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1 lowing 3 months of PTX therapy for recurrent liver metastases.
2 atocellular carcinomas, were also mutated in liver metastases.
3 regressions in primary tumors and colorectal liver metastases.
4 SCs to form a premetastatic niche to promote liver metastases.
5 r (166)Ho radioembolization in patients with liver metastases.
6 lications of radioembolization of colorectal liver metastases.
7 loid cells can be used to target established liver metastases.
8 e of invasive tumors and no apparent lung or liver metastases.
9 to liver endothelial cells and formation of liver metastases.
10 colorectal cancer patient with nonresectable liver metastases.
11 premetastatic niche that ultimately promoted liver metastases.
12 ients with metastatic colorectal cancer with liver metastases.
13 patic peritoneal metastasis and hematogenous liver metastases.
14 e limited response rates in the treatment of liver metastases.
15 vacizumab in patients with colorectal cancer liver metastases.
16 est (90)Y study for patients with colorectal liver metastases.
17 ue of hepatic USG for detecting asymptomatic liver metastases.
18 as reduced in CTC compared to tumor cells in liver metastases.
19 eived (90)Y radioembolization for colorectal liver metastases.
20 PanNETs associated with a different risk for liver metastases.
21 marker for metastatic activity of colorectal liver metastases.
22 glass microsphere treatments for colorectal liver metastases.
23 sed cell death in primary CTCL tumors and in liver metastases.
24 ncer, both CVX-060 and regorafenib inhibited liver metastases.
25 tumors, adjacent normal tissues, and matched liver metastases.
26 ic tumors and to accelerate the formation of liver metastases.
27 h as hepatocellular carcinoma and colorectal liver metastases.
28 dict response to neoadjuvant chemotherapy in liver metastases.
29 and a potential target for interference with liver metastases.
30 between primary colorectal tumors and their liver metastases.
31 t detection of bone lesions, lymph node, and liver metastases.
32 = 0.035) were independently associated with liver metastases.
33 nagement strategies exist for neuroendocrine liver metastases.
34 of two primary CRC tumors and their matched liver metastases.
35 ase recurrence after resection of colorectal liver metastases.
36 n bile ducts induced cholangiocarcinoma with liver metastases.
37 as performed in mice bearing patient-derived liver metastases.
38 eight fresh human colorectal carcinoma (CRC) liver metastases.
39 portantly, ADPh prevented the development of liver metastases.
40 y, for the detection and characterization of liver metastases.
41 patients also had synchronous resections of liver metastases.
42 ents with colorectal cancer with synchronous liver metastases.
43 fibroblasts associated with human colorectal liver metastases.
44 e quality and in the detection of colorectal liver metastases.
45 that obtained after resection of colorectal liver metastases.
46 on 538 to glycine (D538G), was identified in liver metastases.
47 for salvage patients with colorectal cancer liver metastases.
48 (PanNETs) associated with the development of liver metastases.
49 tratified by PD-L1 status, world region, and liver metastases.
50 ut was explicitly related to the presence of liver metastases.
51 at population, and in patients with baseline liver metastases.
52 kinase inhibitors and patients with baseline liver metastases.
53 iable imaging modality that allows to assess liver metastases.
54 positive patients and patients with baseline liver metastases.
55 consisting of patients receiving therapy for liver metastases.
56 of primary liver tumors and melanoma-derived liver metastases.
57 on of prior systemic therapy and presence of liver metastases.
58 ic lineages of two CRC patients with matched liver metastases.
59 alterations in pancreatic primary tumors and liver metastases.
60 le toxicity profile in salvage patients with liver metastases.
61 construction algorithms for the detection of liver metastases.
63 et the inclusion criteria: 17 had colorectal liver metastases, 1 had hepatocellular carcinoma, 1 had
64 ersus BCP was seen in patients with baseline liver metastases (13.3 months [11.6-NE] with ABCP [52 of
67 with 473 procedures (139 HCC, 198 colorectal liver metastases, 61 neuroendocrine liver metastases, an
68 rlying hepatic diagnoses included colorectal liver metastases (69%), hepatocellular carcinoma (18%),
69 patocellular carcinoma (18%), non-colorectal liver metastases (7%), and intrahepatic cholangiocarcino
70 1), preoperative chemotherapy for colorectal liver metastases (70%, 82%, 89%, P < 0.001) and median o
71 92.4% vs. 69.7% and 89.4%, respectively) and liver metastases (97.3% vs. 92.1% and 94.8%, respectivel
72 give patients with nonresectable colorectal liver metastases a 5-year overall survival comparable to
73 ion is also prevalent in human breast cancer liver metastases, a setting in which results with anti-a
74 ersus nonanatomical resection for colorectal liver metastases, according to KRAS mutational status.
