Panobinostat Maintenance After HSCT fo High-risk AML and MDS

Myelodysplastic Syndromes (MDS) Clinical Trial

Official title:

A Randomized, Multicenter Phase III Study to Assess the Efficacy of Panobinostat Maintenance Therapy vs. Standard of Care Following Allogeneic Stem Cell Transplantation in Patients With High-risk AML or MDS (ETAL-4 / HOVON-145)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04326764
• Other study ID #: ETAL-4 / HOVON-145
• Status: Terminated
• Phase: Phase 3
• Start date: July 24, 2018
• Est. completion date: February 13, 2023

Study information

• Verified date: February 2023
• Source: Goethe University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Aim of this prospective randomized trial is to compare maintenance treatment with panobinostat interspersed with donor lymphocyte infusions (DLI) versus the standard approach of pre-emptive DLI alone in patients with poor-risk AML/MDS having favorably received an allogeneic HSCT followed by engraftment, donor chimerism and hematopoietic reconstitution.

Description:

Allogeneic hematopoietic stem cell transplantation (HSCT) has been shown to improve the outcome of poor-risk AML and MDS in both younger and older patients. Reduced-intensity conditioning (RIC) regimen have partially abrogated the problem of regimen-related toxicity. However, graft-versus-host disease (GvHD) remains a major cause of non-relapse morbidity and mortality. Despite a strong graft versus leukemia (GvL) effect after allogeneic HSCT, the relapse rate after transplantation in poor-risk leukemia patients is still too high, necessitating new approaches to exploit GvL in a more optimized way. In addition, minimizing the GvHD reaction remains an important goal. One attractive strategy may be the administration of epigenetic therapy early after HSCT in order to optimize the GvL effect, to provide a direct anti-leukemic effect, and to control GvHD. Two preceding phase I/II studies have suggested that post-transplant administration of the histone deacetylase (HDAC) inhibitor panobinostat may be associated with a reduced relapse rate, while allowing for control of GvHD. Based on these two studies, the hypothesis of the present trial is that panobinostat can be an effective drug in preventing relapse by optimizing GvL in MDS and AML patients with high-risk features after HSCT, while at the same time reducing GvHD. It has been designed to test this hypothesis in a prospective randomized trial comparing maintenance with panobinostat interspersed with donor lymphocyte infusions (DLI) versus the standard approach of pre-emptive DLI alone in patients with poor-risk AML/MDS having favorably received an allogeneic HSCT followed by engraftment, donor chimerism and hematopoietic reconstitution.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 52
• Est. completion date: February 13, 2023
• Est. primary completion date: February 13, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Adult patients (18-70 years of age)
• AML (except acute promyelocytic leukemia with PML-RARA and AML with BCR-ABL1) according to WHO 2016 classification with high-risk features defined as one or more of

the following criteria:

• refractory to or relapsed after at least one cycle of standard chemotherapy
• > 10% bone marrow blasts at day 14-21 of the first induction cycle
• adverse risk according to ELN 2017 risk stratification by genetics (Appendix 2) regardless of stage
• secondary to MDS or radio-/chemotherapy
• MRD positive before HSCT based on flow cytometry or PCR or
• MDS with excess blasts (MDS-EB) according to the WHO 2016 classification, or high-risk or very high-risk according to IPSS-R and First allogeneic HSCT scheduled within the next 4-6 weeks using one of the following

donors, conditioning regimens and strategies for GvHD prophylaxis:

1. Matched sibling or matched unrelated donor (i.e. 10/10 or 9/10 HLA-matched) or haploidentical family donor

2. Conditioning regimens:

1. Reduced-intensity conditioning:

a. Fludarabine/Melphalan b. Fludarabine/Busulfan2 (FB2) (2) Myeloablative conditioning:

1. Fludarabine/Busulfan4 (FB4)

2. Busulfan/Cyclophosphamide (BU/CY)

3. Fludarabine/TBI 8 Gy

4. Cyclophosphamide/TBI 12 Gy (3) Fludarabine/Cyclophosphamide/TBI 2 Gy in combination with post-Tx cyclophosphamide (TP-CY) only (4) Thiotepa/Busulfan/Fludarabine (TBF) in the context of an haploidentical HSCT only (5) In case of active disease at HSCT, salvage chemotherapy prior to conditioning is permitted

c. Strategies for GvHD prophylaxis:

1. HLA-matched donors:

a. CSA + MMF +/- ATG b. CSA + MTX +/- ATG c. PT-CY + CSA

2. Haploidentical donors:

d. PT-CY + CSA + MMF

• No history of significant cardiac disease and absence of active symptoms, otherwise documented left ventricular EF = 40%
• Written informed consent for registration

Exclusion Criteria:

• Prior treatment with a DAC inhibitor
• Hypersensitivity to the active substance or to any of the excipients of panobinostat
• HIV or HCV antibody positive
• Psychiatric disorder that interferes with ability to understand the study and give informed consent, and/or impacts study participation or follow-up.
• Female patients who are pregnant or breast feeding
• History of another primary malignancy that is currently clinically significant or currently requires active intervention

Related Conditions & MeSH terms

• Acute Myeloid Leukaemia (AML)
• Leukemia, Myeloid, Acute
• Myelodysplastic Syndromes
• Myelodysplastic Syndromes (MDS)
• Preleukemia

Intervention

Drug:
• Panobinostat
Panobinostat should be taken orally once on each scheduled day at about the same time, either with or without food. Each dose of panobinostat should be taken with a cup of water. The capsules should be swallowed as whole. If vomiting occurs during the course of treatment, no re-dosing is allowed before the next scheduled dose. If one dose is forgotten during the morning on a scheduled treatment day then the missed dose should be taken on that same day within 12 hours. After more than 12 hours, that day's dose should be withheld, and the patient should wait to take panobinostat until the next schedule treatment day. The patient should then continue treatment with the original dosing schedule. Panobinostat will be administered at a dose of 20 mg three times weekly (TIW) every second week and will be dosed on a flat scale of mg/day and not by weight or body surface area. Panobinostat will be dispensed as a 20 mg capsule or as two 10 mg capsules.

