Irradiation-based Myeloablative Conditioning Followed by Treg/Tcon Immunotherapy in HSCT
Primary Purpose
Acute Myeloid Leukemia, Acute Lymphoid Leukemia, Myeloproliferative Disorders
Status
Unknown status
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
High dose irradiation conditioning + Treg/Tcon
Sponsored by
About this trial
This is an interventional treatment trial for Acute Myeloid Leukemia
Eligibility Criteria
Inclusion Criteria:
- AML and ALL in complete remission and with high-risk of relapse
- AML and ALL primarily chemoresistant or relapsed;
- Chronic Myeloid Leukemia in accelerated or blastic phase;
Patients affected by
- Multiple myeloma,
- Non Hodgkin lymphoma,
- Hodgkin lymphoma,
- Chronic myeloproliferative syndrome,
- Chronic Lymphoid Leukemia,
- Other Hematological malignancy at high-risk of relapse or detectable disease and where a HSCT is indicated.
- Age <75 years
- ECOG ≤ 2
- Acceptable lung, liver, kidney, and heart function and absence of relevant psichiatric diseases
- Signature of the informed consent
Exclusion Criteria:
- Age >75 years
- ECOG > 2
- Not acceptable lung, liver, kidney, and heart function and presence of relevant psichiatric diseases
- Pregnancy
- No signature of the informed consent
Sites / Locations
- University of PerugiaRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
High dose irradiation conditioning + Treg/Tcon
Arm Description
High dose irradiation based conditioning regimens followed by infusion of donor regulatory and conventional T cells and purified CD34+ hematopoietic stem cell transplantation
Outcomes
Primary Outcome Measures
chronic GvHD/relapse-free survival
To evaluate if irradiation based myeloablative conditioning followed by Treg/Tcon adoptive immunotherapy improve chronic GvHD/relapse-free survival (GRFS) after allogeneic HSCT in patients affected by acute leukemias or other hematologic malignancies where HSCT is indicated. GRFS will be assessed in subgroups of patients separated according to HLA-matching with the donor and type of disease (acute myeloid lekemia, acute lymphoid leukemia, other)
Secondary Outcome Measures
full donor-type engraftment
neutrophil and platelet engraftment measured by neutrophil counts >500/mmc for 3 consecutive days and platelets count >20000/mmc with 7 consecutive without platelet transfusion
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03977103
Brief Title
Irradiation-based Myeloablative Conditioning Followed by Treg/Tcon Immunotherapy in HSCT
Official Title
Antileukemic Activity of Allogeneic Hematopoietic Stem Cell Transplantation With Fractionated Total Body Irradiation or Total Marrow and Lymph Node Irradiation Followed by Adoptive Immunotherapy With Regulatory and Conventional T Cells
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 2014 (undefined)
Primary Completion Date
February 28, 2023 (Anticipated)
Study Completion Date
February 28, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Of Perugia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
To evaluate if hyper-fractionated TBI or TMLI followed by Treg/Tcon adoptive immunotherapy improve cGvHD/disease free survival after allogeneic HSCT in patients affected by high-risk acute leukemias or other hematologic malignancy where HSCT is indicated.
Detailed Description
Improving cGvHD/disease free survival in patients with high-risk acute leukemias or other hematologic malignancy where HSCT is indicated with the use of a regulatory T cell based protocol. Hyper-fractionated Total Body Irradiation or Total Marrow and Lymphoid Irradiation based conditioning will be followed by the infusion of T regulatory and T conventional cell adoptive immunotherapy and a purified CD34+ hematopoietic stem cell graft. Incidence of Non Relapse Mortality, Relapse, acute Graft versus Host Disease, chronic Graft versus Host Disease, as well as probability of cGvHD/disease free survival will be assessed in patient subpopulations separated according to HLA-matching with the donor (HLA-matched HSCT and HLA-haploidentical HSCT) and type of disease (acute myeloid leukemia, acute lymphoid leukemia, lymphoma, multiple myeloma, myeloproliferative disease, and other).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia, Acute Lymphoid Leukemia, Myeloproliferative Disorders, Lymphoma, Multiple Myeloma, Other Hematologic Malignant Neoplasms
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
High dose irradiation conditioning + Treg/Tcon
Arm Type
Experimental
Arm Description
High dose irradiation based conditioning regimens followed by infusion of donor regulatory and conventional T cells and purified CD34+ hematopoietic stem cell transplantation
Intervention Type
Biological
Intervention Name(s)
High dose irradiation conditioning + Treg/Tcon
Intervention Description
High dose irradiation based conditioning regimens followed by infusion of donor regulatory and conventional T cells and purified CD34+ hematopoietic stem cell transplantation
Primary Outcome Measure Information:
Title
chronic GvHD/relapse-free survival
Description
To evaluate if irradiation based myeloablative conditioning followed by Treg/Tcon adoptive immunotherapy improve chronic GvHD/relapse-free survival (GRFS) after allogeneic HSCT in patients affected by acute leukemias or other hematologic malignancies where HSCT is indicated. GRFS will be assessed in subgroups of patients separated according to HLA-matching with the donor and type of disease (acute myeloid lekemia, acute lymphoid leukemia, other)
Time Frame
2 years
Secondary Outcome Measure Information:
Title
full donor-type engraftment
Description
neutrophil and platelet engraftment measured by neutrophil counts >500/mmc for 3 consecutive days and platelets count >20000/mmc with 7 consecutive without platelet transfusion
Time Frame
30 days
Other Pre-specified Outcome Measures:
Title
cumulative incidence of grades ≥ 2 acute GvHD
Description
cumulative incidence of grades ≥ 2 acute GvHD according to NIH consesus criteria
Time Frame
6 months
Title
cumulative incidence of extensive chronic GvHD
Description
cumulative incidence of extensive chronic GvHD according to revised NIH consesus criteria (Jagasia et al. BBMT 2015)
Time Frame
2 years
Title
cumulative incidence of non-relapse mortality
Description
cumulative incidence of non-relapse mortality, defined as death by any cause in the absence of relapse, as competitive risk versus relapse
Time Frame
2 years
Title
cumulative incidence of relapse
Description
cumulative incidence of relapse, defined as disease recurrence according to marrow morphology, flow cytometry, cytogenetics, fluorescence in situ hybridization and/or polymerase chain reaction, as competitive risk versus non-relapse mortality
Time Frame
2 years
10. Eligibility
Sex
All
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
AML and ALL in complete remission and with high-risk of relapse
AML and ALL primarily chemoresistant or relapsed;
Chronic Myeloid Leukemia in accelerated or blastic phase;
Patients affected by
Multiple myeloma,
Non Hodgkin lymphoma,
Hodgkin lymphoma,
Chronic myeloproliferative syndrome,
Chronic Lymphoid Leukemia,
Other Hematological malignancy at high-risk of relapse or detectable disease and where a HSCT is indicated.
