Evidence map›Paper›PMID 28412222›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2017

Targeted drug distribution in tumor extracellular fluid of GD2-expressing neuroblastoma patient-derived xenografts using SN-38-loaded nanoparticles conjugated to the monoclonal antibody 3F8.

Carles Monterrubio, Sonia Paco, Nagore G Olaciregui, Guillem Pascual-Pasto, Monica Vila-Ubach, Maria Cuadrado-Vilanova, M Mar Ferrandiz, Helena Castillo-Ecija, Romina Glisoni, Nataliya Kuplennik and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 46 citations in OpenAlex.

  1. Antibody-conjugated polymer nanoparticles for brain cancer.Drug delivery and translational research · 2025
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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

17 authors at 4 institutions in 4 countries.

Carles MonterrubioInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Sonia PacoInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Nagore G OlacireguiInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Guillem Pascual-PastoInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Monica Vila-UbachInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Maria Cuadrado-VilanovaInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
M Mar FerrandizInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Helena Castillo-EcijaInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Romina GlisoniCONICET-Department of Pharmaceutical Technology, Faculty of Pharmacy and Biochemistry, Universidad de Buenos Aires, CP1113 Buenos Aires, Argentina.
Nataliya KuplennikLaboratory of Pharmaceutical Nanomaterials Science, Department of Materials Science and Engineering, Technion-Israel Institute of Technology, 3200003 Haifa, Israel.
Achim JungbluthMemorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Carmen de TorresInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Cinzia LavarinoInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
N K V CheungMemorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Jaume MoraInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain.
Alejandro SosnikLaboratory of Pharmaceutical Nanomaterials Science, Department of Materials Science and Engineering, Technion-Israel Institute of Technology, 3200003 Haifa, Israel.
Angel M CarcabosoInstitut de Recerca Sant Joan de Deu, 08950 Barcelona, Spain; Department of Pediatric Hematology and Oncology, Hospital Sant Joan de Deu, 08950 Barcelona, Spain. Electronic address: amontero@fsjd.org.
Hospital Sant Joan de Déu Barcelona · ESMemorial Sloan Kettering Cancer Center · USTechnion – Israel Institute of Technology · ILConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Neuroblastoma is a pediatric solid tumor with high expression of the tumor associated antigen disialoganglioside GD2. Despite initial response to induction therapy, nearly 50% of high-risk neuroblastomas recur because of chemoresistance. Here we encapsulated the topoisomerase-I inhibitor SN-38 in polymeric nanoparticles (NPs) surface-decorated with the anti-GD2 mouse mAb 3F8 at a mean density of seven antibody molecules per NP. The accumulation of drug-loaded NPs targeted with 3F8 versus with control antibody was monitored by microdialysis in patient-derived GD2-expressing neuroblastoma xenografts. We showed that the extent of tumor penetration by SN-38 was significantly higher in mice receiving the targeted nano-drug delivery system when compared to non-targeted system or free drug. This selective penetration of the tumor extracellular fluid translated into a strong anti-tumor effect prolonging survival of mice bearing GD2-high neuroblastomas in vivo.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, NeoplasmAntineoplastic Agents, PhytogenicCamptothecinCell Line, TumorChild, PreschoolDrug LiberationExtracellular FluidGene Expression Regulation, NeoplasticHumansImmunoglobulin GIrinotecanMaleMice, Nude3F8 antibodyAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, NeoplasmAntineoplastic Agents, PhytogenicCamptothecinImmunoglobulin GIrinotecanN-Acetylgalactosaminyltransferases(N-acetylneuraminyl)-galactosylglucosylceramide N-acetylgalactosaminyltransferaseGD2-targeted nanoparticlesIntratumor drug distributionIrinotecan (PubChem CID: 60838).Irinotecan/SN-38MicrodialysisNeuroblastomaPDX modelsSN-38 (PubChem CID: 104842)Tumor extracellular fluid

Identifiers

PMID28412222
PMCPMC5564453
OpenAlexW2607369599

What OpenQuestion holds

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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.