Evidence map›Paper›PMID 31435922›Full record

Trial reportMethods in molecular biology (Clifton, N.J.)2020

Sonoporation for Augmenting Chemotherapy of Pancreatic Ductal Adenocarcinoma.

Jason Castle, Spiros Kotopoulis, Flemming Forsberg

Abstract readClinical Trial, Phase IClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Methods in molecular biology (Clifton, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

3 authors.

Jason CastleGeneral Electric Research, Niskayuna, NY, USA. castle@ge.com.
Spiros KotopoulisNational Centre for Ultrasound in Gastroenterology, Haukeland University Hospital, Bergen, Norway.
Flemming ForsbergThomas Jefferson University, Philadelphia, PA, USA.

Funding

Optimizing Ultrasound Enhanced Delivery of TherapeuticsR01CA199646 · NCI · THOMAS JEFFERSON UNIVERSITY · PI FORSBERG, FLEMMING · 2016 to 2023
$2.9M
NCI NIH HHS R01 CA199646
6 · The paper itself

Abstract

Pancreatic cancer is the third most common cancer diagnosed in the United States, with more than 53,000 new cases in 2017. It is the fourth leading cause of cancer-related death in both men and women. Nonetheless, there has been no significant improvement in survival for pancreatic ductal adenocarcinoma (PDAC) patients over the past 30+ years. For this reason, there is a considerable and urgent clinical need to develop innovative strategies for effective drug delivery and treatment monitoring, resulting in improved outcomes for patients with PDAC.This chapter describes the development of contrast-enhanced ultrasound image-guided drug delivery (CEUS-IGDD or sonoporation) to be that method and to translate it from the lab to the clinic. The initial clinical focus has been on a Phase I clinical trial for enhancing the effectiveness of standard chemotherapeutics for treatment of inoperable PDAC, which demonstrated a median survival increase from 8.9 months to 17.6 months in ten subjects augmented with sonoporation compared to 63 historical controls (p = 0.011). Recent efforts to optimize this platform and move forward to a larger Phase II clinical trial will be described.

Indexed as

AnimalsCarcinoma, Pancreatic DuctalContrast MediaDrug Delivery SystemsFemaleHumansMaleMiceMicrobubblesPancreatic NeoplasmsUltrasonographyXenograft Model Antitumor AssaysContrast MediaAugmented chemotherapy deliveryContrast-enhanced ultrasound imagingHuman clinical trialPancreatic ductal adenocarcinomaSonoporation

Identifiers

PMID31435922
PMCPMC7418147

What OpenQuestion holds

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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.