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1 nces in 60-month life expectancy (restricted mean survival time).
2 es in the RCTs were compared with restricted mean survival time.
3 Survival was assessed with restricted mean survival time.
4 ctional regression model, and the restricted mean survival time.
5 ibed masses and yielded a 30% enhancement in mean survival time.
6 the liver and kidney, and a 20% reduction in mean survival time.
7 e-care facility was associated with a longer mean survival time.
8 iology (ASA) score (difference in restricted mean survival time 0.12 years [95% CI 0.07-0.16; P < 0.0
9 rejected when transplanted into BALB/c mice (mean survival time: 10+/-0.8 days), normal C57BL/6 mice
10 ificantly prolonged in TLR4(-/-) recipients (mean survival time=10.6 and 14.3 days, respectively).
11 fully MHC-mismatched DBA/2 skin allografts (mean survival time, 12 days; n = 6) compared with the wi
12 transplants was more rapid than skin grafts (mean survival time, 12.9 vs. 26.6 days), and islet graft
17 e showed significantly (P < 0.005) shortened mean survival time (16.2 +/- 5.3 months) compared to the
18 l time: 10+/-0.8 days), normal C57BL/6 mice (mean survival time: 16.5+/-2.1 days) as well as CD8-KO m
19 n the vitamin K antagonist group (restricted mean survival time, 1608 days vs. 1680 days; difference,
20 grafts were vigorously rejected by DKO mice (mean survival time 17 +/- 7, n = 8) as compared with wil
21 acute rejection of class I-disparate hearts (mean survival time, 19+/-7.21 vs. 38+/-8.19; P=0.025) bu
23 erved with either weekly regimen (restricted mean survival time 24.4 months [97.5% CI 23.0-26.0] in g
24 sion who underwent resection of cancer had a mean survival time 25.5 months shorter than that of pati
25 ival of the kidney capsule islet xenografts (mean survival time = 26.5 +/- 7.8 days vs. 15.2 +/- 5.3
27 who received chemotherapy alone (restricted mean survival time 34.5 months [95% CI 32.0-37.0] with s
28 6) recipients survived significantly longer (mean survival time, 38 +/- 8 days) compared with those t
29 efit of bevacizumab was recorded (restricted mean survival time 44.6 months [95% CI 43.2-45.9] in the
30 diated (600 rads), naive C57BL/6 recipients (mean survival time = 48.9 +/- 17.1 days), and three of t
31 n unimmunized cyclosporine-treated controls (mean survival time = 5.5 +/-1.7 vs. 54.7 +/-3.8 days, P
32 b group after 3 years (P = 0.005; Restricted Mean Survival Time = 5.9 months, 95% CI = 1.4-10.4 month
34 RCCs, and all grew progressively but slowly (mean survival times, 57 to >100 days) in vivo after intr
35 n group (difference calculated as restricted mean survival time, 7.4 days; 95% confidence interval [C
37 f CsA (1.0 mg/kg/day) alone was ineffective (mean survival time=7.0+/-0.7 vs. 6.4+/-0.6 days in treat
38 chemotherapy alone (difference in restricted mean survival time, 72 days; 95% confidence interval, 36
40 grafts were rejected by C57Bl/6 recipients (mean survival time=8.2 and 9.3 days, respectively), graf
46 te liver failure significantly prolonged the mean survival time and resolved the liver injury when co
48 tom resolution were calculated as restricted mean survival times and accounted for censored observati
49 rtant difference in revision-free restricted mean survival time, and a reduced relative risk of reope
51 evidenced by increased mortality, shortened mean survival time, and increased bacterial load in the
52 ve incidences, cause-specific HR, restricted mean survival time, and life-years lost at 10 and 20 yea
53 overall survival, risk of death, restricted mean survival time, and palliative care, hospice, and ac
55 ort study assesses the utility of restricted mean survival time as a method for quantifying time to n
56 rds, so we used the difference in restricted mean survival time as the primary estimate of effect.
