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1 e kinase is a clinically validated target in mantle cell lymphoma.
2 ents with indolent non-Hodgkin's lymphoma or mantle cell lymphoma.
3 VcR-CVAD produced high ORR and CR rates in mantle cell lymphoma.
4 in the clinic to treat multiple myeloma and mantle cell lymphoma.
5 , used for treatment of multiple myeloma and mantle cell lymphoma.
6 elapsing and refractory multiple myeloma and mantle cell lymphoma.
7 formed the treatment of multiple myeloma and mantle cell lymphoma.
8 ma, B-cell chronic lymphocytic leukemia, and mantle cell lymphoma.
9 nhibitor PD0332991 in patients with relapsed mantle cell lymphoma.
10 ody) in patients with relapsed or refractory mantle cell lymphoma.
11 s to evaluate this regimen in follicular and mantle cell lymphoma.
12 ent of patients with relapsed and refractory mantle cell lymphoma.
13 e-agent antitumour activity in patients with mantle cell lymphoma.
14 treatment of multiple myeloma and recurring mantle cell lymphoma.
15 acytic lymphoma, marginal zone lymphoma, and mantle cell lymphoma.
16 specific tumors, such as Kaposi sarcoma and mantle cell lymphoma.
17 te for the treatment of multiple myeloma and mantle cell lymphoma.
18 as clinical activity in multiple myeloma and mantle cell lymphoma.
19 se for the treatment of multiple myeloma and mantle cell lymphoma.
20 remission (PR) in a patient with refractory mantle cell lymphoma.
21 file in patients with relapsed or refractory mantle cell lymphoma.
22 ture on high-dose therapeutic approaches for mantle cell lymphoma.
23 had follicular lymphoma, and one patient had mantle cell lymphoma.
24 ab and idelalisib in relapsed follicular and mantle cell lymphoma.
25 ilability of this procedure to patients with mantle cell lymphoma.
26 llogeneic and autologous transplantation for mantle cell lymphoma.
27 n particular refractory multiple myeloma and mantle cell lymphoma.
28 ated in patients with relapsed or refractory mantle cell lymphoma.
29 ngle-group studies in relapsed or refractory mantle cell lymphoma.
30 ngle-agent therapy in relapsed or refractory mantle cell lymphoma.
31 tients with chronic lymphocytic leukemia and mantle-cell lymphoma.
32 : Burkitt lymphoma, follicular lymphoma, and mantle-cell lymphoma.
33 l types of non-Hodgkin's lymphoma, including mantle-cell lymphoma.
34 in 111 patients with relapsed or refractory mantle-cell lymphoma.
35 gle-agent efficacy in relapsed or refractory mantle-cell lymphoma.
36 tuximab is effective for older patients with mantle-cell lymphoma.
37 R-CHOP in patients with previously untreated mantle-cell lymphoma.
38 clinical trial of adoptive immunotherapy for mantle-cell lymphoma.
39 imus in patients with relapsed or refractory mantle-cell lymphoma.
40 vity in patients with relapsed or refractory mantle-cell lymphoma.
41 atio for ibrutinib in relapsed or refractory mantle-cell lymphoma.
42 ersus temsirolimus in relapsed or refractory mantle-cell lymphoma.
43 rituximab was active as initial therapy for mantle-cell lymphoma.
44 ibody, are active in patients with recurrent mantle-cell lymphoma.
45 ially approved for the treatment of relapsed mantle-cell lymphoma.
46 ve outcomes in patients with newly diagnosed mantle-cell lymphoma.
47 n patients with relapsed indolent B-cell and mantle cell lymphomas.
48 detectable nuclear LEF1 expression, as were mantle cell lymphoma (0 of 5), marginal zone lymphoma (0
49 ma, 0/8 follicular center cell lymphoma, 0/4 mantle cell lymphoma, 0/4 anaplastic large cell (Ki-1+)
50 mide and rituximab in patients with relapsed mantle cell lymphoma (A051201) and relapsed follicular l
51 patients had intermediate-risk or high-risk mantle-cell lymphoma according to clinical prognostic fa
52 f 56 unclustered IgH-CCND1 translocations in mantle cell lymphoma across the ~ 344-kb bcl-1 breakpoin
53 in 33 patients with relapsed and refractory mantle cell lymphoma after nonmyeloablative conditioning
54 a randomised, phase 2 study of patients with mantle cell lymphoma aged 18 years or older at 67 clinic
55 s deregulated by chromosome translocation in mantle cell lymphoma and a subset of multiple myeloma.
