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Monitoring
Summary of Prescibing Information
PALOMA Pooled Analysis: Laboratory Abnormalities
Laboratory abnormalities* observed in pooled data set from 3 randomised studies (N=872)1
Adapted from Palbace. Local product document. version 7. 2023
The median duration of PALBACE® treatment across the pooled data set at the time of the final OS analysis was 14.8 months.1
*Note: Laboratory results are graded according to the NCI CTCAE version 4.0 severity grade.
†Letrozole or fulvestrant.
ALT, alanine aminotransferase; AST, aspartate aminotransferase; FUL, fulvestrant; LET, letrozole; N, total number of patients; NA, not applicable; NCI CTCAE, National Cancer Institute Common Toxicity Criteria for adverse events; OS, overall survival; PALOMA, PALbociclib: Ongoing trials in the Management of breast cAncer; WBC, white blood cell
Reference:
Please click the Prescribing Information link to view the safety and adverse events information of PALBACE®.
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With RCT data, PALBACE® RWE can help improve the understanding of outcomes in patients with HR+/HER2- mBC
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