ReviewCancer chemotherapy and pharmacology2025
Mechanisms of resistance to antibody-drug conjugates in cancer: molecular barriers and pharmacological solutions.
Review in Cancer chemotherapy and pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Targeted proteoform degradation for precision drug design, delivery, and therapy.Drug delivery · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Antibody-drug conjugates (ADCs) are a potential category of specialized cancer therapeutics that integrate monoclonal antibodies (mAbs) with cytotoxic drugs. These therapies seek to provide very effective pharmaceuticals directly to neoplastic cells, enhancing the therapeutic index compared to traditional chemotherapy. Despite their clinical success, ADCs face significant challenges, particularly in the form of resistance mechanisms that limit their effectiveness. Resistance can arise through various pathways, including antigen-related alterations, impaired drug internalization, and inefficient payload release. Other factors that complicate ADC penetration and efficacy are tumor microenvironment factors, including hypoxia and acidic pH. This review discusses the mechanistic origin of ADC resistance, and investigates the major biological, chemical, and pharmacokinetic variables related to treatment failure. We also indicate the new approaches to fighting resistance, such as next-generation ADCs designs, drug combination therapies, and tumor microenvironment modulation. Lastly, we talk about the possibility of new payloads, better linkers, and other possible drug delivery systems that could further the ADC efficacy to combat cancer.
Indexed as
Identifiers
41335143What Socratic holds
Registered trials
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 Socratic graph.