56 , and Sept 30, 2014, 11 patients (three with mantle cell lymphoma and eight with follicular lymphoma)
58 in the biology, pathogenesis, and therapy of mantle cell lymphoma and identifies ongoing areas of cli
59 by nonstereotyped FL BCRs and by the Igs of mantle cell lymphoma and multiple myeloma and suggest th
60 nhibitor of the UPS, bortezomib, in treating mantle cell lymphoma and multiple myeloma has demonstrat
62 rash (two [67%] of three) for patients with mantle cell lymphoma and neutropenia (five [63%] of eigh
63 complex 1 (mTORC1) inhibitors, are active in mantle cell lymphoma and other lymphoid neoplasms, but r
65 alignant B cells isolated from patients with mantle cell lymphoma and Waldenstrom macroglobulinemia.
66 ezomib showed promising activity in relapsed mantle-cell lymphoma and encouraging results in other B-
68 seven of 15 with indolent NHL, and two with mantle-cell lymphoma) and seven of nine patients treated
69 s efficiently lysed primary B-cell leukemia, mantle cell lymphoma, and multiple myeloma in vitro.
70 vity of temsirolimus in lymphomas other than mantle cell lymphoma, and supports further evaluation of
71 tment of chronic lymphocytic leukemia (CLL), mantle cell lymphoma, and Waldenstrom macroglobulinemia.
73 this review is to update recent advances in mantle cell lymphoma biology with prognostic and potenti
74 2 trials have shown single-agent activity in mantle-cell lymphoma, breast cancer, liposarcoma, and te
75 than R-CHOP in patients with newly diagnosed mantle-cell lymphoma but at the cost of increased hemato
76 ycin (mTOR) pathway is a validated target in mantle cell lymphoma, but has not been extensively evalu
77 fferentiated embryonic stem cells, B-CLL and mantle cell lymphoma, but not in major adult tissues apa
80 s in human chronic lymphocytic leukaemia and mantle cell lymphoma cell lines, and patients treated wi
84 othesised that adding rituximab could target mantle cell lymphoma cells associated with redistributio
85 ent-derived acute lymphoblastic leukemia and mantle cell lymphoma cells, whereas the IgG1 analogue wa
88 nrolled patients with relapsed or refractory mantle-cell lymphoma confirmed by central pathology in 2
90 cell precursor acute lymphoblastic leukemia, mantle cell lymphoma, diffuse large B cell lymphoma, and
91 l lymphocytic lymphoma, plasma cell myeloma, mantle cell lymphoma, diffuse large B-cell lymphoma, ALK
92 ular lymphoma, chronic lymphocytic leukemia, mantle cell lymphoma, diffuse large B-cell lymphoma, and
93 in a host of B-cell malignancies, including mantle cell lymphoma, diffuse large B-cell lymphoma, Wal
95 e B-cell lymphoma, Richter's transformation, mantle cell lymphoma, follicular lymphoma, and chronic l
97 ed for the treatment of multiple myeloma and mantle cell lymphoma; however, in other hematologic mali
99 r treatment of relapsed multiple myeloma and mantle cell lymphoma) in dy(3K)/dy(3K) mice and in conge
100 ed specific recognition of primary B-CLL and mantle cell lymphoma, including rare drug effluxing chem
102 tatus > 16%, lactate dehydrogenase > 1N 38%, Mantle Cell Lymphoma International Prognostic Index (low
103 ased on the clinical factors included in the Mantle Cell Lymphoma International Prognostic Index (MIP
105 is associated with clinical characteristics (Mantle Cell Lymphoma International Prognostic Index [MIP
106 be shorter for patients presenting with high Mantle Cell Lymphoma International Prognostic Index or l
107 imilar model was created with miR-615-3p and Mantle Cell Lymphoma International Prognostic Index scor
108 I of 2, and 49% with IPI of 3 to 5), as were Mantle Cell Lymphoma International Prognostic Index scor
110 variable analysis, these risk groups and the Mantle Cell Lymphoma International Prognostic Index were
111 ostic value of miR-29 is comparable with the Mantle Cell Lymphoma International Prognostic Index.
112 ignificantly different OS independent of the Mantle Cell Lymphoma International Prognostic Index.
