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Combination Salvage Therapy With Venetoclax and Decitabine in Relapsed/Refractory AML

Phase 2
Recruiting
Conditions
MDS
AML
Interventions
Registration Number
NCT06156579
Lead Sponsor
University Hospital Tuebingen
Brief Summary

The goal of this prospective, phase II single center, one arm, open label clinical trial is to test the efficacy and feasibility of a combination salvage therapy with Venetoclax and intensified Decitabine in patients with newly diagnosed AML (acute myeloid leukemia) and primary induction failure and patients with relapse of AML/MDS IB2 (myelodysplastic neoplasm with increased blasts 2) after chemotherapy. The primary endpoint is hematologic remission after treatment with Decitabine and Venetoclax. Participants eligible for the trial will receive a treatment of ten days of Decitabine and twenty-eight days of Venetoclax for one or two cycles, after which hematological remission will be assessed. Follow up will include the first one hundred days after end of treatment.

Detailed Description

This is a prospective, phase II single center one arm, open label clinical trial testing the efficacy and feasibility of a combination salvage therapy with Venetoclax and intensified Decitabine in relapsed or refractory AML and MDS IB2. Enrolled will be twenty-seven patients with newly diagnosed AML and primary induction failure to conventional anthracycline-based induction chemotherapy, as well as patients with a relapse of AML oder MDS IB2 after chemotherapy. Patients will receive a combination therapy of ten days of Decitabine and twenty-eigt days of Venetoclax. If hematologic remission is not achieved after one cycle of treatment, patients receive a second cycle. After treatment, a follow-up period of 100 days will ensue. The main aim of the trial is the assessment of hematologic remission after combining Venetoclax with a time-dense immediate application of the hypomethylating agent Decitabine after failure of a chemotherapy approach, thus additionally altering backbone treatment modalities from chemotherapy to epigenetic and anti-BCL2 (B-cell lymphoma 2) treatment. A first assessment of safety and feasibility will take place after the treatment of three patients and a second assessment for safety, feasibility and efficacy/futility after nine patients.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
27
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
TreatmentVenetoclaxSalvage therapy with Venetoclax and intensified Decitabine
TreatmentDecitabineSalvage therapy with Venetoclax and intensified Decitabine
Primary Outcome Measures
NameTimeMethod
Rate of hematological remissionsmeasured after the first and second cycle (each cycle is 28 days)

Hematologic remission (defined as morphologically leukemia-free state (MLFS), complete remission (CR), complete remission with incomplete hematological recovery (CRi) or complete remission with partial hematological recovery (CRh)) as best response in bone marrow aspiration cytomorphology\*) after one or two cycles of Decitabine/Venetoclax.

\* or bone marrow pathology, if aspiration morphology not available, not representative or not judged sufficiently reliable by treating physician

Secondary Outcome Measures
NameTimeMethod
Overall survivalday 100 after end of treatment

defined as rate of patients alive at day 100 after end of treatment (and time dependent)

Early Mortalityday 30 after start of treatment

Defined as patients no longer alive at day 30 after start of treatment

Rate of CTCAEs ≥ Grade 3observed during the first and second cycle (each cycle is 28 days) and until day 30 after therapy application

evaluated by the incidence of CTCAEs ≥ Grade 3

Time to hematopoietic recovery in daysafter each chemotherapy treatment cycle (28 days), defined as the time from the start of the cycle until recovery

hematopoietic recovery defined as absolute neutrophil counts ≥0.5 and ≥1.0 x 109/L; platelets ≥50 and ≥100 x 109/L)

Rate of MRD-negativity (measurable residual disease)measured at each remission assessment (C1D15, C1D28, C2D28, Follow Up)

MRD including qPCR for established MRD markers and NGS for exploratory MRD markers is evaluated at each remission assessment

Rate of infectious complications CTCAEs ≥ grade 3measured during the first and second cycle and the first 30 days after end of treatment (each cycle is 28 days)

evaluated by the incidence of infections CTCAEs ≥ grade 3

Time to transplant in daysuntil day 100 after end of treatment

defined as days from diagnosis of primary induction failure or relapse to infusion of allogeneic hematopoietic stem cells

Progression-free survivalday 100 after end of treatment

defined as rate of patients alive without hematological progression at day 100 after end of treatment (and time dependent)

Quality of Life (European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ C30))at screening and at the end of cycle one and two (one cycle is 28 days) and at follow up (day 100 after end of treatment)

evaluated with the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ C30) at screening, and at the end of cycle one and two, as well as at follow up; scale scores ranging from 0 to 100 with higher scores indicating better outcomes

Hospitalisation daysDay 1 of therapy until day 30 after end of treatment

Hospitalisation days, defined as days in hospital (days in the outpatient clinic are not counted) from day 1 of therapy until day 30 after end of treatment

ECOG prior to start of conditioning for transplantbetween end of treatment and follow up

ECOG prior to start of conditioning for transplant in all patients who proceed to alloHSCT

Trial Locations

Locations (1)

University Hospital

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Tuebingen, Baden-Wuerttemberg, Germany

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