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1 ity, which has been associated with superior antitumor efficacy.
2 phery to mild hyperthermia and increases RFA antitumor efficacy.
3 een by alpha-GalCer that might attenuate its antitumor efficacy.
4 channel-modulating agents have demonstrated antitumor efficacy.
5 5TNFR mitigates TNF toxicity without loss of antitumor efficacy.
6 lockade synergized with vaccine in eliciting antitumor efficacy.
7 e CD27 (mCD27) with agonist mAbs can mediate antitumor efficacy.
8 and adaptive immunity will result in better antitumor efficacy.
9 of transferred T cells can lead to improved antitumor efficacy.
10 ic T cells, with trafficking correlated with antitumor efficacy.
11 its poor bioavailability in vivo limits its antitumor efficacy.
12 IDO targeting for ethyl pyruvate to achieve antitumor efficacy.
13 immunization strategies to achieve enhanced antitumor efficacy.
14 ivalent to those associated with preclinical antitumor efficacy.
15 ncer, beta-lap synergized with IR to promote antitumor efficacy.
16 n-7 receptor, heightened apoptosis, and poor antitumor efficacy.
17 ed enhancement of CD8+ T-cell activation and antitumor efficacy.
18 repeats), has significant antiangiogenic and antitumor efficacy.
19 irect intracerebral inoculation in mice, and antitumor efficacy.
20 s that target multiple pathways for enhanced antitumor efficacy.
21 of CD25(hi) T cells did not further improve antitumor efficacy.
22 tments, limiting tolerance opposing systemic antitumor efficacy.
23 or-specific CD8 T-cell activity and improved antitumor efficacy.
24 y using this approach, without compromise to antitumor efficacy.
25 intratumoral virus delivery/penetration and antitumor efficacy.
26 zing transgene would increase virus-mediated antitumor efficacy.
27 t of these receptors is critical for optimal antitumor efficacy.
28 n effective approach to assess potential for antitumor efficacy.
29 ant effect of preexisting immunity on vector antitumor efficacy.
30 increased ER stress and would enhance their antitumor efficacy.
31 lue of (89)Zr-bevacizumab PET for everolimus antitumor efficacy.
32 9 tumors in BALB/c mice, EC131 showed marked antitumor efficacy.
33 ombination with chemotherapy, would increase antitumor efficacy.
34 F, and IFN-gamma were essential for complete antitumor efficacy.
35 d intratumoral delivery of CTLs and improved antitumor efficacy.
36 )-derived T cells, their function, and their antitumor efficacy.
37 d to characterize their in vitro and in vivo antitumor efficacy.
38 with immune therapy may result in increased antitumor efficacy.
39 munostimulatory molecules have shown limited antitumor efficacy.
40 cells with a costimulator can enhance their antitumor efficacy.
41 duced neutropenia and anemia while retaining antitumor efficacy.
42 the tumor microenvironment, eliciting potent antitumor efficacy.
43 uppressive immune-modulating agents (IMs) on antitumor efficacy.
44 CTL combined with CTLA4 blockade might boost antitumor efficacy.
45 cargoes in tumor cells, leading to enhanced antitumor efficacy.
46 ting that sequential schedules could improve antitumor efficacy.
47 elf-tumor antigen positively correlated with antitumor efficacy.
48 rapalogs-mediated immune modulation on their antitumor efficacy.
49 rapy of lung cancer with improved safety and antitumor efficacy.
50 therapy and chemotherapy to receive superior antitumor efficacy.
51 early exhaustion of CAR T cells that limits antitumor efficacy.
52 al small-molecular drug, leading to enhanced antitumor efficacy.
53 mcitabine as an optimal protocol to maximize antitumor efficacy.
54 fic chemosensitivity patterns and to monitor antitumor efficacy.
55 tor T-cell responses, to augment therapeutic antitumor efficacy (66% reduction in tumor growth; P = .
56 od mononuclear cells or T cells enhanced the antitumor efficacy achieved by the parental counterpart.
57 ped a mouse CD19-specific CAR to investigate antitumor efficacy against a syngeneic B cell lymphoma c
58 icular, compound 48 demonstrated significant antitumor efficacy against established HT29 human colon
59 standard chemotherapy drug for GBM increased antitumor efficacy against glioblastoma in experimental
60 ilencing with RIG-I signaling confers potent antitumor efficacy against pancreatic cancer by breaking
61 rophic for leu-arg, is tumor-seeking and has antitumor efficacy against the major types of cancer.
