The DOI matches its Crossref record.
76MO Efficacy of RLY-4008, a highly selective FGFR2 inhibitor in patients (pts) with an FGFR2-fusion or rearrangement (f/r), FGFR inhibitor (FGFRi)-naïve cholangiocarcinoma (CCA): ReFocus trial
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Many biomedical publications are false.
“and many biomedical publications are false (173).”
From Artificial Intelligence for Drug Discovery: Are We There Yet? (2024) · cites this paper as [173]
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Artificial Intelligence for Drug Discovery: Are We There Yet?
Hasselgren, C., & Oprea, T. I. (2024) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-040323-040828 · Cited by 236
Clinical development and management of adverse events associated with FGFR inhibitors
Subbiah, V., & Verstovšek, S. (2023) · Cell Reports Medicine · doi:10.1016/j.xcrm.2023.101204 · Cited by 68
Self-citationValéry, M., Vasseur, D., Fachinetti, F., Boilève, A., Smolenschi, C., Tarabay, A., Antoun, L., Perret, A., Fuerea, A. C., Pudlarz, T., et al. (2023) · Cancers · doi:10.3390/cancers15184446 · Cited by 44
Self-citationUnresectable biliary tract cancer: Current and future systemic therapy
Zhang, D., Dorman, K., Westphalen, C. B., Haas, M., Ormanns, S., Neumann, J. H. L., Seidensticker, M., Ricke, J., Toni, E. N. D., Klauschen, F., et al. (2024) · European Journal of Cancer · doi:10.1016/j.ejca.2024.114046 · Cited by 28
Grivas, P. D., Garralda, E., Meric‐Bernstam, F., et al. (2024) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-24-0012 · Cited by 13
Self-citationNew perspectives in biliary tract cancers
Goetze, T. O., Roderburg, C., Friedrich, F. W., & Trojan, J. (2024) · ESMO Gastrointestinal Oncology · doi:10.1016/j.esmogo.2024.100092 · Cited by 8
Update for: New developments in systemic therapy for advanced biliary tract cancer
Morizane, C., Ueno, M., Ikeda, M., Okusaka, T., Ishii, H., & Furuse, J. (2025) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyaf016 · Cited by 8
Metadata
- Authors
- Park, J. O., Wai Meng, D. T., Hollebecque, A., Borad, M., Goyal, L., Schram, A., Cassier, P., Kamath, S. D., Dotan, E., Kim, R., Sahai, V., Liao, C.-Y., Millward, M., Roda Perez, D., Blakesley, R., Wolf, B., Subbiah, V., Kelley, R. K., & Oh, D.-Y.
- Affiliations
- Samsung Medical Center (KR)
- Institut Gustave Roussy (FR)
- Mayo Clinic (US)
- Massachusetts General Hospital (US)
- Memorial Sloan Kettering Cancer Center (US)
- Centre Léon Bérard (FR)
- Cleveland Clinic (US)
- Fox Chase Cancer Center (US)
- University of South Florida (US)
- University of Michigan (US)
- University of Chicago (US)
- The University of Western Australia (AU)
- Relay Therapeutics (United States) (US)
- The University of Texas MD Anderson Cancer Center (US)
- University of California, San Francisco (US)
- Seoul National University Hospital (KR)
- Venue
- Annals of Oncology
- Publisher
- Elsevier BV
- Published
- 2022-11
- Volume
- 33
- Pages
- S1461-S1462
- ISSN
- 0923-7534 (ISSN-L)
- OpenAlex
- W4310754092
- Cited by
- 7
- References
- 0
- Citations by year
- 2025: 1 · 2024: 3 · 2023: 3
- FWCI
- 1.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Annals of Oncology (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Cholangiocarcinoma and Gallbladder Cancer Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fibroblast Growth Factor Research
- Health Sciences › Medicine › Surgery › Pediatric Hepatobiliary Diseases and Treatments
- Keywords
- RLY-4008, FGFR2 inhibitor, FGFR2 fusion, FGFR2 rearrangement, cholangiocarcinoma, off-target toxicity, objective response rate, duration of response
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