Evidence map›Paper›PMID 26310541›Full record

ArticleLeukemia2016

Risk of non-hematologic cancer in individuals with high-count monoclonal B-cell lymphocytosis.

B M Solomon, K G Chaffee, J Moreira, S M Schwager, J R Cerhan, T G Call, N E Kay, S L Slager, T D Shanafelt

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Risk of Incident Melanoma Among Individuals With Low-Count Monoclonal B-Cell Lymphocytosis.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  4. Article
  5. Clinical Risks for Chronic Lymphocytic Leukemia.Journal of the National Comprehensive Cancer Network : JNCCN · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Chronic Lymphocytic Leukemia.Cold Spring Harbor perspectives in medicine · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. The Treatment of Chronic Lymphatic Leukemia.Deutsches Arzteblatt international · 2019
    Review
  20. Review
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 4 institutions in 1 country.

B M SolomonUniversity of South Dakota Sanford School of Medicine, Vermillion, SD, USA.
K G ChaffeeMayo Clinic Department of Health Sciences Research, Rochester, MN, USA.
J MoreiraNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
S M SchwagerMayo Clinic Department of Medicine, Rochester, MN, USA.
J R CerhanMayo Clinic Department of Health Sciences Research, Rochester, MN, USA.
T G CallMayo Clinic Department of Medicine, Rochester, MN, USA.
N E KayMayo Clinic Department of Medicine, Rochester, MN, USA.
S L SlagerMayo Clinic Department of Health Sciences Research, Rochester, MN, USA.
T D ShanafeltMayo Clinic Department of Medicine, Rochester, MN, USA.
Mayo Clinic in Arizona · USMayo Clinic in Florida · USAvera Health · USNorthwestern University · US

Funding

Molecular Epidemiology of NHL and CLLR01CA092153 · NCI · MAYO CLINIC ROCHESTER · PI CERHAN, JAMES R · 2003 to 2012
$6.7M
NCI NIH HHS R01 CA092153NCI NIH HHS R01 CA92153
6 · The paper itself

Abstract

It is unknown whether individuals with monoclonal B-cell lymphocytosis (MBL) are at risk for adverse outcomes associated with chronic lymphocytic leukemia (CLL), such as the risk of non-hematologic cancer. We identified all locally residing individuals diagnosed with high-count MBL at Mayo Clinic between 1999 and 2009 and compared their rates of non-hematologic cancer with that of patients with CLL and two control cohorts: general medicine patients and patients who underwent clinical evaluation with flow cytometry but who had no hematologic malignancy. After excluding individuals with prior cancers, there were 107 high-count MBL cases, 132 CLL cases, 589 clinic controls and 482 flow cytometry controls. With 4.6 years median follow-up, 14 (13%) individuals with high-count MBL, 21 (4%) clinic controls (comparison MBL P<0.0001), 18 (4%) flow controls (comparison MBL P=0.0001) and 16 (12%) CLL patients (comparison MBL P=0.82) developed non-hematologic cancer. On multivariable Cox regression analysis, individuals with high-count MBL had higher risk of non-hematologic cancer compared with flow controls (hazard ratio (HR)=2.36; P=0.04) and borderline higher risk compared with clinic controls (HR=2.00; P=0.07). Patients with high-count MBL appear to be at increased risk for non-hematologic cancer, further reinforcing that high-count MBL has a distinct clinical phenotype despite low risk of progression to CLL.

Indexed as

B-LymphocytesAdolescentAdultAgedAged, 80 and overFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellLymphocytosisMaleMiddle AgedNeoplasmsProportional Hazards ModelsRisk

Identifiers

PMID26310541
PMCPMC4839962
OpenAlexW1873634461

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.