Evidence map›Paper›PMID 40985869›Full record

ArticleInternational journal of cancer2026

Adult T-cell leukemia/lymphoma in French Guiana (1990-2019): Epidemiology, clinical features, and HTLV-1 genetic diversity in the two main ethnic populations.

Jill-Léa Ramassamy, Patricia Tortevoye, Balthazar Ntab, Gabriel Carles, Jean-Pierre Droz, Pierre Couppié, Giovanni Begliomini, Jean-Francois Carod, N'detodji-Bill Wankpo, Karim Abdelmoumen and 7 more

Abstract read
In one paragraph

Article in International journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

17 authors.

Jill-Léa RamassamyInstitut Pasteur, Université de Paris-Cité, CNRS UMR 3569, Unité d'Épidémiologie et Physiopathologie des Virus Oncogènes, Paris, France.ORCID https://orcid.org/0000-0003-2006-2236
Patricia TortevoyeInstitut Pasteur, Université de Paris-Cité, CNRS UMR 3569, Unité d'Épidémiologie et Physiopathologie des Virus Oncogènes, Paris, France.
Balthazar NtabDépartement de l'Information Médicale, Centre Hospitalier de l'Ouest Guyanais, Franck Joly, Saint-Laurent-du-Maroni, French Guiana, France.
Gabriel CarlesService de Gynécologie-Obstétrique, Centre Hospitalier de l'Ouest Guyanais, Franck Joly, Saint-Laurent-du-Maroni, French Guiana, France.
Jean-Pierre DrozMedical Oncology, Claude-Bernard Lyon-1 University, Lyon, France.ORCID https://orcid.org/0000-0002-2431-0463
Pierre CouppiéDepartment of Dermatology, Cayenne Hospital, French Guiana, France.ORCID https://orcid.org/0000-0002-4213-2867
Giovanni BegliominiInstitut Pasteur, Université de Paris-Cité, CNRS UMR 3569, Unité d'Épidémiologie et Physiopathologie des Virus Oncogènes, Paris, France.ORCID https://orcid.org/0009-0000-3729-8224
Jean-Francois CarodLaboratoire de Biologie Médicale, Centre Hospitalier de l'Ouest Guyanais, Franck Joly, Saint-Laurent-du-Maroni, Guyane, France.ORCID https://orcid.org/0000-0002-7472-7160
N'detodji-Bill WankpoOncology Program, Centre Hospitalier de l'Ouest-Guyane, Franck Joly, Saint-Laurent du Maroni, French Guiana, France.
Karim AbdelmoumenDepartment of Dermatology, Cayenne Hospital, French Guiana, France.ORCID https://orcid.org/0000-0003-1177-643X
Philippe V AfonsoInstitut Pasteur, Université de Paris-Cité, CNRS UMR 3569, Unité d'Épidémiologie et Physiopathologie des Virus Oncogènes, Paris, France.ORCID https://orcid.org/0000-0002-4828-3797
Olivier CassarInstitut Pasteur, Université de Paris-Cité, CNRS UMR 3569, Unité d'Épidémiologie et Physiopathologie des Virus Oncogènes, Paris, France.ORCID https://orcid.org/0000-0001-5331-6357
Antoine TalarminTransmission, Reservoir and Diversity of Pathogens Unit, Institut Pasteur de Guadeloupe, Les Abymes, Guadeloupe, France.ORCID https://orcid.org/0000-0002-7611-2725
Olivier HermineDepartment of Hematology, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris, INSERM UMR 1151 and CNRS, Institut Necker, Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0003-2574-3874
Loïc EpelboinInfectious and Tropical Diseases Unit, Cayenne Hospital and French Guiana University, French Guiana, France.ORCID https://orcid.org/0000-0002-3481-5991
Ambroise MarçaisDepartment of Hematology, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris, INSERM UMR 1151 and CNRS, Institut Necker, Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0002-6844-7920
Antoine GessainInstitut Pasteur, Université de Paris-Cité, CNRS UMR 3569, Unité d'Épidémiologie et Physiopathologie des Virus Oncogènes, Paris, France.ORCID https://orcid.org/0000-0001-6840-4413

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult T-cell leukemia/lymphoma (ATL) is a rare and aggressive malignancy caused by human T-cell leukemia virus type 1 (HTLV-1). French Guiana, located in northeastern South America, is a region of high HTLV-1 endemicity with a multiethnic population. We conducted a comprehensive 30-year study of ATL cases diagnosed between 1990 and 2019, capturing nearly all confirmed ATL cases in the territory (n = 137). The predominant subtypes were lymphoma (58%) and acute ATL (36%). Striking ethnic disparities emerged: 69% of patients were Maroons, and the median age at diagnosis was 43 years among Maroons versus 58 years among Creoles. Survival outcomes were uniformly poor, with median overall survival of 2.7 months for acute and 5.2 months for lymphoma ATL. In multivariate analysis, acute ATL subtype and hepatosplenomegaly at diagnosis were independently associated with worse survival. Complete HTLV-1 genome sequences were obtained for seven ATL cases, and phylogenetic analysis of complete genomes revealed strong ethnic clustering: all Creole strains belonged to the Transcontinental subtype, while all Maroon strains belonged to the West African subtype. Moreover, HTLV-1 seroprevalence in the general population was measured among 1078 Creoles tested in 1998, with a prevalence of 3.1%, markedly lower and occurring at older ages compared to previously published data for the Maroon population. Our findings highlight pronounced disparities in ATL epidemiology by ethnic group and emphasize the need for targeted prevention, early diagnosis, and improved care in high-risk populations.

Indexed as

HTLV-I InfectionsHuman T-lymphotropic virus 1Leukemia-Lymphoma, Adult T-CellSouth American PeopleAdultAgedFemaleFrench GuianaGenetic VariationHumansMaleMiddle AgedPhylogenyYoung Adultadult T‐cell leukemia/lymphoma (ATL)cancer epidemiologyethnic health disparitieshuman T‐lymphotropic virus type 1 (HTLV‐1)South America

Identifiers

PMID40985869
PMCPMC12811218

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.