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1 receiving treatment (less than one-third of those estimated to be eligible).
2 ded at least one PMT visit within 12 months were determined to be eligible.
3 rmance status of 0 or 1, and at least one measurable lesion to be eligible.
5 ts (OR, 0.56; 95% CI, 0.38-0.82; P = .003) were less likely to be eligible after screening visit 1.
7 We screened 1193 patients; 178 were found to be eligible and were randomly assigned to treatment groups
9 o hundred eighty-five (86%) of the patients were determined to be eligible, and 47 (14%) were not eligible.
10 p performance status of 0-2, at least one measurable lesion to be eligible, and who were ineligible for intensive chemoth
11 or further interventions, 9 were certified and 9 were found to be eligible, but declined certification.
12 y 11.9% of ICA+ but GAA- and ICA512AA- relatives were found to be eligible by DPT criteria for trial entry.
13 t of rapid ART initiation specifically among patients known to be eligible for ART before treat all.
18 dividuals) and 13 MN studies (2,097 individuals) were found to be eligible for inclusion in a meta-analysis.
20 Of 110 studies identified, 25 trials were shown to be eligible for inclusion in the meta-analysis.
25 d OR = 0.15; 95% CI: 0.09, 0.24; P < .001) were less likely to be eligible for LCS under previous guidelines.
26 as racial and ethnic minority groups are still less likely to be eligible for lung cancer screening.
27 lt travelers were included; providers considered 6612 (16%) to be eligible for MMR vaccine at the time of pretravel consu
29 Racial/ethnic minorities were significantly less likely to be eligible for screening yet had higher odds of developin
30 participate in the study; 1,375 APA members were determined to be eligible for study participation.
31 up I patients had smaller tumors (P =.01), were more likely to be eligible for surgical treatment (P =.005), and had a be
39 ype 1 infection, blacks were 65% less likely than nonblacks to be eligible for treatment (28.1% > 17.0%; relative risk, 1
40 h frontline nivolumab who were clinically stable and judged to be eligible for treatment beyond RECIST v1.1-defined progr
41 ing is provision of real-world estimates of patients likely to be eligible for triaging, but these are challenging to obt
49 d OR = 0.15; 95% CI: 0.10, 0.23; P < .001) were less likely to be eligible under the revised guidelines.