ReviewCancer chemotherapy and pharmacology2025
Anlotinib in cancer therapy: mechanisms of action, clinical applications, and future perspectives.
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 2 papers.
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
2 citing papers in PubMed.
- Primary sarcomatoid urothelial carcinoma of the ureter: A case report and literature review.Urology case reports · 2026Article
- Consolidation thoracic radiotherapy following quadruple induction with benmelstobart, anlotinib, and chemotherapy for extensive-stage small cell lung cancer: rationale and protocol of a phase II study.Translational lung cancer research · 2026Article
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
No grant is acknowledged in the PubMed record.
Abstract
This comprehensive review examines anlotinib, a novel multi-target receptor tyrosine kinase inhibitor with potent antitumor activity. Anlotinib selectively inhibits multiple targets including VEGFR1-3, PDGFR-α, c-Kit, and FGFR1-3, demonstrating superior inhibitory effects compared to other tyrosine kinase inhibitors. The review explores anlotinib’s multifaceted mechanisms of action: inhibition of angiogenesis through disruption of VEGF/PDGF/FGF pathways, suppression of tumor cell migration and invasion via modulation of various signaling cascades, induction of apoptosis through multiple pathways, inhibition of lymphangiogenesis primarily through VEGFR-3 modulation, and positive modulation of the tumor microenvironment. The article further discusses anlotinib’s promising ability to overcome chemoresistance through regulation of drug efflux systems, pro-survival signaling, cancer stemness, and autophagy. The review highlights the synergistic effects of anlotinib in combination therapies with radiochemotherapy, immune checkpoint inhibitors, and targeted drugs across multiple cancer types. Despite its promising efficacy, challenges including low response rates and potential for acquired resistance remain. Future research directions should focus on optimizing dosing regimens, identifying predictive biomarkers, exploring novel combinations, investigating resistance mechanisms, and evaluating anlotinib’s potential in neoadjuvant or adjuvant settings. This extensive analysis provides insights into anlotinib’s therapeutic potential in solid tumors and hematological malignancies, paving the way for more effective and personalized cancer treatment strategies.
Indexed as
Identifiers
40944871What 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.