Evidence map›Paper›PMID 26089090›Full record

ReviewThe AAPS journal2015

Versatility of Particulate Carriers: Development of Pharmacodynamically Optimized Drug-Loaded Microparticles for Treatment of Peritoneal Cancer.

Jessie L-S Au, Ze Lu, M Guillaume Wientjes

Open access · bronzeAbstract readReview
In one paragraph

Review in The AAPS journal, 2015. 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
2.4field-weighted citation impact, top 13% 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, 18 citations in OpenAlex.

  1. Targeted Radium Alpha Therapy in the Era of Nanomedicine: In Vivo Results.International journal of molecular sciences · 2024
    Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Therapeutic Effect of α-EmittingTranslational oncology · 2018
    Article
  8. Review
  9. Intraperitoneal chemotherapy of ovarian cancer by hydrogel depot of paclitaxel nanocrystals.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Article
  10. Review
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 at 1 institution in 1 country.

Jessie L-S AuOptimum Therapeutics LLC, 1815 Aston Avenue, Suite 107, Carlsbad, California, 92008, USA, jau@optimumtx.com.
Ze Lu
M Guillaume Wientjes
Optimum Therapeutics (United States) · US

Funding

Multiscale computational models for developing combination cancer therapyR01GM100487 · NIGMS · OPTIMUM THERAPEUTICS, LLC · PI AU, JESSIE L.-S., WIENTJES, M GUILLAUME · 2011 to 2014
$1.3M
Capturing dynamic and inter-dependent biointerfaces in nanotechnology designsR01EB015253 · NIBIB · OPTIMUM THERAPEUTICS, LLC · PI AU, JESSIE L.-S., WIENTJES, M GUILLAUME · 2011 to 2014
$1.1M
Tumor-priming Microparticles for Pancreatic CancerR44CA103133 · NCI · OPTIMUM THERAPEUTICS, LLC · PI LU, ZE · 2006 to 2012
$1.1M
Apoptosis Inducing to Enhance Tumor TargetingR43CA103133 · NCI · OPTIMUM THERAPEUTICS, LLC · PI LU, ZE · 2003 to 2004
$496k
NCATS NIH HHS X01TR000329NCI NIH HHS R43/R44CA103133NCI NIH HHS R44 CA103133NIBIB NIH HHS R01 EB015253NIBIB NIH HHS R01EB015253NIGMS NIH HHS R01 GM100487NIGMS NIH HHS R01GM100487NINDS NIH HHS X01NS069198
6 · The paper itself

Abstract

Intraperitoneal (IP) chemotherapy confers significant survival benefits in cancer patients. However, several problems, including local toxicity and ineffectiveness against bulky tumors, have prohibited it from becoming a standard-of-care. We have developed drug-loaded, tumor-penetrating microparticles (TPM) to address these problems. TPM comprises two components and uses the versatile PLGA or poly(lacticco-glycolic acid) copolymer to provide tumor-selective adherence and pharmacodynamically optimized fractionated dosing to achieve the desired tumor priming (which promotes particle penetration into tumors) plus immediate and sustained antitumor activity. Preclinical studies show that TPM is less toxic and more effective against several IP metastatic tumors with different characteristics (fast vs. slow growing, porous vs. densely packed structures, wide-spread vs. solitary tumors, early vs. late stage, with or without peritoneal carcinomatosis or ascites), compared to the intravenous paclitaxel/Cremophor micellar solution that has been used off-label in previous IP studies. TPM further requires less frequent dosing. These encouraging preclinical results have motivated the follow-up clinical development of TPM. We are working with National Institutes of Health on the IND-enabling studies.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicDrug CarriersDrug DesignHumansInjections, IntraperitonealMicrospheresPaclitaxelPeritoneal NeoplasmsPolyethylene GlycolsPolymersAntineoplastic Agents, PhytogeniccremophorDrug CarriersPaclitaxelPolyethylene GlycolsPolymers

Identifiers

PMID26089090
PMCPMC4540721
OpenAlexW820717085

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.