Clinical and cost outcomes of pre-emptive plerixafor administration in patients with multiple myeloma undergoing stem cell mobilization.

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ID: 28447
2019
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Abstract
The stem cell mobilization agent plerixafor significantly improves CD34 stem cell procurement in patients with multiple myeloma undergoing autologous stem cell transplant. We compared mobilization success rates and costs of two regimens of plerixafor administration: pre-emptive (P-PL, initiated the evening prior to the first day of stem cell collection) and standard (S-PL, initiated the evening prior to the second day of stem cell collection in the event of inadequate collection on the first day).Patients with multiple myeloma undergoing mobilization were categorized as either P-PL or S-PL. Stem cell collection success was evaluated using logistic regression models. Associated costs were aggregated in terms of average collections per patient in each mobilization option (patient level), and escalated to a panel of 5000 patients (population level).299 patients were evaluable; 241 received P-PL and 58 received S-PL. Patients receiving P-PL had higher median CD34 count pre-collection and higher median total CD34 cell harvest on the first collection (6.75 × 10/kg for P-PL, 1.96 × 10/kg for S-PL; P<0.01). In multivariable analyses, P-PL remained significantly associated with the ability to collect ≥2 × 10/kg CD34 on the first day (OR = 4.05, 95% CI, 1.19-13.83, P = 0.03) and ≥5x10/kg CD34 in total (OR = 3.09, 95% CI, 1.04-9.23, P = 0.04). P-PL saved $11,248 (46%) per patient compared with S-PL.P-PL significantly enhanced collection efficiency, with most patients completing collection in 1 day, resulting in substantial cost savings.
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andritsos2019clinicalleukemia Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Andritsos, Leslie A;Huang, Ying;Abraham, Ivo;Huff, Keith;Scrape, Scott R;Fan, Tao;Alkhatib, Nimer;Hofmeister, Craig C;Drea, Edward;McBride, Ali;
Journal Leukemia research
Year 2019
DOI
S0145-2126(19)30160-2
URL
Keywords Keywords not found

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