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1 PCNSL in immunocompetent patients is associated with uni
2 PCNSL incidence was higher in Asians/Pacific Islanders t
3 PCNSL is an uncommon tumor, and only four randomized tri
4 PCNSL is highly dependent on BCR signaling, and ibrutini
5 PCNSL patients without evidence of radiographic disease
7 xpression and function were assessed in AIDS-PCNSL biopsy samples and in EBV+ human B-cell tumors tha
8 rimary central nervous system lymphoma (AIDS-PCNSL) is due in part to the intrinsic resistance of thi
12 nome-wide gene expression comparison between PCNSL and non-CNS DLBCL was performed, the latter consis
18 mpetent adults with histologically confirmed PCNSL after experiencing high-dose methotrexate-based ch
19 utive patients with histologically confirmed PCNSL were collected concurrently with magnetic resonanc
21 a true "CNS signature" because we contrasted PCNSL with wide-spectrum non-CNS DLBCL on a genomic scal
22 single-center phase-2 study, newly diagnosed PCNSL patients received 5 to 7 cycles of chemotherapy wi
23 ht consecutive patients with newly diagnosed PCNSL seen at Memorial Sloan-Kettering Cancer Center (MS
24 Forty-four patients with newly diagnosed PCNSL were treated with induction MT-R, and patients who
25 is feasible in patients with newly diagnosed PCNSL without evidence of significant related neurotoxic
28 ncreased the probability for differentiating PCNSL and atypical glioblastoma compared with the evalua
29 e diagnostic performance for differentiating PCNSL from glioblastoma was evaluated by using logistic
31 g a preclinical animal model of human EBV(+) PCNSL with subsequent translation to patients with EBV(+
32 Enhanced expression of EBV-TK mRNA in EBV(+) PCNSL tumors by radiation therapy occurred in a dose-dep
33 have developed a preclinical model of EBV(+) PCNSL to explore strategies that specifically target EBV
37 wledge that dose-intensive consolidation for PCNSL is feasible in the multicenter setting and yields
38 eral biologic contexts with implications for PCNSL, including CNS tropism (ECM and adhesion-related p
39 splant recipients had elevated incidence for PCNSL compared with the general population (standardized
40 d that this appears to be a prerequisite for PCNSL development, we find no evidence that pleomorphic
42 h ibrutinib alone, including patients having PCNSL with CD79B and/or MYD88 mutations, and 86% of eval
46 ally analyze reported studies on HDC/ASCT in PCNSL and discuss its current role and future perspectiv
49 tein level of ECM-related SPP1 and CHI3L1 in PCNSL cells was demonstrated by immunohistochemistry.
50 )(q22) and BCL6 rearrangements are common in PCNSL and predict for decreased OS independent of deep s
51 hough intraocular involvement is frequent in PCNSL and clinically marked by slowly progressive visual
52 ed studies detected high EBV copy numbers in PCNSL tumour tissue, and low copy numbers in AIDS cases
57 , including those with primary CNS lymphoma (PCNSL) (outside the area of neoplastic involvement) cont
59 response assessment of primary CNS lymphoma (PCNSL) are critical to ensure comparability among clinic
61 s with newly diagnosed primary CNS lymphoma (PCNSL) in order to establish a predictive model that cou
66 ed on 31 patients with primary CNS lymphoma (PCNSL) treated between 1986 and 1992 with methotrexate (
74 imary central nervous system (CNS) lymphoma (PCNSL) and primary testicular lymphoma (PTL) are rare ex
75 imary central nervous system (CNS) lymphoma (PCNSL) is a diffuse large B-cell lymphoma (DLBCL) confin
77 Primary central nervous system lymphoma (PCNSL) in HIV patients has declined in incidence and the
78 Primary central nervous system lymphoma (PCNSL) is a rare but often rapidly fatal form of non-Hod
79 Primary central nervous system lymphoma (PCNSL) is an aggressive B cell lymphoma that occurs in i
80 in primary central nervous system lymphoma (PCNSL) is caused mostly by intraocular lymphomatous invo
82 Primary central nervous system lymphoma (PCNSL) risk is greatly increased in immunosuppressed hum
83 Primary central nervous system lymphoma (PCNSL) that arises in immune-deficient patients is an ag
84 Primary central nervous system lymphoma (PCNSL) treatment includes 2 phases: induction and consol
85 sed primary central nervous system lymphoma (PCNSL) using induction immunochemotherapy (rituximab, hi
92 rs, we have analyzed V(H) gene of 5 cases of PCNSL, all confirmed by histological studies to be Epste
95 of ITSS allowed reliable differentiation of PCNSL and atypical glioblastoma in most patients, and th
96 To identify targetable genetic features of PCNSL and PTL, we characterized their recurrent somatic
103 advances have improved our understanding of PCNSL, the need for additional collaborative research is
110 t nivolumab is active in relapsed/refractory PCNSL and PTL and support further investigation of PD-1
114 tive Radiation Therapy Oncology Group (RTOG) PCNSL clinical trials was used to test the RPA classific
115 17 cancer registries (1987-2014), we studied PCNSL and systemic non-Hodgkin lymphoma (NHL) in 288 029
117 is with the program SigPathway revealed that PCNSL is characterized notably by significant differenti
119 rminal center formation in the brain tissue, PCNSL is derived from a B cell with features associated
120 tion is an effective therapeutic approach to PCNSL, but neurotoxicity is a delayed risk of this appro
121 e III EBV gene expression profile similar to PCNSL that develops in some immune-deficient patients.
122 ncluding all Abs derived from IGHV4-34 using PCNSL, recognized galectin-3, which was upregulated on m
125 TSS was significantly lower in patients with PCNSL (32% [six of 19]) than in those with glioblastoma
126 c results in 95% (18 of 19) of patients with PCNSL and 96% (27 of 28) of patients with atypical gliob
129 Vs were significantly lower in patients with PCNSL than in those with glioblastoma (P < .01, respecti
130 brain biopsy specimens from 24 patients with PCNSL to investigate the expression of B cell-attracting
131 diagnosed (with no prior WBRT) patients with PCNSL treated with osmotic BBBD and intra-arterial (IA)
133 eficiency virus (HIV)-negative patients with PCNSL were entered on study and received two (n = 20) or
144 Compared to other recipients, those with PCNSL had increased risk of death (adjusted hazard ratio
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