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. Author manuscript; available in PMC: 2019 Nov 1.
Published in final edited form as: Int J Radiat Oncol Biol Phys. 2018 Jul 2;102(3):536–542. doi: 10.1016/j.ijrobp.2018.06.041

Table 1.

Total CTC-detectable CTC-undetectable p-value
n=48 n=20 n=28
Age at enrollment (median, range) 69.5 years (55–89 years) 70.5 years (59–89 years) 67.5 years (55–84 years) 0.63
Sex (female) 26 (54%) 14 (70%) 12 (43%) 0.08
Race 0.86
 Caucasian 37 (77%) 16 (80%) 21 (75%)
 African American 9 (19%) 3 (15%) 6 (21%)
 Other 2 (4%) 1 (5%) 1 (4%)
Smoking status 0.49
 Current 12 (25%) 4 (20%) 8 (29%)
 Former 34 (71%) 16 (80%) 18 (64%)
 Never 2 (4%) 0 (0%) 2 (7%)
 Pack-years (median, range) 40 (3.5–165) 37.5 pack-years (4.5–75 pack-years) 45 pack-years (3.5–165 pack-years)
Tumor size (median, range) 1.4 cm (0.5–3.8) 1.2 cm (0.5–3.2 cm) 1.75 cm (0.9–3.8 cm) 0.08
Tumor SUV (median, range) 3 (0.8–19.9) 2.6 (0.8–12.7) 3.1 (0.8–19.9) 0.40
T stage 0.31
 1a 35 (73%) 17 (85%) 18(64%)
 1b 10 (21%) 2 (10%) 8 (29%)
 2a 3 (6%) 1 (5%) 2 (7%)
Prior history NSCLC 0.01
 Yes 10 (21%) 8 (40%) 2 (7%)
 No 38 (79%) 12 (60%) 26 (93%)

Detection and monitoring of CTCs may be useful in patients with early stage NSCLC when definitive tissue diagnosis cannot be confirmed by biopsy. We present a pilot prospective assessment of 48 clinical stage I NSCLC patients treated with SBRT undergoing serial CTC monitoring with a novel, telomerase-based assay. Our results suggest that CTC monitoring in this patient population is feasible and potentially useful in enhancing clinical diagnosis and detection of recurrent or progressive disease.