Palbociclib Pfizer

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HomeAboutMode of actionEfficacyPALOMA-2Trial design overviewPatient baseline characteristicsProgression-free survival (primary endpoint)Overall survival (secondary endpoint)Tumour control (secondary endpoint)PALOMA-3Trial design overviewPatient baseline characteristicsProgression-free survival (primary endpoint)Overall survival (secondary endpoint)Tumour control (secondary endpoint)Real World EvidenceP-REALITY study designP-REALITY patients characteristicsP-REALITY real-world progression-free survivalP-REALITY overall survivalP-REALITY strengthsSafetyImportant Safety InformationSafetySafety overviewPooled ARsPooled laboratory abnormalitiesPALOMA-2 AEsPALOMA-3 AEsSelected safety featuresPalbociclib long-term safetyGI and liver toxicitiesEffect of Palbociclib on QTc intervalElderly patientsVisceral disease patientsDose reduction effect on efficacyDosingRecommended dosing scheduleRecommended dose modifications for AEsOne scheduled monitoring provisionMedical InformationVisit the Pfizer Medical Information Africa Website for Healthcare ProfessionalsSubmit a medical question to Pfizer

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Selected safety featuresPalbociclib Pfizer long-term safety

In an exploratory, long-term pooled analysis, there was no evidence of cumulative or delayed toxicity with up to 5 years of treatment withPalbociclib Pfizer in combination with letrozole or Palbociclib Pfizer in combination with fulvestrant in 1st line or later1

Cumulative Event Rates Over Time for Haematologic Adverse Events1Explore More PALOMA-2 AEs See AE tables PALOMA-3 AEs See AE tables
AE = adverse event; AR = adverse reaction; ALT = alanine aminotransferase; AST = aspartate aminotransferase; ECG = electrocardiogram; ET = endocrine therapy; SmPC = Summary of Product Characteristics. References:Finn R, et al. Oncologist. 2021;26:e749–e755.
Selected safety features

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