Evidence map›Paper›PMID 38234840›Full record

ArticlemedRxiv : the preprint server for health sciences2023

Investigative needle core biopsies for multi-omics in Glioblastoma.

Kenny K H Yu, Sreyashi Basu, Gerard Baquer, Ryuhjin Ahn, Jennifer Gantchev, Sonali Jindal, Michael S Regan, Zaki Abou-Mrad, Michael C Prabhu, Marc J Williams and 39 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

49 authors at 6 institutions in 1 country.

Kenny K H Yu
Sreyashi Basu
Gerard Baquer
Ryuhjin Ahn
Jennifer Gantchev
Sonali Jindal
Michael S Regan
Zaki Abou-Mrad
Michael C Prabhu
Marc J Williams
Alicia D D'Souza
Seth W Malinowski
Kelsey Hopland
Yuval Elhanati
Sylwia A Stopka
Alexei Stortchevoi
Zhong He
Jingjing Sun
Yulong Chen
Alexsandra B Espejo
Kin Hoe Chow
Smitha Yerrum
Pei-Lun Kao
Brittany Parker Kerrigan
Lisa Norberg
Douglas Nielsen
GBM TeamLab
Vinay K Puduvalli
Jason Huse
Rameen Beroukhim
Yon Son Betty Kim
Sangeeta Goswami
Adrienne Boire
Sarah Frisken
Michael J Cima
Matthias Holdhoff
Calixto-Hope G Lucas
Chetan Bettegowda
Stuart S Levine
Tejus A Bale
Cameron Brennan
David A Reardon
Frederick F Lang
E Antonio Chiocca
Keith L Ligon
Forest M White
Padmanee Sharma
Viviane Tabar
Nathalie Y R Agar
Brigham and Women's Hospital · USThe University of Texas MD Anderson Cancer Center · USMemorial Sloan Kettering Cancer Center · USJohns Hopkins University · USHarvard–MIT Division of Health Sciences and Technology · USMassachusetts Institute of Technology · US

Funding

Genetic evolution of glioblastomas during radiation and temozolomide therapyR01CA188228 · NCI · DANA-FARBER CANCER INST · PI BEROUKHIM, RAMEEN, CHAKRAVARTI, ARNAB · 2015 to 2025
$6.9M
High-resolution genome-wide mapping of structural mutations in prostate cancerK08CA122833 · NCI · DANA-FARBER CANCER INST · PI BEROUKHIM, RAMEEN · 2007 to 2011
$697k
NCI NIH HHS K08 CA122833NCI NIH HHS R01 CA188228
6 · The paper itself

Abstract

Glioblastoma (GBM) is a primary brain cancer with an abysmal prognosis and few effective therapies. The ability to investigate the tumor microenvironment before and during treatment would greatly enhance both understanding of disease response and progression, as well as the delivery and impact of therapeutics. Stereotactic biopsies are a routine surgical procedure performed primarily for diagnostic histopathologic purposes. The role of investigative biopsies - tissue sampling for the purpose of understanding tumor microenvironmental responses to treatment using integrated multi-modal molecular analyses ('Multi-omics") has yet to be defined. Secondly, it is unknown whether comparatively small tissue samples from brain biopsies can yield sufficient information with such methods. Here we adapt stereotactic needle core biopsy tissue in two separate patients. In the first patient with recurrent GBM we performed highly resolved multi-omics analysis methods including single cell RNA sequencing, spatial-transcriptomics, metabolomics, proteomics, phosphoproteomics, T-cell clonotype analysis, and MHC Class I immunopeptidomics from biopsy tissue that was obtained from a single procedure. In a second patient we analyzed multi-regional core biopsies to decipher spatial and genomic variance. We also investigated the utility of stereotactic biopsies as a method for generating patient derived xenograft models in a separate patient cohort. Dataset integration across modalities showed good correspondence between spatial modalities, highlighted immune cell associated metabolic pathways and revealed poor correlation between RNA expression and the tumor MHC Class I immunopeptidome. In conclusion, stereotactic needle biopsy cores are of sufficient quality to generate multi-omics data, provide data rich insight into a patient's disease process and tumor immune microenvironment and can be of value in evaluating treatment responses. One sentence summary: Integrative multi-omics analysis of stereotactic needle core biopsies in glioblastoma.

Identifiers

PMID38234840
PMCPMC10793534
OpenAlexW4390461456

What OpenQuestion holds

Textmetadata
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.