scholarly journals PCN465 VIRTUAL COMMUNITY ENGAGEMENT AMONG WOMEN RECEIVING PALBOCICLIB FOR HR+/ HER2- METASTATIC BREAST CANCER: DATA FROM THE MADELINE STUDY

2019 ◽  
Vol 22 ◽  
pp. S527
Author(s):  
D. Richardson ◽  
L. Zhan ◽  
M. Reynolds ◽  
D. Odom ◽  
L. McRoy ◽  
...  
2010 ◽  
Vol 28 (15_suppl) ◽  
pp. 1058-1058
Author(s):  
T. Foukakis ◽  
T. Fornander ◽  
T. Lekberg ◽  
H. Hellborg ◽  
J. Adolfsson ◽  
...  

2014 ◽  
Vol 37 (12) ◽  
pp. 748-755 ◽  
Author(s):  
Volkmar Müller ◽  
Stefan Fuxius ◽  
Claus-Christoph Steffens ◽  
Christian Lerchenmüller ◽  
Birgit Luhn ◽  
...  

Author(s):  
Kristina F. Byers, PharmD, BCOP

The treatment landscape of hormone receptor–positive (HR+), human epidermal growth factor receptor 2–negative (HER2–) metastatic breast cancer has been modernized by the identification of cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors. Because the majority of HR+ breast cancers will develop resistance to endocrine therapies (tamoxifen and aromatase inhibitors), newer treatment options are necessary to restore endocrine sensitivity and prolong survival. Ribociclib and abemaciclib are two of three CDK4/6 inhibitors currently approved for first- and second-line treatment of HR+/HER2– metastatic breast cancer. Data from large, phase III clinical trials have demonstrated an improvement in both progression-free and overall survival with the addition of ribociclib or abemaciclib to endocrine-based therapy, establishing a new frontline standard of care. Treatment with ribociclib and abemaciclib provide a convenient oral treatment option that is both efficacious and well tolerated.


2018 ◽  
Vol 53 (5) ◽  
pp. 501-509 ◽  
Author(s):  
Kaitlin Rascon ◽  
Goran Flajc ◽  
Carmine De Angelis ◽  
Xinli Liu ◽  
Meghana V. Trivedi ◽  
...  

Objective: To review the chemistry, pharmacology, pharmacokinetics, safety, and efficacy of ribociclib (LEE011, Kisqali) in hormone receptor–positive/human epidermal growth factor receptor-2–negative (HR+/HER2−) metastatic breast cancer. Data Sources: A PubMed search was performed using the terms ‘Ribociclib’, ‘Kisqali’, and ‘LEE011’ between May 2018 and November 2018. References of published articles and reviews were also assessed for additional information. Study Selection and Data Extraction: English-language preclinical and clinical studies on the chemistry, pharmacology, pharmacokinetics, safety, and efficacy of ribociclib were evaluated. Data Synthesis: Ribociclib, a cyclin-dependent kinase (CDK) 4/6 inhibitor, is Food and Drug Administration (FDA) approved in combination with endocrine therapy for treatment of HR+/HER2− advanced or metastatic breast cancer in premenopausal/perimenopausal and postmenopausal women. Three phase III trials have evaluated ribociclib in combination with endocrine therapy, including letrozole, anastrozole, tamoxifen, and fulvestrant. These studies found that ribociclib 600 mg/d, 21 days on, 7 days off, leads to a significantly greater median progression-free survival (PFS), ranging from 8 to 13 months. Ribociclib is well tolerated in elderly patients, maintains health-related quality of life, and significantly reduces pain scores. The dose-limiting toxicities found in phase I studies were neutropenia, thrombocytopenia, and QTc prolongation. Common adverse effects seen in phase III trials include neutropenia, leukopenia, nausea, diarrhea, vomiting, and fatigue. Relevance to Patient Care and Clinical Practice: Literature on the safety and efficacy of ribociclib as well as its place in therapy in comparison to other FDA-approved CDK4/6 inhibitors for breast cancer is discussed. Conclusions: Ribociclib, when added to endocrine therapy, significantly improves PFS and has manageable toxicity in premenopausal/perimenopausal and postmenopausal women with HR+/HER2− advanced breast cancer.


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