Treosulfan-based Conditioning in Paediatric Patients With Haematological Malignancies

NCT ID: NCT02333058

Last Updated: 2020-05-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-11-21
• Study Completion Date: 2019-09-30

Brief Summary

The primary goal of this study is to evaluate an alternative myeloablative, but reduced toxicity conditioning regimen in children, to describe the safety and efficacy of intravenous (i.v.) Treosulfan administered as part of a standardised Fludarabine-containing conditioning and to contribute to the current pharmacokinetic model to be able to finally give age (or body surface area) dependent dose recommendations. The treatment regimens given in the protocol MC-FludT.17/M are based on sufficient clinical safety and efficacy data. Considering the vital indication for allogeneic haematopoietic stem cell transplantation of the selected patient population, the risk-benefit assessment is therefore reasonably in favour of the study conduct.

Detailed Description

The protocol MC-FludT.17/M is a clinical phase II trial to describe the safety and efficacy of Treosulfan-based conditioning therapy prior to allogeneic haematopoietic stem cell transplantation (allo-HSCT) in at least 70 paediatric patients with haematological malignancies (male and female children with haematological malignant diseases as acute lymphoblastic leukaemias (ALL), acute myeloid leukaemias (AML), myelodysplastic syndromes (MDS) and juvenile myelomonocytic leukaemias (JMML), requiring myeloablative conditioning treatment with following allo-HSCT).

Treosulfan dose per day is to be calculated by using body surface area (BSA). Two background conditioning regimens with Treosulfan are allowed: One regimen consists of a standardised Fludarabine-containing regimen and the other consists of an intensified regimen with Fludarabine and ThioTEPA.

Freedom from transplant (treatment)-related mortality (TRM), defined as death from any transplant-related cause from the day of first administration of study medication until day +100 after HSCT is the primary objective of the trial.

Moreover, the current pharmacokinetic (PK) model should be contributed to be able to finally give age (or BSA) dependent dose recommendations.

Conditions

Acute Lymphoblastic Leukaemias (ALL); Acute Myeloid Leukaemias (AML); Myelodysplastic Syndromes (MDS); Juvenile Myelomonocytic Leukaemias (JMML)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treosulfan

Treosulfan dose per day is to be calculated by using BSA. One dose of Treosulfan per day on three consecutive days (day -6, day -5 and day -4) as intravenous (i.v.) infusion, given over 2 hours.

Two background conditioning regimens with Treosulfan are allowed: One regimen consists of a standardised Fludarabine-containing regimen (regimen A) and the other consists of an intensified regimen with Fludarabine and ThioTEPA (regimen B). The investigator decides for each individual patient whether to treat the patient with regimen A or with regimen B.

Treosulfan: i.v., BSA adapted: 10, 12 or 14 g/m²/day within 120 min to be administered prior to Fludarabine; Fludarabine: i.v., 30 mg/m2/day on days from -7 to -3 prior to HSCT; ThioTEPA (Regimen B): i.v., 2 x 5mg/kg/day on day -2.

Group Type: EXPERIMENTAL

Treosulfan

Intervention Type: DRUG

Treosulfan dose per day is to be calculated by using BSA:

One dose of Treosulfan per day on three consecutive days (day -6, day -5 and day -4) as intravenous (i.v.) infusion, given over 2 hours.

Two background conditioning regimens with Treosulfan are allowed: One regimen consists of a standardised Fludarabine-containing regimen (regimen A) and the other consists of an intensified regimen with Fludarabine and ThioTEPA (regimen B). The investigator decides for each individual patient whether to treat the patient with regimen A or with regimen B.

Treosulfan: i.v., BSA adapted: 10, 12 or 14 g/m²/day within 120 min to be administered prior to Fludarabine; Fludarabine: i.v., 30 mg/m2/day on days from -7 to -3 prior to HSCT; ThioTEPA (Regimen B): i.v., 2 x 5mg/kg/day on day -2.

Interventions

Treosulfan

Treosulfan dose per day is to be calculated by using BSA:

One dose of Treosulfan per day on three consecutive days (day -6, day -5 and day -4) as intravenous (i.v.) infusion, given over 2 hours.

Two background conditioning regimens with Treosulfan are allowed: One regimen consists of a standardised Fludarabine-containing regimen (regimen A) and the other consists of an intensified regimen with Fludarabine and ThioTEPA (regimen B). The investigator decides for each individual patient whether to treat the patient with regimen A or with regimen B.

Treosulfan: i.v., BSA adapted: 10, 12 or 14 g/m²/day within 120 min to be administered prior to Fludarabine; Fludarabine: i.v., 30 mg/m2/day on days from -7 to -3 prior to HSCT; ThioTEPA (Regimen B): i.v., 2 x 5mg/kg/day on day -2.

Intervention Type: DRUG

Other Intervention Names

Treograft®; Ovastat®

Eligibility Criteria

Inclusion Criteria

1. Haematological malignant disease i.e. ALL, AML, MDS or JMML, indicated for allo-HSCT.

2. Indication for first allo-HSCT or second allo-HSCT due to disease relapse, graft failure, or secondary malignancy after previous HSCT.

3. Available matched sibling donor (MSD), matched family donor (MFD) or matched unrelated donor (MUD). For bone marrow (BM) and peripheral blood (PB) match is defined as 9/10 or 10/10 allele match after four digit typing in human leucocyte antigens (HLA)-A, B, C, DRB1 and DQB1.

