ArticleJournal of cheminformatics2026
Cosynllm: predicting drug combination synergy with LLM-generated descriptions.
Article in Journal of cheminformatics, 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
6 authors.
Funding
Abstract
Drug combination therapy is a well-established strategy for treating complex diseases. However, the vast combinatorial space renders exhaustive experimental screening impractical and costly. Recent studies have shown that deep learning techniques can effectively prioritize synergistic drug combinations by leveraging their powerful nonlinear modeling and automatic feature extraction capabilities. Meanwhile, Large Language Models (LLMs) offer great promise in drug discovery. In this paper, we propose CoSynLLM, an LLM-assisted predictive framework for predicting drug combination synergy. We fully leverage the latent knowledge embedded in LLMs to generate semantic-level chemical information, complemented by drug fingerprints to incorporate explicit structural details, while cell line gene expression profiles represent the cellular context. To effectively merge drug and cell line representations, a hierarchical feature fusion strategy is employed to progressively integrate features through multiple stages for predicting drug combination synergy. Extensive experiments on two benchmark datasets, NCI-ALMANAC and O'Neil, demonstrate that CoSynLLM achieves competitive performance, highlighting its effectiveness in predicting drug combination synergy. In summary, CoSynLLM effectively identifies synergistic drug combinations, offering a robust and practical computational framework for predicting drug combination synergy.
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.