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Long-Term Cause-Specific Mortality in Hodgkin Lymphoma Patients

  • Simone de Vries
  • , Michael Schaapveld
  • , Cécile P.M. Janus
  • , Laurien A. Daniëls
  • , Eefke J. Petersen
  • , Richard W.M. van der Maazen
  • , Josée M. Zijlstra
  • , Max Beijert
  • , Marten R. Nijziel
  • , Karijn M.S. Verschueren
  • , Leontien C.M. Kremer
  • , Anna M. van Eggermond
  • , Pieternella J. Lugtenburg
  • , Augustinus D.G. Krol
  • , Judith M. Roesink
  • , Wouter J. Plattel
  • , Dick Johan van Spronsen
  • , Gustaaf W. van Imhoff
  • , Jan Paul de Boer
  • , Berthe M.P. Aleman
  • Flora E. van Leeuwen
  • Netherlands Cancer Institute
  • Netherlands Comprehensive Cancer Organization (IKNL)
  • Leiden University Medical Centre
  • University Medical Centre Utrecht
  • Radboud University Medical Center
  • VU University Medical Center
  • University Medical Centre Groningen
  • Catharina Hospital
  • Dr. Bernard Verbeeten Instituut
  • Princess Máxima Center for Pediatric Oncology

Research output: Contribution to journalArticleAcademicpeer-review

86 Citations (Scopus)
101 Downloads (Pure)

Abstract

BACKGROUND: Few studies have examined the impact of treatment-related morbidity on long-term, cause-specific mortality in Hodgkin lymphoma (HL) patients.

METHODS: This multicenter cohort included 4919 HL patients, treated before age 51 years between 1965 and 2000, with a median follow-up of 20.2 years. Standardized mortality ratios, absolute excess mortality (AEM) per 10 000 person-years, and cause-specific cumulative mortality by stage and primary treatment, accounting for competing risks, were calculated.

RESULTS: HL patients experienced a 5.1-fold (AEM = 123 excess deaths per 10 000 person-years) higher risk of death due to causes other than HL. This risk remained increased in 40-year survivors (standardized mortality ratio = 5.2, 95% confidence interval [CI] = 4.2 to 6.5, AEM = 619). At age 54 years, HL survivors experienced similar cumulative mortality (20.0%) from causes other than HL to 71-year-old individuals from the general population. Whereas HL mortality statistically significantly decreased over the calendar period (P < .001), solid tumor mortality did not change in the most recent treatment era. Patients treated in 1989-2000 had lower 25-year cardiovascular disease mortality than patients treated in 1965-1976 (4.3% vs 5.7%; subdistribution hazard ratio = 0.65, 95% CI = 0.46 to 0.93). Infectious disease mortality was not only increased after splenectomy but also after spleen irradiation (hazard ratio = 2.81, 95% CI = 1.55 to 5.07). For stage I-II, primary treatment with chemotherapy (CT) alone was associated with statistically significantly higher HL mortality (P < .001 for CT vs radiotherapy [RT]; P = .04 for CT vs RT+CT) but lower 30-year mortality from causes other than HL (15.8%, 95% CI = 9.7% to 23.3%) compared with RT alone (36.9%, 95% CI = 34.0% to 39.8%, P = .001) and RT and CT combined (29.8%, 95% CI = 26.8% to 32.9%, P = .02).

CONCLUSIONS: Compared with the general population, HL survivors have a substantially reduced life expectancy. Optimal selection of patients for primary CT is crucial, weighing risks of HL relapse and long-term toxicity.

Original languageEnglish
Pages (from-to)760-769
Number of pages10
JournalJournal of the National Cancer Institute
Volume113
Issue number6
DOIs
Publication statusPublished - 1 Jun 2021

Bibliographical note

Publisher Copyright: © The Author(s) 2020. Published by Oxford University Press.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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