Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents

Risk factors of CMV replication in early period after allo-HSCT (D0‑D100) were – myeloablative conditioning – HR 3.74 (1.67–8.37), р = 0.001; unrelated donor – HR 2.18 (0.86–5.26), р = 0.10; HLA-matched donor – HR 0.24 (0.05–1.06), р = 0,06. In late posttransplant period (from D+100) significant ris...

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Main Authors: S. N. Shiriaev, N. V. Stancheva, Ye. V. Morozova, I. M. Barkhatov, M. Yu. Averianova, S. V. Razumova, O. V. Goloshchapov, A. B. Chukhlovin, L. S. Zubarovskaya, B. V. Afanasiev
Format: Article
Language:Russian
Published: ABV-press 2014-09-01
Series:Onkogematologiâ
Subjects:
Online Access:https://oncohematology.abvpress.ru/ongm/article/view/114
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spelling doaj-3841984d2cd742d4808711bef857b5d72021-07-29T09:03:04ZrusABV-pressOnkogematologiâ1818-83462014-09-0192455210.17650/1818-8346-2014-9-2-45-52129Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescentsS. N. Shiriaev0N. V. Stancheva1Ye. V. Morozova2I. M. Barkhatov3M. Yu. Averianova4S. V. Razumova5O. V. Goloshchapov6A. B. Chukhlovin7L. S. Zubarovskaya8B. V. Afanasiev9Raisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRaisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, I. P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of RussiaRisk factors of CMV replication in early period after allo-HSCT (D0‑D100) were – myeloablative conditioning – HR 3.74 (1.67–8.37), р = 0.001; unrelated donor – HR 2.18 (0.86–5.26), р = 0.10; HLA-matched donor – HR 0.24 (0.05–1.06), р = 0,06. In late posttransplant period (from D+100) significant risk factors of CMV-reactivation were (according to multivariate analysis) myeloablative conditioning – HR 13.17 (3.00–57.86), р = 0.001; combination of pretransplant remission of leukemia and using cyclosporine and methotrexate – HR 0.13 (0.03–0.50), р = 0.003; combination of aGVHD and CMV reactivation in early posttransplant period – HR 2.71 (0.86–8.50), р = 0.088; using of bone marrow – HR 0.37 (0.12–1.19), р = 0.095. We revealed the significant association of aGVHD and CMV-reactivation –OR 2.91 (1.07–7.92), р=0.006, and increased rate of cGVHD in patients with CMV replication at third month after allo-HSCT OR – 2.29 (1.03–5.08), р = 0.066. We revealed a tend to decreasing relapse risk in patients who had CMV-replication – HR 0.07 (0.004–1.17), р = 0.06. Cumulative incidence of CMV-disease was 28 %. CMV-disease was lethal in 44 % patients.https://oncohematology.abvpress.ru/ongm/article/view/114acute lymphoblastic leukemiaacute myeloblastic leukemiacytomegalovirusallogeneic hematopoietic stem cell transplantation
collection DOAJ
language Russian
format Article
sources DOAJ
author S. N. Shiriaev
N. V. Stancheva
Ye. V. Morozova
I. M. Barkhatov
M. Yu. Averianova
S. V. Razumova
O. V. Goloshchapov
A. B. Chukhlovin
L. S. Zubarovskaya
B. V. Afanasiev
spellingShingle S. N. Shiriaev
N. V. Stancheva
Ye. V. Morozova
I. M. Barkhatov
M. Yu. Averianova
S. V. Razumova
O. V. Goloshchapov
A. B. Chukhlovin
L. S. Zubarovskaya
B. V. Afanasiev
Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
Onkogematologiâ
acute lymphoblastic leukemia
acute myeloblastic leukemia
cytomegalovirus
allogeneic hematopoietic stem cell transplantation
author_facet S. N. Shiriaev
N. V. Stancheva
Ye. V. Morozova
I. M. Barkhatov
M. Yu. Averianova
S. V. Razumova
O. V. Goloshchapov
A. B. Chukhlovin
L. S. Zubarovskaya
B. V. Afanasiev
author_sort S. N. Shiriaev
title Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
title_short Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
title_full Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
title_fullStr Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
title_full_unstemmed Risk factors of CMV replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
title_sort risk factors of cmv replication after allogeneic hematopoietic stem cell transplantation in children and adolescents
publisher ABV-press
series Onkogematologiâ
issn 1818-8346
publishDate 2014-09-01
description Risk factors of CMV replication in early period after allo-HSCT (D0‑D100) were – myeloablative conditioning – HR 3.74 (1.67–8.37), р = 0.001; unrelated donor – HR 2.18 (0.86–5.26), р = 0.10; HLA-matched donor – HR 0.24 (0.05–1.06), р = 0,06. In late posttransplant period (from D+100) significant risk factors of CMV-reactivation were (according to multivariate analysis) myeloablative conditioning – HR 13.17 (3.00–57.86), р = 0.001; combination of pretransplant remission of leukemia and using cyclosporine and methotrexate – HR 0.13 (0.03–0.50), р = 0.003; combination of aGVHD and CMV reactivation in early posttransplant period – HR 2.71 (0.86–8.50), р = 0.088; using of bone marrow – HR 0.37 (0.12–1.19), р = 0.095. We revealed the significant association of aGVHD and CMV-reactivation –OR 2.91 (1.07–7.92), р=0.006, and increased rate of cGVHD in patients with CMV replication at third month after allo-HSCT OR – 2.29 (1.03–5.08), р = 0.066. We revealed a tend to decreasing relapse risk in patients who had CMV-replication – HR 0.07 (0.004–1.17), р = 0.06. Cumulative incidence of CMV-disease was 28 %. CMV-disease was lethal in 44 % patients.
topic acute lymphoblastic leukemia
acute myeloblastic leukemia
cytomegalovirus
allogeneic hematopoietic stem cell transplantation
url https://oncohematology.abvpress.ru/ongm/article/view/114
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