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Adverse event reporting can be found at the bottom of the page

Dosing           DosingIBRANCE® Dosing
 
Monitoring Requirements
Safety            
SafetyIBRANCE® Safety ProfileNeutropeniaAdverse Event Management
Real World EvidenceReal World EvidenceIBRANCE® Real World EvidenceIRIS (UK) StudyROIS
 
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Clinical TrialsIBRANCE® Clinical TrialsIBRANCE® PALOMA-2 Trial
 
IBRANCE® PALOMA-3 Trial
Patient ProfilesThe Ibrance® PatientPatient ProfilesAllison - Postmenopausal with comorbiditiesBecky - Postmenopausal with bone-only diseaseELEVATE MasterclassSupport and ResourcesSupport and ResourcesIBRANCE Service SupportMaterials
 
Videos

The content of this website has been produced in line with the IBRANCE® Summary of Product Characteristics. IBRANCE® (palbociclib) Prescribing Information for the UK click here.  Adverse event reporting information can be found at the bottom of the page.

The IBRANCE®Patient - Meet Becky

IBRANCE® is indicated for the treatment of patients with HR+/HER2– locally advanced or metastatic breast cancer and is suitable for pre-, peri- or postmenopausal women. IBRANCE® should be used in combination with an AI or in combination with fulvestrant in women who have received prior endocrine therapy. For pre- or perimenopausal women, the endocrine therapy  should be combined with an LHRH agonist.1

Click for more information on the Randomised controlled trial PALOMA-2, Real world evidence
 P-REALITY X studies
Click here for Safety Information.
Click to return to Patient Profiles or to visit Allison.

This is a fictional patient and images are illustrative only.

*Data cut-off: 31 May 2017. In PALOMA-2, the primary endpoint was investigator-assessed PFS.2

†PALOMA clinical trials. Based on pooled data from 872 patients who received IBRANCE® in combination with ET (n=527 in combination with letrozole and n=345 in combination with fulvestrant).2,3 ‡ROIS (N=191) and IRIS UK cohort (N=255). Safety data were not reported in P-REALITY X.4,5

§ IBRANCE® should be taken for 3 weeks on and 1 week off, in combination with either an AI or fulvestrant 500 mg IM. In pre- or perimenopausal women, the ET should be combined with an LHRH agonist.

||Full blood count should be monitored prior to the start of IBRANCE® therapy and at the beginning of each cycle, as well as on Day 15 of the first two cycles, and as clinically indicated.1

All patients should also be monitored for pulmonary symptoms indicative of ILD/pneumonitis, signs and symptoms of infection, deep vein thrombosis and pulmonary embolism. Patients with moderate or severe hepatic and renal impairment should be closely monitored for signs of toxicity.1

AI : aromatase inhibitor
CI: confidence interval
ET : endocrine therapy
HER2 : human epidermal growth factor receptor 2
HER2—: human epidermal growth factor receptor 2-negative
HR+: hormone receptor positive
HR : hormone receptor
IM : intramuscular
IRIS: IBRANCE real-world insights
LHRH : luteinising hormone-releasing hormone
mBC : metastatic breast cancer
mPFS : median progression-free survival
PFS : progression-free survival
P-REALITY X : palbociclib real-world first-line comparative effectiveness study extended
PSM : propensity score matching
QoL : quality of life
RCT : randomised controlled trial
RWE : real world evidence

ReferencesIBRANCE® (palbociclib) Summary of Product Characteristics. click hereRugo HS, et al. Breast Cancer Res Treat. 2019;174:719–729.Diéras V, et al. J Natl Cancer Inst. 2019;111:419–430.Palmieri C, et al. Br J Cancer. 2023;129:852–860.Pfizer Ltd. Data on file. IBRANCE Real-World Insights (IRIS) UK results, 2020.
 

PP-IBR-GBR-6702. January 2026

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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