ReviewActa pharmaceutica Sinica. B2026
Emerging organoids and organoids-on-chip platforms for translational development of antibody‒drug conjugates and next-generation bioconjugates.
Review in Acta pharmaceutica Sinica. B, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The rapid evolution of antibody‒drug conjugates (ADCs) and emerging X-drug conjugates (XDCs) has revolutionized targeted cancer therapy, yet their clinical translation is severely bottlenecked by the lack of human-relevant preclinical models. To bridge this translational gap, patient-derived organoids and organoids-on-chip (OoC) platforms recapitulate key features of human tumor biology, offering powerful tools for investigating cancer heterogeneity and improving the predictive evaluation of bioconjugated therapeutics. In this review, we systematically summarize the current landscape and challenges of ADCs and XDCs development across existing preclinical models, critically discuss the concepts, biological principles and application potential of organoid- and OoC-based systems, and highlight recent global policy developments and collaborative initiatives shaping their translational implementation. Finally, we highlight key challenges and future perspectives for leveraging organoids and OoCs in the druggability assessment, optimization, and translational development of ADCs and XDCs.
Indexed as
Identifiers
What 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.