Evidence map›Paper›PMID 35406431›Full record

ArticleCancers2022

Impact of Mogamulizumab in Real-Life Advanced Cutaneous T-Cell Lymphomas: A Multicentric Retrospective Cohort Study.

Marie Jouandet, Inès Nakouri, Lawrence Nadin, Alice Kieny, Mahtab Samimi, Henri Adamski, Gaëlle Quéreux, Guillaume Chaby, Anne Dompmartin, Jean-Matthieu L'Orphelin

Abstract 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Clinical and Real-World Effectiveness of Mogamulizumab: A Narrative Review.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Review
  7. 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

10 authors.

Marie JouandetDepartment of Dermatology, Caen-Normandie University Hospital, 14000 Caen, France.
Inès NakouriDepartment of Dermatology, Caen-Normandie University Hospital, 14000 Caen, France.
Lawrence NadinBiostatistics and Clinical Research Unit, Caen-Normandy University Hospital, 14000 Caen, France.
Alice KienyDepartment of Dermatology, Strasbourg Civil Hospital, 67000 Strasbourg, France.
Mahtab SamimiDepartment of Dermatology, Centre Hospitalier Régional et Universitaire de Tours, 37000 Tours, France.
Henri AdamskiDepartment of Dermatology, Centre Hospitalier Universitaire Ponchaillou, 35000 Rennes, France.
Gaëlle QuéreuxDepartment of Dermatology, Nantes University Hospital, 44000 Nantes, France.
Guillaume ChabyDepartment of Dermatology, Amiens-Picardie University Hospital, 80000 Amiens, France.
Anne DompmartinDepartment of Dermatology, Caen-Normandie University Hospital, 14000 Caen, France.
Jean-Matthieu L'OrphelinDepartment of Dermatology, Caen-Normandie University Hospital, 14000 Caen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvanced mycosis fungoides (MF) and Sézary syndrome (SS) are rare, aggressive cutaneous T-cell lymphomas that may be difficult to treat. Mogamulizumab is a recent monoclonal antibody targeting the CCR4 receptor expressed on the surface of Sézary cells. It can be prescribed in MF/SS stages III to IV in the second line after systemic therapy or in stages IB-II after two unsuccessful systemic therapies. We lack data on long-term efficiency and potential side effects in real-life conditions. Our study aims to determine efficacy considering the median PFS of advanced CTCL with mogamulizumab. Secondary objectives were to consider tolerance and estimate delay until side effects appeared.

methodsData on patients with advanced cutaneous T-cell lymphomas were collected since French Authorization, in six French university hospitals. Patients were followed until they stopped mogamulizumab because of relapse or toxicity. For those still treated by mogamulizumab, the end point was 1 September 2021. We excluded 3 patients as they had already been included in the MAVORIC study and data was not available.

resultsThe median time of follow-up was 11.6 months. Of the 21 patients included, we reported four full-response patients, eight in partial response, one in stability, three in progression, and five were deceased. One patient had visceral progression, and seven had new lymphadenopathy. Progression-free survival was estimated at 22 months. Twenty patients presented adverse events, of which 10 were severe, i.e., grade III-IV. The median time between the introduction of mogamulizumab and the first adverse event was 21 days.

conclusionsOur study suggests that mogamulizumab can give patients with advanced refractory CTCL a consequent PFS, estimated at 22 months. The long-term safety of mogamulizumab was determined to be acceptable since we reported few grade III-IV AEs, comparable with other studies. No other study using real-life data has been performed to investigate the AEs of mogamulizumab.

Indexed as

adverse eventscutaneous T-cell lymphomamogamulizumabmycosis fungoidesSézary

Identifiers

PMID35406431
PMCPMC8996883

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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.