Outcomes of patients with Down syndrome and acute leukemia: A retrospective observational study. Issue 40 (8th October 2021)

• Record Type: Journal Article
• Authors: Schmidt, Madalina-Petronela; Colita, Anca; Ivanov, Anca-Viorica; Coriu, Daniel; Miron, Ingrith-Crenguta
• Other Names: Alqasim. Alauldeen Mudhafar Zubair section editor.
• Is Part Of: Medicine. Volume 100:Issue 40(2021)
• Publication Date: 2021-10-08
• Subjects: acute leukemia -- Down syndrome -- outcomes -- survival; Medicine -- Periodicals; Medicine -- Periodicals; Médecine -- Périodiques; Geneeskunde; Medicine; Periodicals; Periodicals; 610.5
• DOI: 10.1097/MD.0000000000027459
• Languages: English
• ISSNs: 0025-7974

Abstract

Abstract : Abstract: Children with Down syndrome (DS) have a higher risk of developing acute leukemia than do those without DS. There are few studies in the literature about outcome, survival, and difficulties of treating patients with DS and acute leukemia in a developing country. This study aimed to analyze the outcome, response to treatment, survival, treatment complications, and causes of death in patients with DS and acute leukemia compared with those in patients with acute leukemia without DS diagnosed in the same period of time. We conducted a retrospective observational analysis including a cohort of 21 patients with DS and acute leukemia diagnosed between 2009 and 2018 in 3 hemato-oncology centers (2 pediatric centers and 1 adult hematology center). A group of patients with DS-acute lymphoblastic leukemia (DS-ALL) was analyzed and compared with a group of 165 patients with acute lymphoblastic leukemia without DS, and a group of patients with DS-acute myeloid leukemia (DS-AML) was analyzed and compared with a group of 50 patients with acute myeloid leukemia without DS, which was diagnosed during the same period of time (2009–2018) and treated under similar conditions in terms of both treatment protocols and economic resources. The overall survival rates in children with DS-ALL and DS-AML were 35.7% and 57.1%, respectively ( P = .438). The overall survival rate was significantly worse in children with DS-ALL than in those with acute lymphoblastic leukemia without DS (35.71% vs 75.80%, P = .001). We noted that treatment-related mortality in the patients with DS-ALL was high (50%) (infections and toxicities related to chemotherapy); this result was significantly different from that for patients with leukemia without DS ( P < .0001). The relapse rate was higher in patients with DS-ALL but not significantly higher than that in patients without DS ( P = .13). In contrast, the overall survival rate was better for patients with DS-AML than for those with acute myeloid leukemia without DS (57.1% vs 45.1%, P = .47). Because of the particularities of the host, we suggest that DS-ALL and DS-AML should be considered as independent diseases and treated according to specific protocols with therapy optimization per the minimal residual disease.