Evidence map›Paper›PMID 30420717›Full record

ArticleCancer gene therapy2019

A model of breast cancer meningeal metastases: characterization with in vivo molecular imaging.

Darshini Kuruppu, Deepak Bhere, Christian T Farrar, Khalid Shah, Anna-Liisa Brownell, Kenneth K Tanabe

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Darshini KuruppuDepartment of Surgery, Massachusetts General Hospital, Boston, MA, USA.
Deepak BhereDepartment of Neurosurgery, Brigham & Women's Hospital, Boston, MA, USA.ORCID 0000-0003-4142-5518
Christian T FarrarDepartment of Radiology, Massachusetts General Hospital, Boston, MA, USA.
Khalid ShahDepartment of Neurosurgery, Brigham & Women's Hospital, Boston, MA, USA.
Anna-Liisa BrownellDepartment of Radiology, Massachusetts General Hospital, Boston, MA, USA.
Kenneth K TanabeDepartment of Surgery, Massachusetts General Hospital, Boston, MA, USA. ktanabe@partners.org.
Massachusetts General Hospital · USBrigham and Women's Hospital · US

Funding

Novel oncolytic HSV-1 therapy for breast cancer meningeal metastasesR21CA186054 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI KURUPPU, KUMUDU DARSHINI · 2014 to 2015
$416k
NCI NIH HHS R21 CA186054
6 · The paper itself

Abstract

Meningeal metastasis is a fatal complication of breast cancer which affects 8-15% of patients who experience severe neurological complications of cranial nerves, cerebrum, and spinal cord. Survival once diagnosed is less than 4 months. Currently there is no cure. Aggressive multimodal radiation, intra-CSF, or systemic chemotherapy is palliative. Investigation of urgently needed new treatment modalities is hindered by the lack of suitable animal models to effectively study tumor growth kinetics. We present a model of meningeal metastases where tumor growth and associated neurological symptoms have been characterized over 3 weeks by sequential molecular imaging, tumor growth kinetics, and histopathology. Meningeal metastases were induced by stereotaxic injection of human breast cancer cells (MDA-MB-231-Rluc) into the lateral ventricle. Tumor identified by Gd-MRI and Rluc-bioluminescence depict growth in 3 phases, namely lag, exponential, and plateau phase. Invasive tumor growth was highlighted by changes in contrast distribution in the meninges, ventricle and brain compartments over time where moderate contrast uptake in the early growth phase gave rise to a heavy tumor burden in the base of the brain in the latter phases. Tumor growth was accompanied with debilitating neurological symptoms and change in body mass. Tumor was confirmed by ex vivo histology. The reliability of the model to study novel therapeutics was confirmed by oncolytic virus delivered into the lateral ventricle showed potential for treatment. This effective and reliable model resembles human disease progression and is ideally suited to investigate novel treatments.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorFemaleHumansMeningeal NeoplasmsMiceMice, NudeMolecular ImagingNeoplasm Metastasis

Identifiers

PMID30420717
OpenAlexW2899987028

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.