Locations

Country	Name	City	State
Germany	Klinikum Augsburg	Augsburg
Germany	University Hospital Bonn	Bonn
Germany	Universtity Hospital Dresden	Dresden
Germany	University Hospital Frankfurt	Frankfurt
Germany	University Hospital Hamburg-Eppendorf	Hamburg
Germany	University Hospital Jena	Jena	Thüringen
Germany	Universitätsklinikum Leipzig	Leipzig	Thüringen
Germany	Otto-von-Guericke University	Magdeburg
Germany	Universitätsmedizin Mainz	Mainz
Germany	Klinikum Mannheim	Mannheim
Germany	Philipps-Universität Marburg	Marburg
Germany	University Hospital Münster	Münster
Germany	Klinikum Nürnberg Nord	Nürnberg
Germany	Robert Bosch Krankenhaus	Stuttgart	Baden-Württemberg
Netherlands	Amsterdam University Medical Center - VUMC	Amsterdam
Netherlands	University Medical Center Groningen	Groningen
Netherlands	Maastricht University Medical Center	Maastricht
Netherlands	Radboud UMC	Nijmegen
Netherlands	Erasmus University Medical Center	Rotterdam

Sponsors (4)

Lead Sponsor	Collaborator
Goethe University	Polish Adult Leukemia Group, Schweizerische Arbeitsgemeinschaft für klinische Krebsforschung, Stichting Hemato-Oncologie voor Volwassenen Nederland

Countries where clinical trial is conducted

Germany,  Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival (OS)	OS is measured from date of randomization to the date of death or date of last follow up. Observations of patients alive at last follow up will be censored at date of last follow up.	5 years
Secondary	Event-free survival (EFS)	EFS is defined as time interval from randomization until relapse of MDS or AML, any treatment of molecular relapse (except DLI) or death from any cause, whichever occurs first. Observations of patients without any event will be censored at time of last follow up.	5 years
Secondary	Disease-free survival (DFS)	DFS is defined as time interval from randomization until relapse of MDS or AML, or death from any cause, whichever occurs first. Observations of patients without any event will be censored at time of last follow up.	5 years
Secondary	Cumulative incidence of hematologic relapse	Remission duration is defined as time from randomization until relapse (including any treatment (except DLI) of molecular relapse). Death in complete remissions (CR) is considered as competing event for relapse. Patients for whom no relapse nor death in CR was observed will be censored at date of last follow up.	5 years
Secondary	Cumulative incidence, time and cause of non-relapse mortality (NRM)	Time to NRM is defined as time from randomization until death in CR from any cause. Relapse is considered as competing event for NRM. Patients for whom no death in CR nor relapse was observed will be censored at date of last follow up.	5 years
Secondary	Cumulative incidence of new onset or aggravation of acute GvHD grade III-IV	Cumulative incidence of new onset or aggravation acute GvHD grade III-IV is calculated as number of patients who newly experienced acute GvHD grade III-IV after randomization or whose preexisting lower grade acute GvHD aggravated to grade 3 or 4 divided by all patients in the analysis set. Cumulative incidence is calculated separately for each arm.	5 years
Secondary	Cumulative incidence and maximal grade of severity of chronic GvHD requiring systemic treatment within one year after HSCT	Acute and chronic GvHD will be graded according to NIH consensus criteria. In case of chronic GvHD, evaluation forms provided by the NIH Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host-Disease should be used.; Time to chronic GvHD requiring systemic treatment is defined time from randomization until date of first diagnosis of chronic GvHD requiring systemic treatment. Relapse and death in CR without chronic GvHD requiring systemic treatment are considered as competing events. Patients for whom no chronic GvHD, nor relapse, nor death in CR was observed will be censored at date of last follow up.	1 year
Secondary	Percentage of patients who are free of systemic immunosuppressive therapy at one and two years after HSCT	Percentage of patients who are free of systemic immunosuppressive therapy is calculated as number of patients who are free of systemic immunosuppressive therapy at the respective time point divided by the total number of patients in the analysis set multiplied by 100. The percentage is calculated separately for each arm.	2 years
Secondary	Percentage of patients completing the one year study treatment and duration of panobinostat administration in patients who discontinue study treatment prematurely	Percentage of patients completing the one year study treatment is calculated as number of patients completing the one year study treatment divided by the total number of patients in the analysis set multiplied by 100. The percentage is calculated for the panobinostat arm only.; The duration of panobinostat administration is calculated from date of first administered dose of study medication until date of last administered dose of study medication.	1 year
Secondary	Percentage of patients with minimal residual disease (MRD) conversion from baseline to 6 months after HSCT	Percentage of patients with MRD conversion from baseline to 6 months after HSCT is calculated as number of patients who were MRD positive at baseline and are MRD negative at 6 months after HSCT divided by the number of patients who were MRD positive at baseline.; Patients who were MRD negative at baseline will not be considered in this endpoint.	6 months
Secondary	Patient-reported HRQoL during panobinostat maintenance therapy	Patient reported health-related quality of life will be assessed using the cancer generic 'European Organization for Research and Treatment of Cancer' quality of life questionnaire.	4 years