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1 e frequency of FoxP3 cells did not influence median overall survival.
2 ociated with an improvement of 3.7 months in median overall survival.
3 ared with matched controls with de novo AML (median overall survival, 1.2 years v 2.9 years; P = .06)
4 herapy (HR 0.58 [95% CI 0.36-0.94], p=0.026; median overall survival 10.7 months [95% CI 6.5-18.9] vs
5 iotherapy (0.59 [95% CI 0.36-0.96], p=0.034; median overall survival 11.6 months [95% CI 6.5-20.5] vs
7 and 336 in the docetaxel plus placebo group; median overall survival 12.6 months [95% CI 10.6-15.1] v
8 lso had improved survival with atezolizumab (median overall survival 12.6 months vs 8.9 months; HR 0.
9 fference in overall survival between groups (median overall survival 12.8 months [95.5% CI 10.5-14.3]
10 ee survival (11.1 months [95% CI 9.7-12.9]), median overall survival (25.6 months [23.1-34.3]), 1-yea
11 treatment medium entropy of less than 7.356 (median overall survival, 33.2 vs 11.7 months; P = .0002)
12 = .0002), coarse entropy of less than 7.116 (median overall survival, 33.2 vs 11.7 months; P = .0002)
13 , and medium uniformity of 0.007 or greater (median overall survival, 33.2 vs 11.7 months; P = .0002)
14 nk p=0.030), as well as significantly longer median overall survival (37.5 months [26-not reached] vs
16 nt groups in the overall patient population (median overall survival 8.8 months [95% CI 7.4-9.6] in t
30 squamous cell lung cancer (mSqCLC) increased median overall survival by 1.6 months (hazard ratio, 0.8
31 metastatic colorectal cancer that increases median overall survival by 6 weeks compared with placebo
33 tients with WDTC was associated with shorter median overall survival compared with matched controls (
45 eived previous concurrent chemoradiotherapy, median overall survival for the 538 (65%) of 829 patient
48 ents with metastatic soft-tissue sarcoma and median overall survival for those treated is 12-16 month
53 With a median follow-up of 36.7 months, the median overall survival from the date of the first rando
57 was evident in epithelioid histology, with a median overall survival gain of 5.4 months (HR, 0.70; 95
58 FS (GemErlo 11.4 months; Gem 11.4 months) or median overall survival (GemErlo 24.5 months; Gem 26.5 m
59 ration between 4 and 8 weeks had the longest median overall survival (group B: 40.4 months) compared
60 .5 months (range, 2.6+ to 22.3+ months), and median overall survival had not been reached (range, 4.6
61 6.8) for those assigned to ipilimumab alone; median overall survival had not been reached in either g
63 At a minimum follow-up of 36 months, the median overall survival had not been reached in the nivo
64 an follow-up of approximately 23 months, the median overall survival has not been reached in either s
70 f 50.3 months (IQR 32.9-68.0), the estimated median overall survival in group A has not been reached,
76 ance therapy until progression, improved the median overall survival in patients with platinum-sensit
78 Based on pretreatment stratification data, median overall survival in the chemotherapy plus bevaciz
79 up, 81 in the active symptom control group), median overall survival in the docetaxel group was 5.2 m
84 er a median follow-up time of 11 months, the median overall survival in the RT cohort was 10.7 months
88 598 (91%) patients with BRAF(V600E) disease, median overall survival in the vemurafenib group was 13.
89 e 57 (9%) patients with BRAF(V600K) disease, median overall survival in the vemurafenib group was 14.
90 well tolerated and associated with promising median overall survival in these patients with heavily p
91 to 50.2% diagnosed in 1988 and 2010, and the median overall survival increased for both PTR and non-P
92 22.4 months (95% CI, 5.4 to 37.6 months) and median overall survival is 34.8 months (95% CI, 14.8 mon
93 l, rCBV was low in nine (47%) patients, with median overall survival (mOS) of 591 days, and high rCBV
94 n improved the outcomes of patients with HT (median overall survival, not reached v 1.7 years) but no
95 ard of care based on a 1.4-month increase in median overall survival observed in a randomized trial.
