Definitive liver radiotherapy for intrahepatic cholangiocarcinoma with extrahepatic metastases Journal Article


Authors: De, B.; Upadhyay, R.; Liao, K.; Kumala, T.; Shi, C.; Dodoo, G.; Abi Jaoude, J.; Corrigan, K. L.; Manzar, G. S.; Marqueen, K. E.; Bernard, V.; Lee, S. S.; Raghav, K. P. S.; Vauthey, J. N.; Tzeng, C. W.; Tran Cao, H. S.; Lee, G.; Wo, J.; Hong, T. S.; Crane, C. H.; Minsky, B. D.; Smith, G. L.; Holliday, E. B.; Taniguchi, C. M.; Koong, A. C.; Das, P.; Javle, M.; Ludmir, E. B.; Koay, E.
Article Title: Definitive liver radiotherapy for intrahepatic cholangiocarcinoma with extrahepatic metastases
Abstract: Introduction: Tumor-related liver failure (TRLF) is the most common cause of death in patients with intrahepatic cholangiocarcinoma (ICC). Though we previously showed that liver radiotherapy (L-RT) for locally advanced ICC is associated with less frequent TRLF and longer overall survival (OS), the role of L-RT for patients with extrahepatic metastatic disease (M1) remains undefined. We sought to compare outcomes for M1 ICC patients treated with and without L-RT. Methods: We reviewed ICC patients that found to have M1 disease at initial diagnosis at a single institution between 2010 and 2021 who received L-RT, matching them with an institutional cohort by propensity score and a National Cancer Database (NCDB) cohort by frequency technique. The median biologically effective dose was 97.5 Gy (interquartile range 80.5-97.9 Gy) for L-RT. Patients treated with other local therapies or supportive care alone were excluded. We analyzed survival with Cox proportional hazard modeling. Results: We identified 61 patients who received L-RT and 220 who received chemotherapy alone. At median follow-up of 11 months after diagnosis, median OS was 9 months (95% confidence interval [CI] 8-11) and 21 months (CI: 17-26) for patients receiving chemotherapy alone and L-RT, respectively. TRLF was the cause of death more often in the patients who received chemotherapy alone compared to those who received L-RT (82% vs. 47%; p = 0.001). On multivariable propensity score-matched analysis, associations with lower risk of death included duration of upfront chemotherapy (hazard ratio [HR] 0.82; p = 0.005) and receipt of L-RT (HR: 0.40; p = 0.002). The median OS from diagnosis for NCDB chemotherapy alone cohort was shorter than that of the institutional L-RT cohort (9 vs. 22 months; p < 0.001). Conclusion: For M1 ICC, L-RT associated with a lower rate of death due to TRLF and longer OS versus those treated with chemotherapy alone. Prospective studies of L-RT in this setting are warranted. © 2023 The Author(s). Published by S. Karger AG, Basel. This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission.
Keywords: adult; cancer chemotherapy; cancer survival; human tissue; aged; major clinical study; cisplatin; treatment duration; gemcitabine; paclitaxel; cancer patient; cancer radiotherapy; follow up; local therapy; cohort analysis; data base; cause of death; liver failure; liver metastasis; intrahepatic cholangiocarcinoma; human; male; female; article; mortality risk; tumor related liver failure
Journal Title: Liver Cancer
Volume: 12
Issue: 3
ISSN: 2235-1795
Publisher: Karger  
Date Published: 2023-08-01
Start Page: 198
End Page: 208
Language: English
DOI: 10.1159/000530134
PROVIDER: scopus
PMCID: PMC10427952
PUBMED: 37593365
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Christopher   Crane
    202 Crane