Evidence map›Paper›PMID 37672566›Full record

ArticleScience translational medicine2023

Intratumoral drug-releasing microdevices allow in situ high-throughput pharmaco phenotyping in patients with gliomas.

Pierpaolo Peruzzi, Christine Dominas, Geoffrey Fell, Joshua D Bernstock, Sarah Blitz, Debora Mazzetti, Mykola Zdioruk, Hassan Y Dawood, Daniel V Triggs, Sebastian W Ahn and 13 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Science translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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.

NCT04135807 early_phase1recruitingnot on this map

A Pilot Study of an Implantable Microdevice for In Situ Evaluation of Drug Response in Patients With Primary Brain Tumors

TypeinterventionalSponsorOliver JonasRan2020 to 2028Enrolled12ConditionsGrade II Glioma, Grade III Glioma, Grade IV Glioma, AstrocytomaArmsMicrodevice
NCT07352566 phase4not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Utilization of a Cutaneous Therapy In Situ Microdevice

TypeinterventionalSponsorUniversity of California, San FranciscoRan2026 to 2030Enrolled10ConditionsPsoriasis, Atopic DermatitisArmsIn situ cutaneous microdevice, Triamcinolone, 5-Fluorouracil, Calcipotriene, Tapinarof
3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
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  4. Recent Advances in Targeted Therapies for Adult Gliomas.Current neurology and neuroscience reports · 2026
    Review
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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

23 authors.

Pierpaolo PeruzziDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0001-5034-2963
Christine DominasDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.
Geoffrey FellDepartment of Data Science, Dana Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA.ORCID 0000-0001-6436-6691
Joshua D BernstockDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0002-7814-3867
Sarah BlitzHarvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA.ORCID 0000-0001-9129-9447
Debora MazzettiDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.
Mykola ZdiorukDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0002-4275-2724
Hassan Y DawoodDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0002-2190-5146
Daniel V TriggsDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.
Sebastian W AhnDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.
Sharath K BhagavatulaDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.ORCID 0000-0002-9194-0932
Shawn M DavidsonLewis-Sigler Institute of Integrative Genomics, Princeton University, Princeton, NJ 08540, USA.ORCID 0000-0002-3475-0382
Zuzana TatarovaDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.ORCID 0000-0002-3128-7214
Michael PannellDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0001-9557-1997
Kyla TrumanDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0001-9519-6023
Anna BallDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0009-0000-7725-4330
Maxwell P GoldDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Veronika PisterDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0002-8051-4890
Ernest FraenkelDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0001-9249-8181
E Antonio ChioccaDepartment of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Road, Boston, MA 02115, USA.ORCID 0000-0001-5183-1670
Keith L LigonDepartment of Pathology, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.ORCID 0000-0002-7733-600X
Patrick Y WenDivision of Neuro-Oncology, Dana Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02115, USA.ORCID 0000-0002-0774-7700
Oliver JonasDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.ORCID 0000-0003-2512-2007

Funding

TRD 3 - Enabling Technologies for Intraprocedural GuidanceP41EB028741 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI Nobuhiko Hata, CLARE M TEMPANY · 2021 to 2026
$10.7M
Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
Using implantable microdevices for deep phenotyping of multiple drug responses in brain tumor patientsR01CA283905 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Oliver Jonas · 2023 to 2026
$3.3M
Identifying therapeutic pathways targeting medulloblastoma-immune cell interactionsU01CA253547 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FRAENKEL, ERNEST, MESIROV, JILL P. · 2021 to 2025
$2.7M
Implantable microdevices with integrated optical imaging for high-throughput in situ tumor response and drug sensitivity measurementR37CA224144 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI JONAS, OLIVER · 2018 to 2023
$2.4M
Harnessing Artificial MicroRNA Clusters Against Glioblastoma Epigenetic Plasticity and Resistance to TherapyR01NS116144 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI PERUZZI, PIER PAOLO · 2020 to 2025
$2.1M
In Situ characterization and manipulation of tumor immune cell metabolomics using implantable microdevicesR01CA223150 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI JONAS, OLIVER · 2018 to 2022
$1.9M
NCI NIH HHS R01 CA223150NCI NIH HHS R01 CA283905NCI NIH HHS R37 CA224144NCI NIH HHS U01 CA253547NIBIB NIH HHS P41 EB028741NIGMS NIH HHS T32 GM087237NINDS NIH HHS R01 NS116144
6 · The paper itself

Abstract

The lack of reliable predictive biomarkers to guide effective therapy is a major obstacle to the advancement of therapy for high-grade gliomas, particularly glioblastoma (GBM), one of the few cancers whose prognosis has not improved over the past several decades. With this pilot clinical trial (number NCT04135807), we provide first-in-human evidence that drug-releasing intratumoral microdevices (IMDs) can be safely and effectively used to obtain patient-specific, high-throughput molecular and histopathological drug response profiling. These data can complement other strategies to inform the selection of drugs based on their observed antitumor effect in situ. IMDs are integrated into surgical practice during tumor resection and remain in situ only for the duration of the otherwise standard operation (2 to 3 hours). None of the six enrolled patients experienced adverse events related to the IMD, and the exposed tissue was usable for downstream analysis for 11 out of 12 retrieved specimens. Analysis of the specimens provided preliminary evidence of the robustness of the readout, compatibility with a wide array of techniques for molecular tissue interrogation, and promising similarities with the available observed clinical-radiological responses to temozolomide. From an investigational aspect, the amount of information obtained with IMDs allows characterization of tissue effects of any drugs of interest, within the physiological context of the intact tumor, and without affecting the standard surgical workflow.

Indexed as

GlioblastomaGliomaDrug Delivery SystemsDrug LiberationHumansTemozolomideTemozolomide

Identifiers

PMID37672566
PMCPMC10754230

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Registered trials

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.