MedPath

Methods of T Cell Depletion Trial (MoTD)

Phase 2
Recruiting
Conditions
Acute Myeloid Leukemia
Myelodysplastic Syndromes
Non Hodgkin Lymphoma
Hodgkin Lymphoma
Chronic Myelogenous Leukemia
Myelofibrosis
Acute Lymphoblastic Leukemia
Chronic Myelomonocytic Leukemia
Multiple Myeloma
Interventions
Registration Number
NCT04888741
Lead Sponsor
University of Birmingham
Brief Summary

A multi-centre phase II trial of GvHD prophylaxis following unrelated donor stem cell transplantation comparing Thymoglobulin vs. Calcineurin inhibitor or Sirolimus-based post-transplant cyclophosphamide.

Detailed Description

This is a prospective, phase II, adaptive, multicentre, randomised clinical trial in patients undergoing reduced intensity conditioned (RIC) unrelated donor allogeneic stem cell transplantation (allo-SCT). The trial will compare the novel graft-versus-host disease (GvHD) prophylaxis regimens of post-transplant cyclophosphamide (PTCy) + Calcineurin inhibitor (CNI) (PTCy-CNI) or PTCy + Sirolimus to a current standard-of-care involving the use of T-cell depletion with Thymoglobulin. Patients will be minimised at randomisation by their randomising centre, disease risk score (low/intermediate or high/very high) and human leukocyte antigen (HLA) match (10/10 or 9/10). Patients eligible for entry into the trial will be randomised on a 1:1:1 ratio to receive either one of the experimental treatment arms or the control arm.

The primary objective is to compare GvHD-free, relapse-free Survival (GRFS) in patients treated with the GvHD prophylaxis regimens PTCy-CNI, PTCy-Sirolimus or T-cell depletion with Thymoglobulin.

The secondary objectives are to evaluate the cumulative incidence of acute GvHD (aGvHD), the cumulative incidence of moderate and severe chronic GvHD (cGvHD), the cumulative incidence of non-relapse mortality (NRM), overall survival (OS), progression-free survival (PFS), immune suppression-free survival, the cumulative incidence of engraftment, the incidence of full donor chimerism, the cumulative incidence of infection requiring inpatient admission, the number of inpatient days, the timing and dose of donor lymphocyte infusion (DLI), the cumulative incidence of Epstein-Barr virus (EBV) related-post transplant lymphoproliferative disease (PTLD), the number of doses rituximab administered for EBV reactivation, quality of life (QoL), the cumulative incidence of haemorrhagic cystitis, the cumulative incidence of cytomegalovirus (CMV) viraemia and CMV end-organ disease and safety and tolerability.

The scientific research will address the questions about how plasma biomarkers for GvHD predict GvHD and non-relapse mortality following T-cell depleted methods of transplantation and how the different methods of T-cell depletion impact on immune function and re-constitution.

Outcome Measures

Primary Outcome Measure:

• GvHD-free, relapse-free survival at 1 year

Secondary Outcome Measures:

* Cumulative incidence of acute grade II-IV and III-IV GvHD at 1 year

* Cumulative incidence of moderate and severe chronic GvHD at 1 year

* Cumulative incidence of NRM at 1 year

* Overall survival at 1 year

* Progression-free survival at 1 year

* Immune suppression-free survival at 1 year

* Cumulative incidence of engraftment at 1 year

* The incidence of full donor chimerism at 100 days

* The cumulative incidence of infection requiring inpatient admission at 1 year

* The number of inpatient days during first 12 months

* The timing and dose of DLI for mixed chimerism, persistent disease or relapse

* Cumulative incidence of EBV-related PTLD

* The number of doses of rituximab administered for EBV reactivation during first 12 months

* QoL measured by FACT-BMT questionnaire at baseline, 6 months and 12 months

* Cumulative incidence of patients with haemorrhagic cystitis at 1 year

* Cumulative incidence of CMV viremia and CMV end-organ disease at 1 year

* Safety defined as the incidence of ≥ grade 3 toxicities reported as per the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.0

* Tolerability defined to be the number of patients able to complete therapy as scheduled

Exploratory Outcome Measures:

The scientific research will address the following questions:

1. Do plasma biomarkers for GvHD predict GvHD and non-relapse mortality following T-cell depleted methods of transplantation?

