Evidence map›Paper›PMID 33683501›Full record

ArticleInvestigational new drugs2021

A phase Ib, open label, dose escalation trial of the anti-CD37 monoclonal antibody, BI 836826, in combination with ibrutinib in patients with relapsed/refractory chronic lymphocytic leukemia.

Alexey V Danilov, Stephen E Spurgeon, Tanya Siddiqi, Anne-Marie Quinson, Daniela Maier, Dionne Smith, Jennifer R Brown

Open access · hybridAbstract readClinical Trial, Phase IComparative 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. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Molecularly targeted therapy and immunotherapy in leukemias.Journal of hematology & oncology · 2026
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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

7 authors at 5 institutions in 2 countries.

Alexey V DanilovCity Of Hope National Medical Center, Duarte, CA, USA.
Stephen E SpurgeonKnight Cancer Institute at Oregon Health & Science University, Portland, OR, USA.
Tanya SiddiqiCity Of Hope National Medical Center, Duarte, CA, USA.
Anne-Marie QuinsonBoehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany.
Daniela MaierBoehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany.
Dionne SmithBoehringer Ingelheim Pharmaceuticals Inc, Ridgefield, CT, USA.
Jennifer R BrownDana-Farber Cancer Institute, Boston, MA, USA. Jennifer_Brown@dfci.harvard.edu.ORCID 0000-0003-2040-4961
Boehringer Ingelheim (Germany) · DECity Of Hope National Medical Center · USBoehringer Ingelheim (United States) · USDana-Farber Cancer Institute · USOregon Health & Science University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BI 836826 is a chimeric immunoglobulin G1 antibody targeting CD37, a transmembrane protein expressed on normal and malignant B cells. This open-label, phase Ib, dose-escalation study was conducted to determine the recommended phase II dose (RP2D) of BI 836826 + ibrutinib in patients with relapsed/refractory chronic lymphocytic leukemia (CLL). Eligible patients received 420 mg/day of ibrutinib with escalating doses of BI 836826. BI 836826 was administered in 4-week cycles. After Cycle 12, patients achieving complete response (CR), CR with incomplete marrow recovery, or minimal residual disease-negative partial response could continue to receive BI 836826 + ibrutinib every 4 weeks for ≤ 12 additional cycles. Patients received either 100 mg (n = 3) or 200 mg (n = 3) BI 836826 + ibrutinib. In the 100 mg BI 836826 cohort, one patient received two cycles and two patients received 22 cycles of BI 836826. In the 200 mg BI 836826 cohort, patients received 12, 16 and 20 cycles of BI 836826, respectively. All patients discontinued BI 836826 and continued ibrutinib outside the trial. No dose-limiting toxicities were reported in the maximum tolerated dose (MTD) evaluation period. As the trial was discontinued before the MTD was reached, the RP2D was not determined. Grade 3/4 adverse events (AEs) were predominantly hematological. Pseudomonal bacteremia was the only drug-related AE of special interest. BI 836826 + ibrutinib did not exceed the MTD at doses up to 200 mg in patients with CLL. However, RP2D and MTD were not formally established, as the sponsor discontinued the trial.

Indexed as

AdenineAgedAntibodies, Monoclonal, HumanizedAntigens, NeoplasmAntineoplastic Combined Chemotherapy ProtocolsDose-Response Relationship, DrugFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMaximum Tolerated DoseMiddle AgedPiperidinesTetraspaninsAdenineAntibodies, Monoclonal, HumanizedAntigens, NeoplasmBI 836826CD37 protein, humanibrutinibPiperidinesTetraspaninsBI 836826CD37Chronic lymphocytic leukemiaPhase IbRelapsed

Identifiers

PMID33683501
PMCPMC8279974
OpenAlexW3135527931

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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.