PQA 01 - PQA 01 Lung Cancer/Thoracic Malignancies and Diversity, Equity and Inclusion in Healthcare Poster Q&A
2047 - Pretreatment Maximum Standard Uptake Value (SUV max) on Positron Emission Tomography (PET) and the Risk of Distant Failure for Patients with Stage I Non-Small Cell Lung Cancer (NSCLC) Receiving Stereo
N. Haldar1, A. L. Fekete2, S. Jain3, P. A. Brower4, J. Martin5, L. N. McLean1, and M. Werner-Wasik1; 1Department of Radiation Oncology, Sidney Kimmel Medical College of Thomas Jefferson University, Philadelphia, PA, 2Philadelphia College of Osteopathic Medicine, Philadelphia, PA, 3Drexel University College of Medicine, Philadelphia, PA, 4Jefferson Abington Hospital, Abington, PA, 5Thomas Jefferson University Hospital, Philadelphia, PA
Purpose/Objective(s): Characterization of tumor metabolism may help predict response to treatment and future treatment selection. Positron-emission tomography (PET) is used to identify hypermetabolic tissue by measuring the uptake of radioactive fluorodeoxyglucose as a surrogate marker of tumor invasiveness. Here we report a retrospective cohort study looking at rates of distant and locoregional failure based on pre-treatment standard-uptake-value maximum (SUV max) or SUV max change post-treatment for tumors < 5cm in size receiving stereotactic-body-radiation-therapy (SBRT). Materials/
Methods: Patients with T1-2 N0 M0 NSCLC treated definitively with SBRT from 2016-2022 at our institution were identified. Patients included in the study had available pre-treatment PET scans and at least 2 years of follow-up. All patients received SBRT with 6 MV photons. Two separate cohorts were created, one with patients with SUV max of their lesion >6.2 and one with SUV max <6.2. Of patients with available both pre-and post-treatment PET, another 2 cohorts were created, for those with a reduction or an increase in post-treatment SUV max. Comparisons between the two groups were conducted with a Fischer’s exact test.Demographic and treatment data were collected. Results: A total of 60 patients were identified as having pre-treatment PET studies. The average age was 78 (67-98), 71%(n=43) were Caucasian, 20% were African American (n=12), 1.6% Asian (n=1), 1.6% Hispanic (n=1), 4.8% Other (n=3). Twenty percent of patients (n=11) received a prescription dose of 60Gy delivered in 5 fractions, 25% (n=15) received 54 Gy in 3 fractions, 13% (n=8) received 55Gy in 5 fractions, 32% (n=15) received 50 Gy in 5 fractions, 10% (n=6) received 48 Gy in 4 fractions. Sixteen pts had SUV maximum > 6.2 and 44 had SUV max <6.2. Of the 57 patients with both pre and post-treatment PET studies, sixty-three percent (n=36) of pts had a decrease in SUV max on post-treatment PET while 37% (n=21) of patients had an increase. Patients with pre-treatment SUV max > 6.2 did not have a significantly increased chance for locoregional recurrence: 44% (7/16) compared to those with SUV max < 6.2, 32% (14/44), p =0.29. However, patients with SUV max > 6.2 had an increased chance of distant failure compared to those with SUV max <6.2 (44% vs 16%, respectively, p=0.03). The correlation of locoregional recurrence between the cohorts with increase versus decrease in SUV max post-treatment did not reach statistical significance (52% vs 28%, respectively, p=0.058). Conclusion: The SUV max of NSCLC tumors can predict response to ablative radiation treatment. An SUV max >6.2 prior to treatment was associated with an increased probability of distal failure. Increased risk of locoregional failure with an increase in SUV max post-treatment was not demonstrated but will be further explored in subsequent analyses.