Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience

We report the national data on the outcomes of hematopoietic stem cell transplantation (HSCT) for thalassemia major (TM) patients in Turkey on behalf of the Turkish Pediatric Stem Cell Transplantation Group. We retrospectively enrolled 1469 patients with TM who underwent their first HSCT between 198...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2022-05, Vol.57 (5), p.760-767
Hauptverfasser: Yesilipek, M. Akif, Uygun, Vedat, Kupesiz, Alphan, Karasu, Gulsun, Ozturk, Gulyuz, Ertem, Mehmet, Şaşmaz, İlgen, Daloğlu, Hayriye, Güler, Elif, Hazar, Volkan, Fisgin, Tunç, Sezgin, Gülay, Kansoy, Savaş, Kuşkonmaz, Barış, Akıncı, Burcu, Özbek, Namık, İnce, Elif Ünal, Öztürkmen, Seda, Küpesiz, Funda Tayfun, Yalçın, Koray, Anak, Sema, Bozkurt, Ceyhun, Karakükçü, Musa, Küpeli, Serhan, Albayrak, Davut, Öniz, Haldun, Aksoylar, Serap, Okur, Fatma Visal, Albayrak, Canan, Yenigürbüz, Fatma Demir, Bozkaya, İkbal Ok, İleri, Talia, Gürsel, Orhan, Karagün, Barbaros Şahin, Kintrup, Gülen Tüysüz, Çelen, Suna, Elli, Murat, Aksoy, Basak Adaklı, Yılmaz, Ebru, Tanyeli, Atila, Akyol, Şule Turan, Siviş, Zuhal Önder, Özek, Gülcihan, Uçkan, Duygu, Kartal, İbrahim, Atay, Didem, Akyay, Arzu, Bilir, Özlem Arman, Çakmaklı, Hasan Fatih, Kürekçi, Emin, Malbora, Barış, Akbayram, Sinan, Demir, Hacı Ahmet, Kılıç, Suar Çakı, Güneş, Adalet Meral, Zengin, Emine, Özmen, Salih, Antmen, Ali Bülent
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Sprache:eng
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Zusammenfassung:We report the national data on the outcomes of hematopoietic stem cell transplantation (HSCT) for thalassemia major (TM) patients in Turkey on behalf of the Turkish Pediatric Stem Cell Transplantation Group. We retrospectively enrolled 1469 patients with TM who underwent their first HSCT between 1988 and 2020 in 25 pediatric centers in Turkey. The median follow-up duration and transplant ages were 62 months and 7 years, respectively; 113 patients had chronic graft versus host disease (cGVHD) and the cGVHD rate was 8.3% in surviving patients. Upon the last visit, 30 patients still had cGvHD (2.2%). The 5-year overall survival (OS), thalassemia-free survival (TFS) and thalassemia-GVHD-free survival (TGFS) rates were 92.3%, 82.1%, and 80.8%, respectively. cGVHD incidence was significantly lower in the mixed chimerism (MC) group compared to the complete chimerism (CC) group ( p  
ISSN:0268-3369
1476-5365
DOI:10.1038/s41409-022-01613-w