| Added by | standudu |
|---|---|
| Group name | EquipeCTCS |
| Item Type | Journal Article |
| Title | Pharmacokinetic Variability Drives Palbociclib-Induced Neutropenia in Metastatic Breast Cancer Patients: Drug-Drug Interactions Are the Usual Suspects |
| Creator | Leenhardt et al. |
| Author | Fanny Leenhardt |
| Author | Ludovic Gauthier |
| Author | Marie Alexandre |
| Author | Séverine Guiu |
| Author | Nelly Firmin |
| Author | Marie Viala |
| Author | Gerald Lossaint |
| Author | Chloé Gautier |
| Author | Caroline Mollevi |
| Author | Matthieu Gracia |
| Author | Litaty Mbatchi |
| Author | Alexandre Evrard |
| Author | William Jacot |
| Abstract | Palbociclib is a good candidate for therapeutic drug monitoring (TDM) due to its narrow therapeutic range and frequency of toxicities, particularly high-grade neutropenia. In this prospective, bicentric clinical trial, we evaluated the palbociclib exposure-toxicity relationship and determined the relevant sources of palbociclib pharmacokinetic variability, including drug-drug interactions (DDI). We followed 58 patients (mean age: 62.9 years) for 1 year. The geometric median of palbociclib plasma trough concentration (Ctrough) was 74.1 ng/mL. Neutropenia occurred in 70.7% of patients (high grade in 67.2% of patients). High-grade neutropenia occurrence during the first two palbociclib cycles was higher in patients with lower neutrophil count at initiation (p = 0.002). Palbociclib plasma Ctrough was correlated with high-grade neutropenia occurrence during the first two cycles (p = 0.024, OR 5.51). Co-treatment with agents that may interfere with palbociclib PK significantly influenced palbociclib Ctrough (p < 0.05). CYP3A4/P-glycoprotein inhibitors increased by 25% palbociclib Ctrough (p = 0.035), while antacids reduced it by 20% (p = 0.036). However, DDI did not have any significant effect on high-grade neutropenia occurrence (p > 0.05). This study confirms the major role of TDM to manage palbociclib safe use from the first week of treatment, particularly the significant incidence of hematological toxicity. Moreover, this first dedicated prospective study confirmed the importance of characterizing co-treatments to limit the DDI risk with oral-targeted therapies. |
| Publication | Pharmaceutics |
| Volume | 14 |
| Issue | 4 |
| Pages | 841 |
| Date | 2022-04-11 |
| Journal Abbr | Pharmaceutics |
| Language | eng |
| DOI | 10.3390/pharmaceutics14040841 |
| ISSN | 1999-4923 |
| Short Title | Pharmacokinetic Variability Drives Palbociclib-Induced Neutropenia in Metastatic Breast Cancer Patients |
| Library Catalog | PubMed |
| Extra | PMID: 35456675 PMCID: PMC9032884 |
| Tags | clinic, corresponding, first-last-corresponding, last, marque |
| Date Added | 2022/07/29 - 11:37:01 |
| Date Modified | 2022/08/01 - 16:21:33 |
| Notes and Attachments | PubMed entry (Attachment) Texte intégral (Attachment) |
Institut de Recherche en Cancérologie de
