Evidence map›Paper›PMID 26475754›Full record

ArticleCytotherapy2015

Hematopoietic progenitor cell mobilization with "just-in-time" plerixafor approach is a cost-effective alternative to routine plerixafor use.

Lauren Veltri, Aaron Cumpston, Alexandra Shillingburg, Sijin Wen, Jin Luo, Sonia Leadmon, Kathy Watkins, Michael Craig, Mehdi Hamadani, Abraham S Kanate

Open access · greenAbstract read
In one paragraph

Article in Cytotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Lauren VeltriSection of Hematology/Oncology, Department of Internal Medicine, West Virginia University, Morgantown, West Virginia, USA.
Aaron CumpstonDepartment of Pharmacy, West Virginia University, Morgantown, and West Virginia Osborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia, USA.
Alexandra ShillingburgDepartment of Pharmacy, West Virginia University, Morgantown, and West Virginia Osborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia, USA.
Sijin WenDepartment of Biostatistics, West Virginia University, Morgantown, West Virginia, USA.
Jin LuoDepartment of Biostatistics, West Virginia University, Morgantown, West Virginia, USA.
Sonia LeadmonOsborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia, USA.
Kathy WatkinsOsborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia, USA.
Michael CraigOsborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia, USA.
Mehdi HamadaniDivision of Hematology-Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Abraham S KanateOsborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, West Virginia, USA. Electronic address: askanate@hsc.wvu.edu.
West Virginia University · USMedical College of Wisconsin · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
NIGMS NIH HHS U54 GM104942NIGMS NIH HHS U54GM104942
6 · The paper itself

Abstract

BACKGROUND

aimsHematopoietic cell mobilization with granulocyte-colony stimulating factor (G-CSF) and plerixafor results in superior CD34+ cell yield compared with G-CSF alone in patients with myeloma and lymphoma. However, plerixafor-based approaches may be associated with high costs. Several institutions use a "just-in-time" plerixafor approach, in which plerixafor is only administered to patients likely to fail mobilization with G-CSF alone. Whether such an approach is cost-effective is unknown.

methodsWe evaluated 136 patients with myeloma or lymphoma who underwent mobilization with 2 approaches of plerixafor utilization. Between January 2010 and October 2012, 76 patients uniformly received mobilization with G-CSF and plerixafor. Between November 2012 and June 2014, 60 patients were mobilized with plerixafor administered only to those patients likely to fail mobilization with G-CSF alone.

resultsThe routine plerixafor group had a higher median peak peripheral blood CD34+ cell count (62 versus 29 cells/μL, P < 0.001) and a higher median day 1 CD34+ yield (2.9 × 10(6) CD34+ cells/kg versus 2.1 × 10(6) CD34+ cells/kg, P = 0.001). The median total CD34+ collection was higher with routine plerixafor use (5.8 × 10(6) CD34+ cells/kg versus 4.5 × 10(6) CD34+ cells/kg, P = 0.007). In the "just-in-time" group, 40% (n = 24) completed adequate collection without plerixafor. There was no difference in mobilization failure rates. The mean plerixafor doses used was lower with "just-in-time" approach (1.3 versus 2.1, P = 0.0002). The mean estimated cost in the routine plerixafor group was higher (USD 27,513 versus USD 23,597, P = 0.01). DISCUSSION: Our analysis demonstrates that mobilization with a just-in-time plerixafor approach is a safe, effective, and cost-efficient strategy for HPC collection.

Indexed as

AdultAgedAntigens, CD34BenzylaminesCost-Benefit AnalysisCyclamsFemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHeterocyclic CompoundsHumansLymphomaMaleMiddle AgedMultiple MyelomaAntigens, CD34BenzylaminesCyclamsGranulocyte Colony-Stimulating FactorHeterocyclic Compoundsplerixaforautologous transplantationcostjust in timemobilizationplerixafor

Identifiers

PMID26475754
PMCPMC4700501
OpenAlexW2185365349

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.