| Literature DB >> 33184452 |
Maryam Khan1, Raheel Iftikhar2, Tariq Ghafoor1, Fayyaz Hussain1, Qamar Un Nisa Chaudhry1, Syed Kamran Mahmood1, Nighat Shahbaz1, Mehreen Ali Khan1, Tariq Azam Khattak1, Ghassan Umair Shamshad1, Jahanzeb Rehman1, Sundas Ali3, Zunaira Shah4, Abdul Rafae5, Muhammad Farhan1, Faiz Anwer6, Parvez Ahmed7.
Abstract
Management of rare hematological disorders pose unique diagnostic and therapeutic challenges due to unusual occurrence and limited treatment options. We retrospectively identified 45 patients receiving matched related donor transplant for rare hematological disorders from 2006 to 2019. Patients were divided into two groups (1) malignant and (2) non malignant. The malignant disorder group included four patients while the nonmalignant group included 41 patients divided into immune dysregulation (n = 23), bone marrow failure (n = 10), metabolic (n = 5), and bleeding diathesis (n = 3). Twenty-six (57.8%) patients received myeloablative conditioning (MAC) and 16 (35.6%) received reduced intensity conditioning (RIC), while 3 (6.6%) patients with severe combined immunodeficiency received stem cell infusion alone without conditioning. The cumulative incidence (CI) of grade II-IV acute GVHD (aGVHD) was 39.1% (n = 18) and chronic GVHD (cGVHD) 15.2% (n = 7). There was no primary graft failure while CI of secondary graft failure was 9%. Overall survival (OS) and disease-free survival (DFS) was 82.2% and 77.8% respectively. Group wise OS was 75% in the malignant group, 82.6% in the immune dysregulation group, 80% in patients with metabolic disorders and bone marrow failure, while 100% in patients with bleeding diathesis. This retrospective analysis shows that hematopoietic stem cell transplant can be a feasible treatment option for rare hematological disorders.Entities:
Year: 2020 PMID: 33184452 DOI: 10.1038/s41409-020-01126-4
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483