Modern Hodgkin lymphoma treatments to reduce second cancer risks: Influence of risk-adapted screening.

A Aislinn Macklin-Doherty (Institute of Cancer Research / Royal Marsden Hospital, London, United Kingdom) D David Cunningham I Ian Chau A Andrew Tom Bates (University Hospital Southampton, Southampton, United Kingdom) M Mark Bower (Department of Oncology, Imperial College London, London, United Kingdom) A A Murray Brunt (School of Medicine, Keele University, Keele, Staffordshire, United Kingdom) G George Follows (14Department of Haematology, Addenbrooke’s Hospital NHS Trust, Cambridge, United Kingdom) C Christopher Fox (14School of Medicine, University of Nottingham, Nottingham, United Kingdom) J John A. Frew (Northern Centre for Cancer Care (NCCC), Newcastle upon Tyne, United Kingdom) J John G. Gribben (6Barts Cancer Institute, Queen Mary University of London, London, United Kingdom) P Peter Hoskin (Mount Vernon Cancer Center and University of Manchester Manchester UK) C Clive Irwin (Department of Oncology, University Hospital Coventry, Coventry, United Kingdom) L Lisa Lowry (12Somerset NHS Foundation Trust, Taunton, United Kingdom) J John Radford (15University of Manchester, Christie NHS Foundation Trust and NIHR Manchester Biomedical Research Centre, Manchester, United Kingdom) I Isabel Syndikus (Clatterbridge Cancer Centre NHS Foundation Trust, Wirral, United Kingdom) E Emma Thomas (Leeds Cancer Centre, St. James' Hospital, Leeds, United Kingdom) A Anjali Zarkar (Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom) M Michael Jones A Amy Berrington de Gonzalez A Anthony Swerdlow

Abstract

7053 Background: Second primary malignancies (SPMs) are the leading cause of long-term treatment-related mortality in Hodgkin Lymphoma (HL). Although substantial improvements have been made to treatments over recent decades, few studies have demonstrated reduced SPM risk, particularly following modern treatments, and how risks should inform screening. Methods: We assembled a national cohort of 7,428 women treated for HL aged <36 across England & Wales 1954-2010, with 99% complete follow-up until 2018. We analyzed SPM incidence from national cancer registry linkage. Treatment data were collated from >250 treatment centers. Standardized incidence ratios (SIRs) and Absolute Excess Risks (AERs) for SPMs were calculated, and multivariable analyses (Hazard Ratios, HR) were undertaken to assess the impact of changes in treatment and assess changing incidence trends over time. Results: Twelve hundred women (16%) developed 1,467 SPMs with mean follow-up of 22 years (range 0-62 years). Overall SIR to develop any SPM was 3.3 (95% CI 3.1-3.5), with breast cancer contributing the greatest excess risk (AER 30.8 95% CI 27.7-34.1). Radiotherapy use halved from 1954-1980 to 2000-2010 (98% to 47%) and mean dose dropped from 48Gy to 33Gy. Conversely chemotherapy use doubled from 55% to 97%, with anthracyclines used in 94% and classic alkylators in 31% of treatments in the most recent period compared with 6% and 48% respectively pre-1980. Radiotherapy conferred the greatest treatment-specific risk factor for SPMs, (SIR 3.5 95% 3.3-3.7), with a strong dose-response relationship trend (HR 1.01/Gy p<0.001), and highest relative risks seen in those treated with radiotherapy aged <15years (SIR 7.4 (95% CI 5.7-9.1). There was a 25% reduction in SPM risk from the earliest treatment period (<1990) to most recent (2000-2010) and 34% reduction in solid SPM risk (Table). The decrease in risk for SPMs became smaller and non-significant after adjusting for reduced radiotherapy use and dose (HR 0.89, p trend 0.11). There was no attenuation after adjustment for chemotherapy. Despite declining risks, risks remained significantly elevated beyond 40 years after treatment. Conclusions: Modern HL treatments are associated with a substantial reduction in SPM risks, which appears to be largely attributable to decreased radiotherapy use and dose. However large persistent excess risks, particularly for breast and lung cancers, underscore the need for targeted screening in high-risk survivors treated in more recent eras. Risk of SPMs by treatment era. SPMs & treatments Treated <1990HR (ref) Treated 1990-1999HR (95% CI) Treated 2000-2010HR (95% CI) p trend All SPMs Any treatment 1.0 0.77 (0.65-0.90 0.75 (0.57-0.99) 0.001 Adjusted for radiotherapy & dose 1.0 0.83 (0.69-1.00) 0.90 (0.63-1.28) 0.11 Solid SPMs Any treatment 1.0 0.71 (0.60-0.85) 0.66 (0.48-0.90) <0.001 Adjusted for radiotherapy & dose 1.0 0.79 (0.65-0.96) 0.81 (0.55-1.20) 0.03

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 7053-7053
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

A

Aislinn Macklin-Doherty

Institute of Cancer Research / Royal Marsden Hospital, London, United Kingdom

D

David Cunningham

I

Ian Chau

A

Andrew Tom Bates

University Hospital Southampton, Southampton, United Kingdom

M

Mark Bower

Department of Oncology, Imperial College London, London, United Kingdom

A

A Murray Brunt

School of Medicine, Keele University, Keele, Staffordshire, United Kingdom

G

George Follows

14Department of Haematology, Addenbrooke’s Hospital NHS Trust, Cambridge, United Kingdom

C

Christopher Fox

14School of Medicine, University of Nottingham, Nottingham, United Kingdom

J

John A. Frew

Northern Centre for Cancer Care (NCCC), Newcastle upon Tyne, United Kingdom

J

John G. Gribben

6Barts Cancer Institute, Queen Mary University of London, London, United Kingdom

P

Peter Hoskin

Mount Vernon Cancer Center and University of Manchester Manchester UK

C

Clive Irwin

Department of Oncology, University Hospital Coventry, Coventry, United Kingdom

L

Lisa Lowry

12Somerset NHS Foundation Trust, Taunton, United Kingdom

J

John Radford

15University of Manchester, Christie NHS Foundation Trust and NIHR Manchester Biomedical Research Centre, Manchester, United Kingdom

I

Isabel Syndikus

Clatterbridge Cancer Centre NHS Foundation Trust, Wirral, United Kingdom

E

Emma Thomas

Leeds Cancer Centre, St. James' Hospital, Leeds, United Kingdom

A

Anjali Zarkar

Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom

M

Michael Jones

A

Amy Berrington de Gonzalez

A

Anthony Swerdlow