Publication

Safety of Same-day Pegfilgrastim Administration in Metastatic Castration-resistant Prostate Cancer Treated With Cabazitaxel With or Without Carboplatin

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Last modified
  • 05/15/2025
Type of Material
Authors
    Mehmet Asim Bilen, Emory UniversityDiana H. Cauley, The University of Texas MD Anderson Cancer CenterBradley J Atkinson, The University of Texas MD Anderson Cancer CenterHsiang-Chun Chen, The University of Texas MD Anderson Cancer CenterDiana H. Kaya, The University of Texas MD Anderson Cancer CenterXuemei Wang, The University of Texas MD Anderson Cancer CenterRaghu Vikram, The University of Texas MD Anderson Cancer CenterShi-Ming Tu, The University of Texas MD Anderson Cancer CenterPaul G. Corn, The University of Texas MD Anderson Cancer CenterJeri Kim, The University of Texas MD Anderson Cancer Center
Language
  • English
Date
  • 2017-06-01
Publisher
  • Elsevier: 12 months
Publication Version
Copyright Statement
  • © 2016 Elsevier Inc.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1558-7673
Volume
  • 15
Issue
  • 3
Start Page
  • E429
End Page
  • E435
Grant/Funding Information
  • This work was supported in part by the National Institutes of Health through MD Anderson Cancer Center’s Support Grant CA016672 (Clinical Trials Support Resource).
Abstract
  • Although myeloid growth factors are commonly used to treat metastatic castration-resistant prostate cancer, the optimal timing of administration has not been well studied. We demonstrate that same-day pegfilgrastim administration after cabazitaxel treatment with or without carboplatin in patients with metastatic castration-resistant prostate cancer is feasible. Furthermore, we observed that the rate of urinary tract inflammation was higher than that reported anecdotally. Introduction Although myeloid growth factors are commonly used to treat metastatic castration-resistant prostate cancer (mCRPC), the optimal timing of administration has not been well studied. We assessed the effects of same-day pegfilgrastim, a neutrophil stimulator, after cabazitaxel treatment with or without carboplatin in patients with mCRPC. We also evaluated the frequency of urinary tract inflammation during treatment. Patients and Methods Between September 2010 and September 2014, 151 consecutive patients with mCRPC underwent cabazitaxel treatment with or without the addition of carboplatin at a single institution. We assessed absolute neutrophil count recovery, incidence of neutropenia, neutropenic fever, antibiotic usage, treatment delays or discontinuation, dose reduction, and hospitalization with pegfilgrastim administration. Radiologists blinded to therapy reviewed computed tomography scans to detect urinary tract inflammation. Results The median patient age was 69 years (range, 41-88 years); 78% of patients were white, and 54% had a Gleason score ≥ 9. Median overall survival was 9 months (95% confidence interval, 8-11 months). One patient (< 1%) had neutropenia; 38 patients (25%) had infection. During cycle 1, a significantly higher proportion of patients receiving pegfilgrastim after 24 hours developed infection than did those receiving pegfilgrastim the same day (26% vs. 6%; P = .01). Conclusion Same-day pegfilgrastim administration after cabazitaxel treatment with or without carboplatin in patients with mCRPC is feasible. The urinary tract inflammation rate (21%) was higher than that reported anecdotally. Results need to be prospectively validated.
Author Notes
  • Address for Correspondence: Jeri Kim, M.D., Department of Genitourinary Medical Oncology, Unit 1374, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030-3721, USA. Tel: +1-713-563-7237; Fax: +1-713-745-1625; jekim@mdanderson.org
Keywords
Research Categories
  • Health Sciences, Radiology
  • Biology, Biostatistics

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