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1 f disease in patients with diffuse malignant pleural mesothelioma.
2 in the palliation of patients with malignant pleural mesothelioma.
3 e or placebo in patients with nonepithelioid pleural mesothelioma.
4 tedanib or placebo in unresectable malignant pleural mesothelioma.
5 exist for second-line treatment of malignant pleural mesothelioma.
6 in relapsed mesothelin-expressing malignant pleural mesothelioma.
7 ents with previously untreated, unresectable pleural mesothelioma.
8 heckpoint therapy is now standard of care in pleural mesothelioma.
9 fety profile in patients with nonepithelioid pleural mesothelioma.
10 ovement in overall survival in patients with pleural mesothelioma.
11 the complex genomic background of malignant pleural mesothelioma.
12 ed 68 with advanced ASS1-deficient malignant pleural mesothelioma.
13 ent option for previously untreated advanced pleural mesothelioma.
14 nds) as maintenance therapy in patients with pleural mesothelioma.
15 measurable relapsed or refractory malignant pleural mesothelioma.
16 ld improve overall survival in patients with pleural mesothelioma.
17 ty in patients with PD-L1-positive malignant pleural mesothelioma.
18 on in patients with ASS1-deficient malignant pleural mesothelioma.
19 therapy for patients with advanced malignant pleural mesothelioma.
20 talc pleurodesis in patients with malignant pleural mesothelioma.
21 os and silica seemed to increase the risk of pleural mesothelioma.
22 e treatment of recurrent and/or unresectable pleural mesothelioma.
23 best available serum biomarker of malignant pleural mesothelioma.
24 rol groups and 1,026 patients with malignant pleural mesothelioma.
25 e of action for asbestos in the induction of pleural mesothelioma.
26 modality therapy in stage I to III malignant pleural mesothelioma.
27 apeutic option in the treatment of malignant pleural mesothelioma.
28 estos and 76 patients with surgically staged pleural mesothelioma.
29 ng of the tumor cells in 36 of 38 samples of pleural mesothelioma.
30 rom those with exposure to asbestos who have pleural mesothelioma.
31 h cisplatin alone in patients with malignant pleural mesothelioma.
32 ing CD8+ T cells in malignant peritoneal and pleural mesotheliomas.
33 d were significantly higher in patients with pleural mesothelioma (105+/-7 ng per milliliter in the D
34 s were significantly higher in patients with pleural mesothelioma (694+/-37 ng per milliliter in the
36 s with histologically confirmed unresectable pleural mesothelioma, aged 18 years or older, with an Ea
37 ble locally advanced or metastatic malignant pleural mesothelioma, an Eastern Cooperative Oncology Gr
38 investigated the presence of osteopontin in pleural mesothelioma and determined serum osteopontin le
39 Patients with measurable advanced malignant pleural mesothelioma and disease progression after one o
40 ars) with unresectable epithelioid malignant pleural mesothelioma and ECOG performance status 0-1 wer
41 dality therapy in the treatment of malignant pleural mesothelioma and identify prognostic factors.
42 h cisplatin is approved for the treatment of pleural mesothelioma and is active in malignant peritone
43 engineering strategy in a model of malignant pleural mesothelioma and validate our findings in a matc
45 ins contribute to the malignant phenotype of pleural mesotheliomas and indicate that interventions de
46 has been reported in varying proportions of pleural mesotheliomas and other tumours, but data are co
47 eous pneumothorax in patients with malignant pleural mesotheliomas and primary lung tumors, and bilat
48 ients with pleural effusion due to malignant pleural mesothelioma, and talc pleurodesis might be pref
51 The successful treatment of unresectable pleural mesothelioma awaits the discovery of active drug
52 rkers for tazemetostat activity in malignant pleural mesothelioma beyond BAP1 inactivation could help
54 type I IGF receptor in a subset of malignant pleural mesothelioma cell lines and determined the corre
55 ere, we report the data of a large malignant pleural mesothelioma cohort within a (68)Ga-FAPI46 PET o
57 , every 3 wk) for the treatment of malignant pleural mesothelioma did not result in survival benefit
58 y approved first-line treatments for diffuse pleural mesothelioma (DPM) are ipilimumab-nivolumab or p
59 n diverse cancer types, notably in malignant pleural mesothelioma (DPM), and has also been identified
60 ICB) is standard of care in advanced diffuse pleural mesothelioma (DPM), but its role in the perioper
61 results are in favor of an increased risk of pleural mesothelioma for subjects exposed to both asbest
62 ients with chemotherapy-naive nonepithelioid pleural mesothelioma from August 1, 2017, to August 15,
64 d quality of life in patients with malignant pleural mesothelioma have, to our knowledge, not been as
66 ctive review of patients with a diagnosis of pleural mesothelioma in the period 2019-2021, analysing
68 d Affymetrix U133A microarray analysis on 99 pleural mesotheliomas, in which multivariate analysis sh
70 literature of clinical studies in malignant pleural mesothelioma, including phase II trials of the n
77 edition of the TNM staging classification of pleural mesothelioma is an update in the TNM staging, re
78 sed immunotherapy in patients with malignant pleural mesothelioma is feasible, well-tolerated, and ca
82 eadily detected in genomic DNA isolated from pleural mesothelioma lines; however, levels of SV40 T/t
83 ype was highly significant for patients with pleural mesothelioma (median survival 7.9 y versus 2.4 y
85 y proposed frontline therapies for malignant pleural mesothelioma (MPM) are very costly, yet their im
87 malignant mesothelial tissues and malignant pleural mesothelioma (MPM) cell lines as compared to ben
88 r TTFields, we applied TTFields to malignant pleural mesothelioma (MPM) cells forming TNTs in vitro.
