Transplantation and cellular therapy · 2026
Outcomes of Acquired Aplastic Anemia after HLA-Identical Sibling Donor Transplantation in Pakistan: A Multicentre Study on Behalf of the Pakistan Blood and Marrow Transplant Group.
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Khan Maryam, Samad Shafaq Abdul, Altaf Sadaf, Ghani Danyal, Sarwar Shahzad, Chaudhry Qamar Un Nisa, Mehmood Syed Kamran, Farzana Tasneem, Zaidi Uzma, Ali Natasha, Shahbaz Nighat, Khan Mehreen Ali, Awais Kashaf Ad Duja, Adil Salman, Mir Muhammad Ayaz, Ghafoor Tariq, Khattak Tariq Azam, Batool Aliya, Bukhari Syed Nasir Abbas, Khurram Sana, Satti Tariq Mahmood, Tariq Hira, Ahmed Parvez, Iftikhar Raheel
Аннотация
Haematopoietic stem cell transplantation (HSCT) from an HLA-identical sibling is the primary curative therapy for acquired aplastic anemia (AA). Outcomes from large cohorts in low- and middle-income countries (LMIC) are scarce. To evaluate survival outcomes of patients with acquired AA undergoing matched sibling donor (MSD) HSCT in Pakistan and to identify key transplant- and patient-related factors influencing outcomes in a resource-limited, LMIC setting. Multicenter retrospective cohort study. We retrospectively analyzed 596 consecutive patients with acquired AA who underwent HSCT from an HLA-identical sibling donor at seven Pakistani centers between January 2001 and August 2023. Patients receiving haploidentical, unrelated, or other alternative-donor grafts were excluded. Overall survival (OS) was estimated using Kaplan-Meier method. Univariable and multivariable Cox regression identified predictors of OS; logistic regression identified predictors of graft failure. Median age at transplant was 18 yr (IQR:13 to 24), median time to neutrophil and platelet engraftment was 12 d (11 to 14 d) and 19 d (14 to 28 d), respectively. Primary graft failure occurred in 39 (6.6%) and secondary graft failure in 52 (8.8%) patients. Incidence of acute and chronic graft-versus-host disease was 70 (11.2%) and 97 (19%), respectively. At a median follow-up of 59.4 mo (95% CI 47.9 to 68.4), OS was 69.6%. The leading cause of mortality was graft failure and poor graft function in 91 (49.4%) followed by sepsis in 60 (32.6%) patients. On multivariable Cox regression, RCC <20 (adjusted HR 0.43, 95% CI 0.25 to 0.73, P = .002), CsA + MMF prophylaxis (adjusted HR 2.57, 95% CI 1.47 to 4.51, P = .001), and BMH + PBSC stem cell source (adjusted HR 0.61, 95% CI 0.36 to 1.07, P = .001) were independent predictors of OS. MSD-HSCT achieves durable survival for AA patients in resource-limited settings. Early referral strategies, infection control, and optimization of graft characteristics are required to improve survival in these settings.