TY - JOUR
T1 - Patterns of care and outcomes of definitive external beam radiotherapy and radioembolization for localized hepatocellular carcinoma
T2 - A propensity score-Adjusted analysis
AU - Bitterman, Danielle S.
AU - Sanford, Nina N.
AU - Niemierko, Andrzej
AU - Mahal, Brandon A.
AU - Qadan, Motaz
AU - Ganguli, Suvranu
AU - Blaszkowsky, Lawrence S.
AU - Zhu, Andrew X.
AU - Hong, Theodore S.
AU - Devlin, Phillip M.
AU - Goyal, Lipika
AU - Wo, Jennifer Y.
N1 - Funding Information:
S.G. reports a consulting role for Sirtex Medical, Medtronic, Boston Scien-tific, and BTG. A.X.Z. reports a consulting role for Eisai, Bristol-Myers Squibb, Merck & Co., Novartis, Sanofi, AstraZeneca, Bayer, Exelixis, and Eli Lilly and Company. He receives research funding from Eli Lilly and Co., Bayer, Bristol-Myers Squibb, Novartis, and Merck & Co. T.S.H. reports a consulting role for Clinical Genomics and EMD Serono. He receives research funding from Novartis, Taiho Pharmaceutical, and AstraZeneca. L.G. receives research funding from Taiho Pharmaceutical. The remaining authors declare no conflicts of interest.
Publisher Copyright:
© 2019 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2019/7/1
Y1 - 2019/7/1
N2 - Objectives:Most localized hepatocellular carcinoma (HCC) patients are not surgically operable or transplantation candidates, increasing the role for nonsurgical therapies. Ablative external beam radiotherapy (XRT) and transarterial radioembolization (TARE) are emerging radiotherapeutic treatments for localized HCC. We sought to evaluate their utilization and efficacy in a large nationwide cohort.Materials and Methods:We conducted an observational study of 2685 patients from the National Cancer Database (NCDB) diagnosed with American Joint Committee on Cancer 7th edition clinical stage I to III HCC between 2004 and 2015, treated with definitive-intent XRT delivered in 1 to 15 fractions or TARE. The association between treatment modality (XRT vs. TARE) and overall survival (OS) was defined using propensity score-weighted Kaplan-Meier estimators and propensity score-weighted multivariable Cox regressions.Results:Among 2685 patients, 2007 (74.7%) received TARE and 678 (25.3%) received XRT, with increasing usage for both from 2004 to 2015 (Ptrend<0.001), but with overall greater uptake and absolute usage of TARE. Patients who received TARE were more likely to have elevated alpha fetoprotein and more advanced stage (P<0.05 for all). Median OS was 14.5 months for the entire cohort. XRT was associated with an OS advantage compared with TARE on propensity score-unadjusted analysis (adjusted hazard ratio [AHR], 0.89; 95% confidence interval, 0.79-1.00; P=0.049), but not on propensity score-Adjusted analysis (AHR, 0.99; 95% confidence interval, 0.86-1.13; P=0.829).Conclusions:Our study demonstrates that while both XRT and TARE usage have increased with time, there was greater uptake and absolute use of TARE. We found no difference in survival between XRT and TARE after propensity score adjustment..
AB - Objectives:Most localized hepatocellular carcinoma (HCC) patients are not surgically operable or transplantation candidates, increasing the role for nonsurgical therapies. Ablative external beam radiotherapy (XRT) and transarterial radioembolization (TARE) are emerging radiotherapeutic treatments for localized HCC. We sought to evaluate their utilization and efficacy in a large nationwide cohort.Materials and Methods:We conducted an observational study of 2685 patients from the National Cancer Database (NCDB) diagnosed with American Joint Committee on Cancer 7th edition clinical stage I to III HCC between 2004 and 2015, treated with definitive-intent XRT delivered in 1 to 15 fractions or TARE. The association between treatment modality (XRT vs. TARE) and overall survival (OS) was defined using propensity score-weighted Kaplan-Meier estimators and propensity score-weighted multivariable Cox regressions.Results:Among 2685 patients, 2007 (74.7%) received TARE and 678 (25.3%) received XRT, with increasing usage for both from 2004 to 2015 (Ptrend<0.001), but with overall greater uptake and absolute usage of TARE. Patients who received TARE were more likely to have elevated alpha fetoprotein and more advanced stage (P<0.05 for all). Median OS was 14.5 months for the entire cohort. XRT was associated with an OS advantage compared with TARE on propensity score-unadjusted analysis (adjusted hazard ratio [AHR], 0.89; 95% confidence interval, 0.79-1.00; P=0.049), but not on propensity score-Adjusted analysis (AHR, 0.99; 95% confidence interval, 0.86-1.13; P=0.829).Conclusions:Our study demonstrates that while both XRT and TARE usage have increased with time, there was greater uptake and absolute use of TARE. We found no difference in survival between XRT and TARE after propensity score adjustment..
KW - hepatocellular carcinoma
KW - radioembolization
KW - radiotherapy
KW - stereotactic body radiotherapy
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U2 - 10.1097/COC.0000000000000560
DO - 10.1097/COC.0000000000000560
M3 - Article
C2 - 31166209
AN - SCOPUS:85067415855
SN - 0277-3732
VL - 42
SP - 564
EP - 572
JO - American Journal of Clinical Oncology: Cancer Clinical Trials
JF - American Journal of Clinical Oncology: Cancer Clinical Trials
IS - 7
ER -