Evidence map›Paper›PMID 31358485›Full record

ArticleClinical lymphoma, myeloma & leukemia2019

A Phase I Study of the Safety and Feasibility of Bortezomib in Combination With G-CSF for Stem Cell Mobilization in Patients With Multiple Myeloma.

Armin Ghobadi, Mark A Fiala, Michael Rettig, Mark Schroeder, Geoffrey L Uy, Keith Stockerl-Goldstein, Peter Westervelt, Ravi Vij, John F DiPersio

Abstract readClinical Trial, Phase I
In one paragraph

Article in Clinical lymphoma, myeloma & leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Armin GhobadiDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO. Electronic address: arminghobadi@wustl.edu.
Mark A FialaDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Michael RettigDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Mark SchroederDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Geoffrey L UyDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Keith Stockerl-GoldsteinDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Peter WesterveltDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Ravi VijDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
John F DiPersioDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Washington University in St. Louis · US

Funding

Washington University Institute of Clinical and Translational Sciences (KL2) KL2TR002346 · NCATS · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 2017 to 2026
$14.0M
BM NICHE DISRUPTION AND IMMUNOTHERAPY IN HEMATOLOGICAL MALIGNANCIESR50CA211466 · NCI · WASHINGTON UNIVERSITY · PI Michael Rettig · 2016 to 2026
$2.3M
NCATS NIH HHS KL2 TR002346NCI NIH HHS R50 CA211466
6 · The paper itself

Abstract

backgroundWe previously reported that administration of bortezomib (BTZ) after 4 days of granulocyte colony-stimulating factor (G-CSF) significantly augments mobilization in mice. We hypothesized that administration of BTZ at peak G-CSF mobilization in patients with multiple myeloma (MM) would be safe, augment mobilization, and have an in vivo purging effect on circulating myeloma cells. PATIENTS AND

methodsThis was a phase I study using 3 dose levels of BTZ. G-CSF was administered for 5 days. On the evening of the fourth day, a single dose of BTZ was administered. Peripheral blood was drawn 1 to 2 hours before and 15 to 18 hours after BTZ administration (before day 5 G-CSF administration) to analyze the mobilization effect of BTZ. Standard apheresis was then performed starting on day 5. After mobilization, patients underwent autologous stem cell transplantation (ASCT) per institutional guidelines.

resultsTen patients were enrolled. There were no dose-limiting toxicities. Median peripheral blood CD34

conclusionAdministration of 1 dose of BTZ at peak G-CSF mobilization was safe and well tolerated, enhanced stem cell mobilization, and did not affect graft viability. The mobilization effect of BTZ at peak G-CSF mobilization shown in this phase I study needs to be confirmed in a larger randomized trial.

Indexed as

AgedAntigens, CD34Antineoplastic Combined Chemotherapy ProtocolsBortezomibFeasibility StudiesFemaleGraft SurvivalGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedMultiple MyelomaOutcome Assessment, Health CareAntigens, CD34BortezomibGranulocyte Colony-Stimulating FactorAutologous stem cell transplantationBortezomibG-CSFMobilizationMultiple myeloma

Identifiers

PMID31358485
PMCPMC7497838
OpenAlexW2942967291

What OpenQuestion holds

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Registered trials

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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.