Volume 28, Issue 6 e14842
ORIGINAL ARTICLE

Initiation of Haploidentical Stem Cell Transplantation With Post-Transplant Cyclophosphamide in Children: A Low–Middle-Income Country Institutional Experience

Syed Ibrahim Bukhari

Corresponding Author

Syed Ibrahim Bukhari

Department of Oncology, Aga Khan University, Karachi, Pakistan

Correspondence:

Syed Ibrahim Bukhari ([email protected])

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Javeria Saeed

Javeria Saeed

Department of Surgery, Aga Khan University, Karachi, Pakistan

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Zehra Fadoo

Zehra Fadoo

Department of Oncology, Aga Khan University, Karachi, Pakistan

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Asim Fakhruddin Belgaumi

Asim Fakhruddin Belgaumi

Department of Oncology, Aga Khan University, Karachi, Pakistan

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Naureen Allani

Naureen Allani

Department of Oncology, Aga Khan University, Karachi, Pakistan

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Sadaf Altaf

Sadaf Altaf

Department of Oncology, Aga Khan University, Karachi, Pakistan

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First published: 19 August 2024

Funding: The authors received no specific funding for this work.

ABSTRACT

Background

Haploidentical hematopoietic stem cell transplant (HSCT) is a curative treatment especially for countries where bone marrow registries are nonexistent. We present our experience with haploidentical HSCT in pediatric patients.

Methods

Retrospective data collected and analyzed for patients ≤18 years, from January 2017 to December 2022.

Results

The cohort consisted of 20 patients with median age at transplant of 61.5 (IQR: 124) months. Fourteen (70%) were malignant and 6 (30%) were benign diseases. Donors were father in majority (9/20; 45%). Stem cell source was peripheral blood 8, marrow 8, and combined 4. c-specific antibodies were positive in 6 (30%). Median CD34 cell dose infused: 9.35 × 106/kg. Median engraftment time: 15 (IQR: 17) days. Acute and chronic graft-versus-host disease (GVHD) occurred in 12/20 (60%) and 5/20 (25%), respectively. Complications included infection/sepsis (14/20; 70%), cytomegalovirus reactivation (14/20; 70%), sinusoidal obstruction syndrome (1/20; 5%), primary graft failure (PGF) (6/20; 30%), and secondary graft failure (4/20; 20%). PGF was more common in benign conditions (p = 0.003) and less prevalent in cases with aGVHD (p = 0.007). aGVHD was more common in malignant conditions (p = 0.007). Overall survival (OS), relapse-free survival (RFS), and treatment-related mortality (TRM) were 40%, 50%, and 35%, respectively. Median time of survival and relapse were 8 (IQR: 15) and 9 (IQR: 13) months, respectively.

Conclusion

OS was comparable to that of other low–middle-income countries. GVHD was a major challenge, along with sepsis and CMV infection. Half of the leukemias relapsed. Graft failure was a major concern in nonmalignant diseases.

Conflicts of Interest

The authors declare no conflicts of interest.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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