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Hematologic safety of palbociclib in combination with endocrine therapy in patients with benign ethnic neutropenia and advanced breast cancer

Cancer Jun 26, 2021

Lynce F, Blackburn MJ, Zhuo R, et al. - This single-arm, open-label, investigator-initiated study (PALINA) was undertaken to determine the hematologic safety of palbociclib (a cyclin-dependent kinase 4/6 inhibitor) in African American females suffering from hormone receptor (HR)-positive/human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer (ABC). These patients with a baseline absolute neutrophil count ≥1000/mm 3 were administered palbociclib (125 mg daily; 21 days on and 7 days off) plus endocrine therapy. Febrile neutropenia or permanent study cessation due to neutropenia did not occur. Occurrence of grade 3 and 4 neutropenia as well as necessity for a palbociclib dose reduction were found in significantly more patients with the Duffy null vs the wild-type variant. Lower overall relative dose intensity and a lower clinical benefit rate were seen in patients with the Duffy null vs the wild-type variant. Findings indicated the good tolerability of palbociclib in African American women with HR-positive/HER2-negative ABC. There may exist an impact of Duffy null status on the incidence of grade 3 neutropenia, dose intensity, and possibly on clinical benefit.

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