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Pulmonary embolism in acute lymphoblastic leukemia - An observational study of 1685 patients treated according to the NOPHO ALL2008 protocol.
Tuckuviene, Ruta; Bjerg, Cecilie Lundgaard; Jonsson, Olafur Gisli; Langstrom, Satu; Rank, Cecilie Utke; Ranta, Susanna; Saks, Kadri; Trakymiene, Sonata Saulyte; Ruud, Ellen.
Afiliação
  • Tuckuviene R; Department of Pediatrics Aalborg University Hospital Aalborg Denmark.
  • Bjerg CL; Department of Pediatrics Aalborg University Hospital Aalborg Denmark.
  • Jonsson OG; Children's Hospital Landspitali, University Hospital Reykjavik Iceland.
  • Langstrom S; Division of Hematology-Oncology and Stem Cell Transplantation New Children's Hospital and Helsinki University Central Hospital University of Helsinki Helsinki Finland.
  • Rank CU; Pediatric Oncology Research Laboratory and Department of Hematology Rigshospitalet University of Copenhagen Copenhagen Denmark.
  • Ranta S; Department of Women's and Children's Health Karolinska University Hospital, and Childhood Cancer Research Unit Women's and Children's Health Karolinska Institutet Stockholm Sweden.
  • Saks K; Department of Oncohematology Tallinn Children's Hospital Tallinn Estonia.
  • Trakymiene SS; Clinic of Children's diseases Faculty of Medicine Vilnius University Vilnius Lithuania.
  • Ruud E; Department of Pediatric Hematology and Oncology Unit for Pediatric and Adolescent Medicine Oslo University Hospital Oslo Norway.
Res Pract Thromb Haemost ; 4(5): 866-871, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32685896
ABSTRACT

BACKGROUND:

Pulmonary embolism (PE) is a serious complication of acute lymphoblastic leukemia (ALL). We examined the cumulative incidence and clinical presentation of PE in a well-defined cohort of patients with ALL aged 1-45 years treated according to the Nordic Society of Pediatric Hematology and Oncology (NOPHO) ALL2008 protocol.

METHODS:

As part of the mandatory toxicity reporting of NOPHO ALL2008, thromboembolism including PE was reported consecutively. The cumulative incidence of first-time PE was calculated using the Aalen-Johansen estimator during a 2.5-year period from ALL diagnosis. We used Fisher's exact test to examine categorical variables and Cox logistic regression to estimate hazard ratios (HRs) for PE.

RESULTS:

PE was diagnosed in 32 of 1685 patients. The 2.5-year cumulative incidence of first-time PE increased with age 0.43% (95% CI, 0.18-1.03) in children aged 1-9 years, 3.28% (95% CI, 1.72-6.22) in children aged 10-17 years, and 7.22% (95% CI, 4.61-11.21) in adults aged 18-45 years. The majority of PEs, 78% (25/32), occurred during asparaginase treatment. HRs adjusted for age and sex were associated with male sex (HR, 2.4; 95% CI, 1.0-5.6) and older age (10-17 years HR 7.5; 95% CI, 2.5-22.2), 18-45 years HR, 16.5; 95% CI, 6.1-44.5). In two-thirds of the patients (63%; 17/27), PE and its treatment had no impact on the administered doses of asparaginase. PE-associated 30-day mortality was 9.4% (95% CI, 1.9-25.0).

CONCLUSIONS:

Awareness of PE is warranted during ALL treatment. Larger multicenter studies are needed to examine predictors of PE in ALL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prognostic_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prognostic_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2020 Tipo de documento: Article