Evidence map›Paper›PMID 35638548›Full record

ArticleHaematologica2022

High-risk stage IIB Hodgkin lymphoma treated in the H10 and AHL2011 trials: total metabolic tumor volume is a useful risk factor to stratify patients at baseline.

Cédric Rossi, Marc André, Jehan Dupuis, Franck Morschhauser, Bertrand Joly, Julien Lazarovici, Hervé Ghesquières, Aspasia Stamatoullas, Emmanuelle Nicolas-Virelizier, Pierre Feugier and 13 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Classical Hodgkin Lymphoma Today.Mediterranean journal of hematology and infectious diseases · 2026
    Review
  4. Review
  5. Article
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  8. 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

23 authors at 20 institutions in 5 countries.

Cédric RossiDepartment of Hematology, Dijon-Bourgogne University Hospital, Dijon; INSERM unit 1231, University of Burgundy Franche-Comté, France. cedric.rossi66@gmail.com.
Marc AndréDepartment of Hematology, CHU UCL Namur, Université Catholique de Louvain, Yvoir, Belgium.
Jehan DupuisLymphoid Malignancies Unit, Henri Mondor University Hospital (AP-HP), Créteil, France.
Franck MorschhauserGroupe de Recherche sur les formes Injectables et les Technologies Associées (GRITA), Department of Haematology, CHU Lille, Université de Lille, Lille.
Bertrand JolyDepartment of Hematology, Hospital Sud Francilien, Corbeille-Essonnes, France.
Julien LazaroviciDepartment of Hematology, Université Paris-Saclay, Gustave Roussy, Villejuif, France.
Hervé GhesquièresDepartment of Hematology, Centre Hospitalier Lyon Sud and Université Claude Bernard Lyon-1, Pierre-Bénite, France.
Aspasia StamatoullasDepartment of Hematology, Centre Henri Becquerel, Rouen, France.
Emmanuelle Nicolas-VirelizierDepartment of Hematology, Centre Léon Bérard, Lyon, France.
Pierre FeugierHospital of Nancy, Vandoeuvre les Nancy, France.
Anne-Claire GacDepartment of Haematology, Institut d'hématologie de Basse Normandie, Caen, France.
Hannah MoattiDepartment of Hematology, CHU Paris-GH St-Louis Lariboisière F-Widal - Hôpital Saint-Louis, Paris, France.
Luc-Matthieu ForneckerDepartment of Haematology, University Hospital of Strasbourg, Strasbourg, France.
Bénédicte DeauDepartment of Hematology, CHU Cochin, Paris, France.
Clémentine JoubertLymphoma Academic Research Organisation, CHU Lyon-Sud, Lyon, France.
Catherine FortpiedEuropean Organisation for Research and Treatment of Cancer, Brussels, Belgium.
John RaemaekersDepartment of Haematology, Radboud University Medical Center, Nijmegen, Netherlands.
Massimo FedericoCHIMOMO department, University of Modena and Reggio Emilia, Policlinico, Modena, Italy.
Salim KanounNuclear Medecine Unit, Institut universitaire du cancer Toulouse-Oncopole, Toulouse, France.
Michel MeignanLYSA Imaging, University Hospital H Mondor, Creteil, France.
Alexandra Traverse-GlehenDepartment of Pathology, Centre Hospitalier Lyon Sud and Université Claude Bernard Lyon-1, Pierre- Bénite, France.
Anne-Ségolène CottereauNuclear Medecine Department, Hôpital Cochin, AP-HP, Université de Paris, France.
René-Olivier CasasnovaDepartment of Hematology, Dijon-Bourgogne University Hospital, Dijon; INSERM unit 1231, University of Burgundy Franche-Comté, France.
Hôpital Lyon Sud · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Sud Francilien · FRCentre Hospitalier Universitaire Henri-Mondor · FRCentre Léon Bérard · FRCHU Dinant Godinne UCL Namur · BEEuropean Organisation for Research and Treatment of Cancer · BEHôpital Cochin · FRHôpital Saint-Louis · FRHôpitaux Universitaires de Strasbourg · FRInserm · FRInstitut universitaire du cancer de Toulouse Oncopole · FRLaboratoire National Henri Becquerel · FRLymphoma Study Association · FRRadboud University Nijmegen · NLUniversité de Bourgogne · FRUniversité de Caen Normandie · FRUniversité de Lille · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stage IIB Hodgkin lymphoma (HL) patients, with a mediastinum-to-thorax (M/T) ratio of ≥0.33 or extranodal localization have a poor prognosis and are treated either as limited or advanced stage. We compared these two approaches in patients included in two randomized phase III trials enrolling previously untreated early (H10) or advanced stage HL (AHL2011). We included HL patients with Ann-Arbor stage IIB with M/T ≥0.33 or extranodal involvement enrolled in the H10 or AHL2011 trials with available positron emission tomography at baseline (PET0) and after two cycles of chemotherapy (PET2). Baseline total metabolic tumor volume (TMTV) was calculated using the 41% SUVmax method. PET2 response assessment used the Deauville score. One hundred and fourty-eight patients were eligible, including 83 enrolled in the AHL2011 trial and 65 in the H10 trial. The median TMTV value was 155.5 mL (range, 8.3-782.9 mL), 165.6 mL in AHL2011 and 147 mL in H10. PET2 positivity rates were 16.9% (n=14) and 9.2% (n=6) in AHL2011 and H10 patients, respectively. With a median follow-up of 4.1 years (95% confidence interval [CI]: 3.9-4.4), overall 4-year PFS was 88.0%, 87.0% in AHL2011 and 89.2% in H10. In univariate and mutivariate analyses, baseline TMTV and PET2 response influenced significantly progression-free survival (hazard ratio [HR]=4.94, HR=3.49 respectively). Notably, among the 16 patients who relapsed, 13 (81%) had a baseline TMTV baseline ≥155 mL. Upfront ABVD plus radiation therapy or upfront escBEACOPP without radiotherapy provide similar patient's outcome in high-risk stage IIB HL. TMTV is useful to stratify these patients at baseline.

Indexed as

Hodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsBleomycinClinical Trials, Phase III as TopicDacarbazineDoxorubicinHumansPrognosisRandomized Controlled Trials as TopicRisk FactorsTumor BurdenVinblastineBleomycinDacarbazineDoxorubicinVinblastine

Identifiers

PMID35638548
PMCPMC9713544
OpenAlexW4282037574

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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 OpenQuestion graph.