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Hematopoietic stem cell transplantation does not increase the risk of infection-related complications for pediatric patients with Hodgkin and non-Hodgkin lymphomas: A multicenter nationwide study.
Zajac-Spychala, O; Wachowiak, J; Czyzewski, K; Dziedzic, M; Wysocki, M; Zalas-Wiecek, P; Szmydki-Baran, A; Hutnik, L; Matysiak, M; Malas, Z; Badowska, W; Gryniewicz-Kwiatkowska, O; Gietka, A; Dembowska-Baginska, B; Semczuk, K; Dzierzanowska-Fangrat, K; Bartnik, M; Ociepa, T; Urasinski, T; Fraczkiewicz, J; Salamonowicz, M; Kalwak, K; Gorczynska, E; Chybicka, A; Irga-Jaworska, N; Bien, E; Drozynska, E; Chelmecka-Wiktorczyk, L; Balwierz, W; Zak, I; Pierlejewski, F; Mlynarski, W; Urbanek-Dadela, A; Karolczyk, G; Stolpa, W; Sobol-Milejska, G; Plonowski, M; Krawczuk-Rybak, M; Musial, J; Chaber, R; Gamrot-Pyka, Z; Woszczyk, M; Tomaszewska, R; Szczepanski, T; Kowalczyk, J; Styczynski, J.
Afiliação
  • Zajac-Spychala O; Department of Pediatric Oncology, Hematology and Transplantology, University of Medical Sciences, Poznan, Poland.
  • Wachowiak J; Department of Pediatric Oncology, Hematology and Transplantology, University of Medical Sciences, Poznan, Poland.
  • Czyzewski K; Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
  • Dziedzic M; Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
  • Wysocki M; Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
  • Zalas-Wiecek P; Department of Microbiology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
  • Szmydki-Baran A; Department of Pediatric Hematology and Oncology, Medical University, Warszawa, Poland.
  • Hutnik L; Department of Pediatric Hematology and Oncology, Medical University, Warszawa, Poland.
  • Matysiak M; Department of Pediatric Hematology and Oncology, Medical University, Warszawa, Poland.
  • Malas Z; Division of Pediatric Hematology and Oncology, Children Hospital, Olsztyn, Poland.
  • Badowska W; Division of Pediatric Hematology and Oncology, Children Hospital, Olsztyn, Poland.
  • Gryniewicz-Kwiatkowska O; Department of Oncology, Children's Memorial Health Institute, Warszawa, Poland.
  • Gietka A; Department of Oncology, Children's Memorial Health Institute, Warszawa, Poland.
  • Dembowska-Baginska B; Department of Oncology, Children's Memorial Health Institute, Warszawa, Poland.
  • Semczuk K; Department of Microbiology, Children's Memorial Health Institute, Warszawa, Poland.
  • Dzierzanowska-Fangrat K; Department of Microbiology, Children's Memorial Health Institute, Warszawa, Poland.
  • Bartnik M; Department of Pediatrics, Hemato-Oncology and Gastroenterology, Pomeranian Medical University, Szczecin, Poland.
  • Ociepa T; Department of Pediatrics, Hemato-Oncology and Gastroenterology, Pomeranian Medical University, Szczecin, Poland.
  • Urasinski T; Department of Pediatrics, Hemato-Oncology and Gastroenterology, Pomeranian Medical University, Szczecin, Poland.
  • Fraczkiewicz J; Department of Pediatric Stem Cell Transplantation, Hematology and Oncology, Medical University, Wroclaw, Poland.
  • Salamonowicz M; Department of Pediatric Stem Cell Transplantation, Hematology and Oncology, Medical University, Wroclaw, Poland.
  • Kalwak K; Department of Pediatric Stem Cell Transplantation, Hematology and Oncology, Medical University, Wroclaw, Poland.
  • Gorczynska E; Department of Pediatric Stem Cell Transplantation, Hematology and Oncology, Medical University, Wroclaw, Poland.
  • Chybicka A; Department of Pediatric Stem Cell Transplantation, Hematology and Oncology, Medical University, Wroclaw, Poland.
  • Irga-Jaworska N; Department of Pediatrics, Hematology and Oncology, Medical University, Gdansk, Poland.
  • Bien E; Department of Pediatrics, Hematology and Oncology, Medical University, Gdansk, Poland.
  • Drozynska E; Department of Pediatrics, Hematology and Oncology, Medical University, Gdansk, Poland.
  • Chelmecka-Wiktorczyk L; Department of Pediatric Oncology and Hematology, Collegium Medicum, University Children's Hospital, Jagiellonian University, Krakow, Poland.
  • Balwierz W; Department of Pediatric Oncology and Hematology, Collegium Medicum, University Children's Hospital, Jagiellonian University, Krakow, Poland.
  • Zak I; Department of Microbiology, Collegium Medicum, University Children's Hospital, Jagiellonian University, Krakow, Poland.
  • Pierlejewski F; Department of Pediatric Oncology, Hematology and Diabetology, Medical University, Lodz, Poland.
  • Mlynarski W; Department of Pediatric Oncology, Hematology and Diabetology, Medical University, Lodz, Poland.
  • Urbanek-Dadela A; Division of Pediatric Hematology and Oncology, Children Hospital, Kielce, Poland.
  • Karolczyk G; Division of Pediatric Hematology and Oncology, Children Hospital, Kielce, Poland.
  • Stolpa W; Division of Pediatric Oncology, Hematology and Chemotherapy, Department of Pediatric, Silesian Medical University, Katowice, Poland.
  • Sobol-Milejska G; Division of Pediatric Oncology, Hematology and Chemotherapy, Department of Pediatric, Silesian Medical University, Katowice, Poland.
  • Plonowski M; Department of Pediatric Oncology and Hematology, Medical University, Bialystok, Poland.
  • Krawczuk-Rybak M; Department of Pediatric Oncology and Hematology, Medical University, Bialystok, Poland.
  • Musial J; Department of Pediatric Oncohematology, Children Hospital, Rzeszow, Poland.
  • Chaber R; Department of Pediatric Oncohematology, Children Hospital, Rzeszow, Poland.
  • Gamrot-Pyka Z; Division of Pediatric Hematology and Oncology, Chorzow Pediatric and Oncology Center, Chorzow, Poland.
  • Woszczyk M; Division of Pediatric Hematology and Oncology, Chorzow Pediatric and Oncology Center, Chorzow, Poland.
  • Tomaszewska R; Department of Pediatric Hematology and Oncology, Silesian Medical University, Zabrze, Poland.
  • Szczepanski T; Department of Pediatric Hematology and Oncology, Silesian Medical University, Zabrze, Poland.
  • Kowalczyk J; Department of Pediatric Hematology, Oncology and Stem Cell Transplantation, Medical University, Lublin, Poland.
  • Styczynski J; Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Transpl Infect Dis ; 22(4): e13292, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32285579
ABSTRACT

