Author/Authors :
Safayi, S.R. Assisstant Professor of Hematology Oncology- Tehran University of Medical Sciences, Tehran , Shahi, f. Associated Professor of Hematology Oncology- Tehran University of Medical Sciences, Tehran , Ghalamkari, M. Fellowship of Hematology Oncology- Tehran University of Medical Sciences, Tehran , Mirzania, M. Associated Professor of Hematology Oncology- Tehran University of Medical Sciences, Tehran , Khatuni, M. Internal Medicine Specialist - Tehran University of Medical Sciences , Hirmandi Niasar, F. Researcher at Tehran University of Medical Sciences, Tehran
Abstract :
Background: Allogeneic hematopoietic stem cell transplantation (HSCT) is a potentially cure for acute
myeloid leukemia (AML). Patients who undergone HSCT are at increased risk of infection due to impaired
immunity.
Objective: To evaluate the rate of bacterial, viral and fungal infection and its relationship with 2-year
overall survival of AML patients who had undergone HSCT.
Methods: This was a retrospective cross-sectional study of 49 patients who underwent allogenic bone
marrow transplantation (BMT) from full-matched donors at BMT Center, Imam Khomeini Hospital Complex,
Tehran, Iran, from 2006 to 2013. All autologous transplantations and promyelocytic leukemia (PML)
transplantations were excluded.
Results: All patients, except for one, had fever for a mean of 7 days post-transplantation and received
broad-spectrum antibiotic. The rate of severe sepsis was 6.1%. None of the patients developed fungal
infection during admission. The rate of admission due to sepsis after discharge was 27% in the alive
group (mean onset of 54 days), and 73% in the deceased group (mean onset of 52 days) (p<0.05). The
most common site of infection was lung (70%). The rate of cytomegalovirus (CMV) antigenemia (positive
PP65) was 20% during the 2-year period after HSCT.
Conclusion: The rate of infection was a negative prognostic factor for 2-year overall survival. The rate of
CMV antigenemia is less than similar studies (51%), which could be due to full-matched donor-recipients
requiring less immunosuppression.