64 ases, as well as pan-Aurora inhibitors, show antitumor efficacy and are now under clinical investigat
66 geneic mouse tumor models, 1F5 showed potent antitumor efficacy and induction of protective immunity,
70 xel (PTX)-loaded OA02-NPs exhibited superior antitumor efficacy and lower systemic toxicity profile i
71 characterize a human IL-2 mutant with higher antitumor efficacy and lower toxicity than wild type hum
72 ta demonstrate that XmAbCD40 displays potent antitumor efficacy and merits further evaluation for the
73 he disease course, with a view to maximizing antitumor efficacy and minimizing overlapping toxicities
74 (DOX)-loaded SNP (SNP/DOX) shows significant antitumor efficacy and nearly eradicates the tumor, subs
75 oughout tumors correlated well with improved antitumor efficacy and overall survival in two highly me
76 nanochemistry for targeting PI3K to enhance antitumor efficacy and potentially overcome these limita
79 tides in combination with docetaxel improved antitumor efficacy and resulted in lower expression leve
80 odel overexpressing GLUT1, compound 2 showed antitumor efficacy and selective uptake in tumors with n
81 combination is expected to have synergistic antitumor efficacy and significant potential for the tre
82 These effects were associated with increased antitumor efficacy and survival as compared with PI103 a
83 ave yielded promising, yet limited, signs of antitumor efficacy and therefore need to be improved for
85 ng nelfinavir might experience both enhanced antitumor efficacy and unexpected adverse toxicity given
87 onucleotides with low doses of docetaxel has antitumor efficacy, and it may be an effective treatment
91 ct displayed comparable in vitro and in vivo antitumor efficacy as bivalent Herceptin/rGel conjugate.
92 is safe and well tolerated with evidence of antitumor efficacy assessed radiologically and serologic
93 unization with DNA and Ad5 produced superior antitumor efficacy associated with increased TCR avidity
94 tigen, gp100(pmel17/silver locus), improving antitumor efficacy, augmenting systemic CD8+ T-cell resp
96 their intratumoral proliferation and direct antitumor efficacy but did not block their capacity to s
97 ation from 30 to 60 mg/kg sorafenib improved antitumor efficacy but worsened survival due to excessiv
98 The established role of CD8(+) T cells in antitumor efficacy, but CD4(+) T cells in autoimmunity,
99 idity TCRs can be improved to increase their antitumor efficacy, but conventional saturation mutagene
100 gens in solid malignancies where it exhibits antitumor efficacy, but its clinical utility for treatin
101 yde interacts with anthracyclines to enhance antitumor efficacy, bypass resistance mechanisms, improv
102 espite having a shorter serum half-life, had antitumor efficacy comparable with equimolar v-mab; 22-2
103 F-5412 with sunitinib significantly improved antitumor efficacy compared with either agent alone.
104 ing A12 and radiation significantly enhances antitumor efficacy compared with either modality alone.
105 o, we show enhanced expansion and CAR T cell antitumor efficacy, culminating in improvement in surviv
106 quely safe profile of induced cytokines, and antitumor efficacy demonstrated in a number of animal mo
107 was cardioprotective and did not compromise antitumor efficacy, did not increase the frequencies of
109 preexisting immunity in oncolytic Ad vector antitumor efficacy following intratumoral injection of v
110 ing immunity to Ad5 does not affect INGN 007 antitumor efficacy following intratumoral injection, but
112 These results establish proof-of-concept antitumor efficacy for tankyrase inhibitors in APC-mutan
114 with enhanced safety, pharmacokinetics, and antitumor efficacy for the specific treatment of NSCLC t
115 strategies attempts to decouple the observed antitumor efficacy from the on-target liver toxicity.
117 in well-characterized mouse models in which antitumor efficacy has been shown; inhibiting only late
118 erm PDK1 knockdown revealed a lack of potent antitumor efficacy in 3 different mouse models of PTEN-d
119 rgeting these nodes concurrently resulted in antitumor efficacy in a majority of cetuximab-resistant
120 N inhibits glutamine metabolism and provides antitumor efficacy in a murine model of glioblastoma, al
121 mice and demonstrated superior single-agent antitumor efficacy in a PPC-1 mouse xenograft model.
