Literature DB >> 30852834

Cardiovascular disease after childhood acute lymphoblastic leukaemia: a cohort study.

Eva M Hau1, Julien N Caccia2, Rahel Kasteler1, Ben Spycher3, Thomas Suter4, Roland A Ammann2, Nicolas X von der Weid5, Claudia E Kuehni1.   

Abstract

BACKGROUND AND AIMS: Cardiovascular diseases (CVD) increase late morbidity and mortality in survivors of acute lymphoblastic leukaemia (ALL). We compared the risk of CVD in ALL survivors to siblings, examined time trends, quantified treatment-related risks, and investigated whether risk extends beyond patients treated with anthracyclines and chest radiotherapy.
METHODS: The Swiss Childhood Cancer Survivor Study assessed CVD by patient questionnaire in 5-year ALL survivors diagnosed between 1976 and 2005 and their siblings. Participants were asked whether a physician had ever told them that they had hypertension, arrhythmia, heart failure, myocardial infarction, angina pectoris, stroke, thrombosis or valvular problems. We investigated treatment-related risk factors for CVD using multivariable logistic regression, adjusting for demographic and socioeconomic factors, BMI, smoking, diabetes mellitus, alcohol consumption and physical activity.
RESULTS: We contacted 707 survivors and 1299 siblings, 511 (72%) and 709 (55%) of whom responded, respectively. Survivors had a higher risk of developing CVD than siblings (odds ratio [OR] 1.9, 95% confidence interval 1.3–2.8), in particular heart failure (OR 13.9, 1.8–107.4). Compared to patients treated 1976–85, the risk of CVD was 1.4 (0.7–2.8) for those treated 1985–1994 and 1.5 (0.6–3.7) for those treated 1995–2005. The overall CVD risks after anthracycline treatment (OR 3.1, 2.0–4.7), haematopoietic stem cell transplantation (OR 8.0, 2.4–26.9) or relapse (OR 4.1, 1.9–8.8) were increased compared to those of siblings, while the CVD risks of survivors treated without anthracycline or chest radiotherapy were similar (OR 1.0; 0.5–2.0).
CONCLUSIONS: Despite attempts to reduce cardiotoxicity in childhood cancer treatment, CVD risks in ALL survivors treated more recently do not seem to have declined.

Entities:  

Mesh:

Substances:

Year:  2019        PMID: 30852834     DOI: 10.4414/smw.2019.20012

Source DB:  PubMed          Journal:  Swiss Med Wkly        ISSN: 0036-7672            Impact factor:   2.193


  4 in total

1.  Tisagenlecleucel in pediatric and young adult patients with Down syndrome-associated relapsed/refractory acute lymphoblastic leukemia.

Authors:  Theodore W Laetsch; Shannon L Maude; Adriana Balduzzi; Susana Rives; Henrique Bittencourt; Michael W Boyer; Jochen Buechner; Barbara De Moerloose; Muna Qayed; Christine L Phillips; Michael A Pulsipher; Hidefumi Hiramatsu; Ranjan Tiwari; Stephan A Grupp
Journal:  Leukemia       Date:  2022-04-14       Impact factor: 12.883

2.  Excess morbidity and mortality among survivors of childhood acute lymphoblastic leukaemia: 25 years of follow-up from the United Kingdom Childhood Cancer Study (UKCCS) population-based matched cohort.

Authors:  Eleanor Kane; Sally Kinsey; Audrey Bonaventure; Tom Johnston; Jill Simpson; Debra Howell; Alexandra Smith; Eve Roman
Journal:  BMJ Open       Date:  2022-03-07       Impact factor: 2.692

Review 3.  The Role of Nutrition in Primary and Secondary Prevention of Cardiovascular Damage in Childhood Cancer Survivors.

Authors:  Fiorentina Guida; Riccardo Masetti; Laura Andreozzi; Daniele Zama; Marianna Fabi; Matteo Meli; Arcangelo Prete; Marcello Lanari
Journal:  Nutrients       Date:  2022-08-11       Impact factor: 6.706

4.  Temporal changes in gut microbiota profile in children with acute lymphoblastic leukemia prior to commencement-, during-, and post-cessation of chemotherapy.

Authors:  Ling Ling Chua; Reena Rajasuriar; Yvonne Ai Lian Lim; Yin Ling Woo; P'ng Loke; Hany Ariffin
Journal:  BMC Cancer       Date:  2020-02-24       Impact factor: 4.430

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.