TY - JOUR
T1 - Pulmonary diseases in patients with classical Hodgkin lymphoma relative to a matched background population
T2 - A Danish national cohort study
AU - Vandtved, Julie Haugaard
AU - Øvlisen, Andreas Kiesbye
AU - Baech, Joachim
AU - Weinrich, Ulla Møller
AU - Severinsen, Marianne Tang
AU - Maksten, Eva Futtrup
AU - Jakobsen, Lasse Hjort
AU - Glimelius, Ingrid
AU - Kamper, Peter
AU - Hutchings, Martin
AU - Specht, Lena
AU - Dahl-Sørensen, Rasmus
AU - Christensen, Jacob Haaber
AU - El-Galaly, Tarec C
N1 - © 2024 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
PY - 2024/8
Y1 - 2024/8
N2 - Late toxicities can impact survivorship in patients with classical Hodgkin lymphoma (cHL) with pulmonary toxicity after bleomycin-containing chemotherapy being a concern. The incidence of pulmonary diseases was examined in this Danish population-based study. A total of 1474 adult patients with cHL treated with ABVD (doxorubicin, bleomycin, vinblastine and dacarbazine) or BEACOPP (bleomycin, vincristine, etoposide, doxorubicin, cyclophosphamide, procarbazine and prednisone) between 2000 and 2018 were included along with 7370 age- and sex-matched comparators from the background population. Median follow-up was 8.6 years for the patients. Patients with cHL had increased risk of incident pulmonary diseases (HR 2.91 [95% CI 2.30-3.68]), with a 10-year cumulative risk of 7.4% versus 2.9% for comparators. Excess risks were observed for interstitial lung diseases (HR 15.84 [95% CI 9.35-26.84]) and chronic obstructive pulmonary disease (HR 1.99 [95% CI 1.43-2.76]), with a 10-year cumulative risk of 4.1% and 3.5% respectively for patients. No excess risk was observed for asthma (HR 0.82 [95% CI 0.43-1.56]). Risk factors for interstitial lung diseases were age ≥60 years, the presence of B-symptoms and low albumin. These findings document a significant burden of pulmonary diseases among patients with cHL and emphasize the importance of diagnostic work-up of pulmonary symptoms.
AB - Late toxicities can impact survivorship in patients with classical Hodgkin lymphoma (cHL) with pulmonary toxicity after bleomycin-containing chemotherapy being a concern. The incidence of pulmonary diseases was examined in this Danish population-based study. A total of 1474 adult patients with cHL treated with ABVD (doxorubicin, bleomycin, vinblastine and dacarbazine) or BEACOPP (bleomycin, vincristine, etoposide, doxorubicin, cyclophosphamide, procarbazine and prednisone) between 2000 and 2018 were included along with 7370 age- and sex-matched comparators from the background population. Median follow-up was 8.6 years for the patients. Patients with cHL had increased risk of incident pulmonary diseases (HR 2.91 [95% CI 2.30-3.68]), with a 10-year cumulative risk of 7.4% versus 2.9% for comparators. Excess risks were observed for interstitial lung diseases (HR 15.84 [95% CI 9.35-26.84]) and chronic obstructive pulmonary disease (HR 1.99 [95% CI 1.43-2.76]), with a 10-year cumulative risk of 4.1% and 3.5% respectively for patients. No excess risk was observed for asthma (HR 0.82 [95% CI 0.43-1.56]). Risk factors for interstitial lung diseases were age ≥60 years, the presence of B-symptoms and low albumin. These findings document a significant burden of pulmonary diseases among patients with cHL and emphasize the importance of diagnostic work-up of pulmonary symptoms.
KW - bleomycin
KW - hodgkin lymphoma
KW - late effects
KW - obstructive lung diseases
KW - pulmonary diseases
KW - pulmonary fibrosis
KW - Lung Diseases/chemically induced
KW - Doxorubicin/adverse effects
KW - Procarbazine/adverse effects
KW - Humans
KW - Middle Aged
KW - Male
KW - Antineoplastic Combined Chemotherapy Protocols/adverse effects
KW - Incidence
KW - Young Adult
KW - Hodgkin Disease/epidemiology
KW - Adult
KW - Female
KW - Denmark/epidemiology
KW - Adolescent
KW - Aged
KW - Cyclophosphamide/adverse effects
KW - Vincristine/adverse effects
KW - Bleomycin/adverse effects
KW - Cohort Studies
UR - http://www.scopus.com/inward/record.url?scp=85191811569&partnerID=8YFLogxK
U2 - 10.1111/bjh.19475
DO - 10.1111/bjh.19475
M3 - Journal article
C2 - 38685596
SN - 0007-1048
VL - 205
SP - 542
EP - 551
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -