Volume 20, Issue 3 pp. 417-423
Original Article

Haploidentical hematopoietic stem cell transplantation with post-transplant high-dose cyclophosphamide in high-risk children: A single-center study

M. Akif Yesilipek

Corresponding Author

M. Akif Yesilipek

Pediatric Stem Cell Transplantation Unit, Department of Pediatric Hematology, Bahcesehir University School of Medicine, Istanbul, Turkey

M. Akif Yesilipek, Medicalpark Antalya Hastanesi, Cocuk Kemik İligi Nakil Unitesi C Blok Kat 7, 07100 Antalya, Turkey

Tel.: +90 532 2836237

Fax: +90 242 3143156

E-mail: [email protected]

Search for more papers by this author
Vedat Uygun

Vedat Uygun

Pediatric Stem Cell Transplantation Unit, Department of Pediatric Hematology, Bahcesehir University School of Medicine, Istanbul, Turkey

Search for more papers by this author
Gulsun Karasu

Gulsun Karasu

Pediatric Stem Cell Transplantation Unit, Department of Pediatric Hematology, Bahcesehir University School of Medicine, Istanbul, Turkey

Search for more papers by this author
Hayriye Daloglu

Hayriye Daloglu

Pediatric Stem Cell Transplantation Unit, Medicalpark Antalya Hospital, Antalya, Turkey

Search for more papers by this author
Zeynep Dincer

Zeynep Dincer

Pediatric Stem Cell Transplantation Unit, Medicalpark Antalya Hospital, Antalya, Turkey

Search for more papers by this author
First published: 28 December 2015
Citations: 7

Abstract

Recently, haploidentical transplantations have been performed with unmanipulated BM or PBSC. This approach is becoming more widely adopted with the use of PTCY. However, there is limited evidence about this approach in children. We present 15 children who received 16 haploidentical HSCT with unmanipulated BM or PBSC using PTCY for GVHD prophylaxis. Post-transplant CY(50 mg/kg IV) was given on the third and fifth day, and CsA or tacrolimus with MMF or MP was also used for GVHD prophylaxis. All patients engrafted at a median of 16 and 18 days for neutrophil and thrombocyte recovery, respectively. Grades II–III acute GVHD developed in seven patients, and mild chronic GVHD was found in two patients. Two patients died within the first 100 days due to sepsis (TRM 12.5%). Eleven patients are currently alive, with a median follow-up of 12 months (range 6–22 months). The 12-month OS and DFS were 75 ± 10.8% and 68.8 ± 11.6%, respectively. Our results with these high-risk patients are encouraging for haploidentical HSCT in pediatric patients. Future studies should continue to assess haploidentical HSCT, including comparison of other modalities, in a primary pediatric population.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.