Evidence map›Paper›PMID 26768687›Full record

ArticleHaematologica2016

Impact of post-brentuximab vedotin consolidation on relapsed/refractory CD30+ Hodgkin lymphomas: a large retrospective study on 240 patients enrolled in the French Named-Patient Program.

Aurore Perrot, Hélène Monjanel, Réda Bouabdallah, Philippe Quittet, Clémentine Sarkozy, Marc Bernard, Aspasia Stamatoullas, Cécile Borel, Krimo Bouabdallah, Emmanuelle Nicolas-Virelizier and 4 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Outcomes of Brentuximab Vedotin Monotherapy in Refractory/Relapsed Classical Hodgkin's Lymphoma: A Multi-Center Retrospective Study on Survival and Safety.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article
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

14 authors at 13 institutions in 1 country.

Aurore PerrotService d'Hématologie, CHU de Nancy, Université de Lorraine, Vandoeuvre les Nancy, France au.perrot@chu-nancy.fr.
Hélène MonjanelHôpital Saint Louis AP-HP, Université Diderot, Paris, France.
Réda BouabdallahDépartement d'Hématologie, CLCC Institut Paoli Calmettes, Marseille, France.
Philippe QuittetDépartement d'Hématologie Clinique, CHRU Hôpital Lapeyronie, Montpellier, France.
Clémentine SarkozyService Hématologie, Hospices Civils de Lyon, Université Claude Bernard, Pierre-Bénite, France.
Marc BernardService d'Hématologie, Hôpital Pontchaillou, Rennes, France.
Aspasia StamatoullasDépartement d'Hématologie, Centre Henri Becquerel, Rouen, France.
Cécile BorelFédération d'Hématologie, Institut Universitaire du Cancer, Toulouse, France.
Krimo BouabdallahService d'Hématologie, CHU de Bordeaux, Hôpital Haut-Lévèque, Pessac, France.
Emmanuelle Nicolas-VirelizierService de Cancérologie Médicale, CLCC Léon Bérard, Lyon, France.
Marion FournierThe Lymphoma Academic Research Organisation (LYSARC), Centre Hospitalier Lyon Sud, Pierre-Bénite, France.
Franck MorschhauserService d'Hématologie, Hôpital Claude Huriez, Unité GRITA, Université de Lille, Lille, France.
Pauline BriceHôpital Saint Louis AP-HP, Université Diderot, Paris, France.
Lymphoma Study Association (LYSA)
Centre Henri BecquerelCentre Léon Bérard · FRDélégation Paris 7 · FRHôpital Cardiologique du Haut-Lévêque · FRHôpital Lapeyronie · FRHôpital Pontchaillou · FRHôpital Saint-Louis · FRInstitut Paoli-Calmettes · FRInstitut universitaire du cancer de Toulouse Oncopole · FRThe Lymphoma Academic Research Organisation · FRUniversité Claude Bernard Lyon 1 · FRUniversité de Lille · FRUniversité de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brentuximab vedotin was reported to be effective and safe against refractory/relapsed Hodgkin lymphoma in cohorts of between 12 to 102 patients. Herein we report our retrospective analysis of the French experience with brentuximab vedotin used alone to treat 240 refractory/relapsed Hodgkin lymphoma patients enrolled in a named patient program between 2011 and 2013. All patients had histologically documented CD30+ Hodgkin lymphoma; 74% had refractory disease or early relapses. After a median of 3 lines of chemotherapy, brentuximab vedotin was infused intravenously (1.8 mg/kg every 3 weeks). The primary endpoint was best response. Response at the end of treatment, its duration, survival data and toxicity profile were secondary endpoints. Patients received a median of 6 cycles; 68 underwent a consolidation thereafter. The best response was observed after a median of 4 cycles in 145 (60.4%) patients: 33.8% complete response/unconfirmed complete response, 26.7% partial response. Objective responses were observed as decreased (39.3%) in the 28 patients >60 years. The median response duration was 8.4 months. With median follow-up at 16.1 months, median progression-free survival was 6.8 months and this was significantly longer for patients transplanted after brentuximab vedotin (a median of 18,8 months); median overall survival was not reached. No death has been linked to brentuximab vedotin toxicity. The most common adverse events were peripheral sensory neuropathy (29.3%) and hematological toxicity. The results of this analysis support the previously reported brentuximab vedotin efficacy with manageable toxicity. Because of the short-term responses in most patients, a high-dose therapy with stem cell transplantation for responders should be considered as quickly as possible.

Indexed as

AdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBrentuximab VedotinDrug Administration ScheduleDrug Resistance, NeoplasmFemaleFranceGene ExpressionHodgkin DiseaseHumansImmunoconjugatesInjections, IntravenousKi-1 AntigenBiomarkers, TumorBrentuximab VedotinImmunoconjugatesKi-1 Antigen

Identifiers

PMID26768687
PMCPMC5004383
OpenAlexW2298694645

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.