1. Predicted Risks of Cardiovascular Disease Following Chemotherapy and Radiotherapy in the UK NCRI RAPID Trial of Positron Emission Tomography-Directed Therapy for Early-Stage Hodgkin Lymphoma.
- Author
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Cutter DJ, Ramroth J, Diez P, Buckle A, Ntentas G, Popova B, Clifton-Hadley L, Hoskin PJ, Darby SC, Radford J, and Illidge T
- Subjects
- Adolescent, Adult, Aged, Antineoplastic Combined Chemotherapy Protocols adverse effects, Bleomycin therapeutic use, Cardiovascular Diseases diagnostic imaging, Cardiovascular Diseases mortality, Clinical Decision-Making, Dacarbazine therapeutic use, Doxorubicin therapeutic use, Female, Heart Disease Risk Factors, Hodgkin Disease diagnostic imaging, Hodgkin Disease mortality, Hodgkin Disease pathology, Humans, Incidence, Male, Middle Aged, Neoplasm Staging, Predictive Value of Tests, Radiation Dosage, Radiation Injuries diagnostic imaging, Radiation Injuries mortality, Risk Assessment, Time Factors, Treatment Outcome, United Kingdom epidemiology, Vinblastine therapeutic use, Young Adult, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Cardiovascular Diseases epidemiology, Chemoradiotherapy adverse effects, Chemoradiotherapy mortality, Hodgkin Disease therapy, Positron-Emission Tomography, Radiation Injuries epidemiology
- Abstract
Purpose: The contemporary management of early-stage Hodgkin lymphoma (ES-HL) involves balancing the risk of late adverse effects of radiotherapy against the increased risk of relapse if radiotherapy is omitted. This study provides information on the risk of radiation-related cardiovascular disease to help personalize the delivery of radiotherapy in ES-HL., Methods: We predicted 30-year absolute cardiovascular risk from chemotherapy and involved field radiotherapy in patients who were positron emission tomography (PET)-negative following three cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine chemotherapy within a UK randomized trial of PET-directed therapy for ES-HL. Cardiac and carotid radiation doses and chemotherapy exposure were combined with established dose-response relationships and population-based mortality and incidence rates., Results: Average mean heart dose was 4.0 Gy (range 0.1-24.0 Gy) and average bilateral common carotid artery dose was 21.5 Gy (range 0.6-38.1 Gy), based on individualized cardiovascular dosimetry for 144 PET-negative patients receiving involved field radiotherapy. The average predicted 30-year radiation-related absolute excess overall cardiovascular mortality was 0.56% (range 0.01%-6.79%; < 0.5% in 67% of patients and > 1% in 15%), whereas average predicted 30-year excess incidence was 6.24% (range 0.31%-31.09%; < 5% in 58% of patients and > 10% in 24%). For cardiac disease, the average predicted 30-year radiation-related absolute excess mortality was 0.42% (0.79% with mediastinal involvement and 0.05% without) and for stroke, it was 0.14%., Conclusion: Predicted excess cardiovascular risk is small for most patients, so radiotherapy may provide net benefit. However, for a minority of patients receiving high doses of radiation to cardiovascular structures, it may be preferable to consider advanced radiotherapy techniques to reduce doses or to omit radiotherapy and accept the increased relapse risk. Individual assessment of cardiovascular and other risks before treatment would allow personalized decision making about radiotherapy in ES-HL., Competing Interests: Johanna RamrothEmployment: Gilead Sciences (I)Stock and Other Ownership Interests: Gilead Sciences Laura Clifton-HadleyResearch Funding: Various pharmaceutical companies Peter J. HoskinResearch Funding: Varian Medical Systems, Astellas Pharma, Bayer, Roche, Pfizer, Elekta John RadfordStock and Other Ownership Interests: AstraZeneca, ADC TherapeuticsHonoraria: Takeda, ADC TherapeuticsConsulting or Advisory Role: Takeda, Seattle Genetics, NovartisSpeakers' Bureau: Takeda, Seattle Genetics, NovartisResearch Funding: TakedaTravel, Accommodations, Expenses: Takeda, ADC Therapeutics Tim IllidgeConsulting or Advisory Role: Takeda, Nordic NanovectorSpeakers' Bureau: Takeda, Bristol Myers Squibb, RocheResearch Funding: AstraZeneca/MedImmune, MSD OncologyTravel, Accommodations, Expenses: RocheNo other potential conflicts of interest were reported.
- Published
- 2021
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