Evidence map›Paper›PMID 11704789›Full record

ArticleBone marrow transplantation2001

Gene scanning of VDJH-amplified segments is a clinically relevant technique to detect contaminating tumor cells in the apheresis products of multiple myeloma patients undergoing autologous peripheral blood stem cell transplantation.

R López-Pérez, R García-Sanz, D González, A Balanzategui, M C Chillón, I Alaejos, M V Mateos, M D Caballero, M Corral, A Orfão and 2 more

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Article in Bone marrow transplantation, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

R López-PérezHaematology Service, University Hospital of Salamanca and Centre for Cancer Research of Salamanca, Paseo de San Vicente, 58-182, Salamanca, 37007, Spain.
R García-Sanz
D González
A Balanzategui
M C Chillón
I Alaejos
M V Mateos
M D Caballero
M Corral
A Orfão
M González
J F San Miguel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contaminating tumour cells in apheresis products have proved to influence the outcome of patients with multiple myeloma (MM) undergoing autologous stem cell transplantation (APBSCT). The gene scanning of clonally rearranged VDJ segments of the heavy chain immunoglobulin gene (VDJH) is a reproducible and easy to perform technique that can be optimised for clinical laboratories. We used it to analyse the aphereses of 27 MM patients undergoing APBSCT with clonally detectable VDJH segments, and 14 of them yielded monoclonal peaks in at least one apheresis product. The presence of positive results was not related to any pre-transplant characteristics, except the age at diagnosis (lower in patients with negative products, P = 0.04). Moreover, a better pre-transplant response trended to associate with a negative result (P = 0.069). Patients with clonally free products were more likely to obtain a better response to transplant (complete remission, 54% vs 28%; >90% reduction in the M-component, 93% vs 43% P = 0.028). In addition, patients transplanted with polyclonal products had longer progression-free survival, (39 vs 19 months, P = 0.037) and overall survival (81% vs 28% at 5 years, P = 0.045) than those transplanted with monoclonal apheresis. In summary, the gene scanning of apheresis products is a useful and clinically relevant technique in MM transplanted patients.

Indexed as

Blood Component RemovalGene Rearrangement, B-Lymphocyte, Heavy ChainHematopoietic Stem Cell TransplantationAdultAntineoplastic Combined Chemotherapy ProtocolsBone Marrow PurgingCell CountClone CellsCombined Modality TherapyCyclophosphamideDexamethasoneDisease-Free SurvivalGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHumansImmunophenotypingCyclophosphamideDexamethasoneGranulocyte Colony-Stimulating FactorInterferonsMyeloma Proteins

Identifiers

PMID11704789

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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.