96 ll survival between treatment groups, with a median overall survival of 11.3 months (95% CI 9.5-13.4)
97 ol patients treated with dacarbazine (DTIC), median overall survival of 15.0 versus 8.3 months (P = 0
98 tio 1.06, 95% CI 0.88-1.29; p=0.527), with a median overall survival of 18.4 months (95% CI 15.6-22.1
99 h progression-free survival rate of 35%, and median overall survival of 23 months; grade 3 or 4 treat
100 normal AFP levels (<13 ng/dL) and exhibited median overall survival of 23.9 mo (95% CI, 20.1-124.1 m
101 ) across studies with a pooled patient-level median overall survival of 24.2 months (95% CI 21.7-26.8
102 creatic cancer treated with FOLFIRINOX had a median overall survival of 24.2 months-longer than that
103 -dose levels (10(8)-10(9) TCID50), and their median overall survival of 26.5 months compared favorabl
104 73 days, while untreated leukemic mice had a median overall survival of 34 days (P < .001, Mantel-Cox
108 0.87; 95% CI, 0.65 to 1.18; P = .188), with median overall survival of 43.9 months with letrozole ve
110 treated with 200 muCi (90)Y-DOTA-30F11 had a median overall survival of 73 days, while untreated leuk
117 mo (95% confidence interval [CI], 27-49 mo); median overall survival of the 89 patients left for mult
122 at baseline was significantly prognostic for median overall survival (OS) in univariate and multivari
123 atients with >3 CTC/ml had a trend for worse median overall survival (OS) than patients with 0.3-3 CT
125 l (PFS) was 3.7 months (95%CI, 2.4 to 5) and median overall survival (OS) was 10.5 months (95%CI, 6.4
126 sponse duration was 8.3 and 10.7 months, and median overall survival (OS) was 16.5 and 13.6 months, r
138 using point estimates for weighted values of median overall survival, progression-free survival, resp
142 ly significant improvement of 11.8 months in median overall survival, suggesting a potential shift in
143 diation therapy plus chemotherapy had longer median overall survival than did those who received radi
144 arcopenic patients had significantly shorter median overall survival than nonsarcopenic patients (52.
145 ry, or distal CBD adenocarcinomas had longer median overall survival than those with PB type (71.7 vs
146 pectively (hazard ratio, 0.91; P = .18), and median overall survival time was 3.9 years in both treat
150 ition of placebo, significantly improved the median overall survival to 56.5 months and extended the
153 val was 4.1 months (95% CI, 1.5-6.5) and the median overall survival was 10.2 months (95% CI, 2.6-44.
160 free survival was 61 d (range, 25-80 d), and median overall survival was 106 d (range, 37-417 d).
164 ective response rate was 45% versus 31%, and median overall survival was 11.5 versus 8.5 months (HR,
166 l (PFS) was 3.6 months (95% CI, 2 to 4), and median overall survival was 11.8 months (95% CI, 8 to 25
172 For colorectal cancer patients (n = 23), the median overall survival was 13.4 mo (95% CI, 8.2-15.7 mo
173 After a median follow-up of 28.9 months, the median overall survival was 13.6 months longer with ADT
174 d with atezolizumab compared with docetaxel (median overall survival was 13.8 months [95% CI 11.8-15.
175 nterval [CI], 0.91 to 1.45; P=0.25), and the median overall survival was 14.4 months versus 13.2 mont
180 umab (n=241) compared with docetaxel (n=222; median overall survival was 15.7 months [95% CI 12.6-18.
