Evidence map›Paper›PMID 41179189›Full record

ArticleACS omega2025

Evaluation of Antibody-Drug Conjugate Performances Using a Novel HPLC-DAD Method for Tumor-Specific Detection of DM4 and

Giulio Lovato, Miryam Perrucci, Ilaria Cela, Alessia Lamolinara, Arianna Mercatelli, Vincenzo De Laurenzi, Emily Capone, Marcello Locatelli, Gianluca Sala

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Giulio LovatoDepartment of Innovative Technologies in Medicine and Dentistry, Center for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.
Miryam PerrucciDepartment of Innovative Technologies in Medicine and Dentistry, Center for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.
Ilaria CelaDepartment of Innovative Technologies in Medicine and Dentistry, Center for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.
Alessia LamolinaraDepartment of Medicine and Aging Sciences, G. D'Annunzio University of Chieti-Pescara, Chieti 66100, Italy.
Arianna MercatelliDepartment of Innovative Technologies in Medicine and Dentistry, Center for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.
Vincenzo De LaurenziDepartment of Innovative Technologies in Medicine and Dentistry, Center for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.
Emily CaponeCenter for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.
Marcello LocatelliDepartment of Science, University of Chieti-Pescara "G. D'Annunzio", Chieti 66100, Italy.ORCID https://orcid.org/0000-0002-0840-825X
Gianluca SalaDepartment of Innovative Technologies in Medicine and Dentistry, Center for Advanced Studies and Technology (CAST), University of Chieti-Pescara "G. D'Annunzio", Via dei Vestini 31, Chieti 66100, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-drug conjugates (ADCs) are an emerging class of therapeutics that have gained interest in precision medicine for cancer treatment, combining the targeted delivery capabilities of monoclonal antibodies with the potent cytotoxicity of small-molecule drugs. The goal is to enhance the therapeutic window by maximizing tumor cell killing while minimizing off-target toxicity. Pivotal aims are precise delivery of payload in the tumor site and a robust analytical methodology to quantify the accumulation of it. 1959-sss/DM4, a novel ADC targeting highly glycosylated LGALS3BP, which is a protein implicated in tumor progression and metastasis, was developed. This ADC has shown potent and durable antitumor activity in various preclinical models. A high-performance liquid chromatography (HPLC) method according to ICH guidelines for the simultaneous quantification of DM4 and its primary metabolite,

Identifiers

PMID41179189
PMCPMC12572975

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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.