Evidence map›Paper›PMID 37600821›Full record

ArticleFrontiers in immunology2023

Activity of tafasitamab in combination with rituximab in subtypes of aggressive lymphoma.

Maria Patra-Kneuer, Gaomei Chang, Wendan Xu, Christian Augsberger, Michael Grau, Myroslav Zapukhlyak, Kristina Ilieva, Karin Landgraf, Doris Mangelberger-Eberl, Kasra Yousefi and 11 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

21 authors at 7 institutions in 3 countries.

Maria Patra-KneuerTranslational Research, MorphoSys AG, Planegg, Germany.
Gaomei ChangDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
Wendan XuDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
Christian AugsbergerTranslational Research, MorphoSys AG, Planegg, Germany.
Michael GrauDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
Myroslav ZapukhlyakDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
Kristina IlievaTranslational Research, MorphoSys AG, Planegg, Germany.
Karin LandgrafTranslational Research, MorphoSys AG, Planegg, Germany.
Doris Mangelberger-EberlTranslational Research, MorphoSys AG, Planegg, Germany.
Kasra YousefiTranslational Research, MorphoSys AG, Planegg, Germany.
Philipp BerningDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
Katrin S KurzDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus and Dr. Margarete Fischer-Bosch Institute for Clinical Pharmacology, Stuttgart, Germany.
German OttDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus and Dr. Margarete Fischer-Bosch Institute for Clinical Pharmacology, Stuttgart, Germany.
Pavel KlenerInstitute of Pathological Physiology, First Faculty of Medicine, Charles University Prague, Prague, Czechia.
Cyrus KhandanpourDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
Pedro HornaDivision of Hematopathology, Mayo Clinic, Rochester, MN, United States.
Jürgen SchanzerTranslational Research, MorphoSys AG, Planegg, Germany.
Stefan SteidlTranslational Research, MorphoSys AG, Planegg, Germany.
Jan EndellTranslational Research, MorphoSys AG, Planegg, Germany.
Christina HeitmüllerTranslational Research, MorphoSys AG, Planegg, Germany.
Georg LenzDepartment of Medicine A, Hematology, Oncology and Pneumology, University Hospital Münster, Münster, Germany.
MorphoSys (Germany) · DEUniversity Hospital Münster · DECharles University · CZDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DEMayo Clinic · USRobert Bosch Hospital · DEUniversity Hospital Schleswig-Holstein · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite recent advances in the treatment of aggressive lymphomas, a significant fraction of patients still succumbs to their disease. Thus, novel therapies are urgently needed. As the anti-CD20 antibody rituximab and the CD19-targeting antibody tafasitamab share distinct modes of actions, we investigated if dual-targeting of aggressive lymphoma B-cells by combining rituximab and tafasitamab might increase cytotoxic effects. Methods: Antibody single and combination efficacy was determined investigating different modes of action including direct cytotoxicity, antibody-dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP) in Results: Three different sensitivity profiles to antibody monotherapy or combination treatment were observed in Conclusion: This study demonstrates that the combination of tafasitamab and rituximab improves efficacy compared to single-agent treatments in models of aggressive B-cell lymphoma

Indexed as

Burkitt LymphomaLymphoma, Large B-Cell, DiffuseAnimalsAntibodies, Monoclonal, HumanizedLeukocytes, MononuclearMiceMice, Inbred NODMice, SCIDRituximabAntibodies, Monoclonal, HumanizedRituximabtafasitamabantibody therapyCD19CD20lymphomarituximabtafasitamabtumor immunology

Identifiers

PMID37600821
PMCPMC10433160
OpenAlexW4385411023

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.