Multicenter propensity score matched study on allogeneic stem cell transplantation in adult sickle cell disease: Comparison of donor vs. no donor outcomes

C Can Boga (1Baskent University Faculty of Medicine, Hematology/ Adana Adult Bone Marrow Transplantation Center, Adana, Türkiye) B Bahar Sevgili (20Iskenderun State Hospital, Hematology, Hatay, Türkiye) E Emel Gürkan S Suheyl Asma (1Baskent University Faculty of Medicine, Hematology/ Adana Adult Bone Marrow Transplantation Center, Adana, Türkiye) S Selma Ünal N Naci Tiftik (30Mersin University School of Medicine, Hematology, Mersin, Türkiye) G Gül İlhan (5Ministry of Health Antalya State Hospital, Hematology, Antalya, Türkiye) F Funda Kupesiz (6Akdeniz University Faculty of Medicine, Pediatric Hematology, Antalya, Türkiye) Z Zeynep Karakas (2Istanbul University, Istanbul School of Medicine, Pediatric Hematology and Oncology, Istanbul, Türkiye) S Seda Gürcan (8Acibadem Altunizade Hospital, Pediatric Hematology, İstanbul, Türkiye) N Nur Akad Soyer (1Ege University School of Medicine, Pediatric Hematology and Oncology, Izmir, Türkiye) E Elif Kazancı (10SBU Medical Faculty of Bursa, Hematology, Bursa, Türkiye) A Ayse Hilal Eroglu Kucukdiller (16Aydin State Hospital, Hematology, Aydin, Türkiye) İpek Yildiz (28Kartal Training and Reseach Hospital, Hematology, Istanbul, Türkiye) M Mahmut Yeral (1Baskent University Faculty of Medicine, Hematology/ Adana Adult Bone Marrow Transplantation Center, Adana, Türkiye) H Hakan Ozdogu (11Baskent University Hospital, Adana, Türkiye) Y Yesim Aydinok (1Ege University School of Medicine, Pediatric Hematology and Oncology, Izmir, Türkiye)

Abstract

Abstract Background Despite the lack of high-level scientific evidence, allogeneic hematopoietic stem cell transplantation (Allo HPSCT) is routinely performed successfully for adult sickle cell disease (SCD). However, studies on transplanted vs. non-transplant patients for the development of SCD indications are lacking. A controlled evaluation of outcomes among adults undergoing allo-HSCT compared to matched controls without a donor is critical to inform clinical decision-making. This study was to assess the outcome of transplanted vs. non-transplant SCD groups by propensity matched pair analysis. Methods This multicenter, retrospective cohort study on behalf of the Turkish Society of Hematology Hemoglobinopathy Study Group (TSH-HSG) included consecutive SCD patients with donor undergoing Allo HSCT or SCD patients with no donor in 14 centers from Turkiye. Propensity scores were calculated based on nine pretransplant variables (age, vasooclusive crisis, pulmonary hypertension, proteinuria, acute chest syndrome and cerebral event, which are known to be associated mortality). Transplant and non-transplant groups were matched in a 1:1 ratio. Outcomes including complications and mortality were compared using paired test. Results: The group sample sizes of 102 in each group achieved 100% power at a significance level of alpha=0.05 based on group survival means. Among 805 patients with SCD patients, 102 pairs were matched with transplanted group receiving non-myeloablative Fu Bu ATLG and posttransplant cyclophosphamide-containing regimen. The mean follow up time for transplanted group was shorter [47 (IQR 24-75) vs. 202 (IQR 84-241); P< 0.001]. Ninety-seven (95%) of transplanted patients achieved cure with no secondary graft failures. Two (2%) patients developed chronic graft-versus-host disease. Hemoglobin, hemoglobin S value, vasooclusive crisis, acute chest, proteinuria, transfusion need and hospitalization rate were significantly better in transplant group vs. non-transplant group (p< 0.001, for all). Overall survival curve analysis of the groups were estimated as similar via log-rank test (P=0.298). When patients who received transplants from alternative donors are excluded, the difference of survival curves did not change. Conclusion This multicenter propensity score matched study confirms the superiority of transplant over non-transplant group based on hematological parameters, vasooclusive crisis, acute chest, proteinuria, transfusion requirement, and hospitalization rate thus validating current guideline advice for adult SCD.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 6060-6060
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (17)

C

Can Boga

1Baskent University Faculty of Medicine, Hematology/ Adana Adult Bone Marrow Transplantation Center, Adana, Türkiye

B

Bahar Sevgili

20Iskenderun State Hospital, Hematology, Hatay, Türkiye

E

Emel Gürkan

S

Suheyl Asma

1Baskent University Faculty of Medicine, Hematology/ Adana Adult Bone Marrow Transplantation Center, Adana, Türkiye

S

Selma Ünal

N

Naci Tiftik

30Mersin University School of Medicine, Hematology, Mersin, Türkiye

G

Gül İlhan

5Ministry of Health Antalya State Hospital, Hematology, Antalya, Türkiye

F

Funda Kupesiz

6Akdeniz University Faculty of Medicine, Pediatric Hematology, Antalya, Türkiye

Z

Zeynep Karakas

2Istanbul University, Istanbul School of Medicine, Pediatric Hematology and Oncology, Istanbul, Türkiye

S

Seda Gürcan

8Acibadem Altunizade Hospital, Pediatric Hematology, İstanbul, Türkiye

N

Nur Akad Soyer

1Ege University School of Medicine, Pediatric Hematology and Oncology, Izmir, Türkiye

E

Elif Kazancı

10SBU Medical Faculty of Bursa, Hematology, Bursa, Türkiye

A

Ayse Hilal Eroglu Kucukdiller

16Aydin State Hospital, Hematology, Aydin, Türkiye

İpek Yildiz

28Kartal Training and Reseach Hospital, Hematology, Istanbul, Türkiye

M

Mahmut Yeral

1Baskent University Faculty of Medicine, Hematology/ Adana Adult Bone Marrow Transplantation Center, Adana, Türkiye

H

Hakan Ozdogu

11Baskent University Hospital, Adana, Türkiye

Y

Yesim Aydinok

1Ege University School of Medicine, Pediatric Hematology and Oncology, Izmir, Türkiye