BACKGROUND:

Hodgkin (HL) and non-Hodgkin lymphoma (NHL) represent a spectrum of lymphoid malignancies that are often curable with currently applied treatment regimens; however, 15%-30% of lymphoma patients still suffer from relapsed or refractory (rel/ref) disease. Although hematopoietic stem cell transplantation (HSCT) improves outcomes of second-line therapy for lymphoma in childhood, the complication rates in this group of patients, especially infectious complications (IC), remain unclear.

OBJECTIVE:

The aim of this population-based cohort study was a retrospective analysis of incidence, epidemiology and profile of bacterial infections (BI), invasive fungal disease (IFD), and viral infections (VI) in primary or rel/ref lymphoma patients, both HL and NHL. PATIENTS AND

METHODS:

We subdivided lymphoma patients into three groups patients with primary conventional chemotherapy/radiotherapy regimens (group A), patients with rel/ref lymphoma treated with second-line chemotherapy (group B), and rel/ref lymphoma patients who underwent HSCT (group C). The medical records of the patients were biannually reported by each pediatric oncology center, and the data were analyzed centrally.

RESULTS:

Within 637 patients with primary lymphoma, at least one IC was diagnosed in 255 (40.0%), among 52 patients with rel/ref lymphoma 24 (46.2%) ICs were observed, and in transplanted group, 28 (57.1%) out of 49 children were diagnosed with IC (P = .151). The distribution of etiology of IC differed between the patient groups (A, B, C), with a predominance of BI in group A (85.6% vs 72.0% and 47.9%, respectively), VI in group C (9% and 16.0% vs 46.6%, respectively), and IFD in group B (5.4% vs 12.0% vs 5.5%, respectively). Overall, 500 (68.0%) episodes of bacterial IC were diagnosed in the entire group. Apart from HL patients treated with chemotherapy, in all the other subgroups of patients Gram-positives were predominant. The rate of multidrug-resistant bacteria was high, especially for Gram-negatives (41.1% in group A, 62.5% in group B, and 84.6% in group C). The infection-related mortality was comparable for each group.

CONCLUSIONS:

The incidence of IC was comparable during first- and second-line chemotherapy and after HSCT, but their profile was different for primary or re/ref lymphoma and depended on the type of therapy.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Linfoma não Hodgkin / Viroses / Doença de Hodgkin / Transplante de Células-Tronco Hematopoéticas / Infecções Fúngicas Invasivas Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Transpl Infect Dis Assunto da revista: TRANSPLANTE Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Linfoma não Hodgkin / Viroses / Doença de Hodgkin / Transplante de Células-Tronco Hematopoéticas / Infecções Fúngicas Invasivas Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Transpl Infect Dis Assunto da revista: TRANSPLANTE Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Polônia