Evidence map›Paper›PMID 32651443›Full record

ArticleScientific reports2020

Co-administration of H-ferritin-doxorubicin and Trastuzumab in neoadjuvant setting improves efficacy and prevents cardiotoxicity in HER2 + murine breast cancer model.

F Andreata, A Bonizzi, M Sevieri, M Truffi, M Monieri, L Sitia, F Silva, L Sorrentino, R Allevi, P Zerbi and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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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

20 authors at 5 institutions in 1 country.

F Andreata *Nanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.ORCID http://orcid.org/0000-0002-5710-3671
A Bonizzi *Nanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
M SevieriNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
M TruffiNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
M MonieriNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
L SitiaNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
F SilvaNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
L SorrentinoNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
R AlleviNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
P ZerbiPathology Unit, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
B MarchiniPathology Unit, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
E LonghiPathology Unit, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.
R OttriaMedical Chemistry, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy.ORCID http://orcid.org/0000-0003-3379-0582
S CasatiDepartment of Biomedical, Surgical and Dental Sciences, Sezione Di Tossicologia Forense, Università Di Milano, Milan, Italy.ORCID http://orcid.org/0000-0002-5049-7321
R VannaNanomedicine and Molecular Imaging Laboratory, Istituti Clinici Scientifici Maugeri IRCCS, Pavia, Italy.ORCID http://orcid.org/0000-0001-6218-8393
C MorassoNanomedicine and Molecular Imaging Laboratory, Istituti Clinici Scientifici Maugeri IRCCS, Pavia, Italy.
M BelliniNanoBioLab, Department of Biotechnology and Biosciences, Università Di Milano-Bicocca, Milan, Italy.
D ProsperiNanoBioLab, Department of Biotechnology and Biosciences, Università Di Milano-Bicocca, Milan, Italy.
F CorsiNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy. fabio.corsi@icsmaugeri.it.
S MazzucchelliNanomedicine Laboratory, Department of Biomedical and Clinical Sciences "Luigi Sacco", Università Di Milano, Milan, Italy. serena.mazzucchelli@unimi.it.
Luigi Sacco Hospital · ITIstituti Clinici Scientifici Maugeri · ITUniversity of Milano-Bicocca · ITVita-Salute San Raffaele University · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neoadjuvant chemotherapy has been established as the standard of care for HER2-positive breast cancer since it allows cancer down-staging, up to pathological complete response. The standard of care in the neoadjuvant setting for HER2-positive breast cancer is a combination of highly cytotoxic drugs such as anthracyclines and the anti-HER2 monoclonal antibody. Despite this cocktail allows a pathological complete response in up to 50%, their co-administration is strongly limited by intrinsic cardiotoxicity. Therefore, only a sequential administration of anthracyclines and the anti-HER2 treatment is allowed. Here, we propose the anthracycline formulation in H-Ferritin nanocages as promising candidate to solve this unmet clinical need, thanks to its capability to increase anthracyclines efficacy while reducing their cardiotoxicity. Treating a murine model of HER2-positive breast cancer with co-administration of Trastuzumab and H-Ferritin anthracycline nanoformulation, we demonstrate an improved tumor penetration of drugs, leading to increased anticancer efficacy and reduced of cardiotoxicity.

Indexed as

AnimalsAnthracyclinesAntineoplastic Combined Chemotherapy ProtocolsApoferritinsApoptosisCardiotoxicityCell LineDoxorubicinErb-b2 Receptor Tyrosine KinasesFemaleHumansMammary Neoplasms, AnimalMiceMice, Inbred BALB CMitochondriaNeoadjuvant TherapyAnthracyclinesApoferritinsDoxorubicinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumab

Identifiers

PMID32651443
PMCPMC7351752
OpenAlexW3040733000

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.