113 tratified by previous therapy and simplified mantle-cell lymphoma international prognostic index scor
121 elapse rates with this approach suggest that mantle cell lymphoma is susceptible to graft-versus-tumo
126 or bortezomib-resistant, relapsed/refractory mantle-cell lymphoma, lenalidomide has demonstrated effi
127 aluating this compound in four proliferating mantle cell lymphoma lines (Jeko-1, Granta 519, Mino, an
128 of B-cell acute lymphocytic leukemia (ALL), mantle cell lymphoma, marginal zone lymphoma and Sezary
129 ollicular lymphoma (FL) (16.3% [43 of 263]), mantle cell lymphoma (MCL) (6.8% [18 of 263]), and diffu
130 large B-cell lymphoma (DLBCL) (10% [n = 9]), mantle cell lymphoma (MCL) (8% [n = 7]), and mycosis fun
132 ignancy that may be hard to distinguish from mantle cell lymphoma (MCL) and chronic lymphocytic leuke
133 broad panel of lymphoma cell lines including mantle cell lymphoma (MCL) and diffuse large B-cell lymp
134 ate the therapeutic efficacy of atiprimod on mantle cell lymphoma (MCL) and elucidate the mechanism b
135 CLL), T-prolymphocytic leukemia (T-PLL), and mantle cell lymphoma (MCL) and is associated with defect
136 nti-CD74 IgG)] show enhanced cytotoxicity in mantle cell lymphoma (MCL) and other lymphoma/leukemia c
137 ouse model, we demonstrated that adhesion of mantle cell lymphoma (MCL) and other non-Hodgkin lymphom
138 monstrated in tumors derived from Granta-519 mantle cell lymphoma (MCL) and Raji Burkitt lymphoma (BL
142 Y-box 11 (SOX11) expression is specific for mantle cell lymphoma (MCL) as compared with other non-Ho
143 tivation of the translocated CCND1 allele in mantle cell lymphoma (MCL) because of its relocalization
144 et al describe recurrent NOTCH1 mutations in mantle cell lymphoma (MCL) by next-generation sequencing
155 blood-brain barrier and has activity against mantle cell lymphoma (MCL) in the central nervous system
156 cell leukemia (HCL) cases, 15% (5 of 34) of mantle cell lymphoma (MCL) in the leukemic phase, and 16
157 interrogate signaling pathways activated in mantle cell lymphoma (MCL) in vivo, we contrasted gene e
175 ion signature of tumor proliferation rate in mantle cell lymphoma (MCL) is an overriding molecular pr
177 t failure (TTF) and overall survival (OS) in mantle cell lymphoma (MCL) is based on the clinical fact
185 entral nervous system (CNS) dissemination in mantle cell lymphoma (MCL) is low and occurs late in the
189 ed CD19+/CD20+/CD45+ human lymphoma cells in mantle cell lymphoma (MCL) JeKo-1 model, while the same
192 ase (PI3K) pathway activation contributes to mantle cell lymphoma (MCL) pathogenesis, but early-phase
193 matic gene copy number alterations (CNAs) in mantle cell lymphoma (MCL) patients treated first line w
194 spite recent advances in lymphoma treatment, mantle cell lymphoma (MCL) remains incurable, and we are
196 There is consensus that young patients with mantle cell lymphoma (MCL) should receive intensive immu
197 is study, we define the genetic landscape of mantle cell lymphoma (MCL) through exome sequencing of 5
198 cently reported the application of RNAseq to mantle cell lymphoma (MCL) transcriptomes revealing recu
202 rosine kinase, is approved for patients with mantle cell lymphoma (MCL) who have received one prior t
204 ent study, we analyzed telomere length in 73 mantle cell lymphoma (MCL), 55 chronic lymphocytic leuke
205 thesized that 8-NH(2)-Ado would be active in mantle cell lymphoma (MCL), a hematological malignancy c
206 nd apoptotic pathway have been identified in mantle cell lymphoma (MCL), affording the opportunity to
208 randomized trials have compared therapies in mantle cell lymphoma (MCL), and the role of aggressive i
209 nt in chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL), but the extent of internaliz
210 lymphoma (FL), and (3) other NHL, including mantle cell lymphoma (MCL), marginal zone lymphoma (MZL)
212 is clinically approved for the treatment of mantle cell lymphoma (MCL), only limited effects of this
213 , including large B-cell lymphoma (LBCL) and mantle cell lymphoma (MCL), playing an important role in
214 Despite unprecedented clinical activity in mantle cell lymphoma (MCL), primary and acquired resista
