Abstract
After treatment of metastatic lesions with SBRT, scarring and fibrosis may lead to misclassification of treatment response when using non-metabolic imaging. Thus, the metabolic information provided by PET may offer a more accurate assessment of treatment efficacy. However, early radiation changes on PET may falsely lead to concern for progressive disease. Here, we report our SBRT experience with long-term PET follow-up in patients with metastatic melanoma. Thirty-two metastatic melanoma patients treated with SBRT who had evaluable baseline and post-SBRT PETs were identified in our prospectively maintained database from 2008 to 2011. PET metabolic response was evaluated per PERCIST 1.0 criteria: Complete response (CR) was a decrease in the maximum standard uptake value corrected for lean body mass (SUL) to 1.5 times the liver mean + 2 standard deviations, partial response (PR) was a 30% decrease in SUL, progressive disease (PD) was> 30% increase in SUL and stable disease (SD) was any lesion not fitting these criteria. Local control (LC) included CR, PR, and SD. Fifty-six SBRT-treated lesions and 201 pre- and post-SBRT PET scans were analyzed. Median follow-up (f/u) was 1.9 years. Sites of treatment included: 15 musculoskeletal, 14 liver, 14 lung, 11 abdominal, 2 extra abdominal lymph nodes. Median single-fraction equivalent dose (SFED) was 43 Gy (range = 18-56 Gy). A median of 5 PET scans (range = 2-6) were evaluated for each lesion. LC was 89% and 75% and overall survival was 54% and 23% at 1.5 and 3 years, respectively. Median time to CR was 2.8 months (0.7-15 months). CR was achieved in 49 lesions (86%), and 43 lesions maintained CR at last f/u. Median f/u for lesions in continuous CR was 22 months. Overall, rates of PR, SD, and PD were 7%, 5%, and 13%, respectively. SFED > 24 Gy correlated with LC (RR = 1.4, P = 0.006). At initial f/u (median 2 months), the rate of CR was 60%, and 9 lesions (16%) had increased SUL. These 9 lesions resolved to 5 CR, 2 SD, and 2 PD with subsequent f/u. CNS metastases developed after SBRT in 35% (median 6 months). Three patients were alive, two with no evidence of disease, at last follow-up. SBRT produces a complete metabolic response and prolonged local control in the majority of treated patients. Even after an initial rise in SUL, long-term local control is high. These data support the use of SBRT to overcome the inherent radioresistant nature of metastatic melanoma.
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