AI Article Synopsis

  • Granulocyte-colony stimulating factors (G-CSFs) like Lenograstim and Filgrastim are evaluated for their impact on stem cell mobilization and recovery post-transplant.
  • A study involving 248 patients receiving autologous hematopoietic stem cell transplants found that Lenograstim resulted in a higher number of harvested CD34 cells and fewer G-CSF vials used compared to Filgrastim.
  • The use of Lenograstim also led to faster recovery times and significant cost savings per patient due to reduced hospitalization and lower incidence of adverse events.

Article Abstract

Purpose: Granulocyte-colony stimulating factors (G-CSFs) are widely used to mobilize CD34 stem cells and to support the engraftment after hematopoietic stem cell transplantation (HSCT). A budget impact analysis and an incremental cost-effectiveness study of two G-CSFs (Lenograstim and Filgrastim biosimilar), considering engraftment, number of hospitalization days and number of G-CSF vials administered were performed.

Patients And Methods: Between 2009 and 2016, 248 patients undergoing autologous HSCT have been evaluated and divided into three groups (100 Leno-Leno, 93 Leno-Fil, 55 Fil-Fil) according to the type of G-CSF used for hematopoietic stem cell mobilization and hematopoietic stem cell recovery after transplant.

Results: The following statistically significant differences have been observed between Leno-Leno, Leno-Fil, Fil-Fil groups: a higher number of harvested CD34 cells (10.56 vs 8.00 vs 7.20; p=0.0003) and a lower number of G-CSF vials (8 vs 8 vs 9; p=0.00020) used for full bone marrow recovery favoring Lenograstim. No statistically significant differences were found regarding the number of G-CSF vials used for mobilization, apheresis number and CD34 cell peak. The post-transplant hematological recovery was faster in Lenograstim group than Filgrastim group: median time to neutrophil count engraftment (>500/mmc) was 12 vs 13 days; median time for platelets recovery (>20.000/mmc) was 12 vs 15 days (p=0.0001). The use of Lenograstim achieved cost savings of €566/patient over Filgrastim biosimilar, related to a decreased number of days of hospitalization (16 vs 17 days; p=0.00012), a lower overall incidence of adverse events, laboratory tests, transfusions for platelet recovery following discharge.

Conclusion: In our experience, Lenograstim outperforms Filgrastim in terms of effectiveness and lower cost. This study shows a clinical superiority of Lenograstim over Filgrastim suggesting a potential cost savings favoring Lenograstim.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7135199PMC
http://dx.doi.org/10.2147/JBM.S224173DOI Listing

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