TY - JOUR
T1 - Systemic treatment of patients with locally advanced or metastatic cholangiocarcinoma – an Austrian expert consensus statement
AU - Taghizadeh, Hossein
AU - Djanani, Angela
AU - Eisterer, Wolfgang
AU - Gerger, Armin
AU - Gruenberger, Birgit
AU - Gruenberger, Thomas
AU - Rumpold, Holger
AU - Weiss, Lukas
AU - Winder, Thomas
AU - Wöll, Ewald
AU - Prager, Gerald W.
N1 - Publisher Copyright:
Copyright © 2023 Taghizadeh, Djanani, Eisterer, Gerger, Gruenberger, Gruenberger, Rumpold, Weiss, Winder, Wöll and Prager.
PY - 2023/8/30
Y1 - 2023/8/30
N2 - Locally advanced or metastatic cholangiocarcinoma is an aggressive carcinoma with a dismal prognosis. For the first-line treatment of locally advanced or metastatic cholangiocarcinoma, cisplatin/gemcitabine has been the standard of care for more than 10 years. Its combination with the immune checkpoint inhibitor durvalumab resulted in an efficiency improvement in the phase III setting. Regarding the use of chemotherapy in the second line, positive phase III data could only be generated for FOLFOX. The evidence base for nanoliposomal irinotecan (Nal-IRI) plus 5-fluorouracil (5-FU) and leucovorin (LV) is contradictory. After the failure of first-line treatment, targeted therapies can be offered if the molecular targets microsatellite instability-high (MSI-H), IDH1, FGFR2, BRAF V600E, and NTRK are detected. These targeted agents are generally preferable to second-line chemotherapy. Broad molecular testing should be performed, preferably from tumor tissue, at the initiation of first-line therapy to timely identify potential molecular targets.
AB - Locally advanced or metastatic cholangiocarcinoma is an aggressive carcinoma with a dismal prognosis. For the first-line treatment of locally advanced or metastatic cholangiocarcinoma, cisplatin/gemcitabine has been the standard of care for more than 10 years. Its combination with the immune checkpoint inhibitor durvalumab resulted in an efficiency improvement in the phase III setting. Regarding the use of chemotherapy in the second line, positive phase III data could only be generated for FOLFOX. The evidence base for nanoliposomal irinotecan (Nal-IRI) plus 5-fluorouracil (5-FU) and leucovorin (LV) is contradictory. After the failure of first-line treatment, targeted therapies can be offered if the molecular targets microsatellite instability-high (MSI-H), IDH1, FGFR2, BRAF V600E, and NTRK are detected. These targeted agents are generally preferable to second-line chemotherapy. Broad molecular testing should be performed, preferably from tumor tissue, at the initiation of first-line therapy to timely identify potential molecular targets.
UR - http://www.scopus.com/inward/record.url?scp=85170831965&partnerID=8YFLogxK
U2 - 10.3389/fonc.2023.1225154
DO - 10.3389/fonc.2023.1225154
M3 - Journal article
C2 - 37711201
SN - 2234-943X
VL - 13
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 1225154
ER -