TY - JOUR
T1 - Cyclophosphamide is not associated with clinically relevant late pulmonary dysfunction in Dutch survivors of childhood cancer – The DCCSS-LATER 2 PULM sub-study
AU - van Kalsbeek, R. J.
AU - Feijen, E. A.M.
AU - Bresters, D.
AU - Kremer, L. C.M.
AU - Pluijm, S. M.F.
AU - Asogwa, O. A.
AU - Dulmen-den Broeder, E. van
AU - van den Heuvel-Eibrink, M. M.
AU - Janssens, G. O.
AU - Tissing, W. J.
AU - Loonen, J. J.
AU - Neggers, S. J.C.M.M.
AU - van der Pal, H. J.H.
AU - Ronckers, C. M.
AU - Teepen, J. C.
AU - de Vries, A. C.H.
AU - Louwerens, M.
AU - van der Heiden-van der Loo, M.
AU - Prevaes, S. M.P.J.
AU - Versluys, A. B.
N1 - Copyright © 2025 Elsevier Ltd. All rights reserved.
PY - 2025/2
Y1 - 2025/2
N2 - 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.
AB - 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.
KW - Childhood cancer
KW - Cyclophosphamide
KW - Diffusion
KW - Late effects
KW - Long-term follow-up
KW - Lung disease
KW - Pulmonary dysfunction
KW - Pulmonary toxic treatment
KW - Respiratory symptoms
KW - Restriction
KW - Survivorship
KW - Lung Diseases/chemically induced
KW - Follow-Up Studies
KW - Vital Capacity/drug effects
KW - Humans
KW - Child, Preschool
KW - Male
KW - Young Adult
KW - Adult
KW - Female
KW - Netherlands/epidemiology
KW - Child
KW - Cancer Survivors/statistics & numerical data
KW - Neoplasms/drug therapy
KW - Forced Expiratory Volume/drug effects
KW - Respiratory Function Tests/methods
KW - Adolescent
KW - Antineoplastic Agents, Alkylating/adverse effects
KW - Cyclophosphamide/adverse effects
UR - https://www.scopus.com/pages/publications/85214825840
UR - https://www.mendeley.com/catalogue/99c2f694-a728-3399-a32c-d200dd3bdd30/
U2 - 10.1016/j.rmed.2025.107948
DO - 10.1016/j.rmed.2025.107948
M3 - Article
C2 - 39793859
AN - SCOPUS:85214825840
SN - 0954-6111
VL - 237
JO - Respiratory Medicine
JF - Respiratory Medicine
M1 - 107948
ER -