Evidence map›Paper›PMID 33330050›Full record

ArticleFrontiers in oncology2020

Combination of T-Cell Bispecific Antibodies With PD-L1 Checkpoint Inhibition Elicits Superior Anti-Tumor Activity.

Johannes Sam, Sara Colombetti, Tanja Fauti, Andreas Roller, Marlene Biehl, Linda Fahrni, Valeria Nicolini, Mario Perro, Tapan Nayak, Esther Bommer and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

42 citing papers in PubMed, 52 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

Johannes SamRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Sara ColombettiRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Tanja FautiRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Andreas RollerRoche Pharmaceutical Research & Early Development, Roche Innovation Center Basel, Basel, Switzerland.
Marlene BiehlRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Linda FahrniRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Valeria NicoliniRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Mario PerroRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Tapan NayakRoche Pharmaceutical Research & Early Development, Roche Innovation Center Basel, Basel, Switzerland.
Esther BommerRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Anne SchoenleRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Maria KaragianniRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Marine Le ClechRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Nathalie SteinhoffRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Christian KleinRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Pablo UmañaRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Marina BacacRoche Pharmaceutical Research & Early Development, Roche Innovation Center Zurich, Zurich, Switzerland.
Roche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell Bispecific Antibodies (TCBs) elicit anti-tumor responses by cross-linking T-cells to tumor cells and mediate polyclonal T-cell expansion that is independent of T-cell receptor specificity. TCBs thus offer great promise for patients who lack antigen-specific T-cells or have non-inflamed tumors, which are parameters known to limit the response of checkpoint inhibitors. The current study deepens the understanding of TCB mode of action and elaborates on one of the adaptive resistance mechanisms following its treatment

Indexed as

carcinoembryonic antigen T-cell bispecific antibodycombinationhumanized miceimmunotherapyprogrammed death–ligand 1solid tumorsT-cell bispecific antibody

Identifiers

PMID33330050
PMCPMC7735156
OpenAlexW4242716502

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.