Evaluation of Recombinant Humanized Anti-CD25 Monoclonal Antibody for Preventing Graft-versus-host Disease After Haploidentical/matched Unrelated Donor Hematopoietic Stem Cell Transplantation in Patients with Transfusion-dependent Thalassemia

Phase 2RecruitingNCT06657391

Rongrong Liu396 enrolled

Overview

Graft-versus-host disease (GVHD) is a major factor affecting the efficacy and quality of life of alternative donor transplantation in thalassemia major (TM), severely limiting the clinical application of alternative donor transplantation in TM.The purpose of this clinical trial is to evaluate whether recombinant humanized anti-CD25 monoclonal antibody is effective in preventing GVHD and its safety after haploidentical/matched unrelated donor hematopoietic stem cell transplantation. The main questions it aims to answer are: * Does recombinant humanized anti-CD25 monoclonal antibody reduce the incidence of GVHD disease after haploidentical/matched unrelated donor hematopoietic stem cell transplantation? * What medical problems will participants experience when using the recombinant humanized anti-CD25 monoclonal antibody? What is the quality of life after 2 years follow-up? In this clinical trail, participants will be randomly assigned to the intervention group or the control group by researchers in a 2:1 ratio. The intervention group will be given recombinant humanized anti-CD25 monoclonal antibody (1mg/Kg) combined with the standard GVHD prophylaxis after transplantation, while the control group will only receive the standard GVHD prophylaxis. The incidence of GVHD after transplantation in the two groups will be observed. The main evaluation is the clinical efficacy of recombinant humanized anti-CD25 monoclonal antibody in preventing aGVHD.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

396

Conditions

Transfusion Dependent Thalassemia

Eligibility

Sex: ALLMin age: 3 YearsMax age: 20 Years

Medical Language ↔ Plain English

Inclusion Criteria: * patients with transfusion-dependent thalassemia; * patients who are planning to receive matched unrelated donor hematopoietic stem cell transplantation (MUD-HSCT) or HLA haploidentical donor hematopoietic stem cell transplantation (HID-HSCT); * physical condition score (Lansky/Karnofsky score) ≥ 70%; * patients (or legal guardians) voluntarily participate in the study and sign the informed consent form Exclusion Criteria: * patients with HLA-matched hematopoietic stem cell donors and willing to receive HLA-matched hematopoietic stem cell transplantation; * patients with known infectious diseases such as hepatitis B, hepatitis C, AIDS, syphilis, human T-lymphotropic virus, etc.; * patients with serious active bacterial, viral, fungal, malaria or parasitic infections; * patients with autoimmune deficiency diseases; * patients with a history of malignant tumors or current malignant tumors; * patients with important organ diseases or abnormal laboratory tests, including but not limited to: 1) patients with cirrhosis, liver fibrosis or active hepatitis, and/or abnormal liver function tests (alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≥2.5×ULN; alkaline phosphatase ≥2.5×ULN); 2) patients with heart disease, or left ventricular ejection fraction (LVEF) \<60%, or severe iron deposition in the heart; 3) kidney disease, or blood creatinine ≥1.5×ULN with creatinine clearance \<30% of normal level; 4) patients with endocrine dysfunction; * patients with uncorrected bleeding disease; * patients with severe mental illness (such as severe depression, schizophrenia, etc.) or cognitive dysfunction (dementia, delirium, etc.), which are unable to cooperate with the study; * peripheral blood white blood cell (WBC) count \<3×10\^9/L or platelet count \<100×10\^9/L; * patients having received thalidomide treatment within the past 3 months; * patients having received any type of gene and/or cell therapy in the past; * patients with severe allergies; * female patients who are pregnant, breastfeeding, or planning to become pregnant within 1 year of participating in this trial; * patients who are participating in other clinical trials; * other situations that are not suitable for participation in this clinical trial as assessed by the investigator.

Locations (5)

Maoming People's Hospital

Maoming, Guangdong, China

RECRUITING

Liuzhou Workers' Hospital

Liuchow, Guangxi, China

RECRUITING

The First Affiliated Hospital of Guangxi Medical University

Nanning, Guangxi, China

RECRUITING

Yulin Red Cross Hospital

Yulin, Guangxi, China

RECRUITING

Hainan Provincial People's Hospital

Haikou, Hainan, China

RECRUITING

Outcomes

Primary Outcomes

Grade III-IV aGVHD

the incidence of grade III-IV aGVHD within 100 days after HID-HSCT/MUD-HSCT was compared between the intervention group and the control group.

Time frame: within 100 days after HID-HSCT/MUD-HSCT

Secondary Outcomes

Grade II-IV aGVHD

the incidence of grade II-IV aGVHD within 100 days after HID-HSCT/MUD-HSCT was compared between the intervention group and the control group.

Time frame: within 100 days after HID-HSCT/MUD-HSCT

Chronic graft-versus-host disease (cGVHD)

The incidence of cGVHD after HID-HSCT/MUD-HSCT was compared between the intervention group and the control group.

Time frame: 2 years

Overall survival (OS)

Comparison of 2-year OS between the intervention group and the control group.

Time frame: 2 years

Thalassemia-free survival (TFS)

comparison of the 2-year TFS between the intervention group and the control group.

Time frame: 2 years

Transplantation-related mortality (TRM)

comparison of the 2-year TRM between the intervention group and the control group.

Time frame: 2 years

Transplantation-related complications

comparison of the 2-year transplantation-related complications between the intervention group and the control group.

Time frame: 2 years

Infection

comparison of the infection during the transplantation between the intervention group and the control group.

Time frame: 2 years

Immune reconstitution

comparison of the immune reconstitution after transplantation between the intervention group and the control group.

Time frame: 2 years

Quality of life

comparison of the quality of life between the intervention group and the control group by using the Pediatric Quality of Life Inventory Version 4.0 (PedsQL4.0) scale. The scales are comprissed of parallel self-report and parent proxy-report formats: 1. Self-report includes ages 8 to 12, 13 to 18, and 18 to 25, with a total of 23 items. 2. Parent proxy-report assesses parent's perceptions of their child's health-related quality of life. Parent proxy-report (ages 5 to 7) has 23 items, and Parent proxy-report (ages 2 to 4) has 21 items. A 5-point response scale is utilized across self-report for ages and parent proxy-report (0 = never a problem; 1 = almost never a problem; 2 = sometimes a problem; 3 = often a problem; 4 = almost always a problem). Items are reverse-scored and linearly transformed to a 0 to 100 scale (0 = 100, 1 = 75, 2 = 50, 3 =25, 4 = 0), so that higher scores indicate better health-related quality of life.

Time frame: 2 years

Adverse events

comparison of the occurrence of adverse events between the intervention group and the control group.

Time frame: 2 years

Evaluation of Recombinant Humanized Anti-CD25 Monoclonal Antibody for Preventing Graft-versus-host Disease After Haploidentical/matched Unrelated Donor Hematopoietic Stem Cell Transplantation in Patients with Transfusion-dependent Thalassemia

Overview

Conditions

Interventions

Eligibility

Locations (5)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts