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1 vity, and antigen-site density most impacted median survival.
2 oss all age and EF groups had markedly lower median survival.
3 care; prognosis is poor, with 4- to 6-month median survival.
4 hibition of tumor growth and prolonged mouse median survival.
5 accelerates tumour development and shortens median survival.
6 was associated with worsening FEV1 and lower median survival.
7 between injections led to a 10% reduction in median survival.
10 s (median survival=40days), cisplatin alone (median survival=12days) or saline-treated controls (medi
11 ypermetabolism was associated with a reduced median survival [14.6 compared with 21.4 mo, respectivel
12 70%, P<0.01), and a trend for longer overall median survival (15.4 versus 9.3 months, P=0.72) yet not
13 MM patients without prior knowledge of MGUS (median survival, 2.1 years), although MM patients with (
14 0.77-0.96; P < .01) better overall survival (median survival, 2.8 years) than MM patients without pri
16 n in tumor size (P < 0.001) and an increased median survival (207 d; interquartile range [IQR], 132-2
17 HER2-positive subtype displayed the longest median survival (21.0 months); patients with triple-nega
18 urvival was recorded between the two groups (median survival 23.4 months [95% CI 20.9-24.8] with doce
19 vided the most significant survival benefit (median survivals: 24.8 vs 21.0 mo for adjuvant chemother
20 ted with improved survival compared with UR (median survival, 26 months v 21 months, respectively; st
22 patients with EGFR mutations had the longest median survival (3.51 years; 95% CI, 2.89 to 5.5 years),
23 port cells succumbed to bone marrow failure (median survival, 328 days) characteristic of myelodyspla
24 st one MRLN by EUS was associated with lower median survival (353 vs 1050 days, p<0.001) and increase
25 st one MRLN by EUS was associated with lower median survival (353 vs. 1,050 days; P < 0.001) and incr
26 atin in conventional un-PEGylated particles (median survival=40days), cisplatin alone (median surviva
27 those with no high-risk pathologic features (median survivals: 54.6 vs 42.7 mo for adjuvant chemother
30 ached </= 0.2 ng/mL compared with > 4 ng/mL (median survival, 60.4 v 22.2 months, respectively; P < .
32 cant for patients with pleural mesothelioma (median survival 7.9 y versus 2.4 y, P = 0.0012), but not
34 io was 0.98 (95% CI, 0.80 to 1.20; P = .847; median survival, 70 months) for SOC + Cel and 0.86 (95%
44 as been demonstrated to significantly extend median survival and achieve a high rate of complete tumo
48 homa in mice at seemingly similar paces with median survival around 10 and 11 weeks, respectively, co
52 nt to normal level, and significantly longer median survival as compared to free drugs or untargeted
55 g patients with decompensated cirrhosis, the median survival benefit was 31 days, and it was not cost
57 nosis with amyloidosis was 45 months (2-89); median survival by amyloidosis type was localized AL: 64
58 re typically have more indolent disease with median survivals close to 25 years, and Ig-mutated CLL,
62 phase III ABCSG-28 POSYTIVE trial evaluated median survival comparing primary surgery followed by sy
65 -) and Cd74(-/-) mice demonstrated decreased median survival following hyperoxia compared to WT mice.
73 th blank wafer died within 11 days while the median survival for rats treated with systemic TMZ was 1
78 the age- and sex-matched control population; median survivals for patients younger than 60 years are
79 ficantly impaired tumor growth and prolonged median survival from 13 d (phosphate-buffered saline) to
80 phaPD-1, inhibited tumor growth and extended median survival from 28 days (non-treatment control) to
81 these mice was associated with an increased median survival from approximately 5.5 to 7.5 mo and inc
84 graft survival was 185 months (96-269), and median survival from diagnosis with amyloidosis was 45 m
85 om onset was 9.8 years (95% CI 8.8-10.7) and median survival from enrolment was 1.8 years (0.9-2.7).
