Evidence map›Paper›PMID 40079767›Full record

ArticleActa dermato-venereologica2025

Systemic Targeted Therapies in Patients with Relapsed/Refractory Advanced Stage Cutaneous T-cell Lymphoma: A Real-world Single-centre Case Series.

Signe Hedebo, Martin B Pedersen, Lise M Lindahl, Aska Drjlevic-Nielsen, Claus Johansen, Francesco D'Amore, Lars Iversen, Rikke Bech

Abstract read
In one paragraph

Article in Acta dermato-venereologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Subcutaneous Panniculitis-Like T-Cell Lymphoma in Children: Two Case Reports.Clinical, cosmetic and investigational dermatology · 2025
    Article
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.

Signe HedeboDepartment of Dermatology and Venereology Aarhus University Hospital, Aarhus, Denmark; Aarhus University, Aarhus, Denmark. siheha@rm.dk.ORCID 0009-0006-2481-035X
Martin B PedersenAarhus University, Aarhus, Denmark; Department of Hematology Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0001-8261-2374
Lise M LindahlAarhus University, Aarhus, Denmark.
Aska Drjlevic-NielsenDepartment of Dermatology and Venereology Aarhus University Hospital, Aarhus, Denmark; Aarhus University, Aarhus, Denmark.
Claus JohansenDepartment of Dermatology and Venereology Aarhus University Hospital, Aarhus, Denmark; Aarhus University, Aarhus, Denmark.ORCID 0000-0003-0240-5127
Francesco D'AmoreAarhus University, Aarhus, Denmark; Department of Hematology Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0002-4032-6633
Lars IversenDepartment of Dermatology and Venereology Aarhus University Hospital, Aarhus, Denmark; Aarhus University, Aarhus, Denmark; MC2 Therapeutics, Hoersholm, Denmark.ORCID 0000-0003-1816-4508
Rikke Bech1Department of Dermatology and Venereology Aarhus University Hospital, Aarhus, Denmark; Aarhus University, Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous T-cell lymphomas are a heterogeneous group of non-Hodgkin lymphomas. Early stages are often controlled with skin-directed therapy, such as topical corticosteroids, topical chlormethine gel, or UV therapy, whereas advanced stages often warrant a more aggressive approach with systemic antibody targeted therapy including mogamulizumab, brentuximab vedotin, or alemtuzumab. A retrospective cohort case series of 27 patients from Aarhus University Hospital, Denmark is presented, evaluating real-world outcomes of patients with cutaneous T-cell lymphomas treated with intravenous systemic targeted therapies from 2013 to 2023. The median age was 72 and the majority had Sézary syndrome or mycosis fungoides. All patients had relapsed/refractory advanced stage cutaneous T-cell lymphoma. Six patients received mogamulizumab, 12 patients received brentuximab vedotin, and 15 patients received alemtuzumab. Six patients received more than 1 of the systemic targeted treatments. Overall response rates were 78% for mogamulizumab, 65% for brentuximab vedotin, and 61% for alemtuzumab. Median time to progression was 2.5, 4, and 11 months, respectively. In conclusion, this paper offers a unique perspective on the complexities of clinical practice when managing advanced-stage cutaneous T-cell lymphomas and demonstrates the effectiveness of the therapies described, with particular emphasis on the promising results observed with alemtuzumab administered in a low-dose protocol.

Indexed as

AlemtuzumabAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBrentuximab VedotinLymphoma, T-Cell, CutaneousMycosis FungoidesNeoplasm Recurrence, LocalSezary SyndromeSkin NeoplasmsAgedAged, 80 and overDenmarkFemaleHumansMaleMiddle AgedAlemtuzumabAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBrentuximab Vedotinmogamulizumab

Identifiers

PMID40079767
PMCPMC13062062

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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.