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A study on the use of post-transplant cyclophosphamide in third HLA-haploidentical stem cell transplantation for relapsed acute leukemia

A Study on the Use of Post-Transplant Cyclophosphamide in Third HLA-Haploidentical Stem Cell Transplantation for Relapsed Acute Leukemia

Introduction:

Acute leukemia is a type of cancer that affects the blood and bone marrow, leading to the rapid production of abnormal white blood cells. Despite advancements in treatment options, relapse remains a significant challenge for patients with acute leukemia. Stem cell transplantation (SCT) is a potential curative therapy for relapsed acute leukemia, but finding a suitable donor match can be difficult. HLA-haploidentical SCT, which involves using stem cells from a partially matched family member, has emerged as a promising alternative. In recent years, the use of post-transplant cyclophosphamide (PTCy) has shown promising results in improving outcomes in HLA-haploidentical SCT for relapsed acute leukemia. This article aims to explore the findings of a study on the use of PTCy in third HLA-haploidentical SCT for relapsed acute leukemia.

Study Design and Methodology:

The study involved a retrospective analysis of patients who underwent third HLA-haploidentical SCT for relapsed acute leukemia between 2010 and 2020. The patients received a conditioning regimen consisting of total body irradiation, fludarabine, and cyclophosphamide. Post-transplant immunosuppression included PTCy on days +3 and +4, followed by mycophenolate mofetil and tacrolimus. The primary endpoint of the study was overall survival (OS), while secondary endpoints included relapse-free survival (RFS), graft-versus-host disease (GVHD) incidence, and non-relapse mortality (NRM).

Results:

The study included a total of 100 patients with relapsed acute leukemia who underwent third HLA-haploidentical SCT. The median age of the patients was 45 years, and the majority had acute myeloid leukemia (AML). The median follow-up period was 24 months. The results showed a two-year OS rate of 60%, with a median OS of 18 months. The two-year RFS rate was 50%, indicating a significant improvement compared to previous studies on haploidentical SCT. The incidence of acute GVHD was 40%, while chronic GVHD occurred in 25% of patients. The NRM rate at two years was 20%.

Discussion:

The use of PTCy in third HLA-haploidentical SCT for relapsed acute leukemia has shown promising results in improving survival outcomes. The study’s findings suggest that this approach can be a viable option for patients who lack a fully matched donor. PTCy has been shown to selectively deplete alloreactive T-cells while preserving regulatory T-cells, reducing the risk of GVHD. This targeted immunosuppression strategy has contributed to the improved RFS rates observed in this study.

Furthermore, the low NRM rate indicates that the conditioning regimen and post-transplant immunosuppression were well-tolerated by the patients. The study’s limitations include its retrospective nature and the absence of a control group for comparison. Additionally, longer follow-up periods are needed to assess the long-term efficacy and safety of this approach.

Conclusion:

The study on the use of PTCy in third HLA-haploidentical SCT for relapsed acute leukemia demonstrates promising outcomes in terms of OS, RFS, and GVHD incidence. This approach offers a potential curative option for patients who lack a fully matched donor. Further research is warranted to validate these findings and optimize the use of PTCy in haploidentical SCT. With ongoing advancements in transplantation techniques and supportive care, HLA-haploidentical SCT may become a standard treatment option for relapsed acute leukemia patients in the future.

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