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Preventing of GVHD with Post-transplantation Cyclophosphamide, Abatacept, Vedolizumab and Ruxolitinib At Children and Young Adults with Hemoblastosis

Phase 2
Recruiting
Conditions
Biphenotypic Acute Leukemia
Acute Lymphoblastic Leukemia
Myeloblastic Leukemia
Bilinear Leukemia
Malignant Lymphoma, Non-Hodgkin
Myelodysplastic Syndrome
Registration Number
NCT06756152
Lead Sponsor
Federal Research Institute of Pediatric Hematology, Oncology and Immunology
Brief Summary

GVHD prevention using a combination of post-transplantation cyclophosphamide in combination with abatacept, vedolizumab and Ruxolitinib in children and young adults with hematoloblastosis after myeloablative conditioning regimen with treosulfan/TBI, etoposide, fludarabine after HSCT from matched unrelated and haploidentical donors

Detailed Description

Conditioning regimen:

Treosulfan 42 g/m2/course on the days -5, -4, -3 or total body irradiation 12 Gray/course on the days -8, -7, -6 Etoposide 60 mg/kg on the days -6, -5. or Thiotepa 10 mg/kg -6,-5 Fludarabine 150 mg/m2/course on the days -6, -5, -4, -3, -2

Prevention of GVHD:

Cyclophosphamide 80 mg/kg/course on the days +3, +4 Abatacept 10 mg/kg/day on the days +5, +14, +28, +60, +90 Vedolizumab 10 mg/kg/day, max. 300 mg on the days 0, +14, +28, +60

Ruxolitinib 10 mg/m2 per os, from day -3 to day +90 (after HSCT), orally, twice a day.

Donor selection criteria

In case of detection of two or more suitable donors, the choice is made in favor of:

* CMV Compliance

* Sex of donor and recipient

* medical and psychological suitability and desire of the donor

* Compatibility by blood type

Duration of therapy

* 120 days (for patients with high risk of recurrence: positive minimal residual disease before HSCT, non-remission status after HSCT, patients diagnosed with juvenile myelomonocytic leukemia)

* 180 days (for the rest) Time of observation

* follow up during 3 years after HSCT

Criteria for premature stopping of the study

1. The probability of developing acute GVHD II-IV is above 40%, of which III-IV - above 15%

2. The probability of 100-day transplant-associated mortality is higher than 20%. Goal Evaluation Date Intermediate analysis after 1 year from the beginning. The final analysis is scheduled to take place 100 days after the last patient is included.

Data Monitoring and Management

1. Plan of initial examination of the patient

After signing the informed consent and registration, the patient undergoes an examination in accordance with the standard plan of pre-transplantation examination and additional examinations, including:

* Confirmation of remission status, determination of MRD, chimerism according to the protocol 1. Monitoring of donor chimerism in patients with acute leukemia Point Days Lines

1 +30 day general, CD34

* Only if a relapse of the disease is suspected, cm can be sent to study chimerism:

* General

* Chimerism in the sorted MRD fraction 2. Minimal residual disease (MRD) monitoring in patients with ALL +30, +100 days after HSCT - for all patients: MRD (immunophenotyping), Cytogenetics (if it presence)

+ 60, +180 days after HSCT - for patients with MRD + or refractory before HSCT: MRD (immunophenotyping), Cytogenetics (if it presence) 3. Minimal residual disease (MRD) monitoring in patients with AML

+100 days after HSCT - for all patients: MRD (immunophenotyping), Cytogenetics (if it presence)

+ 30, +180 days after HSCT - for patients with MRD + or refractory before HSCT: MRD (immunophenotyping), Cytogenetics (if it presence)

4. Biobanking (KM, blood)

In this protocol, in addition to routine post-transplantation monitoring, the following studies are carried out:

• Study of the subpopulation composition of peripheral blood lymphocytes: B-cells: CD19

T-cells:

CD3/4/8/ TCR/gd CD3/4/8/45RA/CCR7 (CD197) CD3/4/31/45RA CD4/25/127

NK-compartment:

CD3/CD56

TCR repertoire:

Analysis multiplicity: +30, +60, +100, +180, +360 day The amount of blood for analysis is 5 ml in a test tube with EDTA.

* Pathogen-specific immunoreconstitution research - ELISPOT method for evaluating the production of gamma-interferon by peripheral blood mononuclears after incubation with microbial antigens. The main antigens studied are (CMV pp65, EBV, Adenovirus (AdvHexon), BK virus) Multiplicity of analysis of recipients: +30, +60, +100, +180, +360. The amount of blood for analysis on +30 days is 10 ml, subsequently - 5 ml in a test tube with EDTA.

