Evidence map›Paper›PMID 32999828›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2020

Thermosensitive Exosome-Liposome Hybrid Nanoparticle-Mediated Chemoimmunotherapy for Improved Treatment of Metastatic Peritoneal Cancer.

Qijun Lv, Lili Cheng, Yao Lu, Xiaoge Zhang, Yizhen Wang, Junfeng Deng, Jiangbing Zhou, Bo Liu, Jie Liu

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 1 pooled it
20.2field-weighted citation impact, top 1% 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

102 citing papers in PubMed, 1 synthesis or guideline pooled it, 192 citations in OpenAlex.

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42 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 2 countries.

Qijun LvDepartment of General Surgery The Third Affiliated Hospital of Sun Yat-sen University Guangzhou 510120 China.
Lili ChengSchool of Biomedical Engineering Sun Yat-sen University Guangzhou Guangdong 510006 China.
Yao LuSchool of Biomedical Engineering Sun Yat-sen University Guangzhou Guangdong 510006 China.
Xiaoge ZhangSchool of Biomedical Engineering Sun Yat-sen University Guangzhou Guangdong 510006 China.
Yizhen WangDepartment of General Surgery The Third Affiliated Hospital of Sun Yat-sen University Guangzhou 510120 China.
Junfeng DengDepartment of General Surgery The Third Affiliated Hospital of Sun Yat-sen University Guangzhou 510120 China.
Jiangbing ZhouDepartments of Neurosurgery and of Biomedical Engineering Yale University New Haven CT 06510 USA.ORCID https://orcid.org/0000-0002-1201-5360
Bo LiuDepartment of General Surgery The Third Affiliated Hospital of Sun Yat-sen University Guangzhou 510120 China.
Jie LiuSchool of Biomedical Engineering Sun Yat-sen University Guangzhou Guangdong 510006 China.
Sun Yat-sen University · CNYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic peritoneal carcinoma (mPC) is a deadly disease without effective treatment. To improve treatment of this disease, a recently developed hyperthermic intraperitoneal chemotherapy (HIPEC) has emerged as the standard of care. However, the efficacy of this approach is limited by inefficient drug penetration and rapidly developed drug resistance. Herein, a nanotechnology approach is reported that is designed to improve drug delivery to mPC and to augment the efficacy of HIPEC through delivery of chemoimmunotherapy. First, the drug delivery efficiency of HIPEC is determined and it is found that chemotherapy agents cannot be efficiently delivered to large tumors nodules. To overcome the delivery hurdle, genetically engineered exosomes-thermosensitive liposomes hybrid NPs, or gETL NPs, are then synthesized, and it is demonstrated that the NPs after intravenous administration efficiently penetrates into mPC tumors and releases payloads at the hypothermia condition of HIPEC. Last, it is shown that, when granulocyte-macrophage colony-stimulating factor (GM-CSF) and docetaxel are co-delivered, gETL NPs effectively inhibit tumor development and the efficacy is enhanced when HIPEC is co-administered. The study provides a strategy to improve drug delivery to mPCs and offers a promising approach to improve treatment of the disease through combination of locoregional delivery of HIPEC and systemic delivery of chemoimmunotherapy via gETL NPs.

Indexed as

chemoimmunotherapyexosomeshyperthermic intraperitoneal chemotherapymetastatic peritoneal carcinomathermosensitive liposomes

Identifiers

PMID32999828
PMCPMC7509655
OpenAlexW3045740151

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.