122 d show that the nanoparticle yields improved antitumor efficacy in a preclinical human melanoma xenog
123 and also demonstrated superior single-agent antitumor efficacy in a prostate cancer mouse xenograft
124 A-BN-PRO and resulted in a trend of improved antitumor efficacy in a PSA-expressing tumor model.
125 fortunately, intravesical IL-12 did not show antitumor efficacy in a recent clinical study of patient
127 NC280, a cMET inhibitor, resulted in durable antitumor efficacy in a xenograft model that initially d
128 nd an orally bioavailable compound (32) with antitumor efficacy in ALK-driven xenografts in mouse mod
129 y, sustained multi-drug exposure, and potent antitumor efficacy in an ES-2-luc, ovarian cancer i.p. x
130 endent gene expression in vivo, demonstrates antitumor efficacy in an MV-4-11 mouse xenograft model,
131 to Sutent (ED50 = 9 mg/kg) and showed potent antitumor efficacy in an MX-1 human breast carcinoma xen
132 Furthermore, dinaciclib revealed in vivo antitumor efficacy in an orthotopic xenograft mouse mode
133 xcellent activity in vitro and in vivo, with antitumor efficacy in both subcutaneous and orthotopic x
134 is-platinum nanoparticle results in enhanced antitumor efficacy in breast cancer as compared with whe
135 may lead to enhanced and sustained clinical antitumor efficacy in CRCs harboring the BRAF(V600E) mut
136 lly, the CH-NPs showed significantly greater antitumor efficacy in EG.7 and TC-1 tumor-bearing mice c
137 revents the PIP3 rebound and induces greater antitumor efficacy in HER2-amplified and PIK3CA mutant c
138 tudies revealed that FL118 exhibits superior antitumor efficacy in human tumor xenograft models in co
140 characteristics of the drug, with equivalent antitumor efficacy in LNCaP xenografts at 1/3 the dose o
142 eover, in vivo peptide administration showed antitumor efficacy in mice bearing Hepa129 or TC1 tumor
144 eting the constant region of CD44 that shows antitumor efficacy in mice implanted with CD44-expressin
145 ion of these compounds would yield increased antitumor efficacy in multiple myeloma and glioblastoma
146 icles exhibit significantly enhanced in vivo antitumor efficacy in murine 4T1 breast cancer and in K-
147 , navitoclax (ABT-263), have shown promising antitumor efficacy in preclinical and early clinical stu
148 noparticles exhibited significantly improved antitumor efficacy in terms of tumor growth delay in bre
149 armacokinetic (PK) properties and remarkable antitumor efficacy in the BRCA1 mutant MX-1 breast cance
150 x-hA20 has a short serum half-life, it shows antitumor efficacy in tumor-bearing mice comparable with
152 Anti-CD137 agonistic mAb has demonstrated antitumor efficacy in various tumor models and has now e
154 lization, cytotoxicity, tumor targeting, and antitumor efficacy in vitro and in vivo over its nonsens
155 be synergistic with phototherapy to improve antitumor efficacy in vitro and in vivo, offering a new
156 th 17-AAG and doxorubicin exhibited superior antitumor efficacy in vivo in an ErbB2-driven xenograft
157 Most significantly, CMP-L-CA4 had better antitumor efficacy in vivo than its noncleavable (NC) an
158 mitter (125)I-DCIBzL yielded highly specific antitumor efficacy in vivo, suggesting promise for treat
162 agonist to the tumor site can contribute to antitumor efficacy, in the context of adoptive T-cell im
165 tudy was to determine the antiangiogenic and antitumor efficacies of a vasculature-targeting fusion t
166 In severe combined immunodeficient mice, the antitumor efficacies of C1 and C2 were greater toward su
168 ility of the probes to predict the potential antitumor efficacy of 2'-deoxy-2',2'-difluorocytidine (g
170 cally, we analyzed how rapamycin affects the antitumor efficacy of a human papilloma virus E7 peptide
171 These results show the in vitro and in vivo antitumor efficacy of a prototype small molecule inhibit
173 ignificantly increased the expansion and the antitumor efficacy of adoptively transferred pmel-1 CD8(
174 udies in murine models of ACT indicated that antitumor efficacy of adoptively transferred T cells is
175 hat targeting eEF-2 kinase may reinforce the antitumor efficacy of Akt inhibitors such as MK-2206.