89 in paraffin tumor tissues such as malignant pleural mesothelioma (MPM) could yield insights to actio
92 peutic procedures in patients with malignant pleural mesothelioma (MPM) has been a widespread practic
93 ion of the genomic complexities of malignant pleural mesothelioma (MPM) has lagged behind other malig
95 Approved systemic treatments for malignant pleural mesothelioma (MPM) have been limited to chemothe
115 ed in patients with ASS1-deficient malignant pleural mesothelioma (MPM) or non-small-cell lung cancer
117 ry (LA-ICP-TOFMS) to analyze human malignant pleural mesothelioma (MPM) samples at the cellular level
119 ned and tested in 28 patients with malignant pleural mesothelioma (MPM) who underwent lung MRI to dem
121 tor-1 (PAR1, F2R) on the growth of malignant pleural mesothelioma (MPM), using human MPM cells that l
134 rgoing cancer-directed surgery for malignant pleural mesothelioma (MPM); however, it is unclear if th
135 e pathological distinction between malignant pleural mesothelioma (MPM)and adenocarcinoma (ADCA) of t
136 en shown to be highly expressed in malignant pleural mesotheliomas (MPM), was detected in serum using
138 ns and expression levels unique to malignant pleural mesotheliomas (MPMs) and not present in control
140 oncoproteins have been detected in malignant pleural mesotheliomas (MPMs), their role in the pathogen
143 s were aged 18 years or older with malignant pleural mesothelioma of any histology that was relapsed
144 ria In Solid Tumors (RECIST) version 1.0 for pleural mesothelioma or RECIST version 1.1 for peritonea
146 sease) at week 12 in patients with malignant pleural mesothelioma per protocol with BAP1 inactivation
150 ocedure-tract metastases (PTMs) in malignant pleural mesothelioma remains controversial, and clinical
152 ur previous microarray analysis of malignant pleural mesothelioma revealed alterations in components
153 surgically resected lung adenocarcinoma and pleural mesothelioma samples in tissue microarrays to co
155 were significantly higher in the group with pleural mesothelioma than in the group with exposure to
158 system components represent novel malignant pleural mesothelioma therapeutic targets for investigati
159 port on their use of a murine model of human pleural mesothelioma to explore potential factors that l
160 benefit reported in patients with malignant pleural mesothelioma treated in a phase 1 study of vorin
163 vel of 1% or higher, small cell lung cancer, pleural mesothelioma, urothelial carcinoma, esophagogast
164 (18)F-FDG-CI in the assessment of malignant pleural mesothelioma using histopathology as the gold st
166 in patients with BAP1-inactivated malignant pleural mesothelioma was 54% (95% CI 42-67; 33 of 61 pat
168 atients with histologically proven malignant pleural mesothelioma were enrolled (26 male patients and
169 eated patients with PD-L1-positive malignant pleural mesothelioma were enrolled from 13 centres in si
171 ears; 10 women and 29 men) with unresectable pleural mesothelioma were treated with repetitive transa
174 spite several attempts at treating malignant pleural mesothelioma with various modalities, mortality
175 or older, with previously untreated advanced pleural mesothelioma, with an Eastern Cooperative Oncolo