New systemic treatment options for advanced cholangiocarcinoma

Cholangiocarcinoma (CCA) is a rare and aggressive cancer, mostly diagnosed at advanced or metastatic stage, at which point systemic treatment represents the only therapeutic option. Chemotherapy has been the backbone of advanced CCA treatment. More recently, immunotherapy has changed the therapeutic...

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গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Valentina Zanuso (Author), Giulia Tesini (Author), Elena Valenzi (Author), Lorenza Rimassa (Author)
বিন্যাস: গ্রন্থ
প্রকাশিত: Korean Liver Cancer Association, 2024-09-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Valentina Zanuso  |e author 
700 1 0 |a Giulia Tesini  |e author 
700 1 0 |a Elena Valenzi  |e author 
700 1 0 |a Lorenza Rimassa  |e author 
245 0 0 |a New systemic treatment options for advanced cholangiocarcinoma 
260 |b Korean Liver Cancer Association,   |c 2024-09-01T00:00:00Z. 
500 |a 2288-8128 
500 |a 2383-5001 
500 |a 10.17998/jlc.2024.08.07 
520 |a Cholangiocarcinoma (CCA) is a rare and aggressive cancer, mostly diagnosed at advanced or metastatic stage, at which point systemic treatment represents the only therapeutic option. Chemotherapy has been the backbone of advanced CCA treatment. More recently, immunotherapy has changed the therapeutic landscape, as immune checkpoint inhibitors have yielded the first improvement in survival and currently, the addition of either durvalumab or pembrolizumab to standard of care cisplatin plus gemcitabine represents the new first-line treatment option. However, the use of immunotherapy in subsequent lines has not demonstrated its efficacy and therefore, it is not approved, except for pembrolizumab in the selected microsatellite instability-high population. In addition, advances in comprehensive genomic profiling have led to the identification of targetable genetic alterations, such as isocitrate dehydrogenase 1 (IDH1), fibroblast growth factor receptor 2 (FGFR2), human epidermal growth factor receptor 2 (HER2), proto-oncogene B-Raf (BRAF), neurotrophic tropomyosin receptor kinase (NTRK), rearranged during transfection (RET), Kirsten rat sarcoma virus (KRAS), and mouse double minute 2 homolog (MDM2), thus favoring the development of a precision medicine approach in previously treated patients. Despite these advances, the use of molecularly driven agents is limited to a subgroup of patients. This review aims to provide an overview of the newly approved systemic therapies, the ongoing studies, and future research challenges in advanced CCA management. 
546 |a EN 
690 |a cholangiocarcinoma 
690 |a systemic treatment 
690 |a immunotherapy 
690 |a immune checkpoint inhibitors 
690 |a targeted therapy 
690 |a Internal medicine 
690 |a RC31-1245 
655 7 |a article  |2 local 
786 0 |n Journal of Liver Cancer, Vol 24, Iss 2, Pp 155-170 (2024) 
787 0 |n http://www.e-jlc.org/upload/pdf/jlc-2024-08-07.pdf 
787 0 |n https://doaj.org/toc/2288-8128 
787 0 |n https://doaj.org/toc/2383-5001 
856 4 1 |u https://doaj.org/article/1d4c8d9a1d9941468ffd1dfd83b8468d  |z Connect to this object online.