造血干细胞移植受者的COVID-19感染

A. Siniaev, A.O. Grinenko, M. Popova, Y. Rogacheva, A. Spiridonova, Y. Vlasova, A. Smirnova, E. Morozova, K. Lepik, N. Mikhailova, M. D. Vladovskaya, S. Bondarenko, I. Moiseev, A. Kulagin
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引用次数: 1

摘要

目标。目的评估同种异体和自体造血干细胞移植(HSCT)受者COVID-19的病程和结果。材料与方法。该回顾性研究包括44名移植后诊断为COVID-19的成人移植受体(异体移植33例[75%]和自体移植11例[25%])。以急性白血病18例(41%)和淋巴瘤10例(22.7%)为主。自发生COVID-19以来的中位随访时间为231天(1-818天),HSCT后为507.5天(14-3723天)。使用Kaplan-Meier和Log-Rank方法评估总生存期和无进展生存期。结果:从造血干细胞移植开始,COVID-19发展的中位时间为122.5天(-1-3490天)。确诊时3-4级中性粒细胞减少12例(27.2%),1-2级中性粒细胞减少16例(36.4%)。16例(48.4%)同种异体造血移植受者在发生COVID-19时存在活动性移植物抗宿主病(GVHD)。疾病严重程度为轻度19例(43.2%),中度13例(29.5%)。总体而言,COVID-19发病后200天生存率为78.8% (95% CI[63.1-88.4])。贫血(p = 0.02)和血小板减少(p = 0.01)显著降低了COVID-19患者造血干细胞移植后的OS。COVID-19发病时GVHD患者生存率更高(p = 0.02)。结论:造血干细胞移植患者发生COVID-19过程的关键是细胞减少和移植物抗宿主病的出现。总生存率为78.8%。
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COVID-19 infection in hematopoietic stem cell transplant recipients
Objective. To assess the course and outcomes of COVID-19 in recipients of allogeneic and autologous hematopoietic stem cell transplant (HSCT). Materials and Methods. The retrospective study included 44 adult recipients (allogeneic – 33 [75%] and autologous – 11 [25%] of HSCT who diagnosed with COVID-19 after transplantation. Group mostly represented by acute leukemia – 18 (41%) and lymphoma – 10 (22.7%). The median follow-up time since the development of COVID-19 was 231 days (1–818 days), after HSCT – 507.5 days (14–3723 days). Overall and progression-free survival was assessed using the Kaplan–Meier and Log-Rank method. We also evaluated the characteristics of the course of a new coronavirus infection. Results. Median time for the development of COVID-19 from the moment of HSCT was 122.5 days (-1–3490 days). Twelve patients (27.2%) were in grade 3–4 neutropenia at the time of COVID-19 diagnosis, 16 (36.4%) patients were in grade 1–2 neutropenia. Sixteen (48.4%) allo-HSCT recipients had active graft-versus-host disease (GVHD) at the time of COVID-19 development. Disease severity was mild in 19 (43.2%) and moderate in 13 (29.5%) patients. Overall, 200-day survival from the onset of COVID-19 was 78.8% (95% CI [63.1–88.4]). Anemia (p = 0.02) and thrombocytopenia (p = 0.01) significantly decrease OS in patients with COVID-19 after HSCT. Patients with GVHD at the time of COVID-19 onset had a better survival rate (p = 0.02). The timing of COVID-19 development after HSCT did not affect outcomes. Conclusions. The key points of the course of COVID-19 in HSCT recipients are the presence of cytopenia and graft-versus-host disease. Overall survival was 78.8%.
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