Clinical Phase III Trial Treosulfan-based Conditioning Versus Reduced-intensity Conditioning (RIC)

Phase 3

Completed

• Conditions: Acute Myeloid Leukemia; Myelodysplastic Syndrome
• Interventions: Drug: Busulfan; Drug: Treosulfan

• Registration Number: NCT00822393
• Lead Sponsor: medac GmbH

Brief Summary

This randomized allogeneic transplantation protocol compares i.v. Treosulfan-based conditioning therapy with reduced intensity i.v. Busulfan-based conditioning in adult AML and MDS patients at increased risk for standard conditioning therapies. The protocol is based on results of previous phase I/II trials evaluating Treosulfan/Fludarabine conditioning prior to allogeneic haematopoietic stem cell transplantation. The reference arm (reduced intensity i.v. Busulfan/Fludarabine) is considered to be accepted medical practice for the study patient population.

Detailed Description

To compare efficacy and safety of Treosulfan-based conditioning (test) with i.v. Busulfan-based reduced intensity conditioning (reference).

The statistical aim of the study is to show non-inferiority with respect to:

Event-free survival (EFS) within 2 years after transplantation. Events are defined as relapse of disease, graft failure or death (whatever occurs first).

1. Comparative evaluation of incidence of CTC grade III/IV mucositis/stomatitis between day -6 and day +28

2. Comparative evaluation of overall survival (OS) and cumulative incidence of relapse (RI) as well as non-relapse mortality (NRM) and transplantation-related mortality (TRM)within 2 years after transplantation

3. Comparative evaluation of day +28 conditional cumulative incidence of engraftment

4. Comparative evaluation of day +28 and day +100 incidence of complete donor-type chimerism

5. Comparative evaluation of cumulative incidence of acute and chronic GvHD within 2 years after transplantation

6. Comparative evaluation of incidence of other CTC grade III/IV adverse events between day -6 and day +28

Individual patients will be followed-up for at most 2 years after transplantation. Three confirmatory interim evaluations and one final analysis are planned, which allow to stop the trial as soon as the question of non-inferiority is answered (as outlined below). In addition, post-surveillance with respect to OS and EFS will be conducted one year after transplantation of the last randomised patient.

Study Timeline

• Study Start: 2008-11-24
• Study First Submitted: 2009-01-13
• Study First Submitted QC: 2009-01-13
• Study First Posted: 2009-01-14
• Primary Completion: 2018-01-25
• Study Completion: 2018-01-25
• Status Verified: 2020-07
• Last Update Submitted: 2020-07-29
• Last Update Posted: 2020-07-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 570

Inclusion Criteria

1. Patients with acute myeloid leukaemia acc. to WHO, 2008 (AML in complete remission at transplant, i.e. blast counts < 5 % in bone marrow) or myelodysplastic syndrome acc. to WHO, 2008 (MDS with blast counts < 20 % in bone marrow during disease history) indicated for allogeneic haematopoietic progenitor cell transplantation but considered to be at increased risk for standard conditioning therapies according to the following criteria:

   • patients aged ≥ 50 years at transplant and / or
   • patients with a HCT-CI score > 2 [acc. to Sorror et al., 2005]

2. Availability of an HLA-identical sibling donor (MRD) or HLA-identical unrelated donor (MUD). Donor selection is based on molecular high resolution typing (4 digits) of class II alleles of the DRB1 and DQB1 gene loci and molecular (at least) low resolution typing (2 digits) of class I alleles (i.e., antigens) of the HLA- A, B, and C gene loci. In case, no class I and class II completely identical donor (10 out of 10 gene loci) can be identified, one antigen disparity (class I) and/or one allele disparity (class II) between patient and donor are acceptable. Conversely, disparity of two antigens (irrespective of the involved gene loci) cannot be accepted. These definitions for the required degree of histocompatibility apply to the selection of related as well as of unrelated donors.

3. Adult patients of both gender, age 18 - 70 years

4. Karnofsky Index ≥ 60 %

5. Written informed consent

6. Men capable of reproduction and women of childbearing potential must be willing to consent to using a highly effective method of birth control such as condoms, implants, injectables, combined oral contraceptives, IUDs, sexual abstinence or vasectomised partner while on treatment and for at least 6 months thereafter

Exclusion Criteria

1. Patients with acute promyelocytic leukaemia with t(15;17)(q22;q12) and in CR1

2. Patients considered contra-indicated for allogeneic HSCT due to severe concomitant illness (within three weeks prior to scheduled day -6):

