Evidence map›Paper›PMID 35626140›Full record

ArticleCancers2022

Artificial Intelligence Enhances Diagnostic Flow Cytometry Workflow in the Detection of Minimal Residual Disease of Chronic Lymphocytic Leukemia.

Mohamed E Salama, Gregory E Otteson, Jon J Camp, Jansen N Seheult, Dragan Jevremovic, David R Holmes, Horatiu Olteanu, Min Shi

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Cytometry in High-Containment Laboratories.Methods in molecular biology (Clifton, N.J.) · 2024
    Review
  13. Deep Learning in Hematology: From Molecules to Patients.Clinical hematology international · 2024
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. 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

8 authors at 2 institutions in 1 country.

Mohamed E SalamaDivision of Hematopathology, Mayo Clinic, Rochester, MN 55905, USA.
Gregory E OttesonDivision of Hematopathology, Mayo Clinic, Rochester, MN 55905, USA.
Jon J CampBiomedical Imaging, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-8140-7210
Jansen N SeheultDivision of Hematopathology, Mayo Clinic, Rochester, MN 55905, USA.
Dragan JevremovicDivision of Hematopathology, Mayo Clinic, Rochester, MN 55905, USA.
David R HolmesBiomedical Imaging, Mayo Clinic, Rochester, MN 55905, USA.
Horatiu OlteanuDivision of Hematopathology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0001-5783-4485
Min ShiDivision of Hematopathology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-5741-4293
Mayo Clinic · USMayo Clinic in Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flow cytometric (FC) immunophenotyping is critical but time-consuming in diagnosing minimal residual disease (MRD). We evaluated whether human-in-the-loop artificial intelligence (AI) could improve the efficiency of clinical laboratories in detecting MRD in chronic lymphocytic leukemia (CLL). We developed deep neural networks (DNN) that were trained on a 10-color CLL MRD panel from treated CLL patients, including DNN trained on the full cohort of 202 patients (F-DNN) and DNN trained on 138 patients with low-event cases (MRD < 1000 events) (L-DNN). A hybrid DNN approach was utilized, with F-DNN and L-DNN applied sequentially to cases. “Ground truth” classification of CLL MRD was confirmed by expert analysis. The hybrid DNN approach demonstrated an overall accuracy of 97.1% (95% CI: 84.7−99.9%) in an independent cohort of 34 unknown samples. When CLL cells were reported as a percentage of total white blood cells, there was excellent correlation between the DNN and expert analysis [r > 0.999; Passing−Bablok slope = 0.997 (95% CI: 0.988−0.999) and intercept = 0.001 (95% CI: 0.000−0.001)]. Gating time was dramatically reduced to 12 s/case by DNN from 15 min/case by the manual process. The proposed DNN demonstrated high accuracy in CLL MRD detection and significantly improved workflow efficiency. Additional clinical validation is needed before it can be fully integrated into the existing clinical laboratory practice.

Indexed as

artificial intelligencechronic lymphocytic leukemiaflow cytometryminimal residual disease

Identifiers

PMID35626140
PMCPMC9139233
OpenAlexW4281254357

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.