may be able to join

  • Patients over 18 years of age
  • Patients with acute myeloid leukemia
  • Patient with myelodysplastic syndrome
  • Person who has given non-opposition
  • Patient who has signed an authorization to perform a constitutional genetic analysis (in the context of care)
  • Need for effective contraception in patients of childbearing age

Who cannot join

  • Failure to obtain non-opposition
  • Adults under guardianship or safeguard of justice
  • Persons deprived of their liberty
  • Patient participating in another research project
  • Pregnancy in progress

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • Hôpital de la Conception

    Marseille, 13005

    Geoffroy Venton, 0491435817 ext. 33, GEOFFROY.VENTON@ap-hm.fr

    Recruiting

Other trials in France

About this study

Until now, the development of personalized medicine in oncology has relied on the use of somatic biomarkers to help therapists choose the right molecule(s) to administer, based on the genetic and molecular profile of each hematological disease. In this project, investigators propose to extend the strategy of therapeutic individualization to the field of dosage targeting. Today, azacytidine is a standard treatment for patients with acute myeloid leukemia (AML) and/or myelodysplastic syndromes (MDS), usually as monotherapy. According to the treatment regimen, azacytidine is prescribed at a standard dose (DS=75mg/m²/d), administered subcutaneously every day for 7 days. The treatment cycle is repeated every 28 days.

No study has evaluated the relevance of "a priori" dose adjustment on an individual basis, according to each patient's pharmacogenetic data. In current practice, doses are adapted a posteriori, and reduced empirically, following the occurrence of observed toxicity (6 to 71% of patients) (Schuck A et al. 2017). This ex-post adjustment in the face of grade 3-4 toxicity is a loss of chance for the patient. Similarly, under-dosing patients for fear of toxicity is another loss of chance. Investigator's hypothesis is that the optimal dose of azacytidine depends not only on the characteristics of the patient's pathology (risk groups including cytogenetic and molecular biology data), but also on the patient's individual characteristics (genetic status of metabolic enzymes and transporters). A mathematical model of the PK/PD type could, on the basis of early observations of circulating levels, be capable of rapidly predicting the pharmacodynamic repercussions in each patient, thus enabling rapid individualization of dosages. In the future, such a tool could make it possible to propose dosage adjustments rapidly after treatment initiation, before toxicity occurs, by predicting azacytidine exposure levels, themselves correlated with the patient's clinical condition.

Read more

Study design: In this open-label, paucicentric, non-randomized study, patients with AML and/or MDS, all of whom are receiving azacytidine-based chemotherapy as part of their standard treatment regimen, will be included. Each patient will be monitored for toxicities (EORTC), treatment response and progression-free survival. In addition to the standard care described above, each patient will undergo a series of constitutional genetic investigations conducted by NGS on markers linked to azacytidine pharmacokinetics (CDA, dCK). Another series of blood samples will be taken to calculate individual azacytidine pharmacokinetic parameters using a Bayesian approach.

Expected results: This study should make it possible to correlate pharmacogenetics with patient plasma exposure, and ultimately improve the molecule's efficacy/toxicity balance by personalizing dosage regimens, which until now have been carried out on an empirical basis.

Prospects: If the data are validated, a pre-therapeutic ADC assay could predict azacytidine pharmacodynamics and enable individual dose and/or dosage adjustment, as is the case with 5-FU and DPD.

Being tested
genetic study, Pharmacokinetic study, Study of phenotypic activity of cytidine deaminase
Medical subject headings
Myelodysplastic Syndromes

What participants receive

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

  • genetic studyOther

    Blood sampling :

    Cure 1 before starting treatment Cure 3 before starting treatment Cure 6 after completion of treatment

  • Pharmacokinetic studyOther

    Cure 1: after completion of subcutaneous administration of azacytidine A total of 5 samples in the induction phase.

    Cure 3: after completion of subcutaneous administration of azacytidine A total of 5 samples in the induction phase.

    Cure 6: after completion of subcutaneous administration of azacytidine A total of 5 samples in the induction phase.

  • Study of phenotypic activity of cytidine deaminaseOther

    Blood sampling :

    Cure 1 before starting treatment Cure 3 before starting treatment Cure 6 after completion of treatment

Study groups in NCT06886425
Study groupRoleWhat they receive
Blood samplingExperimentalBlood sampling through the differents cures of the patients
Receives: Other: genetic study; Other: Pharmacokinetic study; Other: Study of phenotypic activity of cytidine deaminase

What is being measured

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

  1. Plasma dosage of azacytidine

    assessment of the relationship between azacytidine pharmacokinetic profile and cytidine deaminase status

    Measured: Through study completion, an average of 2 years

Secondary outcomes (2)
  1. phenotypic activity of CDA

    searched by Sanger on a ThermoFischer 3500 Dx Genetic automaton using standard procedures, after identification of the most informative regions (exons, promoters). Haplotypic recombinations will be searched for using Haploview software.

    Measured: Through study completion, an average of 2 years

  2. Determination of ADC genotype

    searched by Sanger on a ThermoFischer 3500 Dx Genetic automaton using standard procedures, after identification of the most informative regions (exons, promoters). Haplotypic recombinations will be searched for using Haploview software.

    Measured: Through study completion, an average of 2 years

Timeline

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

  1. First posted20 Mar 2025
  2. Study start14 Jun 2021
  3. Primary completion1 Jan 2027 (estimated)
  4. Study completion14 Jun 2028 (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
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
70 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06886425
Sponsor's protocol ID
RCAPHM19_0333
Other IDs
2020-A02042-37
Acronym
CDA-AML-MDS
Status last verified
Oct 2026
First submitted
7 Mar 2025
Last updated
28 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing genetic study, Pharmacokinetic study and Study of phenotypic activity of cytidine deaminase in people with Myelodysplastic Syndromes (MDS) and Leukemia Acute Myeloid - AML, run by Assistance Publique Hopitaux De Marseille at 1 site 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 6 inclusion and 5 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 Oct 2026. 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 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 Geoffroy Venton (0491435817 ext. 33, GEOFFROY.VENTON@ap-hm.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Plasma dosage of azacytidine (time frame: Through study completion, an average of 2 years). 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 Oct 2026.

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