215 ediated effects of interleukin-21 (IL-21) in mantle cell lymphoma (MCL), providing a preclinical rati
216 advances in the therapy for newly diagnosed mantle cell lymphoma (MCL), relapsed MCL continues to ha
218 r understanding about antigen involvement in mantle cell lymphoma (MCL), we analyzed the expression l
220 g pathway is involved in the pathogenesis of mantle cell lymphoma (MCL), we investigated the phosphor
221 mong 45 patients with relapsed or refractory mantle cell lymphoma (MCL), with manageable tolerability
243 oxidative stress-mediated drug resistance in mantle cell lymphoma (MCL); however, the biological func
244 mall lymphocytic lymphoma (CLL/SLL; n = 15), mantle cell lymphoma (MCL; n = 15), low-grade follicular
246 co purified DNA methylation signatures of 82 mantle cell lymphomas (MCL) in comparison with cell subp
256 rabine, and rituximab (FFR) in patients with mantle-cell lymphoma (MCL), indolent B-cell non-Hodgkin'
257 have improved the outcome for patients with mantle-cell lymphoma (MCL), most eventually relapse and
258 ctory diffuse large B-cell lymphoma (DLBCL), mantle-cell lymphoma (MCL), transformed follicular lymph
260 attempt to improve outcome in patients with mantle-cell lymphoma (MCL); however, the importance of i
265 le myeloma (n = 2), T-cell lymphoma (n = 3), mantle cell lymphoma (n = 2), small lymphocytic lymphoma
266 sk chronic lymphocytic leukemia (n = 22) and mantle-cell lymphoma (n = 13) received a total lymphoid
268 dge, the clinical features of ocular adnexal mantle-cell lymphoma (OA-MCL) have not previously been e
269 a dramatically regressed, and a patient with mantle cell lymphoma obtained an ongoing partial remissi
270 patients with diffuse large B-cell lymphoma, mantle-cell lymphoma, or follicular lymphoma were enroll
272 t trials with these agents were conducted in mantle cell lymphoma, pancreatic neuroendocrine tumors a
273 tumor biopsies were reviewed by the European Mantle Cell Lymphoma Pathology Panel to determine Ki-67
275 One hundred sixty untreated, stage II-IV mantle cell lymphoma patients <66 years received rituxim
277 patients were 73% and 47%, respectively; for mantle-cell lymphoma patients, they were 69% and 53%, re
278 istence of a graft-versus-lymphoma effect in mantle cell lymphoma providing strong scientific rationa
280 small molecule inhibitor (HDACi) in CLL and mantle cell lymphoma restored the expression of the BTK-
281 stochemical analysis of a cohort of 33 human mantle cell lymphomas shows that elevated expression of
282 tients with chronic lymphocytic leukemia and mantle cell lymphoma signal to apoptosis almost exclusiv
283 igned patients 60 years of age or older with mantle-cell lymphoma, stage II to IV, who were not eligi
284 rapeutic agent for multiple myeloma (MM) and mantle cell lymphoma, suppresses proteosomal degradation
285 nd potentially therapeutic implications, and mantle cell lymphoma treatment approaches and new agents
286 iven to patients with relapsed or refractory mantle cell lymphoma, until disease progression or unacc
287 mphocytic leukemia, follicular lymphoma, and mantle cell lymphoma were 5%-10% higher per 5-year incre
288 with autologous stem cell transplantation in mantle cell lymphoma were discouraging, with no clear su
290 16, 124 patients with relapsed or refractory mantle cell lymphoma were enrolled and all patients rece
291 ed or refractory indolent B-cell lymphoma or mantle cell lymphoma were treated with autologous T cell
294 ents with histologically documented relapsed mantle cell lymphoma who had not received previous lenal
295 , USA, and other countries for patients with mantle cell lymphoma who received one previous therapy.
296 mly assigned 487 adults with newly diagnosed mantle-cell lymphoma who were ineligible or not consider
297 al, and overall survival among patients with mantle-cell lymphoma who were younger than 66 years of a
298 nts with relapsed or refractory indolent and mantle cell lymphoma with adequate organ function were t
299 a/lymphoma 1 (CCND1/BCL1) is present in most mantle cell lymphomas with the t(11;14)(q13;q32) translo
300 een reported in patients with follicular and mantle-cell lymphoma with the combination of bendamustin
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