Haematopoietic Cell Transplants in Adults Acute Lymphoblastic Leukaemia in a Resource-poor Middle East Country

Main Article Content

Khalid Halahleh*
Isra Muradi
Nazmi Kamal
Ayat Taqash
Fareed Barakat
Hadeel Abdelkhaleq
Mohammad Khalil
Lina Halahleh
Waleed Da’na
Nidal Almasri
Mohammad Makoseh
Ammar Alamarneh
Al-Far Rozan
Husam Abu-Jazar
Robert Peter Gale

Abstract

Background: Outcomes of chemotherapy in adults with ALL in resource-poor countries are reportedly worse compared with outcomes in resource-rich countries. There are few comparative data on transplants in these settings.


Methods: Retrospective analysis of 102 consecutive subjects > 18 years with ALL receiving an allotransplant from Jan 2007 to Sept 2022 in Jordan.


Results: Median follow-up is 38 mo ([IQR] 16-80 mo). 81 subjects were men. The median age was 29 y(IQR 22-36 y). 63 were B-cell and 38, were T-cell lineage. 31 had the Ph-chromosome. 68 were in 1st and 34, ≥ 2nd histological complete remission. 97 received intensive conditioning. Donors were an HLA-identical sibling (N = 88) or an HLA-mis-matched relative (N = 14). Grafts were blood cells. Subjects received conventional GvHD prophylaxis, cyclophosphamide (N = 11) or ATG (N = 3). All subjects recovered bone marrow function with complete donor chimerism. 5-year leukemia-free survival (LFS), 58% (47, 69%) and survival, 45% (34, 56%). 45 subjects developed acute and 44, cGvHD. 3-year cumulative incidence of cGvHD was 28% (15, 42%). 5-year CIR was 32% (18, 45%) and 3-year NRM, 25% (15, 35%).


Conclusion: Allotransplant outcomes in adults with ALL in Jordan, a resource-poor country, seem comparable to those reported in resource-rich countries.

Article Details

Halahleh, K., Muradi, I., Kamal, N., Taqash, A., Barakat, F., Abdelkhaleq, H., … Gale, R. P. (2025). Haematopoietic Cell Transplants in Adults Acute Lymphoblastic Leukaemia in a Resource-poor Middle East Country. Journal of Stem Cell Therapy and Transplantation, 006–011. https://doi.org/10.29328/journal.jsctt.1001046
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Copyright (c) 2025 Halahleh K, et al.

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