Evidence map›Paper›PMID 34108180›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Role of Tumor-Infiltrating B Cells in Clinical Outcome of Patients with Melanoma Treated With Dabrafenib Plus Trametinib.

Jan C Brase, Robert F H Walter, Alexander Savchenko, Daniel Gusenleitner, James Garrett, Tobias Schimming, Renata Varaljai, Deborah Castelletti, Ju Kim, Naveen Dakappagari and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

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  16. Genome edited B cells: a new frontier in immune cell therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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

25 authors at 15 institutions in 8 countries.

Jan C Brase *Novartis Pharma AG, Basel, Switzerland.
Robert F H Walter *Department of Pathology, University Hospital Essen, Essen, Germany.ORCID 0000-0003-3725-7064
Alexander Savchenko *Oncology Precision Medicine, Novartis, Cambridge, Massachusetts.
Daniel Gusenleitner *Novartis Institutes for BioMedical Research, Inc., Cambridge, Massachusetts.ORCID 0000-0002-7428-0880
James GarrettNovartis Pharmaceuticals Corporation, Cambridge, Massachusetts.
Tobias SchimmingDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Renata VaraljaiDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0000-0001-6852-6859
Deborah CastellettiNovartis Pharma AG, Basel, Switzerland.
Ju KimNavigate BioPharma Services, Inc. (a Novartis subsidiary), Carlsbad, California.
Naveen DakappagariNavigate BioPharma Services, Inc. (a Novartis subsidiary), Carlsbad, California.
Ken SchultzOncology Precision Medicine, Novartis, Cambridge, Massachusetts.
Caroline RobertGustave Roussy and Paris-Sud-Paris-Saclay University, Villejuif, France.ORCID 0000-0002-9493-0238
Georgina V LongMelanoma Institute Australia and Sydney Medical School, The University of Sydney, and Royal North Shore and Mater Hospitals, Sydney, New South Wales, Australia.ORCID 0000-0001-8894-3545
Paul D NathanMount Vernon Cancer Centre, Northwood, United Kingdom.
Antoni RibasDepartment of Medicine, University of California-Los Angeles, Los Angeles, California.
Keith T FlahertyMassachusetts General Hospital Cancer Center and Harvard Medical School, Boston, Massachusetts.
Boguslawa KaraszewskaPrzychodnia Lekarska Komed, Konin, Poland.
Jacob SchachterThe Ella Lemelbaum Institute for Immuno-Oncology and Melanoma, Sheba Medical Center, Tel Hashomer, and Sackler Medical School, Tel Aviv University, Tel Aviv, Israel.
Antje SuckerDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Kurt W SchmidDepartment of Pathology, University Hospital Essen, Essen, Germany.
Lisa ZimmerDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Elisabeth LivingstoneDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0000-0001-8279-9239
Eduard GasalNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Dirk SchadendorfDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0000-0003-3524-7858
Alexander RoeschDepartment of Dermatology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany. alexander.roesch@uk-essen.de.
Essen University Hospital · DEGerman Cancer Research Center · DELineage Cell Therapeutics (United States) · USNovartis (Switzerland) · CHPrecision for Medicine (United States) · USTris Pharma (United States) · USAmerican Institutes for Research · USMassachusetts General Hospital · USMount Vernon Cancer Centre · GBRoyal North Shore Hospital · AURuhrlandklinik · DESheba Medical Center · ILState University of Applied Sciences in Konin · PLUniversité Paris-Saclay · FRUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAlthough patients with unresectable or metastatic melanoma can experience long-term survival with BRAF- and MEK-targeted agents or immune checkpoint inhibitors over 5 years, resistance develops in most patients. There is a distinct lack of pretherapeutic biomarkers to identify which patients are likely to benefit from each therapy type. Most research has focused on the predictive role of T cells in antitumor responses as opposed to B cells. PATIENTS AND

methodsWe conducted prespecified exploratory biomarker analysis using gene expression profiling and digital pathology in 146 patients with previously untreated

resultsBaseline cell-cycle gene expression signature was associated with progression-free survival (

conclusionsB cells may serve as a potential biomarker to predict clinical outcome in patients with advanced melanoma treated with dabrafenib plus trametinib. As separate studies have shown an opposite effect for B-cell levels and response to immunotherapy, B cells may serve as a potential biomarker to facilitate treatment selection. Further validation in a larger patient cohort is needed.

Indexed as

B-LymphocytesAntineoplastic Combined Chemotherapy ProtocolsHumansImidazolesMelanomaOximesPyridonesPyrimidinonesSkin NeoplasmsTreatment OutcomedabrafenibImidazolesOximesPyridonesPyrimidinonestrametinib

Identifiers

PMID34108180
PMCPMC9401540
OpenAlexW3166541179

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.