Evidence map›Paper›PMID 39562715›Full record

ArticleBone marrow transplantation2025

High-dose chemotherapy with autologous haematopoietic stem cell transplantation in patients with isolated vitreoretinal lymphoma: a LOC network study.

Adam Mainguy, Carole Soussain, Valérie Touitou, Amin Bennedjai, Laurent Kodjikian, Hervé Ghesquières, Gandhi Damaj, Rémy Gressin, Jean-Baptiste Ducloyer, Olivier Chinot and 15 more

Abstract read
In one paragraph

Article in Bone marrow transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. 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

25 authors.

Adam MainguySorbonne Université, Department of Ophthalmology, Pitié-Salpêtrière University Hospital, Paris, France. adam.mainguy@gmail.com.ORCID 0000-0003-0871-7834
Carole SoussainDepartment of Hematology, Institut Curie, site de Saint-Cloud, Saint-Cloud, France.ORCID 0000-0002-2479-0348
Valérie TouitouSorbonne Université, Department of Ophthalmology, Pitié-Salpêtrière University Hospital, Paris, France.
Amin BennedjaiSorbonne Université, Department of Ophthalmology, Pitié-Salpêtrière University Hospital, Paris, France.
Laurent KodjikianDepartment of Ophthalmology, Lyon University Hospital, Lyon, France.
Hervé GhesquièresDepartment of Hematology, Lyon University Hospital, Lyon, France.
Gandhi DamajDepartment of Hematology, Caen University Hospital, Caen, France.ORCID 0000-0002-4689-3882
Rémy GressinDepartment of Hematology, Grenoble University Hospital, Grenoble, France.ORCID 0000-0002-9188-3501
Jean-Baptiste DucloyerNantes University, CHU Nantes, ophthalmology department, Inserm, CIC 1413, Nantes, France.
Olivier ChinotDepartment of Neurooncology, Marseille, University Hospital, Marseille, France.
Anaïs VautierAngers University, Department of Ophthalmology, Angers University Hospital, Angers, France.
Cécile Moluçon-ChabrotDepartment of Hematology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.ORCID 0000-0003-1948-5258
Guido AhleDepartment of Neurology, Hospices Civils de Colmar, Colmar, France.ORCID 0000-0002-0877-2289
Luc TaillandierDepartment of Neurology, Nancy University Hospital, Nancy, France.
Jean Pierre MarolleauDepartment of Hematology, Amiens University Hospital, Amiens, France.
Adrien ChauchetDepartment of Hematology, Besançon University Hospital, Besançon, France.
Fabrice JardinDepartment of Hematology, Centre Henri Becquerel, Rouen, France.
Nathalie CassouxDepartment of Ophthalmology, Institut Curie, site de Saint-Cloud, Saint-Cloud, France.
Denis MalaiseDepartment of Ophthalmology, Institut Curie, site de Saint-Cloud, Saint-Cloud, France.ORCID 0000-0001-7454-819X
Adélaïde ToutéeSorbonne Université, Department of Ophthalmology, Pitié-Salpêtrière University Hospital, Paris, France.
Sara TouhamiSorbonne Université, Department of Ophthalmology, Pitié-Salpêtrière University Hospital, Paris, France.
Magali Le Garff-TavernierDepartment of Hematology, Pitié-Salpêtrière University Hospital, APHP, Sorbonne Université, Paris, France.
Khê Hoang-XuanDepartment of Neurooncology, Pitié-Salpêtrière University Hospital, APHP, Sorbonne Université, Inserm, CNRS, UMR S1127, ICM, IHU, Paris, France.
Sylvain ChoquetDepartment of Clinical Hematology, Pitié-Salpêtrière University Hospital, APHP, Sorbonne Université, Paris, France.ORCID 0000-0002-7791-0470
Caroline HouillierDepartment of Neurooncology, Pitié-Salpêtrière University Hospital, APHP, Sorbonne Université, Inserm, CNRS, UMR S1127, ICM, IHU, Paris, France.ORCID 0000-0003-2931-7522

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite its indolent evolution, vitreoretinal lymphoma (VRL) has a poor prognosis due to a major risk of relapse in the central nervous system (CNS) and may necessitate aggressive therapy. However, the use of high-dose chemotherapy with autologous stem cell transplantation (HCT-ASCT) is poorly documented. We retrospectively analysed from the French LOC network database the adult immunocompetent patients treated with HCT-ASCT for isolated VRL. Thirty-eight patients underwent consolidation with HCT-ASCT for isolated VRL between 2008 and 2019 after induction chemotherapy. Twenty patients had primary VRL, and 18 had an isolated VRL relapse of a primary CNS lymphoma. Three patients underwent HCT-ASCT in first-line treatment, 24 in second-line treatment, and 11 in subsequent lines. At HCT-ASCT, the median age was 61 years, and the median KPS was 90. Thirty-two patients (84%) received high-dose thiotepa-based HCT. One patient (3%) died from HCT-ASCT toxicity. Nineteen (50%) patients relapsed after HCT-ASCT, including 17 cases occurring in the brain. The median progression-free survival, brain-free survival and overall survival from HCT-ASCT were 96, 113 and 92 months, respectively. HCT-ASCT represents an effective therapeutic strategy for select VRL patients, with a tolerable safety profile. However, the risk of subsequent brain relapse remains significant.

Indexed as

Hematopoietic Stem Cell TransplantationRetinal NeoplasmsTransplantation, AutologousAdultAgedFemaleHumansMaleMiddle AgedRetrospective Studies

Identifiers

PMID39562715
PMCPMC11893470

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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.