Evidence map›Paper›PMID 31412798›Full record

ArticleBMC cancer2019

Prognostic role of CD4 T-cell depletion after frontline fludarabine, cyclophosphamide and rituximab in chronic lymphocytic leukaemia.

Martin Gauthier, Françoise Durrieu, Elodie Martin, Michael Peres, François Vergez, Thomas Filleron, Lucie Obéric, Fontanet Bijou, Anne Quillet Mary, Loic Ysebaert

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Influence of polyfunctional TbetFrontiers in immunology · 2025
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  8. Early CAREJHaem · 2024
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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 at 4 institutions in 1 country.

Martin GauthierDepartment of Haematology, Toulouse-Oncopole University Cancer Institute (IUCT-O), 1 Avenue Irene Joliot-Curie, 31059, Toulouse, France.
Françoise DurrieuDepartment of Biology Haematology, Institut Bergonié, Bordeaux, France.
Elodie MartinDepartment of Biostatistics, Institut Claudius Regaud, IU, CT-O, Toulouse, France.
Michael PeresDepartment of Biology Haematology, Toulouse-Oncopole University Cancer Institute (IUCT-O), Toulouse, France.
François VergezDepartment of Biology Haematology, Toulouse-Oncopole University Cancer Institute (IUCT-O), Toulouse, France.
Thomas FilleronDepartment of Biostatistics, Institut Claudius Regaud, IU, CT-O, Toulouse, France.
Lucie ObéricDepartment of Haematology, Toulouse-Oncopole University Cancer Institute (IUCT-O), 1 Avenue Irene Joliot-Curie, 31059, Toulouse, France.
Fontanet BijouDepartment of Medical Haematology, Institut Bergonié, Bordeaux, France.
Anne Quillet MaryInserm UMR1037, Cancer Research Centre of Toulouse, Toulouse, France.
Loic YsebaertDepartment of Haematology, Toulouse-Oncopole University Cancer Institute (IUCT-O), 1 Avenue Irene Joliot-Curie, 31059, Toulouse, France. ysebaert.loic@iuct-oncopole.fr.ORCID http://orcid.org/0000-0003-4102-7261
Institut universitaire du cancer de Toulouse Oncopole · FRInserm · FRInstitut Bergonié · FRInstitut Claudius Regaud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEradication of minimal residual disease (MRD), at the end of Fludarabine-Cyclophosphamide-Rituximab (FCR) treatment, is a validated surrogate marker for progression-free and overall survival in chronic lymphocytic leukaemia. But such deep responses are also associated with severe immuno-depletion, leading to infections and the development of secondary cancers.

methodsWe assessed, blood MRD and normal immune cell levels at the end of treatment, in 162 first-line FCR patients, and analysed survival and adverse event.

resultsMultivariate Landmark analysis 3 months after FCR completion identified unmutated IGHV status (HR, 2.03, p = 0.043), the level of MRD reached (intermediate versus low, HR, 2.43, p = 0.002; high versus low, HR, 4.56, p = 0.002) and CD4 > 200/mm

conclusionsConsolidation/maintenance trials based on detectable MRD after FCR should investigate CD4 T-cell numbers both as a selection and a response criterion, and consolidation treatments should target B-cell/T-cell interactions.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCD4-Positive T-LymphocytesCyclophosphamideFemaleFollow-Up StudiesHumansImmunoglobulin Variable RegionImmunosuppressive AgentsLeukemia, Lymphocytic, Chronic, B-CellLymphocyte CountMaleMiddle AgedMutationNeoplasm, ResidualPrognosisRituximabCyclophosphamidefludarabineImmunoglobulin Variable RegionImmunosuppressive AgentsRituximabVidarabineCD4 T-cellsChemo-immunotherapyChronic lymphocytic LeukaemiaImmunosuppressionMinimal residual disease

Identifiers

PMID31412798
PMCPMC6694602
OpenAlexW2967228333

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.