Evidence map›Paper›PMID 21323738›Full record

ArticleEuropean journal of haematology2011

Analysis of CLLU1 expression levels before and after therapy in patients with chronic lymphocytic leukemia.

Anne Mette Buhl, Danelle F James, Donna Neuberg, Sonia Jain, Laura Z Rassenti, Thomas J Kipps

Open access · greenAbstract read
In one paragraph

Article in European journal of haematology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
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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

6 authors at 2 institutions in 2 countries.

Anne Mette Buhl *Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
Danelle F James *Division of Hematology/Oncology, Department of Medicine, Moores UCSD Cancer Center, University of California San Diego, La Jolla, CA.
Donna NeubergThe CLL Research Consortium, Dana-Farber Cancer Institute, Boston, MA.
Sonia JainDivision of Biostatistics and Bioinformatics, UCSD, La Jolla, CA, USA.
Laura Z RassentiDivision of Hematology/Oncology, Department of Medicine, Moores UCSD Cancer Center, University of California San Diego, La Jolla, CA.
Thomas J KippsDivision of Hematology/Oncology, Department of Medicine, Moores UCSD Cancer Center, University of California San Diego, La Jolla, CA.
University of California, San Diego · USDana-Farber Cancer Institute · US

Funding

Tissue CoreP01CA081534 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KIPPS, THOMAS J · 2000 to 2016
$59.5M
NCI NIH HHS P01 CA081534
6 · The paper itself

Abstract

objectiveChronic lymphocytic leukemia (CLL) is incurable, but therapy leading to eradication of minimal residual disease (MRD) in CLL is associated with improved clinical outcomes. CLL upregulated gene 1 (CLLU1) is solely upregulated in CLL patient samples. We hypothesized that CLLU1 could be used to monitor for residual disease in CLL patient samples after therapy.

methodsWe examined whether the CLLU1 real-time quantitative PCR (RQ-PCR) could detect small numbers of CLL cells in mixtures of normal peripheral blood mononuclear (PBMC) cells. We then performed a retrospective analysis on time-matched cryo-preserved specimens from patients who achieved MRD-negative remissions that underwent serial marrow biopsies for evaluation of residual disease by 4-color flow cytometry. RNA from PBMC samples collected at the time of the marrow assessments was analyzed for CLLU1. Nine patients underwent a total of 46 paired blood and marrow evaluations (median 5 assessments per patient).

resultsCLLU1 RQ-PCR on PBMCs of healthy donors reconstituted with varying amounts of CLL cells demonstrated leukemia cells could be reliably detected with high sensitivities depending on the CLLU1 expression level. Analysis of time-matched samples assessed for CLLU1 levels in the blood by RQ-PCR and residual disease of the marrow determined by 4-color flow cytometry revealed a correlation coefficient of 0.96 (P < 0.0001).

conclusionThe CLLU1 RQ-PCR is a sensitive and specific assay for detecting residual CLL cells after therapy. Assessment of blood CLLU1 levels can be used as a reliable marker of tumor burden and has the potential to complement currently used techniques for MRD monitoring in patients with CLL.

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBone MarrowFlow CytometryGene ExpressionHumansLeukemia, Lymphocytic, Chronic, B-CellMiddle AgedNeoplasm ProteinsNeoplasm, ResidualPolymerase Chain ReactionReference ValuesRetrospective StudiesRNA, Long NoncodingTumor BurdenBiomarkers, TumorCLLU1 lncRNA, humanNeoplasm ProteinsRNA, Long Noncoding

Identifiers

PMID21323738
PMCPMC4114228
OpenAlexW1832105008

What OpenQuestion holds

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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.