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BIOMARKER:

IDH1 mutation + FGFR2 fusion

i
Other names: FGFR2, BEK, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25, Fibroblast growth factor receptor 2, HEL-216, HEL-S-26, Epididymis Luminal Protein 216, Isocitrate Dehydrogenase 1 (NADP+), Epididymis Secretory Protein Li 26, IDH1, Isocitrate Dehydrogenase (NADP(+)) 1, Isocitrate Dehydrogenase 1 (NADP+), Soluble
Entrez ID:
5ms
Real-world testing, treatment patterns, and outcomes following liquid biopsy in advanced cholangiocarcinoma. (ASCO-GI 2024)
FOLFOX (21%), gemcitabine and cisplatin (13%), and capecitabine (11%) were the most common second-line therapies... The rate of actionable molecular alterations detected via ctDNA is 18%, comparable to reports from tissue-based testing. Patients with aCCA are often tested before starting first or second LOT. Patients with ctDNA-detected IDH1 mutations treated with ivosidenib and had a trend toward improved rwTTD and rwTTNT, although it did not reach statistical significance.
Real-world evidence • Clinical • MSi-H Biomarker • Liquid biopsy • Real-world • Metastases • Biopsy
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HER-2 (Human epidermal growth factor receptor 2) • BRAF (B-raf proto-oncogene) • MSI (Microsatellite instability) • RET (Ret Proto-Oncogene) • FGFR2 (Fibroblast growth factor receptor 2) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1)
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BRAF V600E • MSI-H/dMMR • HER-2 amplification • BRAF V600 • HER-2 mutation • IDH1 mutation • RET fusion • FGFR2 mutation • FGFR2 fusion • IDH1 mutation + FGFR2 fusion
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Guardant360® CDx
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cisplatin • gemcitabine • 5-fluorouracil • capecitabine • Tibsovo (ivosidenib) • leucovorin calcium
10ms
Management of biliary tract cancers in older patients: A French multicenter cohort study (ESMO 2023)
They were offered less frequently first-line systemic therapy (87% vs 97%, p<0.0001)(gemcitabine 3% vs 0.3%; gemcis 31% vs 35%; gemox 54% in 2 groups; p=0.007) and molecular profiling (43% vs 65%, p<0.0001) than pts <70...If treated, PFS of older pts was similar to younger pts. Molecular profiling was less often performed in older pts.
Clinical
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HER-2 (Human epidermal growth factor receptor 2) • MSI (Microsatellite instability) • FGFR2 (Fibroblast growth factor receptor 2) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1)
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HER-2 amplification • IDH1 mutation • FGFR2 mutation • FGFR2 fusion • IDH1 mutation + FGFR2 fusion
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gemcitabine
over1year
Immunology and immunotherapy of cholangiocarcinoma. (PubMed, Nat Rev Gastroenterol Hepatol)
We introduce findings from preclinical immunotherapy studies, discuss future immune-mediated treatment options, and provide a summary of results from clinical trials testing immune-based approaches in patients with cholangiocarcinoma. This Review provides a thorough survey of our knowledge on immune signatures and immunotherapy in cholangiocarcinoma.
Review • Journal • IO biomarker
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FGFR2 (Fibroblast growth factor receptor 2) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1)
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IDH1 mutation • FGFR2 mutation • FGFR2 fusion • IDH1 mutation + FGFR2 fusion
over1year
Mutations de l'ADN dans les cholangiocarcinomes : cibler IDH1 et autres mutations. (PubMed, Bull Cancer)
Two lines of chemotherapy are currently recommended in France, with cisplatin-gemcitabine and 5 FU-oxaliplatin as first and second-line treatment respectively, allowing a median survival of approximately one year...To date, only ivosidenib and pemigatinib, targeting IDH1 mutations and FGFR2 fusions respectively, are approved in France for pre-treated patients with these molecular alterations. Many other potentially targetable alterations are found in BTC, including mutations in genes involved in DNA repair, BRAF, HER2 and the recently exploited KRASG12C mutation. This review will focus on targetable mutations in BTC and develop the main molecules that can be used in BTC with these actionable alterations, offering new therapeutic perspectives for these patients, with the ultimate goal of improving their prognosis.
Review • Journal
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HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • FGFR2 (Fibroblast growth factor receptor 2) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1)
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KRAS mutation • KRAS G12C • BRAF mutation • HER-2 mutation • IDH1 mutation • FGFR2 mutation • FGFR2 fusion • KRAS G12 • IDH1 mutation + FGFR2 fusion
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cisplatin • gemcitabine • 5-fluorouracil • oxaliplatin • Pemazyre (pemigatinib) • Tibsovo (ivosidenib)
over2years
ESMO Scale for Clinical Actionability of Molecular Targets driving targeted treatment in patients with cholangiocarcinoma. (PubMed, Clin Cancer Res)
ESCAT represents a tool to guide clinicians in fine-tuning use of molecular profiling data to choose matched targeted therapies. Our data demonstrate that targeted treatment administered per alteration actionability according to ESCAT is associated with improved survival in cholangiocarcinoma, particularly in ESCAT I-II intrahepatic cholangiocarcinoma.
Clinical • Journal
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FGFR2 (Fibroblast growth factor receptor 2) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1)
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IDH1 mutation • FGFR2 mutation • FGFR2 fusion • IDH1 mutation + FGFR2 fusion
3years
Current and Future Systemic Therapies in Biliary Tract Cancer. (PubMed, Visc Med)
Since 2010, chemotherapy with gemcitabine and cisplatin is considered the standard of care in the palliative situation. The current study landscape clearly shows that precision medicine will play an important role in the therapy of biliary malignancies and underlines the importance of early tumor genetic diagnostics. In this article we provide an overview of systemic therapy concepts in the adjuvant and palliative setting.
Review • Journal
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HER-2 (Human epidermal growth factor receptor 2) • BRAF (B-raf proto-oncogene) • FGFR2 (Fibroblast growth factor receptor 2) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1) • NTRK (Neurotrophic receptor tyrosine kinase)
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BRAF mutation • HER-2 amplification • IDH1 mutation • FGFR2 mutation • FGFR2 fusion • BRAF amplification • IDH1 mutation + FGFR2 fusion • NTRK fusion
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cisplatin • gemcitabine