Utility of routine pulmonary function test after autologous hematopoietic cell transplantation in lymphoma.
Humans
Hematopoietic Stem Cell Transplantation
/ adverse effects
Lymphoma
/ therapy
Lymphoma, Non-Hodgkin
/ drug therapy
Carmustine
/ therapeutic use
Etoposide
/ adverse effects
Melphalan
/ therapeutic use
Transplantation, Autologous
Lung Diseases
Transplantation Conditioning
/ adverse effects
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Pulmonary function test
autologous
lymphoma
pFT
transplant
Journal
Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422
Informations de publication
Date de publication:
Dec 2023
Dec 2023
Historique:
medline:
26
12
2023
pubmed:
10
9
2023
entrez:
10
9
2023
Statut:
ppublish
Résumé
This study aims to evaluate the predictive value of routine pulmonary function testing (PFT) at the 12-month mark post-autologous hematopoietic cell transplant (AHCT) in identifying clinically significant lung disease in lymphoma survivors. In 247 patients, 173 (70%) received BEAM (carmustine, etoposide, cytarabine, melphalan), and 49 (20%) received TBC (thiotepa, busulfan, cyclophosphamide) conditioning regimens. Abnormal baseline PFT was noted in 149 patients (60%). Thirty-four patients had a significant decline (reduction of >/= 20% in DLCO or FEV1 or FVC) in post-AHCT PFT, with the highest incidence in the CNS lymphoma group (39%). The incidence of clinically significant lung disease post-transplant was low at 2% and there was no association between abnormal pre- and 1-year post-transplant PFTs with the development of clinical lung disease. While this study illustrates the impact of treatment regimens on PFT changes, it did not demonstrate a predictive value of scheduled PFTs in identifying clinically significant post-AHCT lung disease.
Identifiants
pubmed: 37690007
doi: 10.1080/10428194.2023.2256912
doi:
Substances chimiques
Carmustine
U68WG3173Y
Etoposide
6PLQ3CP4P3
Melphalan
Q41OR9510P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2279-2285Subventions
Organisme : NCI NIH HHS
ID : P01 CA023766
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States