Age <75 years
ECOG ≤ 2
Acceptable lung, liver, kidney, and heart function and absence of relevant psichiatric diseases
Signature of the informed consent
Exclusion Criteria:
Age >75 years
ECOG > 2
Not acceptable lung, liver, kidney, and heart function and presence of relevant psichiatric diseases
Pregnancy
No signature of the informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antonio Pierini, MD, PhD
Phone
+390755784147
Email
antonio.pierini@unipg.it
First Name & Middle Initial & Last Name or Official Title & Degree
Mara Merluzzi, MBioTech
Phone
+393482200239
Email
maramerluzzi@libero.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Velardi, MD, PhD
Organizational Affiliation
University Of Perugia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Perugia
City
Perugia
State/Province
PG
ZIP/Postal Code
06132
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antonio Pierini, MD, PhD
Phone
+390755784147
Email
antonio.pierini@unipg.it
First Name & Middle Initial & Last Name & Degree
Mara Merluzzi, MBioTech
Phone
+393482200239
Email
maramerluzzi@libero.it
First Name & Middle Initial & Last Name & Degree
Cynthia Aristei, MD
First Name & Middle Initial & Last Name & Degree
Maurizio Caniglia, MD
First Name & Middle Initial & Last Name & Degree
Alessandra Carotti, MD
First Name & Middle Initial & Last Name & Degree
Franca Falzetti, MD
First Name & Middle Initial & Last Name & Degree
Antonio Pierini, MD
First Name & Middle Initial & Last Name & Degree
Loredana Ruggeri, MD
First Name & Middle Initial & Last Name & Degree
Adelmo Terenzi, MD
First Name & Middle Initial & Last Name & Degree
Simonetta Saldi, MD
First Name & Middle Initial & Last Name & Degree
Ilaria Capolsini, MD
First Name & Middle Initial & Last Name & Degree
Elena Mastrodicasa, MD
First Name & Middle Initial & Last Name & Degree
Maria Speranza Massei, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
21292771
Citation
Di Ianni M, Falzetti F, Carotti A, Terenzi A, Castellino F, Bonifacio E, Del Papa B, Zei T, Ostini RI, Cecchini D, Aloisi T, Perruccio K, Ruggeri L, Balucani C, Pierini A, Sportoletti P, Aristei C, Falini B, Reisner Y, Velardi A, Aversa F, Martelli MF. Tregs prevent GVHD and promote immune reconstitution in HLA-haploidentical transplantation. Blood. 2011 Apr 7;117(14):3921-8. doi: 10.1182/blood-2010-10-311894. Epub 2011 Feb 3.
Results Reference
background
PubMed Identifier
24923299
Citation
Martelli MF, Di Ianni M, Ruggeri L, Falzetti F, Carotti A, Terenzi A, Pierini A, Massei MS, Amico L, Urbani E, Del Papa B, Zei T, Iacucci Ostini R, Cecchini D, Tognellini R, Reisner Y, Aversa F, Falini B, Velardi A. HLA-haploidentical transplantation with regulatory and conventional T-cell adoptive immunotherapy prevents acute leukemia relapse. Blood. 2014 Jul 24;124(4):638-44. doi: 10.1182/blood-2014-03-564401. Epub 2014 Jun 12.
Results Reference
background
PubMed Identifier
33646302
Citation
Pierini A, Ruggeri L, Carotti A, Falzetti F, Saldi S, Terenzi A, Zucchetti C, Ingrosso G, Zei T, Iacucci Ostini R, Piccinelli S, Bonato S, Tricarico S, Mancusi A, Ciardelli S, Limongello R, Merluzzi M, Di Ianni M, Tognellini R, Minelli O, Mecucci C, Martelli MP, Falini B, Martelli MF, Aristei C, Velardi A. Haploidentical age-adapted myeloablative transplant and regulatory and effector T cells for acute myeloid leukemia. Blood Adv. 2021 Mar 9;5(5):1199-1208. doi: 10.1182/bloodadvances.2020003739.
Results Reference
derived
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Irradiation-based Myeloablative Conditioning Followed by Treg/Tcon Immunotherapy in HSCT
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