Oral Azacitidine Maintenance Post-CPX 351

NCT06349239 | Recruiting

• 1 other identifier: 24Hemato01
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

Approximately 10% of patient develop AML after chemotherapy or radiation for unrelated disease (t-AML) and 20% have AML with an antecedent hematologic disorder (AML-MRC). CPX-351 (Vyxeos), a liposomal formulation of a fixed molar ratio (1:5) daunorubicin and cytarabine, has been approved for treatment of adults with newly diagnosed t-AML or AML-MRC. CPX-351 significantly improved median overall survival. Although induction chemotherapy results in remission in many older patients with AML, relapse is common and overall survival is poor. For patients not eligible for HSCT, maintenance therapies are needed to reduce the risk of relapse and prolong overall survival without causing undue adverse effects or compromising health-related quality of life. Oral azacitidine (ONUREG) has been approved by FDA on September, 2020, to treat adult patients with AML who achieved CR or CRi following intensive induction chemotherapy with or without consolidation and who are not able to complete intensive curative therapy (not candidate to HSCT). The use of oral azacitidine maintenance is an integral part of clinical practice for AML patients who have achieved a first complete remission (CR) or complete remission with incomplete blood count recovery (CRi) after intensive ""3+7"" induction chemotherapy and who are unable to complete intensive curative therapy. But there are few data on its efficacy as a post-CPX-351 maintenance agent in patients with newly diagnosed t-AML or AML-MRC or de novo AML.THe aim of this study is to show the improvement of overall survival with use of oral Azacitidine as maintenance for patients with de novo AML including t-AML or AML-MRC who achieved complete remission or complete remission with incomplete blood count recovery after CPX-351. Long-term product safety is also being studied

Conditions

Acute Myeloid Leukemia

Keywords

ONUREG; AML de novo

Outcome Measures

Primary Outcomes (1)

• overall survival

  evalute overal survival

  from first administration of ONUREG to death from any cause, assessed up to 60 moths

Secondary Outcomes (1)

• Safety and tolerance

  from first administration of ONUREG to death from any cause, assessed up to 60 months

Interventions

No intervention OTHER

Follow-up of disease

Eligibility Criteria

• Age: 64 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patient with de novo AML, therapy-related AML or AML with myelodysplasia related changes in first remission (CR1, CRi1, CRh1 according to IWG) after CPX-351 induction with or without CPX-351 consolidation.

You may qualify if:

• Male or female subjects \> 64 years of age at the time of C1J1 CPX-351
• de novo AML including t-AML or AML-MRC according to WHO 2016
• Should have undergone induction therapy with CPX-351 with or without CPX-351 consolidation
• Patients in first line of treatment
• Should have achieved first CR/CRi/CRh status according to IWG criteria
• ECOG performance status of 0,1,2,3

You may not qualify if:

• Prior bone marrow or stem cell transplantation
• patients having achieved CR/CRi following an added therapy
• Patients alive at the start of the study who did not receive study information or who objected to the collection of data

Sponsors & Collaborators

• Centre Hospitalier Universitaire de Nice: lead

Study Sites (1)

CHU de Nice

Nice, France

RECRUITING

MeSH Terms

Conditions

Leukemia, Myeloid, Acute

Condition Hierarchy (Ancestors)

Leukemia, Myeloid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases

Central Study Contacts

Thomas Cluzeau, Pr

CONTACT

0492039025; cluzeau.t@chu-nice.fr

Caroline Fineli

CONTACT

0617430432; fileni.c@chu-nice.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 22, 2024
• First Posted: April 5, 2024
• Study Start: January 1, 2020
• Primary Completion: January 1, 2025
• Study Completion: January 1, 2025
• Last Updated: April 5, 2024

Record last verified: 2024-03

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)