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NCT Number: NCT04943757

Post-transplantation Benadamustine and Cyclophosphamide in Patients With Refractory Myeloid Malignancies

Prognosis of patients undergoing salvage allogeneic stem cell transplantation for refractory leukemia or other refractory myeloid malignanies is poor. One of the approaches to augment graft-versus-leukemia effect the use of post-transplantation bendamustine in graft-versus-host disease prophylaxis. Despite high frequency of responses and durable remissions after this approach majority of patients develop a serious complication - cytokine release syndrome, which can be life-threatening in some patients. On the other hand post-transplantation cyclophocphamide was reported to abort cytokine release syndrome that sometimes occurs after graft transfusion in patients after haploidentical graft transfusion. The aim of this study is to evaluate if the combination of post-transplantation bendamustine (PTB) and post-transplantation cyclophosphamide (PTCY) facilitates comparable graft-versus leukemia effect to PTB, but with better safety profile and reduced incidence of severe cytokine release syndrome.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with indication for allogeneic hematopoietic stem cell transplantation
  • Patients with 5-10/10 HLA-matched related or unrelated donor available. The donor and recipient must be identical by the following genetic loci: HLA-A, HLA-B, HLA-Cw, HLA-DRB1, and HLA-DQB1.
  • Peripheral blood stem cells or bone marrow as a graft source
  • Diagnosis:

Acute myeloid leukemia Chronic myeloid leukemia, Ph+ Myelodysplastic Syndromes Myeloprolipherative neoplasms

  • Salvage hematopoietic stem cell transplantation defined as:
  • Acute myeloid leukemia: >5% of clonal blasts despite adequate previous induction therapy or allogeneic stem cell transplantation Myelodysplastic Syndrome: >10% of blasts despite previous therapy with -7 or complex karyotype, or p53 mutation Chronic myeloid leukemia: blast crisis or acceleration phase despite at least 3 previous lines of TKIs Myeloprolipherative neoplasms : high tumor burden despite previous therapy, including >20 000 WBC/ ul or splenomegaly >15 cm
  • No severe concurrent illness

Exclusion criteria

  • Moderate or severe cardiac dysfunction, left ventricular ejection fraction <50%
  • Moderate or severe decrease in pulmonary function, FEV1 <70% or DLCO<70% of predicted
  • Respiratory distress >grade I
  • Severe organ dysfunction: AST or ALT >5 upper normal limits, bilirubin >1.5 upper normal limits, creatinine >2 upper normal limits
  • Creatinine clearance < 60 mL/min
  • Uncontrolled bacterial or fungal infection at the time of enrollment
  • Requirement for vasopressor support at the time of enrollment
  • Karnofsky index <30%
  • Pregnancy
  • Somatic or psychiatric disorder making the patient unable to sign informed consent

Treatment and study plan

Bendamustine Hydrochloride

Drug

50 mg/m2 iv Days +3 through +4 after allogeneic hematopoietic stem cell transplantation

Cyclophosphamid

Drug

25 mg/kg iv Days +3 through +4 after allogeneic hematopoietic stem cell transplantation

Primary outcomes

  1. Event-free survival analysis [ Time Frame: 1 year ]

    Time frame: 1 year

    Measure: Kaplan-Meier estimate of death or relapse, or graft failure

Secondary outcomes

  1. - Incidence of Cytokine release syndrome

    Time frame: 100 days

    Proportion of patients with cytokine release syndrome according to ASBMT Consensus Grading for Cytokine Release Syndrome, 2018

  2. Incidence of HSCT-associated adverse events (safety and toxicity)

    Time frame: 100 days

    Toxicity assessment is based on NCI CTC AE 5.0 grades. Veno-occlusive disease incidence and severity assessment is based on EBMT criteria 2016. Transplant-associated microangiopathy incidence assessment is based on Cho et al.

  3. Incidence of acute GVHD grade II-IV

    Time frame: 125 days

    Cumulative incidence of patients with acute GVHD II-IV grade

  4. Incidence of moderate and severe chronic GVHD

    Time frame: 1 year

    Cumulative incidence of patients with moderate and severe chronic GVHD according to NIH 2015 criteria

  5. Relapse rate analysis

    Time frame: 1 year

    Cumulative incidence of patients with relapse

  6. Non-relapse mortality analysis

    Time frame: 1 year

    Cumulative incidence of patients with mortality without hematological relapse of malignancy

  7. Overall survival analysis

    Time frame: 1 year

    Kaplan-Meier estimate of death from all causes

Sponsors and collaborators

Lead sponsor

St. Petersburg State Pavlov Medical University

Other

Registry information

Official study title

Graft-versus-host Disease Prophylaxis With Combination of Post-transplantation Benadamustine and Cyclophosphamide in Patients With Refractory Myeloid Malignancies (PTBCy)

Acronym: PTBCy

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Jun 29, 2021
Registry last updated
Oct 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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