Pulmonary diseases in patients with classical Hodgkin lymphoma relative to a matched background population: A Danish national cohort study

Author:

Vandtved Julie Haugaard12ORCID,Øvlisen Andreas Kiesbye12ORCID,Baech Joachim12ORCID,Weinrich Ulla Møller13ORCID,Severinsen Marianne Tang12ORCID,Maksten Eva Futtrup12ORCID,Jakobsen Lasse Hjort2ORCID,Glimelius Ingrid4ORCID,Kamper Peter5,Hutchings Martin6ORCID,Specht Lena7ORCID,Dahl‐Sørensen Rasmus8ORCID,Christensen Jacob Haaber9,El‐Galaly Tarec C.12910ORCID

Affiliation:

1. Department of Clinical Medicine Aalborg University Aalborg Denmark

2. Department of Hematology, Clinical Cancer Research Center Aalborg University Hospital Aalborg Denmark

3. Department of Respiratory Diseases Aalborg University Hospital Aalborg Denmark

4. Department of Immunology, Genetics and Pathology Uppsala University Hospital Uppsala Sweden

5. Department of Hematology Aarhus University Hospital Aarhus Denmark

6. Department of Hematology, Rigshospitalet Copenhagen Denmark

7. Department of Oncology, Rigshospitalet Copenhagen Denmark

8. Department of Hematology Zealand University Hospital Roskilde Denmark

9. Department of Hematology Odense University Hospital Odense Denmark

10. Department of Medicine Solna, Division of Clinical Epidemiology Karolinska Institute Stockholm Sweden

Abstract

SummaryLate 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.

Publisher

Wiley

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