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1 t Milan criteria provides a high local tumor progression-free survival rate.
2 response rate and the 20-week immune-related progression-free survival rate.
3 mide backbone and has promising response and progression-free survival rates.
5 rate, 71% [5 of 7 patients]; immune-related progression-free survival rate, 67% [4 of 6 patients]).
9 e improved overall radiographic response and progression-free survival rates, although the impact of
10 l patients with high-risk NMIBC, the 10-year progression-free survival rate and disease-specific deat
11 a median follow-up of 41 months, the 3-year progression-free survival rate and overall survival rate
12 time of 42 months, the estimated overall and progression-free survival rates are 68% and 42%, respect
13 with a positive and negative TSE score show progression free survival rates at 6 months of 67 and 0%
14 , does one have a well-documented historical progression-free survival rate at 1 year for comparison
15 l response after induction and difference in progression-free survival rate at 2 years from randomisa
23 ary outcome was the difference in the 3-year progression-free survival rate between randomized groups
28 rable 3-year response, overall survival, and progression-free survival rates for asymptomatic patient
29 f 33 months (range,17-94 months), the 3-year progression-free survival rates for patients with chemor
31 zard ratio [HR] 1.05; 95% CI 0.95-1.17), and progression free survival rates (HR 1.01; 95% CI, 0.92-1
33 more percentage points from the assumed 95% progression-free survival rate in the radiotherapy group
34 ear overall survival rate is 76%, the 3-year progression-free survival rate is 56%, and the 3-year lo
37 all objective response rate of 33%, 12-month progression-free survival rate of 35%, and median overal
38 ulting in a 63% durable CR rate and a 2-year progression-free survival rate of 65% (95% CI, 51% to 79
39 signed to exclude a difference in the 3-year progression-free survival rate of 7 or more percentage p
40 l (24 from Hodgkin's lymphoma), for a 3-year progression-free survival rate of 82.6% and an overall s
41 ival rate of 98% (95% CI 92-99) and a 5-year progression-free survival rate of 83% (76-88) for supram
43 5.9 years (range, 0.5-10 years), the 6-year progression-free survival rate of patients who underwent
44 -84) versus 48% (29-65; p<0.0001) and 5-year progression-free survival rates of 44% (38-50) versus 25
45 had disease progression or died, with 2-year progression-free survival rates of 69 and 55%, respectiv
46 , with estimated 3-year overall survival and progression-free survival rates of 73% (95% confidence i
47 rates of 87%, 64%, 53%, and 22%, and 5-year progression-free survival rates of 83%, 55%, 33%, and 12
50 (22% v 11%; P = .034), but decreased 3-year progression-free survival rates (P < .0001) and 3-year o
52 included objective response rate and 24-week progression-free survival rate (per Response Evaluation
55 ts compared with historical series; however, progression-free survival rates remain disappointing, ra
56 and bevacizumab achieved better overall and progression-free survival rates than sorafenib in unrese
57 abine-docetaxel was associated with a 2-year progression-free survival rate that appears superior to
58 ndpoint versus the historical control 1-year progression-free survival rate used to determine the sam
65 t a median follow-up of 370 days, the 1-year progression-free survival rate was 58.2% (95% CI, 33.1%-
68 findings on a third PET-CT scan; the 3-year progression-free survival rate was 67.5% and the overall
77 ad a major response), the estimated 18 month progression-free survival rate was 86% (95% CI 66-94), a
78 24.2 months (95% CI, 23.4-26.9), the 2-year progression-free survival rate was 88% (95% CI, 75.7-94.
79 6.6 years (range, 0.1-12 years), the 6-year progression-free survival rate was 88% (95% confidence i
85 e was 196 months (16.3 years) and the median progression-free survival rate was 98 months (8.2 years)
88 d objective response rate and immune-related progression-free survival rate were 40% (4 of 10 patient
93 ab-plus-irinotecan groups, estimated 6-month progression-free survival rates were 42.6% and 50.3%, re
94 lts The 8-year time to treatment failure and progression-free survival rates were 44% (95% CI, 39% to
96 3%, 47%, 47%, and 43%, respectively; 24-week progression-free survival rates were 51%, 71%, 38%, and
102 fter a median follow-up of 67 months, 5-year progression-free survival rates were 72% in the inductio
103 14 [95% CI 0.138-0.334]; p<0.0001); 42-month progression-free survival rates were 74.6% (95% CI 65.0-
104 months, respectively; the 1-year overall and progression-free survival rates were 76% and 59%, respec
106 42 months), the 11-year overall survival and progression-free survival rates were 78%, and 72%, respe
110 w-up of 28.9 months, estimated 1- and 2-year progression-free survival rates were 84.1% and 78.6%, re
111 s (range, 19-94), the estimated survival and progression-free survival rates were 85% and 83%, respec
112 With a median follow-up of 23 months, 2-year progression-free survival rates were 86% for interim PET
113 or pembrolizumab and 10.1% for chemotherapy; progression-free survival rates were 9.5% and 2.7%, resp
116 he RVd group progressed; respective 24-month progression-free survival rates were 95.8% and 89.8%.