TY - JOUR
T1 - Molecular profiling and treatment pattern differences between intrahepatic and extrahepatic cholangiocarcinoma
AU - Spencer, Kristen
AU - Pappas, Leontios
AU - Baiev, Islam
AU - Maurer, Jordan
AU - Bocobo, Andrea Grace
AU - Zhang, Karen
AU - Jain, Apurva
AU - De Armas, Anaemy Danner
AU - Reyes, Stephanie
AU - Le, Tri Minh
AU - Rahma, Osama E.
AU - Stanton, Jennifer
AU - Deleon, Thomas T.
AU - Roth, Marc
AU - Peters, Mary Linton
AU - Zhu, Andrew X.
AU - Lennerz, Jochen K.
AU - Iafrate, A. John
AU - Boyhen, Kylie
AU - Vancott, Christine
AU - Roberts, Lewis R.
AU - Lindsey, Stacie
AU - Horick, Nora
AU - Goff, Laura Williams
AU - Mody, Kabir
AU - Borad, Mitesh J.
AU - Shroff, Rachna T.
AU - Kelley, Robin Kate
AU - Javle, Milind M.
AU - Goyal, Lipika
N1 - Publisher Copyright:
© The Author(s) 2023.
PY - 2023/7/1
Y1 - 2023/7/1
N2 - Treatment patterns for intrahepatic cholangiocarcinoma (ICC) and extrahepatic cholangiocarcinoma (ECC) differ, but limited studies exist comparing them. This study examines differences in molecular profiling rates and treatment patterns in these populations, focusing on use of adjuvant, liver-directed, targeted, and investigational therapies. Methods: This multicenter collaboration included patients with ICC or ECC treated at 1 of 8 participating institutions. Retrospective data were collected on risk factors, pathology, treatments, and survival. Comparative statistical tests were 2-sided. Results: Among 1039 patients screened, 847 patients met eligibility (ICC=611, ECC=236). Patients with ECC were more likely than those with ICC to present with early stage disease (53.8% vs 28.0%), undergo surgical resection (55.1% vs 29.8%), and receive adjuvant chemoradiation (36.5% vs 4.2%) (all P<.00001). However, they were less likely to undergo molecular profiling (50.3% vs 64.3%) or receive liver-directed therapy (17.9% vs 35.7%), targeted therapy (4.7% vs 18.9%), and clinical trial therapy (10.6% vs 24.8%) (all P<.001). In patients with recurrent ECC after surgery, the molecular profiling rate was 64.5%. Patients with advanced ECC had a shorter median overall survival than those with advanced ICC (11.8 vs 15.1months; P<.001). Conclusions: Patients with advanced ECC have low rates of molecular profiling, possibly in part because of insufficient tissue. They also have low rates of targeted therapy use and clinical trial enrollment. While these rates are higher in advanced ICC, the prognosis for both subtypes of cholangiocarcinoma remains poor, and a pressing need exists for new effective targeted therapies and broader access to clinical trials.
AB - Treatment patterns for intrahepatic cholangiocarcinoma (ICC) and extrahepatic cholangiocarcinoma (ECC) differ, but limited studies exist comparing them. This study examines differences in molecular profiling rates and treatment patterns in these populations, focusing on use of adjuvant, liver-directed, targeted, and investigational therapies. Methods: This multicenter collaboration included patients with ICC or ECC treated at 1 of 8 participating institutions. Retrospective data were collected on risk factors, pathology, treatments, and survival. Comparative statistical tests were 2-sided. Results: Among 1039 patients screened, 847 patients met eligibility (ICC=611, ECC=236). Patients with ECC were more likely than those with ICC to present with early stage disease (53.8% vs 28.0%), undergo surgical resection (55.1% vs 29.8%), and receive adjuvant chemoradiation (36.5% vs 4.2%) (all P<.00001). However, they were less likely to undergo molecular profiling (50.3% vs 64.3%) or receive liver-directed therapy (17.9% vs 35.7%), targeted therapy (4.7% vs 18.9%), and clinical trial therapy (10.6% vs 24.8%) (all P<.001). In patients with recurrent ECC after surgery, the molecular profiling rate was 64.5%. Patients with advanced ECC had a shorter median overall survival than those with advanced ICC (11.8 vs 15.1months; P<.001). Conclusions: Patients with advanced ECC have low rates of molecular profiling, possibly in part because of insufficient tissue. They also have low rates of targeted therapy use and clinical trial enrollment. While these rates are higher in advanced ICC, the prognosis for both subtypes of cholangiocarcinoma remains poor, and a pressing need exists for new effective targeted therapies and broader access to clinical trials.
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U2 - 10.1093/jnci/djad046
DO - 10.1093/jnci/djad046
M3 - Article
C2 - 37040087
AN - SCOPUS:85164239415
SN - 0027-8874
VL - 115
SP - 870
EP - 880
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 7
ER -