Evidence map›Paper›PMID 18292286›Full record

Trial reportBlood2008

Clinical, biologic, and pathologic features in 157 patients with angioimmunoblastic T-cell lymphoma treated within the Groupe d'Etude des Lymphomes de l'Adulte (GELA) trials.

Nathalie Mourad, Nicolas Mounier, Josette Brière, Emmanuel Raffoux, Alain Delmer, Alfred Feller, Chris J L M Meijer, Jean-François Emile, Réda Bouabdallah, André Bosly and 6 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 136 papers.

0numbers the graph read from it
0cells of the map it votes in
136citing papers in PubMed
13.8field-weighted citation impact, top 1% 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

136 citing papers in PubMed, 337 citations in OpenAlex.

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76 more citing papers are in PubMed but not listed here.

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

16 authors at 13 institutions in 4 countries.

Nathalie MouradInserm U728, Paris, France.
Nicolas Mounier
Josette Brière
Emmanuel Raffoux
Alain Delmer
Alfred Feller
Chris J L M Meijer
Jean-François Emile
Réda Bouabdallah
André Bosly
Jacques Diebold
Corinne Haioun
Bertrand Coiffier
Christian Gisselbrecht
Philippe Gaulard
Groupe d'Etude des Lymphomes de l'Adulte
Université Paris Cité · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire Henri-Mondor · FRHôpital Ambroise-Paré · FRHôpital Robert-Debré · FRHôpital Saint-Louis · FRHôtel-Dieu de Paris · FRInstitut Paoli-Calmettes · FRUCLouvain · BEUniversité Paris-Est Créteil · FRUniversity Hospital Schleswig-Holstein · DEVrije Universiteit Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To evaluate the prognostic significance of clinicobiologic and pathological features in angioimmunoblastic T-cell lymphoma (AITL), 157 AITL patients were retrieved from the GELA LNH87-LNH93 randomized clinical trials. One hundred forty-seven patients received a cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP)-like regimen with intensified courses in half of them. Histologically, 41 cases were classified as "rich in large cells" and 116 as "classic" (including 19 rich in epithelioid cells, 14 rich in clear cells, and 4 with hyperplastic germinal centers). Sixty-two cases were scored for CD10 and CXCL13 expression according to the abundance of positive lymphoid cells. Median age was 62 years, with 81% advanced stage, 72% B symptoms, 65% anemia, 50% hypergammaglobulinemia, and 66% elevated LDH. Overall 7-year survival was 30%. In multivariate analysis, only male sex (P = .004), mediastinal lymphadenopathy (P = .041), and anemia (P = .042) adversely affected overall survival. Increase in large cells and high level of CD10 and CXCL13 did not affect survival. Intensive regimen did not improve survival. In conclusion, AITL is a morphologically heterogeneous T-cell lymphoma commonly expressing CXCL13 and CD10 and carrying few prognostic factors. It portends a poor prognosis even when treated intensively. However, AITL is not always lethal with 30% of patients alive at 7 years.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsChemokine CXCL13CyclophosphamideDoxorubicinHumansImmunoblastic LymphadenopathyLymphoma, T-CellMiddle AgedNeprilysinPrednisonePrognosisRandomized Controlled Trials as TopicRetrospective StudiesSurvival AnalysisVincristineChemokine CXCL13CXCL13 protein, humanCyclophosphamideDoxorubicinNeprilysinPrednisoneVincristine

Identifiers

PMID18292286
PMCPMC2343588
OpenAlexW2015684600

What OpenQuestion holds

Textmetadata
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.