* Virological monitoring by PCR weekly:

Blood: CMV, EBV, ADV by PCR method Chair: ADV MONITORING by PCR is carried out up to 100 days after CGSC. The exception is patients with viremia, or receiving immunosuppressive therapy on day 100.

in case of suspected visceral lesion: cerebrospinal fluid / bal / stool / urine / biopsy / other material

* Biobanking Multiplicity: + 30, +60, +100, +180, +360 Blood in a test tube with EDTA, used 2. Toxicity monitoring:

* Diagnosis and therapy of acute GVHD Clinical diagnosis and staging of acute GVHD is carried out in accordance with standard criteria (Appendix No. 3).

When an isolated rash appears, a skin biopsy is mandatory. When a clinic of acute GVHD appears with damage to the upper and lower gastrointestinal tract (nausea, vomiting, enterocolitis), gastroscopy with a biopsy of the gastric mucosa and colonoscopy with a floor biopsy is reokended.

The biopsy material should also be sent for virological examination. Before starting therapy, a consultation is held with the head of the protocol / appointed expert.

• Criteria for prescribing systemic immunosuppressive therapy: Acute GVHD stage I - therapy is not carried out Acute GVHF stage II-IV - methylprednisolone 1-2 mg / kg / day IV The period for assessing the response to first-line therapy: 72 hours, 7 days, 14 days from the start of therapy.

• Criteria for prescribing second-line therapy: progression of manifestations of O.RTPH after 72 hours or no improvement after 7 days or incomplete resolution of clinical and laboratory manifestations after 14 days

• Diagnosis and therapy of chronic GVHD: Diagnosis and staging of chronic GVHD are performed in accordance with THE NIH criteria (Appendix No. 4). Due to the fact that the development of chronic GVHD is one of the main parameters for the evaluation of the study, the diagnosis and staging of chronic GVHD are performed prospectively, monthly from the day +100, using a structured examination in accordance with Appendix No. 2.

Therapy of chronic GVHD is carried out in accordance with the standard adopted in the clinic

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  1. Patients under the age of 21 years with following diseases:
  • acute lymphoblastic,
  • myeloblastic,
  • biphenotypic,
  • bilinear leukemia,
  • malignant lymphoma,
  • myelodysplastic syndrome,
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Exclusion Criteria

Age over 21 years

  • Patients with ALL outside clinical and hematological remission

  • Clinical status:

    • Lansky/Karnowski index <70% (supplement No.1)
    • Heart function: left ventricular ejection fraction <40% according to ultrasound of the heart1
    • Kidney function: clearance of endogenous creatinine < 70 ml / min
    • Liver function: total bilirubin, ALT, AST, ALP > 2 norms
    • Lung function: lung capacity <50%, for children who cannot carry out of respiratory function - oxygen saturation during pulse oximetry <92%
  • Uncontrolled viral, fungal or bacterial infection.

  • Mental illness of the patient or caregivers, making it impossible to realize the essence of the study and compromising compliance with medical appointments and sanitary and hygienic regime 1 These patients may receive treatment according to the protocol, but the results will be evaluated separately

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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
1. Cumulative Incidence stage II-IV after HSCTup to 100-day

Estimate the probability of developing acute GVHD stage II-IV after HSCT

Kaplan Meier overal survivalup to 100 days

Explore the safety based on an assessment of the frequency of occurrence severe (3-5 degrees) side effects of conditioning- 100-day transplant-associated mortality

Kaplan Meier event free survivalup to 100 days

Explore the safety based on an assessment of the frequency of occurrence severe (3-5 degrees) side effects of conditioning- 100-day transplant-associated mortality

Secondary Outcome Measures
NameTimeMethod
event-free survivalup to 100 days

Probability of developing a relapse of the primary disease, transplantation-associated mortality on the horizon of 100 days, general and event-free survival

Cumulative Incidence of leukocyte engraftmentup to 30 days

Probability and kinetics of engraftment of leukocyte and platelet sprouts of donor origin

Cumulative Incidence of platelet engraftmentup to 30 days

Probability and kinetics of engraftment of leukocyte and platelet sprouts of donor origin

Cumulative Incidence reactivation of CMVup to 6 mouth or up to immunreconstitution

Probability of reactivation of CMV, EBV, AdV, HHV6 infection

box plotup to 1 year

Kinetics of general and pathogen-specific immunoreconstitution

Cumulative Incidence of chronic GVHDup to 1 year

Probability of the development of chronic GVHD, its severity and the nature of the involvement of organs and tissues.

Cumulative Incidence reactivation of EBVup to 6 mouth or up to immunreconstitution

Probability of reactivation of CMV, EBV, AdV, HHV6 infection

Cumulative Incidence reactivation of AdVup to 6 mouth or up to immunreconstitution

Probability of reactivation of CMV, EBV, AdV, HHV6 infection

Cumulative Incidence reactivation of HHV6up to 6 mouth or up to immunreconstitution

Probability of reactivation of CMV, EBV, AdV, HHV6 infection

Trial Locations

Locations (1)

National medical research center of pediatric haematology, oncology and immulogy named after Dmytriy Rogachyov

🇷🇺

Moscow, Russian Federation

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