76 d systemic increases in TIMP1 developed more liver metastases after injections of pancreatic cancer c
77 % of patients with colorectal cancer develop liver metastases after resection of the primary tumor, a
78 ong with the proportion of mice with diffuse liver metastases, an effect ablated by coexpression of N
79 ctable or suboptimally resectable colorectal liver metastases and a WHO performance status of 0-2 wer
80 ighest uptake of FAPI tracer was observed in liver metastases and anal cancer, with an SUV(max) of 9.
83 increasing evidence to support resection of liver metastases and concurrent EHD in selected patients
84 term survival is possible after resection of liver metastases and concurrent EHD, but true cure is ra
87 ified subgroups, such as those patients with liver metastases and those with no response to prior ant
88 number dramatically during establishment of liver metastases and were recruited from bone marrow by
89 riate analysis, (18)F-FDG PET, G3 tumor, >=2 liver metastases, and >=2 prior therapies were independe
90 ine patients with NETs (41 patients with 162 liver metastases, and 18 control subjects with no liver
91 lorectal liver metastases, 61 neuroendocrine liver metastases, and 75 other) for a total of 875 tumor
92 vs 1), age (<50 vs >/=50 years), presence of liver metastases, and histopathological grade (2 vs 3).
93 in established SCLC primary lung tumors, in liver metastases, and in chemotherapy-resistant tumors.
94 response to neoadjuvant chemotherapy in the liver metastases, and inhibition of this protein at both
96 ation was stratified by previous taxane use, liver metastases, and PD-L1 expression on tumour-infiltr
98 0.003) after controlling for CTR, number of liver metastases, and preoperative extrahepatic disease.
99 nd found the combination to inhibit lung and liver metastases, and prolong host survival without toxi
101 d in purine metabolism, were detected in 4/5 liver metastases, and the same four liver metastases sha
102 ng photothermal ablation (PTA) of colorectal liver metastases, and thus increase ablation zones.
105 reason for this unfavorable outcome is that liver metastases are poorly vascularized, limiting the a
106 d immediately after percutaneous ablation of liver metastases are predictors of local treatment failu
109 CL5-promoter activation within the stroma of liver metastases as evidenced by tumor-selective iodide
110 ur knowledge), robust MRI detection of early liver metastases as small as approximately 0.24 mm in di
112 ew the existing approaches to neuroendocrine liver metastases, assess the evidence on which managemen
113 tic castration-resistant prostate cancer and liver metastases assigned to (177)Lu-PSMA alone (n = 31)
115 excluded because of unequivocal evidence of liver metastases at baseline whole-body MRI, two partici
116 between observers 1 and 2 for characterizing liver metastases at per-lesion analysis (kappa coefficie
118 pproximately 75-80% of patients present with liver metastases at the time of their diagnosis, and 20%
121 ected patients with nonresectable colorectal liver metastases benefit from liver transplantation and
123 ulted not only in a higher detection rate of liver metastases but also in a significantly higher lesi
125 e a metastatic CRC mouse model and show that liver metastases can manifest without a lymph node metas
128 ong-term survival to selected patients whose liver metastases cannot be removed in a single procedure
131 f postoperative complications for colorectal liver metastases (CLM) in the era of RAS mutation analys
136 56.8 y; range, 35-79 y) for the treatment of liver metastases (colorectal, n = 23; breast, n = 1; and
138 PGE2 had increased numbers of cecal CSCs and liver metastases compared with controls after intracecal
140 have developed orthotopic colorectal cancer liver metastases (CRCLM) and primary cholangiocarcinoma
142 luate outcomes after resection of colorectal liver metastases (CRLM) and concurrent extrahepatic dise
144 in the treatment of patients with colorectal liver metastases (CRLM) is the Kirsten rat sarcoma viral
145 y-nine patients with unresectable colorectal liver metastases (CRLM) were included in a single-instit
146 tumors (NET), and colorectal carcinoma with liver metastases (CRLM), but not cholangiocarcinoma (CCA
152 lorectal cancer (CRC), it is unknown whether liver metastases derive from cancer cells that first col
153 imary SI-NETs from patients with and without liver metastases detected at the time of surgery and ini
154 established tumors and slowed the growth of liver metastases, driven by cytotoxic T-lymphocyte-media
159 ssue from both primary colorectal tumour and liver metastases from 17 patients was subjected to prote
