Evidence map›Paper›PMID 34258584›Full record

ArticleBlood cancer discovery2021

Tumor burden limits bispecific antibody efficacy through T cell exhaustion averted by concurrent cytotoxic therapy.

Erin W Meermeier, Seth J Welsh, Meaghen E Sharik, Megan T Du, Victoria M Garbitt, Daniel L Riggs, Chang-Xin Shi, Caleb K Stein, Marco Bergsagel, Bryant Chau and 6 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Blood cancer discovery, 2021. 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 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

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11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 2 countries.

Erin W MeermeierDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.ORCID 0000-0002-9709-7624
Seth J WelshDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Meaghen E SharikDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Megan T DuDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Victoria M GarbittDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Daniel L RiggsDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Chang-Xin ShiDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Caleb K SteinDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.
Marco BergsagelDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.ORCID 0000-0003-1523-7388
Bryant ChauDiscovery Biotherapeutics, Bristol Myers Squibb, Redwood City, California.
Matthew L WheelerTumor Microenvironment Thematic Research Center, Bristol Myers Squibb, Redwood City, California.
Natalie BezmanTumor Microenvironment Thematic Research Center, Bristol Myers Squibb, Redwood City, California.
Feng WangDiscovery Biotherapeutics, Bristol Myers Squibb, Redwood City, California.
Pavel StropDiscovery Biotherapeutics, Bristol Myers Squibb, Redwood City, California.
P Leif BergsagelDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona.ORCID 0000-0003-1523-7388
Marta ChesiDepartment of Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona. chesi.marta@mayo.edu.ORCID 0000-0002-4024-8225
Mayo Clinic in Arizona · USBristol-Myers Squibb (Germany) · DE

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel · 2015 to 2026
$25.5M
Project 3 - Modeling Proteasome Inhibitor Response and Resistance in Cell Lines and Patient Samples with Single Cell Analysis of SubpopulationsU54CA224018 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2017 to 2021
$6.0M
Credentialing a Genetically Engineered Clinically-Relevant Mouse Model of Multiple MyelomaR01CA234181 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2019 to 2023
$1.9M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA234181NCI NIH HHS U54 CA224018
6 · The paper itself

Abstract

BCMA-CD3-targeting bispecific antibodies (BsAb) are a recently developed immunotherapy class which shows potent tumor killing activity in multiple myeloma (MM). Here, we investigated a murine BCMA-CD3-targeting BsAb in the immunocompetent Vk*MYC and its IMiD-sensitive derivative Vk*MYC

Indexed as

Antibodies, BispecificMultiple MyelomaAnimalsHumansImmunotherapyMiceT-LymphocytesTumor BurdenAntibodies, Bispecific

Identifiers

PMID34258584
PMCPMC8266040
OpenAlexW3158660900

What OpenQuestion holds

Textmetadata
LicenceTDM
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.