PDCs, small molecule-drug conjugates, and other novel conjugate modalities are emerging as alternatives to ADCs, offering advantages in cost, penetration, and manufacturing for targeted cancer therapy.
Beyond antibodiesPeptide-drug conjugates offer better tumor penetration, simpler manufacturing, and lower cost than antibody-drug conjugates — democratizing targeted cancer therapy
What the researchers found
PDCs, SMDCs, and novel conjugate modalities are emerging as ADC alternatives with advantages in tumor penetration, manufacturing simplicity, cost, and immunogenicity for targeted cancer therapy.
Why it matters
ADCs have transformed cancer therapy but are expensive and imperfect. Alternative conjugates could democratize targeted therapy.
How the study worked
Review of conjugate drug modalities beyond ADCs, covering PDCs, SMDCs, and novel platforms.
What this study cannot tell us
Many alternative conjugates are still preclinical. Head-to-head comparisons with ADCs limited.
How to read the evidence
Review of evolving conjugate therapy landscape.
When this study was published
Published in 2025.
The bigger picture
The conjugate therapy revolution is expanding beyond antibodies to include peptides and small molecules, potentially making targeted cancer therapy more accessible.
Questions still open
- Will PDCs achieve ADC-level clinical success?
- Which conjugate modality is optimal for each tumor type?
- Can manufacturing costs of PDCs compete with generic small molecules?
Common questions
What are peptide-drug conjugates?
Are they better than ADCs?
Read the original research
Challenges and opportunities beyond antibody-drug conjugates: Toward a new era of programmable therapeutic proteins.
Biochemical and biophysical research communications, 794, 153018
Citation
Kurtova, Anastasia I; Iureva, Anna M; Esetov, Nikolay S; Sokol, Daniil V; Fedotova, Polina A; Shipunova, Victoria O. (2026). Challenges and opportunities beyond antibody-drug conjugates: Toward a new era of programmable therapeutic proteins.. Biochemical and biophysical research communications, 794, 153018. https://doi.org/10.1016/j.bbrc.2025.153018