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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]).
8 e improved overall radiographic response and progression-free survival rates, although the impact of
9 a median follow-up of 41 months, the 3-year progression-free survival rate and overall survival rate
10 time of 42 months, the estimated overall and progression-free survival rates are 68% and 42%, respect
11 , does one have a well-documented historical progression-free survival rate at 1 year for comparison
18 ary outcome was the difference in the 3-year progression-free survival rate between randomized groups
21 f 33 months (range,17-94 months), the 3-year progression-free survival rates for patients with chemor
22 zard ratio [HR] 1.05; 95% CI 0.95-1.17), and progression free survival rates (HR 1.01; 95% CI, 0.92-1
23 more percentage points from the assumed 95% progression-free survival rate in the radiotherapy group
24 ear overall survival rate is 76%, the 3-year progression-free survival rate is 56%, and the 3-year lo
27 all objective response rate of 33%, 12-month progression-free survival rate of 35%, and median overal
28 ulting in a 63% durable CR rate and a 2-year progression-free survival rate of 65% (95% CI, 51% to 79
29 signed to exclude a difference in the 3-year progression-free survival rate of 7 or more percentage p
30 l (24 from Hodgkin's lymphoma), for a 3-year progression-free survival rate of 82.6% and an overall s
31 had disease progression or died, with 2-year progression-free survival rates of 69 and 55%, respectiv
32 , with estimated 3-year overall survival and progression-free survival rates of 73% (95% confidence i
33 rates of 87%, 64%, 53%, and 22%, and 5-year progression-free survival rates of 83%, 55%, 33%, and 12
36 (22% v 11%; P = .034), but decreased 3-year progression-free survival rates (P < .0001) and 3-year o
38 included objective response rate and 24-week progression-free survival rate (per Response Evaluation
40 ts compared with historical series; however, progression-free survival rates remain disappointing, ra
41 abine-docetaxel was associated with a 2-year progression-free survival rate that appears superior to
46 t a median follow-up of 370 days, the 1-year progression-free survival rate was 58.2% (95% CI, 33.1%-
49 findings on a third PET-CT scan; the 3-year progression-free survival rate was 67.5% and the overall
56 ad a major response), the estimated 18 month progression-free survival rate was 86% (95% CI 66-94), a
57 6.6 years (range, 0.1-12 years), the 6-year progression-free survival rate was 88% (95% confidence i
60 e was 196 months (16.3 years) and the median progression-free survival rate was 98 months (8.2 years)
63 d objective response rate and immune-related progression-free survival rate were 40% (4 of 10 patient
66 ab-plus-irinotecan groups, estimated 6-month progression-free survival rates were 42.6% and 50.3%, re
67 lts The 8-year time to treatment failure and progression-free survival rates were 44% (95% CI, 39% to
69 3%, 47%, 47%, and 43%, respectively; 24-week progression-free survival rates were 51%, 71%, 38%, and
72 months, respectively; the 1-year overall and progression-free survival rates were 76% and 59%, respec
74 42 months), the 11-year overall survival and progression-free survival rates were 78%, and 72%, respe
78 s (range, 19-94), the estimated survival and progression-free survival rates were 85% and 83%, respec
79 With a median follow-up of 23 months, 2-year progression-free survival rates were 86% for interim PET
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