2. Do PTCy methods increase T cell receptor repertoire diversity (as measured by TCR DNA sequencing) compared to ATG-based T cell depletion?

3. How do the different methods of T-cell depletion impact upon donor Treg reconstitution?

4. How do the different methods of T-cell depletion impact upon thymic function as evaluated by measurement of recent thymic emigrants?

5. Are PTCy methods of TCD associated with better preservation of virus-specific immunity (as measured by tetramer or ex vivo functional immune responses)?

Patient Population

Adults considered suitable for an allo-SCT with the following haematological malignancies will be recruited to this trial:

* Acute Myeloid Leukaemia (AML)

* Acute lymphoblastic leukaemia (ALL)

* Chronic myelomonocytic leukemia (CMML)

* Myelodysplastic syndromes (MDS)

* Non-Hodgkin lymphoma (NHL)

* Hodgkin lymphoma (HL)

* Multiple myeloma (MM)

* Chronic lymphocytic leukaemia (CLL)

* Chronic myeloid leukaemia (CML)

* Myelofibrosis

Sample Size:

Up to 400 patients will be randomised to the MoTD trial across IMPACT centres.

Trial Duration:

Patients will be recruited over 48 months. Patients will be followed up for a minimum of 1 year.

MoTD Trials Office Contact Details:

MoTD trials office, Centre for Clinical Haematology, Queen Elizabeth Hospital, Edgbaston, Birmingham, B15 2TH Tel: 0121 371 7858 Email: MoTD@trials.bham.ac.uk

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
400
Inclusion Criteria
  • Availability of suitably matched unrelated donor (9/10 or 10/10)

  • Planned to receive one of the following RIC protocols:

    • Fludarabine-Melphalan (Fludarabine 120-180mg/m2 IV; melphalan ≤ 150mg/m2 IV)
    • BEAM or LEAM (carmustine 300mg/m2 IV or lomustine 200mg/m2 IV with: etoposide 800 mg/m2 IV; cytarabine 1600mg/m2 IV; melphalan 140mg/m2 IV)
    • Fludarabine-Busulphan (Fludarabine 120-180mg/m2 IV; Busulphan ≤ 8mg/kg PO or 6.4mg/kg IV)
    • Fludarabine- Treosulfan (Fludarabine 150mg/m2 IV; Treosulfan 30g/m2 IV)
  • Planned use of PBSCs for transplantation

  • Planned allo-SCT for one of the following haematological malignancies:

    • AML in CR (patients enrolled onto the COSI trial are not eligible for this study)
    • ALL in CR (patients enrolled onto the ALL-RIC trial are not eligible for this study)
    • CMML <10% blasts
    • MDS <10% blasts (patients enrolled onto the COSI trial are not eligible for this study)
    • NHL in CR/PR
    • HL in CR/PR
    • MM in CR/PR
    • CLL in CR/PR
    • CML in 1st or 2nd chronic phase
    • Myelofibrosis
  • Age 16-70 years

  • Females of and male patients of reproductive potential (i.e., not post-menopausal or surgically sterilised) must agree to use appropriate, highly effective, contraception from the point of commencing therapy until 12 months after transplant

Exclusion Criteria
  • Use of any method of graft manipulation (excluding storage of future DLI)

  • Use of alemtuzumab or any method of T cell depletion except those that are protocol-defined

  • Known hypersensitivity to study drugs or history of hypersensitivity to rabbits

  • Pregnant or lactating women

  • Adults of reproductive potential not willing to use appropriate, highly effective, contraception during the specified period

  • Life expectancy <8 weeks

  • Active HBV or HCV infection

  • Organ dysfunction defined as:

    • LVEF <45%
    • GFR <50ml/min
    • Bilirubin >50µmol/l
    • AST/ALT>3 x ULN
  • Participation in COSI or ALL-RIC trials

  • Contraindication to treatment with the study drugs (Thymoglobulin, cyclophosphamide, sirolimus, ciclosporin and mycophenolate mofetil) as detailed in each study drug SPC.