176 for a combinatorial approach to enhance the antitumor efficacy of an OV, suggesting a strategy to im
177 y offers a general approach to retaining the antitumor efficacy of antibody-drug conjugates, while mi
178 ockdown of NAC1 expression can reinforce the antitumor efficacy of bevacizumab, an inhibitor of angio
180 t and depleting properties contribute to the antitumor efficacy of CD27-targeted immunotherapy, and m
181 7-DMAG-based "pulse" therapy may improve the antitumor efficacy of CD8(+) T effector cells reactive a
192 Investigations in vivo showed equivalent antitumor efficacy of deoxynyboquinone to beta-lapachone
196 6 pathway may be responsible for the reduced antitumor efficacy of erlotinib and other EGFRIs, and bl
197 e the potential of disulfiram to enhance the antitumor efficacy of external-beam gamma-irradiation an
202 Furthermore, bortezomib enhances the in vivo antitumor efficacy of IFN-gamma/TNF-alpha-inducing cytok
203 important obstacle to the evaluation of the antitumor efficacy of immunomodulator Abs in syngeneic m
204 ta pathway is a promising way to improve the antitumor efficacy of ionizing radiation and warrants cl
210 , while Fas signaling blockade preserved the antitumor efficacy of naive cells within mixed populatio
212 r in vitro as well as in vivo studies showed antitumor efficacy of NVP-LDE225 in combination with bor
213 UV irradiation in vitro and potentiated the antitumor efficacy of paclitaxel in a mouse xenograft mo
215 The dual mechanism of action and robust antitumor efficacy of PF-5412 support its clinical devel
217 G2 inhibitors would effectively increase the antitumor efficacy of purine nucleosides by blocking dru
222 by chemotherapy or radiation can enhance the antitumor efficacy of several distinct, cell-based immun
226 severely immunodeficient mice to assess the antitumor efficacy of systemic NBP treatments when combi
228 t pathways of nuclear import that affect the antitumor efficacy of taxanes, suggesting a mechanistic
230 rimary aim of this study was to evaluate the antitumor efficacy of the bromodomain inhibitor JQ1 in p
231 Itraconazole significantly enhanced the antitumor efficacy of the chemotherapeutic agent cisplat
234 of CD4 or CD8 T cells completely eliminated antitumor efficacy of the lymphodepletion/anti-PD-L1 the
242 ork provides direct evidence for the in vivo antitumor efficacy of TRAIL being proportional to system
245 neutralizing anti-VSV antibodies negate the antitumor efficacy of VSV, a concern for repeat VSV admi
247 M demonstrated dramatically enhanced in vivo antitumor efficacy over single treatment on nude mice be
249 ma was well tolerated and produced increased antitumor efficacy relative to the respective monotherap
250 in vivo are limited persistence and reduced antitumor efficacy, relative to CD8(+) T cells with a ce
253 erstanding of the molecular determinants for antitumor efficacy resulting from RAF pathway inhibition
255 Targeted type I interferon elicits powerful antitumor efficacy, similar to wild-type IFN, but withou
259 -induced CD8(+) T-cell immunity and improved antitumor efficacy, suggesting manipulating beta-catenin
260 PF-5412 displayed robust and dose-dependent antitumor efficacy superior to that observed with IgG1/w
261 n was obtained by 20, which exhibited higher antitumor efficacy than 3 in PTEN-negative cancer cells
264 resulting in significantly improved clinical antitumor efficacies that have transformed the clinical
265 rgeted therapies, such as less-than-expected antitumor efficacy that may arise from compensatory incr
266 th acceptable toxicity and promising durable antitumor efficacy that warrant further testing in a ran
267 gamma responses can lead to successful early antitumor efficacy, they may also impair the development
270 tial immunization with DNA and Ad5 maximized antitumor efficacy through TCR avidity enhancement, it p
271 ichia coli by the disk diffusion method, and antitumor efficacy toward the HeLa cell-derived tumor sp
272 ics and in vivo pharmacokinetics that define antitumor efficacy under intermittent dosing conditions.
273 atory target and to address the mechanism of antitumor efficacy using different IgG isotypes of 1F5 i
274 a foreign gene can be selected for enhanced antitumor efficacy via in vivo serial passage within fla
278 use PDA xenografts (+MUC1 or MUC1 null), and antitumor efficacy was further improved when the virus w
285 o determine the mechanisms of chNKG2D T cell antitumor efficacy, we analyzed how chNKG2D T cells alte
286 e binding affinity to p185(her2/neu) and the antitumor efficacy, we have engineered a fusion protein
287 ics (PKs), pharmacodynamics, and preliminary antitumor efficacy were assessed in a phase I study of M
289 decreased human vessel density and improved antitumor efficacy when combined with bevacizumab (anti-
290 r-bearing mice showed significantly improved antitumor efficacy when combined with either 5-aziridiny
291 Compound 50 also showed excellent in vivo antitumor efficacy when dosed orally in an A2780 ovarian
292 Compound 25b exhibited significant in vivo antitumor efficacy when dosed orally in an ALK-positive
293 rime or prime-boost regimens correlated with antitumor efficacy, whereas T cell number and cytokine p
294 erent valencies did not significantly affect antitumor efficacy, whereas the presence of an Fc domain
295 ors targeting EGFR have demonstrated limited antitumor efficacy, which may be explained, in part, by
299 f ATR have been reported showing significant antitumor efficacy, with most advanced ones entering cli
300 idity enhancement eliminated GUCY2C-specific antitumor efficacy, without affecting responding T cell
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