PO.CL08.02 · 临床研究

Low-dose radiation therapy for peripheral joint osteoarthritis: Early U.S. community experience with pain, function, and medication outcomes

编号 5269 展板 6 时间 4/21 09:00–12:00 区域 Section 43 主讲 Emily Schwartz, No Degree
分会场 Effects of Ionizing Radiation on Normal Tissues and FLASH Radiation Research
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作者与单位

Emily Schwartz1, Michael Anderson2, Russell Nevins3, Kelsey Moakler2, Andrew Cohen4, Michael Sinopoli4, Samuel Francis4, Bradley Newby2, Matthew Schwartz5

1University of Miami, Coral Gables, FL,2Comprehensive Cancer Centers of Nevada, Henderson, NV,3Desert Orthopaedic Center, Las Vegas, NV,4Comprehensive Cancer Centers of Nevada, Las Vegas, NV,5University of Nevada, Las Vegas (UNLV), Las Vegas, NV

摘要 Abstract

Background / Significance: Osteoarthritis (OA) causes chronic pain and functional decline in older adults, yet treatment options are limited for patients who cannot tolerate long-term NSAIDs or opioids. Low-dose radiation therapy (LDRT) has shown efficacy in European studies, but U.S. data are sparse. This student-led study reports early outcomes from a community oncology practice implementing LDRT for OA, focusing on pain, function, and analgesic trends. Methods: Thirty patients (55 joints) with OA were treated with LDRT (3 Gy in 5-6 fractions, 0.5 Gy/fraction). Pain was assessed using the Numeric Rating Scale (NRS, 0-10) and patient-assessed global improvement using the von Pannewitz Score (VPS, 0-4) at baseline, end of treatment (EOT), and ~1-month follow-up. Analgesic use was recorded at both time points. Paired t-tests and one-way ANOVA by joint site were used to assess changes. Results: Mean baseline NRS = 8.0 (±1.2); follow-up = 3.3 (±2.1), a mean reduction of 4.7 points (p < 0.001). Eighty-three percent (25/30) achieved ≥2-point improvement; 70% (21/30) ≥3 points; 40% (12/30) ≥5 points. VPS at follow-up indicated moderate improvement in 39%, excellent in 25%, and complete response in 9%. Analgesic use decreased in 23% (7/30), and no patients required escalation or new medications. No ≥ Grade 2 toxicities occurred. Conclusions: LDRT was safe, feasible, and provided substantial pain relief and improved function with parallel reductions in analgesic use. The absence of medication escalation underscores its potential as a non-pharmacologic, opioid-sparing therapy for OA pain. These real-world U.S. data support further prospective evaluation of LDRT in geriatric pain management. Disclosure: No external funding or conflicts of interest. Study conducted under student investigator leadership with faculty supervision.
利益披露 Disclosure
E. Schwartz, None.. M. Anderson, None.. R. Nevins, None.. K. Moakler, None.. A. Cohen, None.. M. Sinopoli, None.. S. Francis, None.. B. Newby, None.. M. Schwartz, None.

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