  • Patient has any other systemic dysfunction (e.g., gastrointestinal, renal, respiratory, cardiovascular) or significant disorder which, in the opinion of the investigator would jeopardise the safety of the patient by taking part in the trial.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control Arm Thymoglobulin + Cyclosporine + MMFThymoglobulinThymoglobulin is given as an intravenous infusion of 2.5 mg/kg/day over 2 days (days -2 and -1; total dose 5 mg/kg) via a central line through a 0.2 micron inline filter. Each dose will be infused over 6-8 hours. No test dose will be given. 30 minutes before Thymoglobulin, the patient should receive methylprednisolone 1mg/kg intravenously, 1g paracetamol PO and 10mg chlorphenamine IV. Patients should be monitored carefully and receive appropriate therapy for any infusion-related or anaphylactic reactions as per local policy. Patients will receive IV/PO cyclosporine according to local policy to begin on day -1 maintaining a trough level of 100-200 µg/L until day 90 before a subsequent taper in the absence of any active GvHD. MMF will be given IV/PO according to local policy at a dose of 1g TDS to begin on day -1 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Control Arm Thymoglobulin + Cyclosporine + MMFMycophenolate MofetilThymoglobulin is given as an intravenous infusion of 2.5 mg/kg/day over 2 days (days -2 and -1; total dose 5 mg/kg) via a central line through a 0.2 micron inline filter. Each dose will be infused over 6-8 hours. No test dose will be given. 30 minutes before Thymoglobulin, the patient should receive methylprednisolone 1mg/kg intravenously, 1g paracetamol PO and 10mg chlorphenamine IV. Patients should be monitored carefully and receive appropriate therapy for any infusion-related or anaphylactic reactions as per local policy. Patients will receive IV/PO cyclosporine according to local policy to begin on day -1 maintaining a trough level of 100-200 µg/L until day 90 before a subsequent taper in the absence of any active GvHD. MMF will be given IV/PO according to local policy at a dose of 1g TDS to begin on day -1 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Control Arm Thymoglobulin + Cyclosporine + MMFCyclosporineThymoglobulin is given as an intravenous infusion of 2.5 mg/kg/day over 2 days (days -2 and -1; total dose 5 mg/kg) via a central line through a 0.2 micron inline filter. Each dose will be infused over 6-8 hours. No test dose will be given. 30 minutes before Thymoglobulin, the patient should receive methylprednisolone 1mg/kg intravenously, 1g paracetamol PO and 10mg chlorphenamine IV. Patients should be monitored carefully and receive appropriate therapy for any infusion-related or anaphylactic reactions as per local policy. Patients will receive IV/PO cyclosporine according to local policy to begin on day -1 maintaining a trough level of 100-200 µg/L until day 90 before a subsequent taper in the absence of any active GvHD. MMF will be given IV/PO according to local policy at a dose of 1g TDS to begin on day -1 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Experimental arm (PTCy + Cyclosporine + MMF)CyclophosphamideCyclophosphamide is given as an IV infusion of 50 mg/kg/day over 2 days (days 3 and 4; total dose 100 mg/kg) together with IV hydration and Mesna, as per local policy. Patients will receive IV/PO cyclosporine according to local policy to begin on day 5 maintaining a trough level of 100-200 µg/L until day 90 before a subsequent taper in the absence of active GvHD. MMF will be given IV/PO according to local policy at a dose of 1g TDS to begin on day 5 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Experimental arm (PTCy + Cyclosporine + MMF)CyclosporineCyclophosphamide is given as an IV infusion of 50 mg/kg/day over 2 days (days 3 and 4; total dose 100 mg/kg) together with IV hydration and Mesna, as per local policy. Patients will receive IV/PO cyclosporine according to local policy to begin on day 5 maintaining a trough level of 100-200 µg/L until day 90 before a subsequent taper in the absence of active GvHD. MMF will be given IV/PO according to local policy at a dose of 1g TDS to begin on day 5 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Experimental arm (PTCy + Cyclosporine + MMF)Mycophenolate MofetilCyclophosphamide is given as an IV infusion of 50 mg/kg/day over 2 days (days 3 and 4; total dose 100 mg/kg) together with IV hydration and Mesna, as per local policy. Patients will receive IV/PO cyclosporine according to local policy to begin on day 5 maintaining a trough level of 100-200 µg/L until day 90 before a subsequent taper in the absence of active GvHD. MMF will be given IV/PO according to local policy at a dose of 1g TDS to begin on day 5 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Experimental arm (PTCy + Sirolimus + MMF)CyclophosphamideCyclophosphamide is given as an IV infusion of 50 mg/kg/day over 2 days (days 3 and 4; total dose 100 mg/kg) together with IV hydration and Mesna, as per local policy. Sirolimus will be initially given PO as a loading dose of 6 mg on day 5 followed by 2 mg daily; doses will be adjusted to maintain a trough level (in whole blood) of 8 to 14 ng/mL until day 60, thereafter 5-8 ng/mL until day 90. In the absence of active GvHD, the dose of sirolimus will be tapered from day 90. We recommend that the daily maintenance dose of sirolimus is reduced empirically to 0.5-1mg daily with concomitant treatment with a triazole anti-fungal agent. MMF will be given IV/O according to local policy at a dose of 1g TDS to begin on day 5 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Experimental arm (PTCy + Sirolimus + MMF)SirolimusCyclophosphamide is given as an IV infusion of 50 mg/kg/day over 2 days (days 3 and 4; total dose 100 mg/kg) together with IV hydration and Mesna, as per local policy. Sirolimus will be initially given PO as a loading dose of 6 mg on day 5 followed by 2 mg daily; doses will be adjusted to maintain a trough level (in whole blood) of 8 to 14 ng/mL until day 60, thereafter 5-8 ng/mL until day 90. In the absence of active GvHD, the dose of sirolimus will be tapered from day 90. We recommend that the daily maintenance dose of sirolimus is reduced empirically to 0.5-1mg daily with concomitant treatment with a triazole anti-fungal agent. MMF will be given IV/O according to local policy at a dose of 1g TDS to begin on day 5 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Experimental arm (PTCy + Sirolimus + MMF)Mycophenolate MofetilCyclophosphamide is given as an IV infusion of 50 mg/kg/day over 2 days (days 3 and 4; total dose 100 mg/kg) together with IV hydration and Mesna, as per local policy. Sirolimus will be initially given PO as a loading dose of 6 mg on day 5 followed by 2 mg daily; doses will be adjusted to maintain a trough level (in whole blood) of 8 to 14 ng/mL until day 60, thereafter 5-8 ng/mL until day 90. In the absence of active GvHD, the dose of sirolimus will be tapered from day 90. We recommend that the daily maintenance dose of sirolimus is reduced empirically to 0.5-1mg daily with concomitant treatment with a triazole anti-fungal agent. MMF will be given IV/O according to local policy at a dose of 1g TDS to begin on day 5 and discontinued on day 35 without taper if there is no evidence of active GvHD. In adults weighing \<55kg, MMF should be given at a lower dose of 0.75g IV/PO TDS.
Primary Outcome Measures
NameTimeMethod
GVHD-free, relapse-free survivalat 1 year