160 ho underwent primary resection of colorectal liver metastases from 2 major hepatobiliary units in the
161 rs, a shift in indications toward colorectal liver metastases from 53% to 77% and a reverse trend in
163 Clinically, immunohistochemical analysis of liver metastases from chemotherapy-naive colon cancer pa
164 rs) who underwent radioembolization to treat liver metastases from colorectal adenocarcinoma between
166 pected of having hepatocellular carcinoma or liver metastases from colorectal cancer and were schedul
167 ring preoperative treatment of patients with liver metastases from colorectal cancer, and its predict
168 cle of treatment in patients with resectable liver metastases from colorectal cancer, within a phase
170 ve for the detection and characterization of liver metastases from NETs than T2-weighted FSE and dyna
171 unexpectedly caused a remarkable increase in liver metastases from neuroblastoma and breast cancer ce
174 ished PET response criteria in patients with liver metastases from pancreatic cancer after treatment
181 patient affected of irresectable colorectal liver metastases (i-CRLM) BACKGROUND:: A renaissance of
182 athologic findings of core liver biopsies of liver metastases identified by needle localization in a
183 then, she had been treated with resection of liver metastases in 2009 and 2010, palliative combinatio
184 6 to 82 years), hemoglobin < 10 g/dL in 17%, liver metastases in 30%, median time from prior chemothe
185 nes was performed from primary tumors and/or liver metastases in 401 patients undergoing CLM resectio
186 icantly reduced whole body, lung, kidney and liver metastases in an experimental metastases mouse mod
188 otherapy and surgery for operable colorectal liver metastases in KRAS exon 2 wild-type patients resul
192 sponses with both regressive and progressive liver metastases in the same patient (best vs. worst res
193 ssociated with CTC shedding from established liver metastases in the training and validation cohorts.
194 (Arp2/3) is required for vessel co-option in liver metastases in vivo and that, in this setting, comb
195 sseminated cancer cells are Lgr5(-) and seed liver metastases in which Lgr5(+) cells then appear, sho
196 ene therapy completely cured established CRC liver metastases in ~50% of mice and provided long-lasti
197 trant metastasis (100% metastasis; with >80% liver metastases) in Kras(G12D)-driven serrated cancer.
198 Intraarterial therapy options for colorectal liver metastases include chemoinfusion via a hepatic art
202 er curatively intended surgery of colorectal liver metastases is feasible and may significantly impro
203 ents with colorectal cancer with synchronous liver metastases is possible but is associated with a wi
205 ot be withheld from patients with colorectal liver metastases lacking intratumoral (99m)Tc-MAA accumu
206 in already established, experimental, murine liver metastases led to diminished metastatic growth.
207 r curatively intended surgery for colorectal liver metastases, liver recurrences occur in more than 6
208 who underwent liver transplantation (LT) for liver metastases (LM) from neuroendocrine tumors (NET) o
209 udy aimed to assess the prognostic impact of liver metastases (LM) in patients with colorectal perito
213 metastases vs as suppressor in prostate and liver metastases) may eventually help us to develop bett
214 -six patients with a total of 435 colorectal liver metastases (mean number of lesions +/- SD, 6.6 +/-
216 t cancer liver metastases, n = 7; colorectal liver metastases, n = 5; hepatocellular carcinoma, n = 8
217 ectable advanced liver tumors (breast cancer liver metastases, n = 7; colorectal liver metastases, n
218 ents with multifocal, bilobar neuroendocrine liver metastases (NELM) after the first transarterial ch
219 : hepatocellular carcinoma (HCC), colorectal liver metastases, neuroendocrine liver metastases, and o
220 cancer (WHO performance status 0 or 1) with liver metastases not suitable for curative resection or
221 ns of 79 colorectal tumors and 23 associated liver metastases, obtained from 2 hospitals in Spain.
223 y mass index: 18.5 kg/m) with neuroendocrine liver metastases of a digestive origin underwent hybrid
224 patients with unresectable, chemorefractory liver metastases of any origin were enrolled in this pha
225 adiation therapy (SIRT) for the treatment of liver metastases of castration-resistant prostate cancer
226 on criteria were Body-Mass index (BMI) > 40, liver metastases of malignant diseases and concurrent or
228 ly, an analogous myeloid subset was found in liver metastases of some colorectal cancer patients.
