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Mashup Score: 7Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics - 2 year(s) ago
Among patients with multiple primary cancers, the prevalence of germline pathogenic variants (PVs) in actionable cancer genes increases with the number of primary cancers (PCs): 13.1% with 2 PCs, 15….
Source: American Cancer Society JournalsCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 1Clinical Research Job: Regulatory Coordinator II - GI Oncology at Dana-Farber Cancer Institute in 450 Brookline Ave, Boston, MA - 3 year(s) ago
Regulatory Coordinator II – GI Oncology job
Source: careers.dana-farber.orgCategories: Latest Headlines, Oncologists2Tweet
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Mashup Score: 8
The findings demonstrate the feasibility of rapid identification of the biologic relevance of somatic mutations, which thus advances clinicians’ ability to make informed treatment decisions.
Source: PubMedCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 8TAS-120 Overcomes Resistance to ATP-Competitive FGFR Inhibitors in Patients with FGFR2 Fusion–Positive Intrahepatic Cholangiocarcinoma - 3 year(s) ago
ATP-competitive fibroblast growth factor receptor (FGFR) kinase inhibitors, including BGJ398 and Debio 1347, show antitumor activity in patients with intrahepatic cholangiocarcinoma (ICC) harboring activating FGFR2 gene fusions. Unfortunately, acquired resistance develops and is often associated with the emergence of secondary FGFR2 kinase domain mutations. Here, we report that the irreversible…
Source: Cancer DiscoveryCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 2
We conducted next generation DNA sequencing on 335 biliary tract cancers and characterized the genomic landscape by anatomic site within the biliary tree. In addition to frequent FGFR2 fusions among patients with intrahepatic cholangiocarcinoma (IHCC), we identified FGFR2 extracellular domain in-frame deletions (EIDs) in 5 of 178 (2.8%) patients with IHCC, including two patients with FGFR2…
Source: Cancer DiscoveryCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 0Functions of FGFR2 corrupted by translocations in intrahepatic cholangiocarcinoma - PubMed - 3 year(s) ago
Cholangiocarcinoma, originating from the biliary duct, represents a subset of liver cancer. With about 8000 new cases of cholangiocarcinoma diagnosed annually in the U.S., these fall into three categories: intrahepatic, peri-hilar, and extrahepatic cholangiocarcinoma. Arising from the epithelium of …
Source: PubMedCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 7Pemigatinib for previously treated, locally advanced or metastatic cholangiocarcinoma: a multicentre, open-label, phase 2 study - 3 year(s) ago
These data support the therapeutic potential of pemigatinib in previously treated patients with cholangiocarcinoma who have FGFR2 fusions or rearrangements.
Source: The Lancet OncologyCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 8Phase II Study of BGJ398 in Patients With FGFR-Altered Advanced Cholangiocarcinoma - PubMed - 3 year(s) ago
Purpose No standard treatment exists for patients with cholangiocarcinoma for whom first-line gemcitabine-based therapy fails. Fibroblast growth factor receptor 2 ( FGFR2) fusions/translocations are present in 13% to 17% of intrahepatic cholangiocarcinomas. BGJ398, an orally bioavailable, selective …
Source: PubMedCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 6
Original Article from The New England Journal of Medicine — Cisplatin plus Gemcitabine versus Gemcitabine for Biliary Tract Cancer
Source: New England Journal of MedicineCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 6Gemcitabine, Cisplatin, and nab-Paclitaxel for the Treatment of Advanced Biliary Tract Cancers - 3 year(s) ago
This open-label, single-arm, phase 2 clinical trial evaluates whether nab-paclitaxel plus gemcitabine-cisplatin prolongs survival vs that for historical populations treated with gemcitabine-cisplatin alone among patients with advanced biliary tract cancers.
Source: jamanetwork.comCategories: Hem/Oncs, Latest HeadlinesTweet
Data from this paper really drives home the point that patients w/ multiple cancers are a unique population. Pathogenic germline mutations were found in 13% of pts w/ 2 cancers and 18% of pts w/ 4 cancers. Germline screening is clearly needed in these pts. https://t.co/dN1o36qsla https://t.co/IStIX8NkGX