GVHD assessment scoring will be performed as per the modified Glucksberg criteria (revised by MAGIC) and the National Institutes of Health (NIH) criteria. GvHD-free, relapse-free survival (GRFS) defined as the time from date of day 0 (defined as the day of stem cell infusion) to the date of first event or death from any cause. An event is defined as GvHD (both acute and chronic), relapse or progression. Patients who are alive and event free at the end of the trial will be censored at their date of last follow-up

Secondary Outcome Measures
NameTimeMethod
Overall survivalat 1 year

Overall survival (OS) is defined as the time from day 0 to date of death, from any cause. Patients who are alive at the end of the trial will be censored at their date last seen.

Cumulative incidence of patients with haemorrhagic cystitisat 1 year

Cumulative incidence of patients with haemorrhagic cystitis measured by blood and urine sample at 1 year

Cumulative incidence of moderate and severe chronic GvHDat 1 year

GVHD assessment scoring will be performed as per the modified Glucksberg criteria (revised by MAGIC) and the National Institutes of Health (NIH) criteria. GvHD-free

Cumulative incidence of acute grade II-IV and III-IV GvHDat 1 year

GVHD assessment scoring will be performed as per the modified Glucksberg criteria (revised by MAGIC) and the National Institutes of Health (NIH) criteria. GvHD-free

The cumulative incidence of infection requiring inpatient admissionat 1 year

The cumulative incidence of infection requiring inpatient admission measured by blood test and tissue culture at 1 year

The timing of mixed chimerism, persistent disease or relapseduring first 12 months

We will be recording the time (days, post-transplant) whenever mixed chimerism, persistent disease or relapse occurred post transplant

Safety defined as the incidence of ≥ grade 3 toxicities reported as per the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) V4.0from the date of commencement of protocol defined treatment until 28 days after the administration of the last dose of IMP.

