Long‐term cause‐specific mortality in adolescent and young adult Hodgkin lymphoma patients treated with contemporary regimens—A nationwide Danish cohort study

Author:

Rossetti Sára1ORCID,Juul Sidsel Jacobsen2ORCID,Eriksson Frank3,Warming Peder Emil4,Glinge Charlotte4,El‐Galaly Tarec Christoffer567,Haaber Christensen Jacob6,Kamper Peter8,de Nully Brown Peter1,Gislason Gunnar Hilmar910,Vestmø Maraldo Maja2,Tfelt‐Hansen Jacob411,Hutchings Martin110

Affiliation:

1. Department of Hematology Copenhagen University Hospital, Rigshospitalet Copenhagen Denmark

2. Department of Clinical Oncology Copenhagen University Hospital, Rigshospitalet Copenhagen Denmark

3. Section of Biostatistics University of Copenhagen Copenhagen Denmark

4. Department of Cardiology, The Heart Centre Copenhagen University Hospital, Rigshospitalet Copenhagen Denmark

5. Department of Hematology Aalborg University Hospital Aalborg Denmark

6. Department of Hematology Odense University Hospital Odense Denmark

7. Department of Clinical Epidemiology Karolinska Institutet Stockholm Sweden

8. Department of Hematology University Hospital of Aarhus Aarhus Denmark

9. Department of Cardiology Herlev and Gentofte Hospital Herlev Denmark

10. Department of Clinical Medicine University of Copenhagen Copenhagen Denmark

11. Department of Forensic Medicine Copenhagen University Hospital, Rigshospitalet Copenhagen Denmark

Abstract

SummaryThe documented treatment‐induced excess mortality in Hodgkin lymphoma (HL) has spurred important treatment changes over recent decades. This study aimed to examine mortality among young HL patients treated with contemporary strategies, including historical data comparison. This nationwide study included 1348 HL patients, diagnosed in 1995–2015 and aged 15–40 at diagnosis. Among the patients, 66.5% had Ann Arbor stage I–II and 33.5% had stage III–IV disease. With a median follow‐up of 14.76 years, 139 deaths occurred, yielding a 5‐year overall survival of 94.6%. Older age, advanced disease, earlier treatment periods and extensive regimens were associated with higher overall mortality risk. The cumulative risk of HL‐related death showed an initial sharp rise, with a plateau at 5.3% 10‐year post‐diagnosis. Deaths due to cardiovascular or pulmonary diseases and second cancers initially had minimal risk, gradually reaching 1.2% and 2.0% at the 20‐year mark respectively. HL cases had a 7.5‐fold higher mortality hazard than the background population. This study suggests that contemporary HL treatment still poses excess mortality risk, but recent changes have notably reduced overall and cause‐specific mortality compared to earlier eras. Balancing treatment efficacy and toxicity remains crucial, but our findings highlight improved outcomes with modern treatment approaches.

Publisher

Wiley

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