Results 81 to 90 of about 8,127 (167)

Ribociclib plus Endocrine Therapy in Early Breast Cancer

open access: yes
Background Ribociclib has been shown to have a significant overall survival benefit in patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer.
Chakravartty, Arunava   +30 more
core   +1 more source

Assessing the Influence of Proton Pump Inhibitors on Clinical Outcomes in Hormone Receptor-Positive Metastatic Breast Cancer Patients Receiving CDK4/6 Inhibitors: Evidence from a Ribociclib-Dominant Cohort

open access: yesMedicina
Background and Objectives: Endocrine therapy combined with CDK4/6 inhibitors are widely recognized as the standard first-line approach for treating hormone receptor-positive HER2-negative (HR+/HER2−) metastatic breast cancer (mBC). Nonetheless, potential
Enes Erul   +5 more
doaj   +1 more source

The effect of ribociclib on the expression levels of miR-141 and CDK4/6-USP51 signaling pathway genes in MCF-7 and MDA-MB-231 cells.

open access: yesPLoS ONE
IntroductionPatients with breast cancer, especially triple-negative breast cancer, have a poor prognosis. There is still no effective treatment for this disease.
Shayeste Sadat Baghermanesh   +2 more
doaj   +1 more source

A Vitiligo-like Cutaneous Reaction Induced by Ribociclib in Advanced Breast Cancer: An Unusual Case Report from Colombia

open access: yesDiseases
Background: Cutaneous toxicities associated with CDK4/6 inhibitors are uncommon but may affect treatment adherence. We present the case of a patient with advanced breast cancer who developed vitiligo-like lesions after initiating ribociclib, contributing
John Fernando Montenegro   +7 more
doaj   +1 more source

METHOD OF PREPARING CRYSTALLINE FORM A OF RIBOCICLIB SUCCINATE

open access: yes
Ribociclib is a kinase inhibitor. The active pharmaceutical ingredient Ribociclib is developed in the form of its succinate salt to improve physicochemical stability, manufacturability, and solid‑state consistency.
Anonymous
core   +1 more source

Preclinical evaluation of ribociclib and its synergistic effect in combination with alpelisib in non-keratinizing nasopharyngeal carcinoma

open access: yes, 2018
Ribociclib is a specific cyclin dependent kinase (Cdk) 4/6 inhibitor that induces G1 arrest by blocking the formation of cyclin D1-Cdk4/6 complex and inhibiting retinoblastoma (RB) phosphorylation. Cyclin D1 is overexpressed in over 90% of nasopharyngeal
Connie W. C. Hui   +5 more
core   +1 more source

Infection associated with CDK4/6 inhibitors: a pharmacovigilance analysis of the FDA adverse event reporting system database

open access: yesFrontiers in Pharmacology
IntroductionCyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors are first-line treatments for hormone receptor-positive/human epidermal growth factor receptor 2-negative breast cancer. With their increasing clinical use, infection-related adverse events (
Jinhua Chen   +4 more
doaj   +1 more source

Ribociclib Approved for Advanced Breast Cancer

open access: yes, 2017
The FDA has approved ribociclib combined with aromatase inhibitor therapy for women with metastatic HR-positive, HER2-negative breast cancer. It is the second CDK 4/6 inhibitor approved for these patients, behind palbociclib; a third is under ...

core   +1 more source

A phase I study of the CDK4/6 inhibitor ribociclib combined with gemcitabine in patients with advanced solid tumors

open access: yesBJC Reports
Background Based on preclinical data showing addition of CDK4/6 inhibitors to gemcitabine was synergistic, ribociclib was evaluated in combination with gemcitabine to determine the maximum tolerated dose (MTD) and dose limiting toxicities (DLT).
Aurora Norman   +12 more
doaj   +1 more source

Considerations for emulations of randomized controlled trials using real-world data: learnings from an emulation of MONALEESA-2

open access: yesJournal of Comparative Effectiveness Research
Aim: The eligibility criteria of randomized controlled trials can exclude groups of patients indicated for the therapy post-approval and the trial populationmay not be generalizable to routine care.We attempted to emulate the MONALEESA-2 trial of ...
Amanda M Kong   +7 more
doaj   +1 more source

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