Matched Unrelated vs. Haploidentical Donor for Allogeneic Stem Cell Transplantation in Patients With Acute Leukemia

Phase 2Active Not RecruitingNCT04232241

Universitätsklinikum Hamburg-Eppendorf167 enrolled

Overview

Primary objective of this open label, two-arm, multicenter, multinational, randomized trial is to compare anti-leukemic activity of allogeneic stem cell transplantation for patients with acute leukemia in complete remission between a 10/10 HLA matched unrelated donor and a haploidentical donor. The hypothesis: Haploidentical stem cell transplantation with post cyclophosphamide induces a stronger anti-leukemic activity in comparison to 10/10 HLA matched unrelated donor and reduces the risk of relapse at 2 years after stem cell transplantation by 10%.

Secondary objectives are to assess and compare the safety and efficacy of study treatments therapy in both study arms on non-relapse mortality (NRM), relapse-free survival (RFS), Overall survival (OS), QOL, toxicity, development of acute and chronic GvDH as well as engraftment and chimerism and impact of measurable residual disease.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

167

Conditions

Acute Myeloid Leukemia in Remission Acute Lymphoblastic Leukemia in Remission Myelodysplastic Syndromes

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria 1. Acute Myeloid Leukemia (AML) intermediate or high risk according to ELN or Acute Lymphoblastic Leukemia (ALL) high risk according to ESMO guidelines in 1. CR or AML/ALL in 2. CR, or high risk MDS (according to IPSS-R) in 1. CR or 2. CR. 2. Patients age: 18 - 70 years at time of inclusion (female and male). 3. Patients understand and voluntarily sign an informed consent form. 4. ECOG ≤ 2. 5. 10/10 HLA-matched unrelated donor and haploidentical (≥ 5/10 and ≤ 8/10 HLA) relative matched donor available at least 4 weeks after completion of induction and/or consolidation therapy. 6. Females/Males who agree to comply with the applicable contraceptive requirements of the protocol. Exclusion Criteria 1. Severe renal, hepatic, pulmonary or cardiac disease, such as: * total bilirubin, SGPT or SGOT \> 3 times upper the normal level * left ventricular ejection fraction \< 30 % * creatinine clearance \< 30 ml/min * DLCO \< 35 % and/or receiving supplementary continuous oxygen 2. Positive serology for HIV. 3. Pregnant or lactating women (positive serum pregnancy test). 4. Age \< 18 and ≥ 71 years. 5. Uncontrolled invasive fungal infection at time of screening (baseline). 6. Serious psychiatric or psychological disorders. 7. Participation in another study with ongoing use of unlicensed investigational product from 28 days before study enrollment. 8. Uncontrolled severe autoimmune disease or uncontrolled other malignancy. 9. Availability of an HLA-identical sibling as donor source.

Locations (24)

LKH-Univ. Klinikum Graz

Graz, Austria

Medizinische Universität Innsbruck

Innsbruck, Austria

Medizinische Universität Wien, Universitätsklinik für Innere Medizin I Einrichtung für Stammzelltransplantation KMT

Vienna, Austria

Institute of Hematology and Blood Transfusion

Prague, Czechia

Turku University Central Hospital

Turku, Finland

University Hospital Düsseldorf

Düsseldorf, Germany

Universitätsklinikum Essen

Essen, Germany

Universitätsklinikum Frankfurt am Main | Medizinische Klinik II

Frankfurt, Germany

Universitätsklinikum Freiburg

Freiburg im Breisgau, Germany

Universitätsklinikum Hamburg-Eppendorf

Hamburg, Germany

...and 14 more locations

Outcomes

Primary Outcomes

Relapse incidence at two years between both arms

The primary efficacy endpoint will be analyzed using cumulative incidence estimation to assess the subdistribution hazard rates for both treatment groups at two years after accounting for competing risk events.

Time frame: 2 years

Secondary Outcomes

Overall survival at two years between both arms

The overall survival at two years between both arms will be presented with Kaplan-Meier's estimates of survival.

Time frame: 2 years

Overall survival for all patients assigned to one of the two treatment arms as time to event endpoint

The overall survival for all patients will be presented with Kaplan-Meier curve. To compare the survival distributions between two arms, log-rank test will be performed, and two-sided p-values will be presented. If applicable, Cox regression model stratified by the types of leukemia, types of complete remission and conditioning will be performed as sensitivity analysis.

Time frame: through study completion, an average of two yeras

Comparison of GVHD/relapse-free survival as Composite endpoint in both arms

The rate of composite endpoint in both arms will be analyzed with the same methods as for the overall survival at two years between both arms.

Time frame: Starting at day +30 (+/- 3 d) to 24 months (+/- 1 mo) after allogenic stem cell transplantation (SCT)

Comparison of non-relapsed mortality (NRM) at 1 and 2 years after allogeneic SCT in both arms

Due to the existence of competing risk events (persisting disease and relapse), NRM of each arm at 1 and 2 years after allogeneic SCT will be analyzed with the same methods as for the primary endpoint

Time frame: At 1 and 2 years after allogeneic SCT

Comparison of acute graft-versus-host disease (aGVHD) on day +100 and 1 year (max grade) after allogeneic SCT according to the Glucksberg scale revised by Przepiorka et al. between both arms

For each time point, the frequency and percentage of aGVHD (maximum grade) of each arm will be presented. To compare the difference between both arms, logistic regression adjusted for covariates and stratification factors will be performed.

Time frame: On day +100 and 1 year (max grade) after allogeneic SCT

Comparison of chronic graft-versus-host disease (cGVHD) according to the NIH consensus criteria of Jagasia et al. at 1 and 2 years after allogeneic SCT between both arms

For each time point, the frequency and percentage of cGVHD of each arm will be presented. To compare the difference between both arms, logistic regression adjusted for the stratification factors will be performed.

Time frame: At 1 and 2 years after allogeneic SCT

Comparison of toxicity of both regimens scored according to the current version of the NCI CTCAE between both arms

Safety will be analyzed with frequency of patients with AEs as described above.

Time frame: through study completion, an average of two yeras

Comparison of immune reconstitution between both arms

Frequency and percentage of patients having immune reconstitution in two arms will be provided. For the comparison between two arms, logistic regression adjusted for the stratification factors will be performed.

Time frame: At day 30, 100, 6 months, 1 year and 2 years after allogenic SCT

Comparison of full donor chimerism between both arms

Frequency and percentage of patients having full donor chimerism in two arms will be provided. For the comparison between two arms, logistic regression adjusted for the stratification factors will be performed.

Time frame: At day 30, 100, 6 months, 1 year and 2 years after allogenic SCT

Evaluation of Sorror Risk Score on outcome after allogeneic SCT

Comorbidity score after Sorror will be assessed prior to randomization and outcome in both arms will be analyzed according the pre-transplant Sorror score.

Time frame: At baseline

Comparison of QOL (FACT-BMT) before and after transplantation at + 100 days, 6 months, 1 year, 2 years between both arms

The means of change in scores at each time point (day 100, 6 months, 1 year and 2 years after transplantation respectively) from baseline and the confidence intervals of each arm will be presented. To compare the difference in QOL scores between both arms, logistic regression adjusted for covariates and stratification factors will be performed for each time point.

Time frame: At day 100, 6 months, 1 year and 2 years after allogenic SCT