Evidence map›Paper›PMID 41906015›Full record

ArticleAnnals of biomedical engineering2026

Development and Pre-clinical Feasibility of a Catheter-Based Platform for Interventional Phase-0 Drug Response Measurements.

Sharath K Bhagavatula, Ellen Maloney, Hidde Ploeger, Sebastian W Ahn, Samantha Martin, Santhosh A Mathew, Sajanlal Panikkanvalappil, Guigen Liu, Oliver Jonas

Abstract read
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Article in Annals of biomedical engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Sharath K BhagavatulaBrigham and Women's Hospital, Boston, MA, 02115, USA. sbhagavatula@bwh.harvard.edu.ORCID http://orcid.org/0000-0002-9194-0932
Ellen MaloneyBrigham and Women's Hospital, Boston, MA, 02115, USA.
Hidde PloegerBrigham and Women's Hospital, Boston, MA, 02115, USA.
Sebastian W AhnBrigham and Women's Hospital, Boston, MA, 02115, USA.
Samantha MartinBrigham and Women's Hospital, Boston, MA, 02115, USA.
Santhosh A MathewBrigham and Women's Hospital, Boston, MA, 02115, USA.
Sajanlal PanikkanvalappilBrigham and Women's Hospital, Boston, MA, 02115, USA.
Guigen Liu *Brigham and Women's Hospital, Boston, MA, 02115, USA.
Oliver Jonas *Brigham and Women's Hospital, Boston, MA, 02115, USA. ojonas@bwh.harvard.edu.

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
Development and optimization of highly effective treatments in patients with head and neck cancer using in situ implantable microdevicesR01CA295683 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Oliver Jonas · 2025 to 2026
$1.4M
Interventional method development for multiplexed personalized drug evaluation using implantable microdevicesR03CA270772 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI BHAGAVATULA, SHARATH · 2023 to 2024
$154k
NCI NIH HHS R01CA295683NCI NIH HHS R03CA270772NIBIB NIH HHS P41EB028741Society of Interventional Radiology Foundation Ernest Ring Grant
6 · The paper itself

Abstract

purposeTo develop and validate a percutaneous Interventional Drug Response Assay (IDRA) catheter capable of intratumoral drug microdosing, adhesive stabilization, and subsequent biopsy retrieval of drug-exposed tissue, enabling minimally invasive in situ drug response measurements.

methodsThe IDRA catheter was designed as a modular platform allowing image-guided insertion, adhesive-based stabilization, microdose drug delivery into four discrete tissue regions, and suction-assisted biopsy retrieval. Feasibility and functionality were assessed across three ex vivo models: a gelatin phantom (n = 15), pork loin (n = 15), and rabbit VX-2 tumors (n = 15), as well as a rabbit VX-2 in vivo model (n = 2). Endpoints included proportion of drug reservoirs yielding intact tissue, sample thickness, and stabilization force. Success was defined as retrieval of ≥ 75% of drug regions with ≥ 3 drug sites per catheter and stabilization within a target force range of 1.5-4 N.

resultsEx vivo success rates were 100% (15/15 catheters) in phantom, 80% (12/15) in pork loin, and 80% (12/15) in VX-2 tumors. Mean tissue thickness exceeded 500 µm in all models (phantom: 860 ± 233 µm; loin: 589 ± 261 µm; VX-2: 637 ± 271 µm). Stabilization forces were within the target range across all tissue types (phantom: 3.4 ± 0.5 N; loin: 2.5 ± 0.6 N; VX-2: 2.8 ± 0.6 N). In vivo, 3-4 drug regions were successfully retrieved per catheter without complications.

conclusionThe IDRA catheter achieved predefined functional endpoints across ex vivo and in vivo models, demonstrating early mechanical and procedural feasibility. If biologically validated, this could serve as a non-surgical platform for microdose-based early human drug response and biomarker testing and personalized oncology applications.

Indexed as

BiopsyCatheterInterventional oncologyMicrodosingPhase−0

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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.