Evidence map›Paper›PMID 33523334›Full record

ArticleInvestigational new drugs2021

A phase Ib, open-label, dose-escalation trial of the anti-CD37 monoclonal antibody, BI 836826, in combination with gemcitabine and oxaliplatin in patients with relapsed/refractory diffuse large B-cell lymphoma.

Monica Balzarotti, Massimo Magagnoli, Miguel Ángel Canales, Paolo Corradini, Carlos Grande, Juan-Manuel Sancho, Francesco Zaja, Anne-Marie Quinson, Valérie Belsack, Daniela Maier and 1 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02624492 (An Open Label Multicenter Phase Ib/II Trial to Determine the Dose of BI 836826 in Combination With Gemcitabine and Oxaliplatin), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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.

NCT02624492 phase2completednot on this map

An Open Label Multicenter Phase Ib/II Trial to Determine the Dose of BI 836826 in Combination With Gemcitabine and Oxaliplatin (GemOx) and the Efficacy of BI 836826-GemOx Versus Rituximab (R)- GemOx (R-GemOx) in Patients With Relapsed/ Refractory Diffuse Large B-cell Lymphoma (DLBCL) Who Are Not Eligible for, or Have Relapsed/Progressed After Autologous/Allogeneic Stem Cell Transplant

TypeinterventionalSponsorBoehringer IngelheimRan2016 to 2018Enrolled21ConditionsLymphoma, Large B-Cell, DiffuseArmsBI 836826, GemOx, Rituximab
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

11 authors at 9 institutions in 5 countries.

Monica BalzarottiOncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milano, Italy.
Massimo MagagnoliOncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milano, Italy.
Miguel Ángel CanalesServicio de Hematologia, Hospital Universitario La Paz, Madrid, Spain.
Paolo CorradiniUniversity of Milan, Milan, Italy.
Carlos GrandeHospital Universitario 12 de Octubre, Madrid, Spain.
Juan-Manuel SanchoClinical Hematology Department, ICO-IJC-Hospital Germans Trias i Pujol, Badalona, Spain.
Francesco ZajaUniversity of Trieste, Ospedale Maggiore, Piazza dell'Ospitale 1, Trieste, Italy.
Anne-Marie QuinsonBoehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA.
Valérie BelsackSCS Boehringer Ingelheim Comm.V, Brussels, Belgium.
Daniela MaierBoehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riß, Germany.
Carmelo Carlo-StellaOncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milano, Italy. carmelo.carlostella@hunimed.eu.ORCID 0000-0003-3144-0124
Humanitas University · ITBoehringer Ingelheim (Belgium) · BEBoehringer Ingelheim (Germany) · DEBoehringer Ingelheim (United States) · USHospital Universitari Germans Trias i Pujol · ESHospital Universitario 12 De Octubre · ESHospital Universitario La Paz · ESUniversity of Milan · ITUniversity of Trieste · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background BI 836826 is a chimeric mouse-human monoclonal antibody directed against human CD37, a transmembrane protein expressed on mature B lymphocytes. This open-label, phase I dose-escalation trial (NCT02624492) was conducted to determine the maximum tolerated dose (MTD), safety/tolerability, and preliminary efficacy of BI 836826 in combination with gemcitabine and oxaliplatin in patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL). Methods Eligible patients received intravenous infusions of BI 836826 on day 8 and gemcitabine 1000 mg/m

Indexed as

AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsDeoxycytidineDose-Response Relationship, DrugFemaleGemcitabineHumansLymphoma, Large B-Cell, DiffuseMaleMaximum Tolerated DoseMiddle AgedOxaliplatinTreatment OutcomeAntibodies, Monoclonal, HumanizedBI 836826DeoxycytidineGemcitabineOxaliplatinBI 836826CD37Diffuse large B-cell lymphomaNon-Hodgkin lymphomaPhase IRelapsed

Identifiers

PMID33523334
PMCPMC8279964
OpenAlexW3127158261

What OpenQuestion holds

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Registered trials

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.