Modern Hodgkin lymphoma treatments to reduce second cancer risks: Influence of risk-adapted screening.
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Aislinn Macklin-Doherty
Institute of Cancer Research / Royal Marsden Hospital, London, United Kingdom
David Cunningham
Ian Chau
Andrew Tom Bates
University Hospital Southampton, Southampton, United Kingdom
Mark Bower
Department of Oncology, Imperial College London, London, United Kingdom
A Murray Brunt
School of Medicine, Keele University, Keele, Staffordshire, United Kingdom
George Follows
14Department of Haematology, Addenbrooke’s Hospital NHS Trust, Cambridge, United Kingdom
Christopher Fox
14School of Medicine, University of Nottingham, Nottingham, United Kingdom
John A. Frew
Northern Centre for Cancer Care (NCCC), Newcastle upon Tyne, United Kingdom
John G. Gribben
6Barts Cancer Institute, Queen Mary University of London, London, United Kingdom
Peter Hoskin
Mount Vernon Cancer Center and University of Manchester Manchester UK
Clive Irwin
Department of Oncology, University Hospital Coventry, Coventry, United Kingdom
Lisa Lowry
12Somerset NHS Foundation Trust, Taunton, United Kingdom
John Radford
15University of Manchester, Christie NHS Foundation Trust and NIHR Manchester Biomedical Research Centre, Manchester, United Kingdom
Isabel Syndikus
Clatterbridge Cancer Centre NHS Foundation Trust, Wirral, United Kingdom
Emma Thomas
Leeds Cancer Centre, St. James' Hospital, Leeds, United Kingdom
Anjali Zarkar
Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom
Michael Jones
Amy Berrington de Gonzalez
Anthony Swerdlow