   • patients with severe renal impairment like patients on dialysis or prior renal transplantation or S-creatinine > 3.0 x ULN or calculated creatinine-clearance < 60 ml/min
   • patients with severe pulmonary impairment, DLCOsb (Hb-adjusted)/or FEV1 < 50 % or severe dyspnoea at rest or requiring oxygen supply
   • patients with severe cardiac impairment diagnosed by echocardiography and LVEF < 40 %
   • patients with severe hepatic impairment indicated by hyperbilirubinaemia > 3 x ULN or ALT / AST > 5 x ULN

3. Active malignant involvement of the CNS

4. HIV-positivity, active non-controlled infectious disease under treatment (no decrease of CRP or PCT) including active viral liver infection

5. Previous allogeneic HSCT

6. Pleural effusion or ascites > 1.0 L

7. Pregnancy or lactation

8. Known hypersensitivity to treosulfan, busulfan and/or related ingredients

9. Participation in another experimental drug trial within 4 weeks prior to day -6 of the protocol

10. Non-cooperative behaviour or non-compliance

11. Psychiatric diseases or conditions that might compromise the ability to give informed consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Busulfan	Busulfan
2	Treosulfan	Treosulfan

Primary Outcome Measures

Name	Time	Method
Event-free survival (EFS)	within 2 years after transplantation

Secondary Outcome Measures

Name	Time	Method
Comparative evaluation of incidence of CTC grade III/IV mucositis/stomatitis between day -6 and day +28	between day -6 and day +28

Trial Locations

Locations (33)

Ospedale Civile Pescara; 🇮🇹 Pescara, Italy

Universitätsklinikum Freiburg; 🇩🇪 Freiburg, Germany

Klinikum Nürnberg, 5. Medizinische Klinik; 🇩🇪 Nürnberg, Germany

Universität Tübingen; 🇩🇪 Tübingen, Germany

Universitätsmedizin Goettingen, Haematolgie und Onkologie; 🇩🇪 Göttingen, Germany

Universitätsklinikum Heidelberg; 🇩🇪 Heidelberg, Germany

Policlinico GB Rossi (Borgo Roma), Div. di Ematologia; 🇮🇹 Verona, Italy

Universitätsklinikum Leipzig, Haematologie, internistische Onkologie; 🇩🇪 Leipzig, Germany

Universitätsklinikum Koeln, Stammzelltransplantation; 🇩🇪 Koeln, Germany

Policlinico Umberto I Univ. La Sapienza; 🇮🇹 Rome, Italy

Johannes-Gutenberg-Universität Mainz, III. Medizinische Klinik; 🇩🇪 Mainz, Germany

Hopital Saint-Louis; 🇫🇷 Paris, France

Silesian Medical University; 🇵🇱 Katowice, Poland

Azienda Ospedaliera Papa Giovanni XXIII; 🇮🇹 Bergamo, Italy

Hematology University of Brescia; 🇮🇹 Brescia, Italy

Scientific Institute H. San Raffaele; 🇮🇹 Milan, Italy

Clinica Ematologica ed Unita di Terapie Cellulari 'Carlo Melzi'; 🇮🇹 Udine, Italy

Klinikum der Universität Würzburg; 🇩🇪 Würzburg, Germany

Medical University of Gdansk; 🇵🇱 Gdansk, Poland

Helsinki University Central Hospital, Dept. of Medicine; 🇫🇮 Helsinki, Finland

Klinikum Rechts der Isar der TU München, III. Med. Klinik; 🇩🇪 Muenchen, Germany

Universität Rostock; 🇩🇪 Rostock, Germany

Klinikum Oldenburg gGmbH; 🇩🇪 Oldenburg, Germany

Stiftung Deutsche Klinik für Diagnostik; 🇩🇪 Wiesbaden, Germany

Centre Hospitalier Lyon Sud; 🇫🇷 Lyon, France

Malteser Krankenhaus St. Franziskus-Hospital; 🇩🇪 Flensburg, Germany

Klinik für Knochenmarktransplantation; 🇩🇪 Essen, Germany

Asklepios Kliniken Hamburg GmbH; 🇩🇪 Hamburg, Germany

Universitätsklinikum Carl Gustav Carus Dresden, Med. Klinik I; 🇩🇪 Dresden, Germany

Klinikum der Universität Regensburg; 🇩🇪 Regensburg, Germany

Universitätsklinikum Münster; 🇩🇪 Münster, Germany

St. Istvan and St. Laszlo Hospital of Budapest; 🇭🇺 Budapest, Hungary

Friedrich-Schiller-Universität Jena; 🇩🇪 Jena, Germany