Evidence map›Paper›PMID 37071273›Full record

ReviewArchives of pharmacal research2023

Antibody drug conjugates as targeted cancer therapy: past development, present challenges and future opportunities.

Ritwik Maiti, Bhumika Patel, Nrupesh Patel, Mehul Patel, Alkesh Patel, Nirav Dhanesha

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Archives of pharmacal research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
8.7field-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

30 citing papers in PubMed, 38 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Ritwik MaitiInstitute of Pharmacy, Nirma University, Ahmedabad, 382481, Gujarat, India.
Bhumika PatelDepartment of Pharmaceutical Chemistry, Institute of Pharmacy, Nirma University, Ahmedabad, 382481, Gujarat, India. bhumika.patel@nirmauni.ac.in.ORCID http://orcid.org/0000-0002-1474-425X
Nrupesh PatelDepartment of Pharmaceutical Analysis, Institute of Pharmacy, Nirma University, Ahmedabad, 382481, Gujarat, India.
Mehul PatelDepartment of Pharmaceutical Chemistry and Analysis, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, CHARUSAT Campus, Changa, 388421, Gujarat, India.
Alkesh PatelDepartment of Pharmacology, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, CHARUSAT Campus, Changa, 388421, Gujarat, India.
Nirav DhaneshaDepartment of Pathology and Translational Pathobiology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, LA, 71103, USA. nirav.dhanesha@lsuhs.edu.
Nirma University · INCharotar University of Science and Technology · INLouisiana State University Health Sciences Center Shreveport · US

Funding

Mechanisms for Deep Vein Thrombosis following StrokeR01HL158546 · NHLBI · LOUISIANA STATE UNIV HSC SHREVEPORT · PI Nirav Dhanesha · 2022 to 2026
$2.2M
American Heart Association Career Development Award (20CDA3560123)American Heart Association-American Stroke Association 20CDA35260123 - NIRAV DHANESHANational Institute of Health NHLBI/NIH (R01HL15854601)NHLBI NIH HHS R01 HL158546
6 · The paper itself

Abstract

Antibody drug conjugates (ADCs) are promising cancer therapeutics with minimal toxicity as compared to small cytotoxic molecules alone and have shown the evidence to overcome resistance against tumor and prevent relapse of cancer. The ADC has a potential to change the paradigm of cancer chemotherapeutic treatment. At present, 13 ADCs have been approved by USFDA for the treatment of various types of solid tumor and haematological malignancies. This review covers the three structural components of an ADC-antibody, linker, and cytotoxic payload-along with their respective structure, chemistry, mechanism of action, and influence on the activity of ADCs. It covers comprehensive insight on structural role of linker towards efficacy, stability & toxicity of ADCs, different types of linkers & various conjugation techniques. A brief overview of various analytical techniques used for the qualitative and quantitative analysis of ADC is summarized. The current challenges of ADCs, such as heterogeneity, bystander effect, protein aggregation, inefficient internalization or poor penetration into tumor cells, narrow therapeutic index, emergence of resistance, etc., are outlined along with recent advances and future opportunities for the development of more promising next-generation ADCs.

Indexed as

Antineoplastic AgentsImmunoconjugatesNeoplasmsAntibodies, MonoclonalHumansAntibodies, MonoclonalAntineoplastic AgentsImmunoconjugatesADCCancer treatmentDARLinkersSite specific conjugationTargeted therapy

Identifiers

PMID37071273
PMCPMC11345756
OpenAlexW4366235055

What OpenQuestion holds

Textmetadata
LicenceTDM
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.