Efficacy and Safety of the CloB2M (Clofarabine Combined With Busulfan and Melphalan) Conditioning Regimen in Allogeneic Hematopoietic Stem Cell Transplantation for Adult Patients With Acute Myeloid Leukemia in First Complete Remission

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorInstitute of Hematology & Blood Diseases Hospital, China

About this trial

This is a single-center, prospective, exploratory clinical study. It plans to enroll 30 adult patients with acute myeloid leukemia (AML) who have achieved first complete remission (CR1) after induction therapy and meet the indications for allogeneic hematopoietic stem cell transplantation (allo-HSCT). The aim is to evaluate the efficacy and safety of allo-HSCT following conditioning regimens with clofarabine, busulfan and melphalan.

Eligibility criteria

Qualifiers

1.Aged from 18 to 60 years inclusive, with no restriction on gender;

2.Patients diagnosed with acute myeloid leukemia (AML, excluding acute promyelocytic leukemia, APL) by bone marrow morphological, immunological and genetic examinations according to the 2022 World Health Organization (WHO) classification, who have achieved first complete remission (CR1) after induction therapy;

AML classified as intermediate or adverse genetic risk according to the 2022 ELN genetic risk stratification;

AML with positive measurable residual disease (MRD) before transplantation;

Disqualifiers

1.Refractory/relapsed AML;

2.Known hypersensitivity to any drugs in the conditioning regimen or their excipients;

3.Major surgery within the past 4 weeks (excluding diagnostic surgical procedures);

4.History of or concurrent other malignant tumors (excluding well-controlled non-melanoma basal cell carcinoma of the skin, breast/cervical carcinoma in situ, and other malignancies well controlled without treatment for more than five years);

Trial design

Treatments tested in this trial

  • CloB2M (Clofarabine Combined With Busulfan and Melphalan) Conditioning Regimen

Treatment groups

30 Participants
are divided into 1 treatment group

Locations

This trial has no locations