1136 - Osteoarthritis (OA): Calculating Lifetime Attributable Oncogenic Risk from Low-Dose Radiotherapy (LDRT)
Presenter(s)
D. Zheng1, A. Lassalle2, B. Marples3, M. T. Milano4, Y. Chen4, and L. S. Constine5; 1University of Rochester Medical Center, Department of Radiation Oncology, Rochester, NY, 2University of Rochester, Rochester, NY, 3Department of Radiation Oncology, University of Rochester, Rochester, NY, 4Department of Radiation Oncology, University of Rochester Medical Center, Rochester, NY, 5Department of Radiation Oncology and Pediatrics, University of Rochester Medical Center, Rochester, NY
Purpose/Objective(s): LDRT is an effective analgesic modality for OA refractory to standard treatments. However, clinical adoption is often hindered by concerns regarding stochastic oncogenic risk. A risk calculator was developed to provide customizable, BEIR VII-based risk estimation for patients with OA, adjustable for age, sex, height, and joint-specific scatter proximity.
Materials/Methods: Utilizing a linear no-threshold model, we calculated LAR for a standard 6-fraction 3.0 Gy regimen. BEIR VII incidence coefficients were used for ages 40-80 years, and extrapolated via linear regression for 85-100. Anthropometric variability was addressed by stratifying joints into three height-based cohorts (<160 cm, 160-185 cm, >185 cm). Site-specific weighting factors were assigned based on ICRP 103 tissue sensitivities, with distal extremities (hand/foot) distinct from intermediate (knee/elbow) and axial (spine/hip/shoulder) joints to account for red bone marrow volumes exposed and truncal scatter volume.
Results: Radiation-induced malignancy risk demonstrated a steep inverse correlation with age and anatomical distance from the trunk. For the foot, LAR at age 70 was negligible (male: 0.07%, female: 0.09%). In the geriatric population (age 80+), LAR for all sites, including high-weighting axial joints, dropped significantly (eg, male spine at 80: 1.0%) as the typical time to develop malignancy exceeds the remaining life expectancy. Conversely, the highest risk profile was identified in short-stature (<160 cm) females age 40 receiving axial treatment (spine LAR: 6.0%). By age 100, statistical risk for all cohorts converged toward zero, reflecting a "stochastic floor."
Conclusion: Anthropometric and age-based stratification reveals that LDRT for OA carries a risk profile frequently lower than the acute morbidity/mortality rates associated with invasive arthroplasty or chronic NSAID use. This granular data supports practice patterns favoring LDRT for distal and geriatric indications. The developed calculator provides a convenient, robust tool for clinicians to discuss case-specific risks with patients and referring providers, facilitating evidence-based informed consent.
Table 1. Comparative OA treatment risk analysis of acute vs. stochastic events (75-year-old male, avg. height)| Treatment | Nature of Risk | Probability |
| Arthroplasty | Acute Death / Morbidity | ~1.0% / ~27% |
| Chronic NSAIDs | Annual GI / Renal Event | ~1.5% |
| LDRT (Foot) | Stochastic (Lifetime) | <0.08% |
| LDRT (Knee) | Stochastic (Lifetime) | ~0.47% |
| LDRT (Spine) | Stochastic (Lifetime) | ~1.32% |