57 ffect and introduce difference in restricted mean survival times as an alternative to identify faster
58 whiB3 mutant strain had significantly longer mean survival times as compared with mice challenged wit
59 ed paclitaxel benefits in terms of increased mean survival time, as well as median survival time.
62 as the difference in the 36-month restricted mean survival time between 2 conventional survival end p
63 how no demonstrable difference in restricted mean survival time between groups after 13.9 years (P =
65 teins that are clinically diverse, producing mean survival times between 2 and 12 years (postdiagnosi
66 expectancy was calculated as the restricted mean survival time (bound by the maximum follow-up of 20
67 accination with YpkA significantly prolonged mean survival time but did not increase overall survival
69 time to hospital, analysed using restricted mean survival time, Cox proportional hazards, and flexib
70 r, in non-high-risk patients, the restricted mean survival time did not differ significantly between
73 an unexposed facilities (adjusted restricted mean survival time difference, 91.2 days [95% CI, 30.6-1
75 isk differences, risk ratios, and restricted mean survival time differences were estimated from inver
77 higher survival rate (75% versus 62.5%) and mean survival time during the first 21 days postchalleng
79 the estimated mean difference in restricted mean survival time for grafts that experienced a DSAEK i
80 d the simulation reproduces the experimental mean survival times for all four sites with activation e
85 l of Balb/c KTx in naive C57BL/6 recipients (mean survival time >100 days vs. 52 days in controls; P<
86 lantation induced indefinite graft survival (mean survival time >140.3+/-12.3 vs. 12.7+/-0.7 control,
88 in allograft survival in CD4-deficient mice (mean survival time, >120 days), but not in CD8-deficient
93 commonly observed, making cure or restricted mean survival time models preferable for analysis of ICI
94 al hazards frailty regression and restricted mean survival time models were fitted using reconstructe
97 controls, 0.5 mg/kg SRL per day extended the mean survival time (MST) from 6.4+/-0.5 days to 12.3+/-3
98 ivo, 20 mg/kg 17359 prolonged survivals to a mean survival time (MST) of 18.3+/-2.6 days (P<0.001) in
100 e incidence as wild-type control mice, their mean survival time (MST) was significantly longer than t
101 SL model demonstrated significantly improved mean survival time (MST) with single fraction whole-brai
102 sis, The incidence of graft rejection, graft mean survival time (MST), and alloimmune responses, and
104 ng renal allograft acceptance: the BMT/renal mean survival time (MST, 76 days) was not significantly
106 heart graft rejection both in the B10-->C3H (mean survival time [MST] 7.8+/-0.2 days; control MST 10.
107 n rapid fashion either LEW heart allografts (mean survival time [MST] = 4.2+/-0.4 days vs. 5.6+/-0.5
108 nsplants of islets from BALB/c into C57BL/6 (mean survival time [MST]: 16.5 vs. 12.0 days; P = 0.004)
109 l of hamster liver xenografts in Lewis rats (mean survival time [MST]=10.5 days, n=6, and MST=9.0 day
111 rafts in Lewis (LEW; RT1l) recipients from a mean survival time of 10.6 +/- 1.9 days in untreated con
114 allograft survival (>200 days) compared to a mean survival time of 15.0+/-2.3 days in controls treate
115 reas xenografts were acutely rejected with a mean survival time of 15.3 days in B cell-deficient mice
119 hazards was seen (p=0.037), with restricted mean survival time of 23.9 months (97.5% CI 22.1-25.6) i
120 val to 30 days was 81.7% (1349/1651), with a mean survival time of 26.5 days (95% CI 26.1-26.9) with
121 RL(lpr) mice had prolonged viability, with a mean survival time of 33.0 wk compared with 22.6 wk in c
122 antation of tumor (1 x 10(5) cells) showed a mean survival time of 35 +/- 4 days, whereas tumor-beari
123 ontrast, tacrolimus + donor BM resulted in a mean survival time of 42 days (P<0.01 compared with tacr
125 ) for frailty with a reduction in restricted mean survival time of 48.8 days and 2.18 (95% CI, 1.40-3
128 ed on exogenous protamine zinc insulin had a mean survival time of 53 days (range, 10-217), a "last e
