Evidence map›Paper›PMID 36523150›Full record

ArticleCancer2023

Staging lymph nodes and blood at diagnosis in mycosis fungoides identifies patients at increased risk of progression to advanced stage: A retrospective cohort study.

Pamela B Allen, Ashley A McCook-Veal, Jeffrey M Switchenko, Darina M Paulino, Tim Niyogusaba, Katelin M Baird, Erica S Tarabadkar, Mary Jo Lechowicz

Open access · greenAbstract read
In one paragraph

Article in Cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 10 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

8 authors at 2 institutions in 1 country.

Pamela B AllenDepartment of Hematology, Winship Cancer Institute, Atlanta, Georgia, USA.ORCID 0000-0002-3959-3662
Ashley A McCook-VealDepartments of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.
Jeffrey M SwitchenkoDepartments of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-5563-9325
Darina M PaulinoDepartment of Hematology, Winship Cancer Institute, Atlanta, Georgia, USA.
Tim NiyogusabaDepartment of Hematology, Winship Cancer Institute, Atlanta, Georgia, USA.
Katelin M BairdDepartment of Hematology, Winship Cancer Institute, Atlanta, Georgia, USA.
Erica S TarabadkarDepartment of Hematology, Winship Cancer Institute, Atlanta, Georgia, USA.
Mary Jo LechowiczDepartment of Hematology, Winship Cancer Institute, Atlanta, Georgia, USA.
Piedmont Cancer Institute · USEmory University · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
NCI NIH HHS L30 CA242774NCI NIH HHS P30 CA138292NIH HHS P30CA138292
6 · The paper itself

Abstract

backgroundRisk factors for progression to advanced-stage mycosis fungoides (MF) are poorly defined.

methodsThe authors performed a single-center, retrospective cohort study among patients with MF at an academic medical center from 1990 to 2020 to identify clinical variables associated with progression to advanced-stage MF (stage IIB-IVB), and 388 patients who had a clinicopathologic diagnosis of early stage (IA-IIA) MF were identified from their cutaneous lymphoma database. Baseline clinical characteristics, laboratory values, imaging, and blood flow cytometry or T-cell receptor gene rearrangement (TCR) data were collected. Logistic regression was used to assess risk factors associated with progression.

resultsOverall, 93 of 388 patients (24.0%) progressed to advanced stage. Patients who progressed had an increased risk of death (hazard ratio, 4.50; 95% CI, 2.89-7.00; p < .001). Progression was associated with a higher overall stage at diagnosis, tumor stage, lymph node stage, low-level blood involvement, as measured with TCR data and/or flow cytometry, and elevated lactate dehydrogenase (LDH). Limitations included missing data for LDH, imaging, peripheral blood TCR data, or flow cytometry assessed at diagnosis.

conclusionsStaging and baseline laboratory assessments with imaging, peripheral blood flow cytometry, TCR data, and LDH in patients who have newly diagnosed MF may identify those who are at risk for progression to advanced stage.

Indexed as

Mycosis FungoidesSezary SyndromeSkin NeoplasmsHumansLymph NodesNeoplasm StagingPrognosisReceptors, Antigen, T-CellRetrospective StudiesReceptors, Antigen, T-Celladvanced stagecutaneous T-cell lymphomaflow cytometrymycosis fungoidesprogressionSezary syndrome

Identifiers

PMID36523150
PMCPMC9852075
OpenAlexW4311677761

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.