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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

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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 - Feb 2025

Keywords

  • Childhood cancer
  • Cyclophosphamide
  • Diffusion
  • Late effects
  • Long-term follow-up
  • Lung disease
  • Pulmonary dysfunction
  • Pulmonary toxic treatment
  • Respiratory symptoms
  • Restriction
  • Survivorship
  • Lung Diseases/chemically induced
  • Follow-Up Studies
  • Vital Capacity/drug effects
  • Humans
  • Child, Preschool
  • Male
  • Young Adult
  • Adult
  • Female
  • Netherlands/epidemiology
  • Child
  • Cancer Survivors/statistics & numerical data
  • Neoplasms/drug therapy
  • Forced Expiratory Volume/drug effects
  • Respiratory Function Tests/methods
  • Adolescent
  • Antineoplastic Agents, Alkylating/adverse effects
  • Cyclophosphamide/adverse effects

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