129 nated mice challenged with yeast cells had a mean survival time of 56 days, compared with <13 days fo
130 nts with none of the adverse genotypes had a mean survival time of 62.1 months, and those with one, t
131 he grafts in this model were rejected with a mean survival time of 7+/-1 days and showed extensive ev
135 d to 56 days, 8.0 mg/kg/q.o.d BQR produced a mean survival time of 83.8 +/0 33.8 days (P < 0.001), wi
136 reater prolongation of graft survival with a mean survival time of 88 days compared with the control
137 ly prolonged Lewis cardiac allografts from a mean survival time of 9.8+/-0.7 days in controls to 19.8
142 une response that significantly improved the mean survival time of mice bearing established lung meta
143 onger tumor growth suppression and increased mean survival time of the mice compared with the treatme
144 p = 0.006)." Kaplan-Meier analysis revealed mean survival times of 9.3 years for PR and 12.65 years
145 ghly correlated with the previously reported mean survival times of animals treated with the same age
149 creased in the docetaxel arm (the restricted mean survival time over 10 years was 9.11 v 8.82 years;
152 (95% CI, 1.9-16.9 months; P = .008) shorter mean survival time restricted after 12.5 years compared
153 th (95% CI, 2.2-18.3 months; P = .02) longer mean survival time restricted at 15 years compared with
155 of post hoc analyses have applied restricted mean survival time (RMST) analysis on the aggregated-lev
157 Overal survival (OS) according to restricted mean survival time (RMST) and median OS, and hazard rati
158 fects of interest were the 7-year restricted mean survival time (RMST) differences between intensive
159 ate or enzalutamide and evaluated restricted mean survival time (RMST) differences in overall surviva
163 h death as a competing event, and restricted mean survival time (RMST) model were used to analyze the
166 rved nonproportional hazards; the restricted mean survival time (RMST) was 6.81 years for 3 years of
168 val, which was measured using the restricted mean survival time (RMST) with propensity score adjustme
171 by the difference (and ratio) of restricted mean survival times (RMST) in oncology randomized trials
172 hazard ratio (aHR) of death, and restricted mean survival times (RMST) were analyzed as of September
173 ival over an 8-year time horizon (restricted mean survival time [RMST]) for each combination of clini
174 P < 0.001, test for difference in restricted mean survival time [RMST]), but no differences were obse
175 survival were compared using the restricted mean survival times (RMSTs) across different age and soc
177 y two distinct quantities) of the restricted mean survival times (RMSTs, expectation of life at a giv
178 Despite reducing FV3 loads and extending the mean survival time, rXlIFN treatments failed to prevent
181 had a significantly higher survival rate and mean survival time than mice immunized with only LVS Del
182 lliation failure had a significantly shorter mean survival time than those without complications (14.
183 death and of death or AIDS-defining illness, mean survival time, the proportion of individuals in nee
184 pient, and eye bank variables and restricted mean survival time through 47 months (1434 days) after D
185 transplantation prolonged cardiac allograft mean survival time to >120 days compared with untreated
186 transplantation prolonged cardiac allograft mean survival time to 25.7+/-0.9 days compared with untr
187 plantation was able to extend the Pd grafts' mean survival time to 32 months for fourteen 4 Pd grafts
189 is such as milestone survival, or restricted mean survival time to capture the value of indolent HCC.
191 10-year area under the curve; ie, restricted mean survival time) to emulate a randomized clinical tri
192 significantly protected, as reflected by the mean survival time versus control grafts (27+/-20 days [
197 nts with tumors that responded to treatment, mean survival time was 15 months (range, 4.5-33.1 months
210 Life expectancy was estimated by restricted mean survival time within 10 years, and QOL status accor