Evidence map›Paper›PMID 39668908›Full record

ArticleDermatologic therapy2024

Increased Risk of Cutaneous T-Cell Lymphoma Development after Dupilumab Use for Atopic Dermatitis.

Jenna Mandel, Jaanvi Mehta, Ramsay Hafer, Mahaa Ayub, Faria Nusrat, Henry Yang, Pierluigi Porcu, Neda Nikbakht

Abstract read
In one paragraph

Article in Dermatologic therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Cutaneous T-cell lymphomas and dupilumab for atopic dermatitis: A systematic review and expert consensus.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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.

Jenna MandelDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
Jaanvi MehtaDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
Ramsay HaferDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
Mahaa AyubDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
Faria NusratDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
Henry YangDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.
Pierluigi PorcuDivision of Hematologic Malignancies and Cellular Therapy, Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA, USA.
Neda NikbakhtDepartment of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA, USA.

Funding

The malignant microenvironment in early cutaneous T-cell lymphomaR03CA252818 · NCI · THOMAS JEFFERSON UNIVERSITY · PI NIKBAKHT, NEDA · 2021 to 2022
$156k
NCI NIH HHS R03 CA252818
6 · The paper itself

Abstract

There have been several reports of dupilumab use and the development of CTCL; however, the risk of CTCL development has not been adequately evaluated at the population level. The objective of this study is to determine whether dupilumab administration for AD is associated with an increased risk of developing CTCL and to identify at-risk populations within this group. This retrospective cohort study used TriNetX, a deidentified medical record database including over 107 million patients, to identify eligible patients. Treatment and control groups were evaluated for the development of CTCL. Patients of any age with a documented diagnosis of AD were included. The treatment cohort included individuals treated with dupilumab, while the control cohort included AD patients treated with alternative therapies. Selected biologics were excluded from both groups. Subgroup analyses were performed to evaluate three age groups and to identify whether the risk of CTCL development was higher within a given time frame after starting dupilumab. We identified a total of 1,181,533 patients with AD. Of these, 19,612 patients were prescribed dupilumab. Both treatment and control groups included 19,612 patients matched for age, race, and sex. The mean age was 32.3 years (

Identifiers

PMID39668908
PMCPMC11635927

What OpenQuestion holds

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Registered trials

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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.