229 growing in the liver in vivo and a subset of liver metastases of uveal melanoma patients express acti
230 sequencing identified mutations enriched in liver metastases of various cancers, including Notch pat
231 laparoscopic liver resection, for colorectal liver metastases, offers significant lower morbidity, an
233 ls with tumor-conditioned myeloid cells from liver metastases or myeloid cell conditioned media down-
237 with non-small cell lung cancer, colorectal liver metastases, or metastatic melanoma who were scanne
239 lizing antibody to mice bearing experimental liver metastases phenocopied neutrophil depletion by red
241 diameter of less than 8 cm for the 2 largest liver metastases predicted time to intrahepatic progress
242 esis, GCLC, becomes overexpressed in patient liver metastases, promotes cell survival under hypoxic a
243 dex, primary tumor location, or treatment of liver metastases, PTR with/without liver treatment impro
244 roups of patients, together with more than 3 liver metastases, R1 resection, and extrahepatic disease
245 ference in OS was also seen in patients with liver metastases randomized to eribulin versus control (
246 o the significantly higher detection rate of liver metastases rather than tumor differentiation grade
248 tients with colorectal carcinoma and bilobar liver metastases received whole-liver radioembolization
249 Methods: Twenty-three mCRC patients with liver metastases refractory to chemotherapy were include
250 m study, 56 patients were enrolled, all with liver metastases refractory to systemic therapy and inel
253 r "radioembolization" and "colorectal cancer liver metastases." Results were described separately for
254 d in 4/5 liver metastases, and the same four liver metastases shared mutations in 32 genes, including
256 analyses suggest that surgical resection of liver metastases should be carefully considered in this
257 margin achieved in patients with colorectal liver metastases should now be considered the standard o
258 Pathway analyses of all mutated genes in liver metastases showed aberrant tumor necrosis factor a
260 not granulocytes, isolated from experimental liver metastases stimulated migration and invasion of MC
261 creatic neuroendocrine tumor with multifocal liver metastases, suggesting that excessive overproducti
262 f (18)F-FLT may limit utility for imaging of liver metastases.Targeting angiogenesis has had some suc
263 venous injection of LV12 cells produced more liver metastases than QRsP-11 cells, whereas the inciden
265 era of effective chemotherapy for colorectal liver metastases, the association between surgical margi
266 ines of systemic therapy and the presence of liver metastases, to receive intravenous gemcitabine 100
267 f a large cohort of patients with colorectal liver metastases treated with (90)Y radioembolization us
268 microenvironment of either primary tumors or liver metastases triggered regression of established tum
271 atients with pathologically proven mCRC (512 liver metastases) underwent Gd-EOB MRI and MDCT imaging.
272 metastases, and 18 control subjects with no liver metastases) underwent MR imaging that included DW,
274 rom explant cultures of CRC patients-derived liver metastases was associated with response to OXA + C
275 stases, whereas progression of nonresectable liver metastases was observed in the chemotherapy group.
276 low passage cultures from primary tumors and liver metastases we show that ATM loss accelerates Kras-
278 years; range 43.6-66.3), with neuroendocrine liver metastases were analyzed by means of distributed p
279 tratumoral (99m)Tc-MAA uptake was rated, and liver metastases were classified according to changes in
281 distant metastases, although in one patient liver metastases were evident on (18)F-FDG but not on (1
282 gnosed with metastatic disease in 2009, when liver metastases were found 1 year after the primary tre
283 patients treated with liver embolization for liver metastases were found, and similar results were de
286 for OS, and (18)F-FDG PET, G3 tumor, and >=3 liver metastases were independent prognostic factors for
287 ctable or suboptimally resectable colorectal liver metastases were randomised in a 1:1 ratio to recei
289 curative resection of at least 4 colorectal liver metastases, were selected from a prospective datab
290 cells demonstrated significant reduction in liver metastases when treated with N(1)-(3-aminopropyl)-
291 or bone metastases, distant lymph nodes, and liver metastases, whereas CT was more sensitive for lung
292 Food and Drug Administration for colorectal liver metastases, whereas institutional review board app
293 in a syngeneic tumor model resulted in fewer liver metastases, whereas PHD3 knockdown induced tumor s
294 ys containing samples from CRC patients with liver metastases who had undergone hepatic resection.
295 ated the second hepatectomy in patients with liver metastases who required a 2-stage hepatectomy.
296 thods: Patients with primary liver cancer or liver metastases who underwent radioembolization with gl
297 However, colony size was greatly reduced in liver metastases with decreased invasion into adjacent t
298 clinical benefit in patients with colorectal liver metastases with liver-dominant disease after chemo
299 ge of the biological phenotype of colorectal liver metastases would be invaluable to inform clinical
300 , chemotherapy type (vinflunine vs taxanes), liver metastases (yes vs no), and number of prognostic f