Methods of T Cell Depletion Trial (MoTD)

Multiple Myeloma Clinical Trial

— MoTD  

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04888741
• Other study ID #: RG_19-116
• Status: Recruiting
• Phase: Phase 2
• Start date: February 22, 2021
• Est. completion date: January 2026

Study information

• Verified date: September 2023
• Source: University of Birmingham
• Contact: MoTD Trial
• Phone: 0121 371 7859
• Email: MoTD[@]trials.bham.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Recruiting
• Enrollment: 400
• Est. completion date: January 2026
• Est. primary completion date: January 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 16 Years to 70 Years

Eligibility

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.

Related Conditions & MeSH terms

• Acute Lymphoblastic Leukemia
• Acute Myeloid Leukemia
• Chronic Myelogenous Leukemia
• Chronic Myelomonocytic Leukemia
• Hodgkin Lymphoma
• Leukemia
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive
• Leukemia, Myeloid
• Leukemia, Myelomonocytic, Chronic
• Leukemia, Myelomonocytic, Juvenile
• Lymphoma
• Multiple Myeloma
• Myelodysplastic Syndromes
• Myelofibrosis
• Non Hodgkin Lymphoma
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Drug:
• Thymoglobulin
GVHD prophylaxis
• Cyclophosphamide
Post transplant cyclophosphamide strategy for GVHD prophylaxis
• Cyclosporine
immunosuppressant
• Sirolimus
immunosuppressant
• Mycophenolate Mofetil
immunosuppressant

Locations

Country	Name	City	State
United Kingdom	Queen Elizabeth Hospital	Birmingham
United Kingdom	Bristol Haematology and Oncology Centre	Bristol
United Kingdom	Addenbrookes Hospital	Cambridge
United Kingdom	University Hospital of Wales	Cardiff	Wales
United Kingdom	Queen Elizabeth Hospital Glasgow	Glasgow
United Kingdom	St Jame's University Hospital	Leeds
United Kingdom	Hammersmith Hospital	London
United Kingdom	King's College Hospital	London
United Kingdom	University College London Hospital	London
United Kingdom	Manchester Royal Infirmary	Manchester
United Kingdom	The Christie	Manchester
United Kingdom	Freeman Hospital	Newcastle Upon Tyne
United Kingdom	Nottingham City Hospital	Nottingham
United Kingdom	Churchill Hospital	Oxford
United Kingdom	Derriford Hospital	Plymouth

Sponsors (2)

Lead Sponsor	Collaborator
University of Birmingham	IMPACT (funded by NHS Blood & Transplant, Anthony Nolan and Leukaemia UK)

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	GVHD-free, relapse-free survival	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	at 1 year
Secondary	Cumulative incidence of acute grade II-IV and III-IV GvHD	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	at 1 year
Secondary	Cumulative incidence of moderate and severe chronic GvHD	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	at 1 year
Secondary	Cumulative incidence of NRM	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.	at 1 year
Secondary	Overall survival	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.	at 1 year
Secondary	Progression-free survival	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.	at 1 year
Secondary	Immune suppression-free survival	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	at 1 year
Secondary	Cumulative incidence of engraftment	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.	at 1 year
Secondary	The incidence of full donor chimerism	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.	at 100 days
Secondary	The cumulative incidence of infection requiring inpatient admission	The cumulative incidence of infection requiring inpatient admission measured by blood test and tissue culture at 1 year	at 1 year
Secondary	The number of inpatient days	The sum of inpatients days	during first 12 months
Secondary	The timing of mixed chimerism, persistent disease or relapse	We will be recording the time (days, post-transplant) whenever mixed chimerism, persistent disease or relapse occurred post transplant	during first 12 months
Secondary	Cumulative incidence of EBV-related PTLD	Measured by blood sample, EBV PCR testing.	during first 12 months
Secondary	The number of doses of Rituximab administered for EBV reactivation	We will collect the number of doses every time the patient will receive Rituximab whenever there is EBV reactivation	during first 12 months
Secondary	QoL measured by FACT-BMT questionnaire	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.	at baseline, 6 months and 12 months
Secondary	Cumulative incidence of patients with haemorrhagic cystitis	Cumulative incidence of patients with haemorrhagic cystitis measured by blood and urine sample at 1 year	at 1 year
Secondary	Cumulative incidence of CMV viremia and CMV end-organ disease	Cumulative incidence of CMV viremia and CMV end-organ disease measured by blood sample at 1 year	at 1 year
Secondary	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	. 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.	from the date of commencement of protocol defined treatment until 28 days after the administration of the last dose of IMP.
Secondary	Tolerability defined to be the number of patients able to complete therapy as scheduled	Tolerability defined to be the number of patients able to complete therapy as scheduled (excluding any patients who discontinued treatment due to toxicities	during first 12 months
Secondary	Dose of Donor lymphocyte infusion (DLI) for mixed chimerism, persistent disease or relapse	We will be collecting the dose of DLI (CD3 Cells/kg) whenever required for mixed chimerism, persistent disease or relapse	during first 12 months