89 There was a significant increase in overall median survival from the 1970s to 2000s (2 vs. 8 months;
103 method, which shows significant extension of median survival in two patient-derived BTIC xenograft mo
107 ression and hinders effective treatment; the median survival is 16 mo despite standard-of-care therap
115 omatic, and this, in combination with a long median survival, led to the initial studies of observing
116 is highly invasive and uniformly fatal, with median survival<20months after diagnosis even with the m
118 Because of their relatively long overall median survival, more aggressive treatments are typicall
119 e III, and 16% had stage IIIb disease with a median survival not reached in stage I, 9.4 years in sta
120 elivered in brain penetrating nanoparticles (median survival not reached; 80% long-term survivors) co
122 advanced cancer diagnosis for patients with median survival of 1 year or less, and progressive disea
123 s reported for patients with ovarian cancer (median survival of 11-14 months), 50-91% for gastric can
126 rtality of 44.4/100 person-years (PYs) and a median survival of 13.5 months after the diagnosis of CM
127 adiation and chemotherapy, only results in a median survival of 14 months, underscoring the importanc
128 oup that received the BCNU alone wafer had a median survival of 15 days, the group that received the
129 8-15 months), 71-86% for colorectal cancer (median survival of 16 months), and 67-75% (median surviv
130 roup that received the TMZ wafer alone had a median survival of 19 days, and the group treated with t
136 (median survival of 16 months), and 67-75% (median survival of 27 months) for peritoneal mesotheliom
137 of 2.7/100 PYs (P < 0.001) and an estimated median survival of 27.0 years after the diagnosis of CMV
138 ts receiving surgical therapy (n = 25) had a median survival of 27.8 months, significantly superior t
139 group treated with the BCNU-TMZ wafer had a median survival of 28 days with 25% of the animals livin
141 ts experience frequent relapses resulting in median survival of 3 to 5 years, requiring more efficien
145 associated with the highest survival with a median survival of 53.0% (range, 26.0-72.0), whereas def
146 compared with controls was observed, with a median survival of 55 d for 277.5 kBq of (212)Pb-daratum
147 on compared to controls was observed, with a median survival of 55 days for 277.5 kBq of (212)Pb-Dara
148 has resulted in marrow CR rates of 55% and a median survival of 6 to 7 months when given to patients
149 n overall response rates of 40% to 50% and a median survival of 6.5 months in a similar refractory-re
150 studied for the creation of the DS-GPA had a median survival of 7 months from the time of initial tre
152 atients (<10 points) demonstrating excellent median survival of 70.6 months, significantly superior t
154 of 11-14 months), 50-91% for gastric cancer (median survival of 8-15 months), 71-86% for colorectal c
155 those who preferred inotropes over LVAD had median survival of 9.0 months (interquartile range, 3.1-
156 and increased risk of death due to lymphoma (median survival of 9.5 years with BCL2 mutations vs 20.4
159 rity of SMZLs show an indolent course with a median survival of approximately 10 years, nearly 30% of
162 s the deadliest form of brain cancer, with a median survival of less than 2 years despite surgical re
164 cancer, which is associated with an overall median survival of less than 5 years from diagnosis.
168 with BA and ibrutinib markedly improved the median survival of mice engrafted with the MCL cells.
169 211At-CD38 at 15 to 45 uCi at least doubled median survival of mice relative to untreated controls (
170 esveratrol treatment significantly increased median survival of mice with HF, lessened cardiac fibros
171 ression in the prostate tumors (n=8); with a median survival of more than 60 days compared to 12 days
173 a onset was rapid in triple-CKO mice, with a median survival of only 12 weeks, and malignant mesothel
180 potent therapeutic effect and prolonged the median survival of TET1-high AML mice over three fold.