184 ths (IQR 5-11) and 210 deaths were reported; median overall survival was 16 months (95% CI 13-not ava
185 val was 6.0 (95% CI, 5.0 to 7.3) months, and median overall survival was 16.6 (95% CI, 11.1 to 20.6)
186 the ipilimumab followed by nivolumab group, median overall survival was 16.9 months (95% CI 9.2-26.5
187 rvival was 8.8 (95% CI, 4.6-15.4) months and median overall survival was 17.5 (95% CI, 13.3-NE) month
188 % CI 51.2-75.5) and, at a subsequent cutoff, median overall survival was 17.5 months (95% CI 13.7-not
193 ion was 11 months (95% CI, 9-13 months), and median overall survival was 18 months (95% CI, 9-27 mont
199 e in overall survival for patients with MRD: median overall survival was 20.1 months (95% CI 18.5-22.
201 was 6.5 months (95% CI, 5.8 to 7.7 months); median overall survival was 21.5 months (95% CI, 16.0 to
210 ing bortezomib and an immunomodulatory drug, median overall survival was 25.5 months (95% CI 19.6-34.
212 onths (T,: 16.6 months; TC, 5.6 months), and median overall survival was 25.7 months (T, not reached;
213 7.5 months (95% CI, 8.6-25.0 months) and the median overall survival was 25.8 months (95% CI, 15.7-25
217 tive tumours in either trial: in LUX-Lung 3, median overall survival was 27.6 months (19.8-41.7) in t
221 old for statistical significance [p<0.0095]; median overall survival was 29.8 months [95% CI 26.9-35.
222 76%) died after discontinuing ibrutinib; the median overall survival was 3.1 months after discontinua
223 a median follow-up of 45 months (IQR 35-58), median overall survival was 30 months (95% CI 24-34) in
227 an follow-up of 20.7 months (IQR 14.2-25.4), median overall survival was 31.4 months (95% CI 28.6-not
228 therapy group in both trials: in LUX-Lung 3, median overall survival was 33.3 months (95% CI 26.8-41.
229 ture, although at the time of this analysis, median overall survival was 33.64 months (95% CI 31.34-n
232 o three risk categories using IMDC criteria, median overall survival was 35.3 months (95% CI 28.3-47.
233 Among propensity score-matched groups, the median overall survival was 37.3 (95% CI, 35.2-38.7) mon
237 s 14.7, 15.4, and 17.3 months, respectively; median overall survival was 49.8, 51.5, and 53.1 months,
239 o [HR], 1.05; 95% CI, 0.90 to 1.23), and the median overall survival was 50.8 and 59.1 months (HR, 0.
242 LR only underwent salvage surgery, and their median overall survival was 58.6 months (95% CI, 28.8 to
246 iotherapy groups, respectively (p=0.58), and median overall survival was 6.9 months (95% CI 5.1-8.3)
250 0.45 [97.5% CI, 0.34 to 0.61]; P<0.001); the median overall survival was 7.7 months (95% CI, 6.0 to 9
256 % confidence interval, 0.35-0.92; P = .021); median overall survival was 8.0 vs 5.2 months, respectiv
264 py did not provide a survival advantage; the median overall survival was 9.1 months (95% confidence i
267 the 16 patients with mast-cell leukemia, the median overall survival was 9.4 months (95% CI, 7.5 to n
273 of overall survival with predefined factors, median overall survival was longer for: patients with ba
276 was 9.1 months (95% CI, 4.9 to 11.7 months); median overall survival was not reached at 14 months.
277 ogression-free survival was 13.7 mo, and the median overall survival was not reached during follow-up
282 an follow-up of 19.8 months (IQR 12.8-25.7), median overall survival was not reached in the nivolumab
296 Outcome by pathologic lymph node status (N, median overall survival) was N0: 224, 26 months; N1: 118
298 n a significant but only marginally improved median overall survival when combined with gemcitabine i
299 Dendritic cell-vaccinated patients showed a median overall survival with metastatic disease of 19.2
300 bjective was to test the hypothesis that the median overall survival would be 33.3% longer among pati
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