4. Patients with ALL or AML in complete morphologic remission (blast counts <5 % in BM) and patients with MDS or JMML with blast counts < 20 % in BM at study entry.

5. Age at time of registration from 28 days to less than 18 years of age.

6. Lansky (patients aged <16 years) or Karnofsky (patients aged ≥ 16 years) performance score of at least 70 %.

7. Written informed consent of the parents/ legal guardians and patient's assent/consent according to national regulations.

8. Females of child-bearing potential or male patients' partners with child-bearing potential must use a highly effective method of contraception (pearl index < 1 %) such as complete sexual abstinence, combined oral contraceptive, hormone intrauterine contraceptive device (IUCD), vaginal hormone ring, transdermal contraceptive patch, contraceptive implant or depot contraceptive injection in combination with a second method of contraception like a condom or a cervical cap / diaphragm with spermicide or surgical sterilisation (vasectomy) in male patients or male partners during the study and at least 6 months thereafter.

9. Negative pregnancy test for females of child-bearing potential.

Exclusion Criteria

1. Third or later allo-HSCT.

2. HSCT from haploidentical or umbilical cord blood donor.

3. Symptomatic involvement of central nervous system (CNS) at study entry.

4. Treatment with cytotoxic drugs within 10 days prior to day 7.

5. Obese paediatric patients with body mass index: weight (kg)/[height (m)]² > 30 kg/m².

6. Solid tumours (e.g. neuroblastoma, peripheral neuroectodermal tumour [PNET], Ewing sarcoma).

7. Fanconi anaemia and other deoxyribonucleic acid (DNA) breakage repair disorders.

8. Impaired liver function indicated by Bilirubin > three times the upper limit of normal (ULN) or aspartate aminotransferase/alanine aminotransferase (AST/ALT) > five times ULN, or active infectious hepatitis.

9. Impaired renal function indicated by estimated glomerular filtration rate ([GFR], according to the Schwartz formula) < 60 mL/min/1,73m2.

10. Impaired cardiac function: severe cardiac insufficiency indicated by left ventricle ejection fraction (LVEF) < 35 %.

11. Requirement for supplementary continuous oxygen.

12. Severe active infection requiring deferral of conditioning.

13. Human immunodeficiency virus (HIV) positivity.

14. Known pregnancy, breast feeding.

15. Known hypersensitivity to Treosulfan and/or Fludarabine.

• Minimum Eligible Age: 28 Days
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Celerion

INDUSTRY

Sponsor Role: collaborator

Syneos Health

OTHER

Sponsor Role: collaborator

medac GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ajay Vora, MD, Prof.

Role: PRINCIPAL_INVESTIGATOR

Great Ormond Street Hospital NHS Trust

Locations

St. Anna Children Hospital

Vienna, , Austria

University Hospital Motol, Charles University, Prague

Prague, , Czechia

University Clinic Düsseldorf

Düsseldorf, , Germany

University Clinic Erlangen-Nürnberg

Erlangen, , Germany

Universitätsklinikum Essen

Essen, , Germany

University Hospital Johann Wolfgang Goethe

Frankfurt, , Germany

University Clinic Hamburg-Eppendorf

Hamburg, , Germany

Medical University Hannover

Hanover, , Germany

University Clinic Heidelberg

Heidelberg, , Germany

University Clinic Jena

Jena, , Germany

University Clinic München

München, , Germany

University Clinic Münster

Münster, , Germany

University Clinic Regensburg

Regensburg, , Germany

University Clinic Ulm

Ulm, , Germany

University Clinic Würzburg

Würzburg, , Germany

Ospedale Bambino Gesu Roma

Rome, , Italy

Ospedale Infantile Regina Margherita Torino

Turin, , Italy

Bydgoszcz Medical University

Bydgoszcz, , Poland

Kraków Medical University

Krakow, , Poland

Lublin Medical University

Lublin, , Poland

Wroclaw Medical University

Wroclaw, , Poland

Birmingham Children's Hospital

Birmingham, , United Kingdom

Central Manchester University Hospital

Manchester, , United Kingdom

Sheffield Children's Hospital

Sheffield, , United Kingdom

Countries

Austria; Czechia; Germany; Italy; Poland; United Kingdom

References

Kalwak K, Mielcarek M, Patrick K, Styczynski J, Bader P, Corbacioglu S, Burkhardt B, Sykora KW, Drabko K, Gozdzik J, Fagioli F, Greil J, Gruhn B, Beier R, Locatelli F, Muller I, Schlegel PG, Sedlacek P, Stachel KD, Hemmelmann C, Moller AK, Baumgart J, Vora A. Treosulfan-fludarabine-thiotepa-based conditioning treatment before allogeneic hematopoietic stem cell transplantation for pediatric patients with hematological malignancies. Bone Marrow Transplant. 2020 Oct;55(10):1996-2007. doi: 10.1038/s41409-020-0869-6. Epub 2020 Mar 20.

Reference Type: DERIVED

PMID: 32203268 (View on PubMed)

Related Links

http://www.medac.de

sponsor's homepage

Other Identifiers

MC-FludT.17/M

Identifier Type: -

Identifier Source: org_study_id