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Cyclophosphamide is not associated with clinically relevant late pulmonary dysfunction in Dutch survivors of childhood cancer – The DCCSS-LATER 2 PULM sub-study

  • R. J. van Kalsbeek
  • , E. A. M. Feijen
  • , D. Bresters
  • , L. C. M. Kremer
  • , S. M. F. Pluijm
  • , O. A. Asogwa
  • , E. van Dulmen-den Broeder
  • , M. M. van den Heuvel-Eibrink
  • , G. O. Janssens
  • , W. J. Tissing
  • , J. J. Loonen
  • , S. J. C. M. M. Neggers
  • , H. J. H. van der Pal
  • , C. M. Ronckers
  • , J. C. Teepen
  • , A. C. H. de Vries
  • , M. Louwerens
  • , M. van der Heiden-van der Loo
  • , S. M. P. J. Prevaes
  • , A. B. Versluys*
  • E. van Dulmen-den Broeder
*Corresponding author for this work
  • Princess Máxima Center for Pediatric Oncology
  • Leiden University
  • University of Amsterdam
  • Utrecht University
  • Radboud University Nijmegen
  • Erasmus University Rotterdam
  • Johannes Gutenberg University Mainz

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: Treatment for childhood cancer may increase the risk of long-term pulmonary complications and dysfunction. Pulmonary surveillance is recommended after established pulmonary toxic exposures, including bleomycin, busulfan, carmustine (BCNU), lomustine (CCNU), radiotherapy to a field exposing the lungs, and pulmonary surgery. However, the role of cyclophosphamide as a pulmonary toxic agent is debated. Aim: To establish whether cyclophosphamide is associated with late pulmonary dysfunction among survivors of childhood cancer. Methods: In this multicenter Dutch Childhood Cancer Survivor Study (DCCSS)-LATER 2 PULM sub-study, we included 828 survivors with a median follow-up of 26.6 years, treated with cyclophosphamide and/or established pulmonary toxic treatment, or neither. Pulmonary function tests were used to measure the primary outcomes of diffusion impairment (diffusing capacity for carbon monoxide (DLCO) z-score), restriction (total lung capacity (TLC) z-score), and obstruction (forced expiratory volume in the first second/forced vital capacity (FEV1/FVC) z-score). Secondary outcomes comprised chronic cough, recurrent respiratory tract infections, shortness of breath, and supplemental oxygen need. Results: Diffusion and restrictive abnormalities were highly prevalent among those treated with established pulmonary toxic treatment, with cyclophosphamide (41.0 % and 50.4 %, respectively) and without (34.3 % and 41.9 %, respectively), and occurred less frequently in survivors treated with cyclophosphamide only (12.9 % and 7.3 %, respectively) or in survivor controls (9.9 % and 12.4 %, respectively). In multivariable analyses, cyclophosphamide did not have a clinically relevant effect on the primary or secondary outcomes. Conclusions: This study suggests that cyclophosphamide is not associated with clinically relevant pulmonary dysfunction in long-term childhood cancer survivors.
Original languageEnglish
Article number107948
JournalRespiratory medicine
Volume237
DOIs
Publication statusPublished - 1 Feb 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Childhood cancer
  • Cyclophosphamide
  • Diffusion
  • Late effects
  • Long-term follow-up
  • Lung disease
  • Pulmonary dysfunction
  • Pulmonary toxic treatment
  • Respiratory symptoms
  • Restriction
  • Survivorship

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