Results 31 to 40 of about 50,237 (216)

Biomarkers of cetuximab resistance in patients with head and neck squamous cell carcinoma

open access: yesCancer Biology & Medicine, 2020
Objective: In patients with head and neck squamous cell carcinoma (HNSCC), cetuximab [a monoclonal antibody targeting epidermal growth factor receptor (EGFR)] has been shown to improve overall survival when combined with radiotherapy in the locally ...
Olivia Leblanc   +14 more
doaj   +1 more source

Economic evaluation of encorafenib with cetuximab in patients with BRAF V600E-mutant metastatic colorectal cancer in France: a cost-effectiveness analysis using data from the BEACON CRC randomised controlled trial

open access: yesBMJ Open, 2022
Objective The BEACON CRC randomised controlled trial (NCT02928224) in BRAF-mutant metastatic colorectal cancer (mCRC) patients showed improved overall survival for the combination treatment of encorafenib (BRAF inhibitor) with cetuximab (EGFR inhibitor ...
David Malka   +10 more
doaj   +1 more source

In vivo efficacy of Palbociclib and Cetuximab in CF555 chordoma xenograft model_CF40

open access: yes, 2021
DrugTargetsPalbociclib + CetuximabCDK4/6 + EGFRDose75mg/kg (Palbociclib) 20mg/kg (Cetuximab)RoutePO (Palbociclib) IP (Cetuximab)Scheduleqd to end (Palbociclib) 2xwklyx6 (Cetuximab) Duration of treatment42 dStrain of miceAthymic NudeTGI (day)98% (Day 42)p-
Dan Freed (4391989)
core   +1 more source

Analysis of the anti-tumor effect of cetuximab using protein kinetics and mouse xenograft models

open access: yesBMC Research Notes, 2011
Background The binding of EGFR and its ligands leads to autophosphorylation of receptor tyrosine kinase as well as subsequent activation of signal transduction pathways that are involved in regulating cellular proliferation, differentiation, and survival.
Matsuo Teppei   +5 more
doaj   +1 more source

In vivo efficacy of Abemaciclib and Cetuximab in SF8894 chordoma xenograft model_CF41

open access: yes, 2021
DrugTargetsAbemaciclib + CetuximabCDK4/6 + EGFRDose50mg/kg (Abemaciclib) 20mg/kg (Cetuximab)RoutePO (Abemaciclib) IP (Cetuximab)Scheduleqd to end (Abemaciclib) 2xwklyx6 (Cetuximab) Duration of treatment42 dStrain of miceAthymic NudeTGI (day)49% (Day 41)p-
Dan Freed (4391989)
core   +1 more source

Cetuximab-sulfo-SMCC-protamine ability to transport two independent siRNAs.

open access: yes, 2018
A-I. Alexa 488 and Alexa 555 control-siRNA were mixed, coupled to cetuximab-sulfo-SMCC-protamine and incubated with the indicated cell lines at 60 nM end concentration overnight (Fig 1 A to I) or 48 h (J to R).
Wolfgang Hartmann (38453)   +9 more
core   +1 more source

Cetuximab associated dermal filler reaction

open access: yes, 2019
A 52-year-old male patient with hyaluronic acid-based dermal fillers injected in his cheeks was diagnosed with glossotonsillary malignancy, and managed with concurrent cetuximab (epidermal growth factor receptor inhibitor) and radiation therapy.
Dzienis, Marcin   +1 more
core   +1 more source

The effect of near-infrared fluorescence conjugation on the anti-cancer potential of cetuximab

open access: yesLaboratory Animal Research, 2018
This study investigated the anti-cancer potential of a near-infrared fluorescence (NIRF) molecule conjugated with Cetuximab (Cetuximab-NIRF) in six-week-old female BALB/c athymic (nu+/nu+) nude mice. A431 cells were cultured and injected into the animals
Ji Young Yun   +5 more
doaj   +1 more source

Advanced Materials for Biologics Delivery to Brain Tumors

open access: yesAdvanced Materials, EarlyView.
Material innovation is central to unlocking the therapeutic potential of biologics against many central nervous system diseases, including brain cancer. By engineering carriers with controlled transport, targeting, and release properties, advanced materials can overcome the blood–brain barrier and tumor microenvironment, improving the delivery of ...
Yuran Feng   +4 more
wiley   +1 more source

Selenium Nanoparticles Selectively Target KRAS G13D to Inhibit Colorectal Cancer

open access: yesAdvanced Science, EarlyView.
The mechanisms of SeNPs therapy in cancer treatment, encompass three parallel actions: (1) seleno‐amino acids, key metabolites, upregulate GPX2 expression, thereby inhibiting tumor metastasis via the GPX2‐HIF1α‐VEGF signaling pathway; (2) selenite (SeO32−), an inorganic metabolite, forms hydrogen bonds with amino acid residues 13–17 of the KRAS G13D ...
Xiaoting Liu   +13 more
wiley   +1 more source

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