Evidence map›Paper›PMID 36658712›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Sustained Intratumoral Administration of Agonist CD40 Antibody Overcomes Immunosuppressive Tumor Microenvironment in Pancreatic Cancer.

Hsuan-Chen Liu, Daniel Davila Gonzalez, Dixita Ishani Viswanath, Robin Shae Vander Pol, Shani Zakiya Saunders, Nicola Di Trani, Yitian Xu, Junjun Zheng, Shu-Hsia Chen, Corrine Ying Xuan Chua and 1 more

Open access · goldFull text read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

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  16. Engineering platforms for localized long-acting immune modulation.The Journal of allergy and clinical immunology · 2024
    Review
  17. Intratumor injected gold molecular clusters for NIR-II imaging and cancer therapy.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

11 authors at 1 institution in 1 country.

Hsuan-Chen LiuDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.ORCID 0000-0001-7857-0204
Daniel Davila GonzalezDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Dixita Ishani ViswanathDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Robin Shae Vander PolDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Shani Zakiya SaundersDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Nicola Di TraniDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Yitian XuCenter for Immunotherapy Research, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Junjun ZhengCenter for Immunotherapy Research, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Shu-Hsia ChenCenter for Immunotherapy Research, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Corrine Ying Xuan ChuaDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.
Alessandro GrattoniDepartment of Nanomedicine, Houston Methodist Research Institute, 6670 Bertner Ave, Houston, TX, 77003, USA.ORCID 0000-0001-7888-422X
Houston Methodist · US

Funding

A nanofluidic platform for tunable drug deliveryR01GM127558 · NIGMS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI GRATTONI, ALESSANDRO, LIU, XUEWU · 2018 to 2021
$1.6M
NIGMS NIH HHS R01 GM127558
6 · The paper itself

Abstract

Agonist CD40 monoclonal antibodies (mAb) is a promising immunotherapeutic agent for cold-to-hot tumor immune microenvironment (TIME) conversion. Pancreatic ductal adenocarcinoma (PDAC) is an aggressive and lethal cancer known as an immune desert, and therefore urgently needs more effective treatment. Conventional systemic treatment fails to effectively penetrate the characteristic dense tumor stroma. Here, it is shown that sustained low-dose intratumoral delivery of CD40 mAb via the nanofluidic drug-eluting seed (NDES) can modulate the TIME to reduce tumor burden in murine models. NDES achieves tumor reduction at a fourfold lower dosage than systemic treatment while avoiding treatment-related adverse events. Further, abscopal responses are shown where intratumoral treatment yields growth inhibition in distant untreated tumors. Overall, the NDES is presented as a viable approach to penetrate the PDAC immune barrier in a minimally invasive and effective manner, for the overarching goal of transforming treatment.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAnimalsAntibodies, MonoclonalCD40 AntigensImmunosuppressive AgentsImmunotherapyMiceTumor MicroenvironmentAntibodies, MonoclonalCD40 AntigensImmunosuppressive Agentsdrug deliveryimmunotherapyimplantable devicepancreatic cancersustained release

Identifiers

PMID36658712
PMCPMC10037694
OpenAlexW4317566998

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read54
identifiers read6
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.