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.
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
- Conditions the study is for
- Myelodysplastic Syndromes (MDS), Leukemia Acute Myeloid - AML
- 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
- Recruiting
Hôpital de la Conception
Marseille, 13005
Geoffroy Venton, 0491435817 ext. 33, GEOFFROY.VENTON@ap-hm.fr
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 group | Role | What they receive |
|---|---|---|
| Blood sampling | Experimental | Blood 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.
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)
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
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.
- First posted20 Mar 2025
- Study start14 Jun 2021
- Primary completion1 Jan 2027 (estimated)
- Study completion14 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Myelodysplastic Syndromes (MDS)Studies of the same condition, open and under way.
- More trials run by Assistance Publique Hopitaux De MarseilleThe 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 70 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assistance Publique Hopitaux De Marseille
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Involvement of CDA and/or dCK Metabolizing Enzymes in the Response to Azacytidine Treatment of Patients With Hematologic Malignancies
- ClinicalTrials.gov ID
- NCT06886425
- Acronym / sponsor ID
- CDA-AML-MDS / RCAPHM19_0333
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 70 participants (estimated)
- Lead sponsor
- Assistance Publique Hopitaux De MarseilleUniversity, hospital or other
- Study start
- 14 Jun 2021 (actual)
- Primary completion
- 1 Jan 2027 (estimated)
- Study completion
- 14 Jun 2028 (estimated)
- First posted
- 20 Mar 2025 (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.
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.
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.
Study design
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Blood sampling | Experimental | Other: genetic study, Other: Pharmacokinetic study, Other: Study of phenotypic activity of cytidine deaminaseBlood sampling through the differents cures of the patients |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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)
Key exclusion criteria (5 listed)
- 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
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 |
|---|---|---|
| genetic studyBlood sampling : Cure 1 before starting treatment Cure 3 before starting treatment Cure 6 after completion of treatment | Other | Blood sampling |
| Pharmacokinetic studyCure 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. | Other | Blood sampling |
| Study of phenotypic activity of cytidine deaminaseBlood sampling : Cure 1 before starting treatment Cure 3 before starting treatment Cure 6 after completion of treatment | Other | Blood sampling |
Primary outcome
Plasma dosage of azacytidine
Time frame: Through study completion, an average of 2 years
assessment of the relationship between azacytidine pharmacokinetic profile and cytidine deaminase status
2 secondary outcomes
phenotypic activity of CDA
Time frame: Through study completion, an average of 2 years
Determination of ADC genotype
Time frame: Through study completion, an average of 2 years
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 Oct 2026.
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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.
1 site in 1 country: see every site and its status.
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.