Evidence map›Paper›PMID 32044093›Full record

ArticleThe Journal of thoracic and cardiovascular surgery2020

Paclitaxel-loaded expansile nanoparticles improve survival following cytoreductive surgery in pleural mesothelioma xenografts.

Ngoc-Quynh Chu, Rong Liu, Aaron Colby, Claire de Forcrand, Robert F Padera, Mark W Grinstaff, Yolonda L Colson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of thoracic and cardiovascular surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Article
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  8. Review
  9. Pilot-scale production of expansile nanoparticles: Practical methods for clinical scale-up.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Ngoc-Quynh ChuDivision of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, Boston, Mass.
Rong LiuDivision of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, Boston, Mass.
Aaron ColbyDepartments of Biomedical Engineering and Chemistry, Boston University, Boston, Mass.
Claire de ForcrandDivision of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, Boston, Mass.
Robert F PaderaDepartment of Pathology, Brigham and Women's Hospital, Boston, Mass.
Mark W GrinstaffDepartments of Biomedical Engineering and Chemistry, Boston University, Boston, Mass.
Yolonda L ColsonDivision of Thoracic Surgery, Department of Surgery, Massachusetts General Hospital, Boston, Mass. Electronic address: ycolson@partners.org.
Massachusetts General Hospital · USBoston University · USBrigham and Women's Hospital · US

Funding

OPTIMIZATION OF NANOPARTICLE TUMOR-LOCALIZATION AND DRUG-LOADINGFOR TREATING MESOTHELIOMAR01CA232056 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI COLSON, YOLONDA L, GRINSTAFF, MARK W. · 2019 to 2023
$2.7M
TUMOR SPECIFIC DELIVERY OF VERTICILLIN A OVERCOMES EPIGENETIC SILENCING RESPONSIBLE FOR DRUG RESISTANCER01CA227433 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI COLSON, YOLONDA L, GRINSTAFF, MARK W. · 2018 to 2022
$2.7M
Treating Peritoneal Malignancies with Paclitaxel-Loaded Expansile NanoparticlesR44CA189215 · NCI · IONIC PHARMACEUTICALS · PI COLBY, AARON HENRY · 2019 to 2020
$2.0M
Fluorescent nanoparticles to improve resections of microscopic pancreatic tumorsR43CA224739 · NCI · IONIC PHARMACEUTICALS · PI COLBY, AARON HENRY · 2018 to 2018
$297k
Prodrug treatment for CMLR43CA224731 · NCI · INHIBIKASE THERAPEUTICS · PI WERNER, MILTON H. · 2017 to 2017
$285k
Improving delivery of paclitaxel to ovarian cancer via expansile nanoparticlesR43CA213538 · NCI · IONIC PHARMACEUTICALS · PI COLBY, AARON HENRY · 2017 to 2017
$283k
Large Scale Synthesis and Biodistribution of Expansile NanoparticlesR43CA189215 · NCI · IONIC PHARMACEUTICALS · PI COLBY, AARON HENRY · 2014 to 2014
$225k
NCI NIH HHS R01 CA227433NCI NIH HHS R01 CA232056NCI NIH HHS R43 CA189215NCI NIH HHS R43 CA213538NCI NIH HHS R43 CA224731NCI NIH HHS R43 CA224739NCI NIH HHS R44 CA189215
6 · The paper itself

Abstract

objectiveMalignant pleural mesothelioma is a lethal malignancy with poor survival and high local recurrence rates despite multimodal therapy with cytoreduction and chemoradiation. We evaluated the antitumor efficacy of a paclitaxel-loaded pH-responsive expansile nanoparticle (PTX-eNP) in 2 clinically relevant murine xenograft models of malignant pleural mesothelioma.

methodsLuciferase-transfected MSTO-211H human mesothelioma cells were injected into the thoracic cavity of immunodeficient Nu/J mice. Tumor burden was monitored by bioluminescent imaging. Animals were randomized into 2 models of disease treatment chemotherapy with PTX-eNPs alone delivered locally for early limited disease or cytoreductive surgery plus local PTX-eNP chemotherapy for advanced disease. Within each disease model, anti-tumor efficacy of PTX-eNP was compared against standard formulation paclitaxel and drug-empty nanoparticles. Influence on survival was calculated. Fluorescently labeled PTX-eNPs and immunohistochemistry evaluated in vivo drug localization to tumor.

resultsIntrathoracic injection of MSTO-211H resulted in large tumor deposits distributed within the pleural space of the murine thoracic cavity. Local multidose treatment with PTX-eNPs alone in limited stage disease more than doubled survival compared with drug-empty nanoparticles (P ≤ .0001) and standard formulation paclitaxel (P = .0004). In the model of advanced disease, local multidose treatment with PTX-eNPs following cytoreductive surgery also prolonged survival by 126% and 69.4% compared with drug-empty nanoparticles (P = .0018) and standard formulation paclitaxel (P = .03457), respectively. Immunohistology demonstrated PTX-eNP accumulation within tumor cells in vitro and in vivo.

conclusionsLocal delivery of paclitaxel via eNPs confers prolonged survival in a murine model of malignant pleural mesothelioma as single modality treatment for limited disease and in combination with cytoreductive surgery for advanced disease.

Indexed as

Cytoreduction Surgical ProceduresLung NeoplasmsMesotheliomaNanoparticlesPaclitaxelPleural NeoplasmsAnimalsCell Line, TumorCombined Modality TherapyDisease Models, AnimalDisease ProgressionHumansMesothelioma, MalignantMicePneumonectomyTumor BurdenPaclitaxeladjuvant chemotherapycytoreductive surgerynanoparticlesnanotechnologypleural mesothelioma

Identifiers

PMID32044093
PMCPMC7354899
OpenAlexW2999423083

What OpenQuestion holds

Textmetadata
LicenceTDM
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.