Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation

Abstract Background The significance of very early chimerism assessment before day + 28, which is considered the moment of engraftment, is still unclear. In this retrospective study, we evaluated the clinical impact of very early chimerism on the clinical outcome after allogeneic haematopoietic stem...

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Main Authors: Monika Lejman, Agnieszka Zaucha-Prażmo, Joanna Zawitkowska, Aleksandra Mroczkowska, Dominik Grabowski, Jerzy R. Kowalczyk, Katarzyna Drabko
Format: Article
Language:English
Published: BMC 2019-11-01
Series:BMC Cancer
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12885-019-6360-3
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spelling doaj-a1745341d37d4cab96355e948cb36e742020-11-25T01:32:28ZengBMCBMC Cancer1471-24072019-11-011911810.1186/s12885-019-6360-3Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantationMonika Lejman0Agnieszka Zaucha-Prażmo1Joanna Zawitkowska2Aleksandra Mroczkowska3Dominik Grabowski4Jerzy R. Kowalczyk5Katarzyna Drabko6Laboratory of Genetic Diagnostics, Department of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinDepartment of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinDepartment of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinLaboratory of Genetic Diagnostics, Department of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinDepartment of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinDepartment of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinDepartment of Pediatric Hematology, Oncology, and Transplantology, Medical University of LublinAbstract Background The significance of very early chimerism assessment before day + 28, which is considered the moment of engraftment, is still unclear. In this retrospective study, we evaluated the clinical impact of very early chimerism on the clinical outcome after allogeneic haematopoietic stem cell transplantation (allo-HSCT) in children with acute lymphoblastic leukaemia (ALL). Methods The study group included 38 boys and 18 girls. Very early chimerism was evaluated on days + 7, + 14, + 21 and + 28 after the transplant. Short tandem repeat polymerase chain reaction (STR PCR) was used to analyse chimerism. Results Overall survival (OS) and event-free survival (EFS) were 84 and 80%, respectively. The OS in the group of 24 patients with complete donor chimerism on day + 14 was 83%, and it did not differ statistically compared to the 32 patients with mixed chimerism on day + 14 (OS was 84%). In our cohort of patients, the matched unrelated donor, male gender of donor, number of transplanted cells above 4.47 × 106 kg and no serotherapy with anti-thymocyte globulin (ATG) were statistically related to a higher level of donor chimerism. The immunophenotypes of disease, age of patient at time HSCT, recipient sex, stem cell source (peripheral blood/bone marrow) and conditioning regimen had no impact on early chimerism. Acute graft versus host disease grades II-IV was diagnosed in 23 patients who presented with donor chimerism levels above 60% on day 7. Conclusions The data presented in this study provide valuable insight into the analysis of very early chimerism in children with ALL treated with HSCT.http://link.springer.com/article/10.1186/s12885-019-6360-3ChimerismEngraftmentQuantitative PCRGvHDAcute lymphoblastic leukaemiaAllogeneic Haematopoietic stem cell transplantation
collection DOAJ
language English
format Article
sources DOAJ
author Monika Lejman
Agnieszka Zaucha-Prażmo
Joanna Zawitkowska
Aleksandra Mroczkowska
Dominik Grabowski
Jerzy R. Kowalczyk
Katarzyna Drabko
spellingShingle Monika Lejman
Agnieszka Zaucha-Prażmo
Joanna Zawitkowska
Aleksandra Mroczkowska
Dominik Grabowski
Jerzy R. Kowalczyk
Katarzyna Drabko
Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
BMC Cancer
Chimerism
Engraftment
Quantitative PCR
GvHD
Acute lymphoblastic leukaemia
Allogeneic Haematopoietic stem cell transplantation
author_facet Monika Lejman
Agnieszka Zaucha-Prażmo
Joanna Zawitkowska
Aleksandra Mroczkowska
Dominik Grabowski
Jerzy R. Kowalczyk
Katarzyna Drabko
author_sort Monika Lejman
title Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
title_short Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
title_full Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
title_fullStr Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
title_full_unstemmed Impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
title_sort impact of early chimerism status on clinical outcome in children with acute lymphoblastic leukaemia after haematopoietic stem cell transplantation
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2019-11-01
description Abstract Background The significance of very early chimerism assessment before day + 28, which is considered the moment of engraftment, is still unclear. In this retrospective study, we evaluated the clinical impact of very early chimerism on the clinical outcome after allogeneic haematopoietic stem cell transplantation (allo-HSCT) in children with acute lymphoblastic leukaemia (ALL). Methods The study group included 38 boys and 18 girls. Very early chimerism was evaluated on days + 7, + 14, + 21 and + 28 after the transplant. Short tandem repeat polymerase chain reaction (STR PCR) was used to analyse chimerism. Results Overall survival (OS) and event-free survival (EFS) were 84 and 80%, respectively. The OS in the group of 24 patients with complete donor chimerism on day + 14 was 83%, and it did not differ statistically compared to the 32 patients with mixed chimerism on day + 14 (OS was 84%). In our cohort of patients, the matched unrelated donor, male gender of donor, number of transplanted cells above 4.47 × 106 kg and no serotherapy with anti-thymocyte globulin (ATG) were statistically related to a higher level of donor chimerism. The immunophenotypes of disease, age of patient at time HSCT, recipient sex, stem cell source (peripheral blood/bone marrow) and conditioning regimen had no impact on early chimerism. Acute graft versus host disease grades II-IV was diagnosed in 23 patients who presented with donor chimerism levels above 60% on day 7. Conclusions The data presented in this study provide valuable insight into the analysis of very early chimerism in children with ALL treated with HSCT.
topic Chimerism
Engraftment
Quantitative PCR
GvHD
Acute lymphoblastic leukaemia
Allogeneic Haematopoietic stem cell transplantation
url http://link.springer.com/article/10.1186/s12885-019-6360-3
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