Evidence map›Paper›PMID 34635566›Full record

ArticleMolecular cancer therapeutics2021

A Novel Brain-Permeant Chemotherapeutic Agent for the Treatment of Brain Metastasis in Triple-Negative Breast Cancer.

Jiaojiao Deng, Sophia B Chernikova, Yuelong Wang, Mirna L Rodriguez, Stephanie J Andersen, Maxine C Umeh-Garcia, Bryanna O Godfrey, Saman S Ahmadian, Wolf-Nicolas Fischer, Kerry J Koller and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 4 institutions in 2 countries.

Jiaojiao Deng *Department of Neurosurgery, Stanford University, Stanford, California.
Sophia B Chernikova *Department of Neurosurgery, Stanford University, Stanford, California.
Yuelong Wang *Department of Neurosurgery, Stanford University, Stanford, California.ORCID 0000-0001-6457-0481
Mirna L RodriguezQuadriga BioSciences, Inc., Los Altos, California.
Stephanie J AndersenDepartment of Neurosurgery, Stanford University, Stanford, California.ORCID 0000-0003-4759-0848
Maxine C Umeh-GarciaDepartment of Neurosurgery, Stanford University, Stanford, California.
Bryanna O GodfreyDepartment of Neurosurgery, Stanford University, Stanford, California.
Saman S AhmadianDepartment of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-4133-7895
Wolf-Nicolas FischerQuadriga BioSciences, Inc., Los Altos, California.
Kerry J KollerQuadriga BioSciences, Inc., Los Altos, California.
Bernd JandeleitQuadriga BioSciences, Inc., Los Altos, California.ORCID 0000-0001-7863-4212
Gordon M RingoldQuadriga BioSciences, Inc., Los Altos, California.
Melanie Hayden GephartDepartment of Neurosurgery, Stanford University, Stanford, California. mghayden@stanford.edu.
Stanford Medicine · USQuadriga Biosciences (United States) · USSichuan University · CNStanford University · US

Funding

Phase 1b/2a Trial of QBS-72S for the Treatment of Newly Diagnosed Glioblastoma Multiforme in Patients with Unmethylated MGMT PromotersR44CA174129 · NCI · QUADRIGA BIOSCIENCES, INC. · PI RINGOLD, GORDON M · 2017 to 2025
$6.0M
Tumor DNA in CSF and novel modeling decode breast cancer - brain metastasesK08NS091527 · NINDS · STANFORD UNIVERSITY · PI HAYDEN GEPHART, MELANIE · 2016 to 2020
$928k
Novel Chemotherapeutics for Brain TumorsR43CA174129 · NCI · QUADRIGA BIOSCIENCES, INC. · PI JANDELEIT, BERND · 2013 to 2013
$288k
NCI NIH HHS R43 CA174129NCI NIH HHS R44 CA174129NINDS NIH HHS K08 NS091527
6 · The paper itself

Abstract

Development of metastases to central nervous system (CNS) is an increasing clinical issue following the diagnosis of advanced breast cancer. The propensity to metastasize to CNS varies by breast cancer subtype. Of the four breast cancer subtypes, triple-negative breast cancers (TNBC) have the highest rates of both parenchymal brain metastasis and leptomeningeal metastasis (LM). LM is rapidly fatal due to poor detection and limited therapeutic options. Therapy of TNBC brain metastasis and LM is challenged by multifocal brain metastasis and diffuse spread of LM, and must balance brain penetration, tumor cytotoxicity, and the avoidance of neurotoxicity. Thus, there is an urgent need for novel therapeutic options in TNBCs CNS metastasis. QBS10072S is a novel chemotherapeutic that leverages TNBC-specific defects in DNA repair and LAT1 (L-amino acid transporter type 1)-dependent transport into the brain. In our study, activity of QBS10072S was investigated

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorHumansMiceNeoplasm MetastasisTriple Negative Breast NeoplasmsAntineoplastic Agents

Identifiers

PMID34635566
PMCPMC8571036
OpenAlexW3206812428

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.