Yeni jenerasyon proteozom inhibitörleriyle olan çevresel nöropati yükünün fda yan etki raporlama sistemi kullanılarak pazarlama sonrası analizi

Translated title of the contribution: Post-marketing analysis of peripheral neuropathy burden with new-generation proteasome inhibitors using the fda adverse event reporting system

Syeda A. Mina, Ibrahim N. Muhsen, Ethan A. Burns, Humaira Sarfraz, Sai Ravi Pingali, Jiaqiong Xu, Shahrukh K. Hashmi

Research output: Contribution to journalArticlepeer-review

Abstract

Proteasome inhibitors (PIs) are an integral component of multiple myeloma therapies. Peripheral neuropathy (PN) is a well-known consequence of PIs, most frequently reported with earlier generations such as bortezomib (BTZ). There is a paucity of data highlighting the risk of developing PN with the new-generation PIs carfilzomib (CFZ) and ixazomib (IZB). This study evaluated reports of PN encountered with all three PIs using the Food and Drug Administration Adverse Event (AE) Reporting System (FAERS). Signal disproportionality analysis was reported using the reporting odds ratio (ROR) with 95% confidence interval (CI). PN was reported in a total of 2.1%, 5.0%, and 10.9% of AEs with CFZ, IZB, and BTZ, respectively. The ROR (95% CI) for PN secondary to BTZ, CFZ, and IZB was 34.10 (32.76-35.49), 6.37 (5.50-7.37), and 14.97 (13.63-16.44), respectively. Compared to BTZ, CFZ and IZB have lower rates of reported PN, with RORs of 0.19 (0.16-0.22) and 0.48 (0.43-0.54), respectively.

Translated title of the contributionPost-marketing analysis of peripheral neuropathy burden with new-generation proteasome inhibitors using the fda adverse event reporting system
Original languageUndefined/Unknown
Pages (from-to)218-221
Number of pages4
JournalTurkish Journal of Hematology
Volume38
Issue number3
DOIs
StatePublished - 2021

Keywords

  • Multiple myeloma
  • Peripheral neuropathy
  • Proteasome inhibitors

ASJC Scopus subject areas

  • Hematology

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