183 cleaved caspase-3, and leads to a prolonged median survival of the mice (36.5 vs. 22.5 d, respective
186 r patients develop brain metastasis, and the median survival of these patients remains less than 6 mo
189 ies also defines better outcome groups, with median survivals of 15.9 versus 9.2 months (P = 0.029) a
190 o characterize the incidence proportions and median survivals of patients with breast cancer and brai
191 ays, resulted in a simulated 31% increase in median survival over a single 400 nCi administration.
192 MD treatment was further shown to extend the median survival period from less than 20days in the cont
199 onths (95% CI, 24.8 to 41.3 months), whereas median survival since the time of SCLC transformation wa
200 ts receiving PRRT had a significantly longer median survival than patients not receiving PRRT (4.4 vs
201 resulted in a significant improvement in the median survival time (24.5 days for saline, 26 days for
202 iously reported IDEC-131-treated allografts, median survival time (35 +/- 31 days) was significantly
203 mice brain with significant increase in the median survival time (36 days) along with no toxicity.
204 , fibrosis, and apoptosis; and prolonged the median survival time 2-fold in the myocyte-specific Lmna
206 was 65% overall, 48% in the BDex+AA cohort (median survival time 821 days), and 76% in patients who
208 ediction was assessed by using difference in median survival time and area under the curve with time-
209 r differentiation according to difference in median survival time between high- and low-risk groups (
216 ose-dependent therapeutic response, with the median survival time increasing from 68 d for the lowest
218 hose with an SUVr of at least 2.5, who had a median survival time of 10.1 (95% CI: 2.4, 15.9; P = .00
219 deaths from lung cancer were documented with median survival time of 10.3 months (interquartile range
221 nths), 71.6% of patients were deceased, with median survival time of 11 months for those who died.
222 tients with SUVr of less than 1.7, who had a median survival time of 23.1 months (95% confidence inte
231 and breast cancer xenografts and doubled the median survival time of TCL1-Tg:p53(-/-) mice, which dev
233 nd initial respiratory impairment, and had a median survival time similar to bulbar onset patients.
235 after a diagnosis of esophageal cancer, the median survival time was 14.9 months (IQR, 7.1-52.3 mo)
240 estimated the time ratio (relative change in median survival time) per 100 working level months (rado
241 on in tumor progression, a 50.0% increase in median survival time, and a 26.6% increase in necrotic p
243 M/DOX liposome-treated group had the longest median survival time, double that of the DOX liposome-tr
248 days), limited weight loss (<5%), and longer median survival times (~18 days) that were significantly
249 h R0, R1 (<1 mm), and R1 (direct) status the median survival times and 5-year survival rates were 41.
253 toma (GBM) is an astrocytic brain tumor with median survival times of <15 months, primarily as a resu
254 ontrol antibody, anti-PD-1, or anti-OX40 had median survival times of 50 days or less, whereas mice g
255 ss (>10%) than the unvaccinated controls and median survival times that were not significantly differ
259 Although current standard therapy extends median survival to ~15 months, most patients do not have
260 static disease during neoadjuvant treatment, median survival was 10.5 months compared with 53 months
261 0.63 (95% CI 0.50-0.79; one-sided p<0.0001); median survival was 10.6 months (95% CI 9.1-12.1) for re
265 me was 28.2 months (range, 4-38 months), and median survival was 16.1 months (range, 0.1-60.3 months)
275 was 20 months (95% CI, 16 to 26 months), and median survival was 49 months (95% CI, 40 months to not
282 l subtype who underwent trimodality therapy, median survival was extended from 14.5 months to 23.4 mo
288 3 [44%] of 1315 in other African countries), median survival was shorter in the other African countri
294 After PSM, the 3-year survival rates and median survival were 44.9% and 27.2 (95% confidence inte
297 acizumab (hazard ratio [HR], 0.86; P = .12); median survival with pemetrexed and bevacizumab was 16.4
298 With a median follow-up of 50.6 months, median survival with pemetrexed was 15.9 months, compare
299 prostate DKO) exhibited a markedly increased median survival with reduced tumor size and proliferatio
300 ificant tumor regression and prolonged mouse median survival without significant change in mouse body