. Safety defined as the incidence of ≥ grade 3 toxicities reported as per the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.0. Details of all AEs will be documented and reported from the date of commencement of protocol defined treatment until 28 days after the administration of the last dose of IMP. Serious AEs will be reported from the date of consent.

Cumulative incidence of NRMat 1 year

Non-relapse mortality (NRM) is defined as the time from day 0 to date of non-relapse death. Patients who die post-relapse from any other cause will be considered a competing risk and patients alive at the end of the trial will be censored at their date last seen.

Progression-free survivalat 1 year

Progression-free survival (PFS) is defined as the time from day 0 to date of first relapse/progression or death from any cause. Patients who are alive and progression free at the end of the trial will be censored at their date last seen.

Cumulative incidence of engraftmentat 1 year

Cumulative incidence of engraftment defined as time from day 0 to date of engraftment (Neutrophil engraftment defined to be the first of 3 consecutive days a neutrophil count ≥ 0.5×〖10〗\^9/L is reached and platelet engraftment defined to be the first of 3 consecutive days an unsupported platelet count ≥ 20×〖10〗\^9/L is reached). Patients who relapse/progress or die prior to relapse, progression or engraftment will be considered a competing risk at their date of relapse/progression for the former and date of death for the latter. Patients alive and engraftment free at the end of the trial will be censored at their date last seen.

The number of inpatient daysduring first 12 months

The sum of inpatients days

The number of doses of Rituximab administered for EBV reactivationduring first 12 months

We will collect the number of doses every time the patient will receive Rituximab whenever there is EBV reactivation

QoL measured by FACT-BMT questionnaireat baseline, 6 months and 12 months

QoL measured by FACT-BMT questionnaire at baseline, 6 months and 12 months. FACT-BMT Questionnaire uses Units on a scale 0-4, higher scores mean a better outcome.

Cumulative incidence of CMV viremia and CMV end-organ diseaseat 1 year

Cumulative incidence of CMV viremia and CMV end-organ disease measured by blood sample at 1 year

Dose of Donor lymphocyte infusion (DLI) for mixed chimerism, persistent disease or relapseduring first 12 months

We will be collecting the dose of DLI (CD3 Cells/kg) whenever required for mixed chimerism, persistent disease or relapse

Immune suppression-free survivalat 1 year

Immune suppression-free survival is defined as time from day 0 to the date of first immunosuppressive agent use. Patients who are alive and immune suppression free at the end of the trial will be censored at their date last seen

The incidence of full donor chimerismat 100 days

Engraftment will be assessed by lineage specific chimerism measurements. Lineage specific chimerism in both whole blood and T-cell compartments (where possible) will be assessed as per local procedure, performed at 3 monthly intervals for the first 12 months post-transplant; at day 100 and then months 6, 9 and 12. Tests should be performed in local laboratories.

Cumulative incidence of EBV-related PTLDduring first 12 months

Measured by blood sample, EBV PCR testing.

Tolerability defined to be the number of patients able to complete therapy as scheduledduring first 12 months

Tolerability defined to be the number of patients able to complete therapy as scheduled (excluding any patients who discontinued treatment due to toxicities

Trial Locations

Locations (15)

Queen Elizabeth Hospital

🇬🇧

Birmingham, United Kingdom

Bristol Haematology and Oncology Centre

🇬🇧

Bristol, United Kingdom

University Hospital of Wales

🇬🇧

Cardiff, Wales, United Kingdom

Manchester Royal Infirmary

🇬🇧

Manchester, United Kingdom

King's College Hospital

🇬🇧

London, United Kingdom

Churchill Hospital

🇬🇧

Oxford, United Kingdom

Addenbrookes Hospital

🇬🇧

Cambridge, United Kingdom

University College London Hospital

🇬🇧

London, United Kingdom

St Jame's University Hospital

🇬🇧

Leeds, United Kingdom

Freeman Hospital

🇬🇧

Newcastle Upon Tyne, United Kingdom

Queen Elizabeth Hospital Glasgow

🇬🇧

Glasgow, United Kingdom

Nottingham City Hospital

🇬🇧

Nottingham, United Kingdom

Hammersmith Hospital

🇬🇧

London, United Kingdom

Derriford Hospital

🇬🇧

Plymouth, United Kingdom

The Christie

🇬🇧

Manchester, United Kingdom

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