AI Article Synopsis

  • Blinatumomab (Blincyto) is a bispecific T-cell engaging antibody used to treat relapsed/refractory acute lymphoblastic leukemia and is delivered through continuous infusion, typically at home.
  • The study focused on potential leakage of blinatumomab due to administration device issues, and found no damage to the filter after testing with the drug solution.
  • However, it was noted that physical stimulation of the infusion solution can cause the formation of precipitate on filters, suggesting that care should be taken during long-term administration to ensure safety and efficacy.

Article Abstract

Blinatumomab (Blincyto injection solution) is classified as a bispecific T-cell engaging (BiTE) antibody and is intended for the treatment of relapsed/refractory acute lymphoblastic leukemia. It requires continuous infusion to maintain therapeutic levels. Therefore, it is often administered at home. Monoclonal antibodies, which are administered intravenously, have the potential to leak depending on the nature of the administration devices. Therefore, we investigated device-associated causes of blinatumomab leakage. We observed no apparent changes to the filter and its materials after exposure to the injection solution and surfactant. From scanning electron microscopic images, precipitate on the surface of the filters was observed after physical stimulation of the injection solution. Therefore, physical stimulations should be avoided during the prolonged administration of blinatumomab. In conclusion, the findings of this study assist in the safe administration of antibodies using portable infusion pumps, taking into consideration the composition of drug excipients and the choice of filter type and structure.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052184PMC
http://dx.doi.org/10.3390/ijms24065729DOI Listing

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