TY - JOUR
T1 - Outcomes of radioembolization for unresectable hepatocellular carcinoma in patients with marginal functional hepatic reserve
AU - Biederman, Derek M.
AU - Posham, Raghuram
AU - Durrani, Raisa J.
AU - Titano, Joseph J.
AU - Patel, Rahul S.
AU - Tabori, Nora E.
AU - Nowakowski, Francis S.
AU - Fischman, Aaron M.
AU - Lookstein, Robert A.
AU - Kim, Edward
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2018/1
Y1 - 2018/1
N2 - Purpose To evaluate the outcomes of radioembolization (RE) as a therapy for unresectable hepatocellular carcinoma (HCC) in patients with marginal functional hepatic reserve. Methods A retrospective review of 471 patients (1/2010–7/2015) treated with RE (Therasphere, BTG, UK) was performed. A total of 36 patients (mean age: 66.1 ± 9.3, male: 86.1%) underwent therapy for HCC with a MELD ≥ 15 (median: 16, range: 15–22). Baseline demographics of the study cohort were as follows: etiology (HCV: 26, 72.2%), cirrhosis (n = 32, 88.9%), ECOG 0 (n = 16, 44.4%), Child-Pugh class (A = 15, B = 19, C = 2), unilobar distribution (n = 27, 75%), AFP > 200 (n = 11, 30.6%), portal vein thrombosis (PVT, n = 7, 19.4%), metastasis (n = 3, 8.3%). Outcomes analyzed included CTCAEv4.03 laboratory toxicities (120-day), imaging response (mRECIST), progression-free survival (PFS), and overall survival (OS). Results A total of 42 treatments were performed with mean dose of 2.02 ± 1.23 GBq. The cumulative grade 3/4 toxicity was 28% overall and 21% for bilirubin at 120-days. The objective response and disease control rates were 48.3% (14/29) and 69% (20/29) respectively. The median (95% CI) PFS was 5.9 (4.4–7.7) months. Ten (27.8%) patients received additional locoregional therapy at a median (IQR) of 138 (102–243) days post RE. The mean (95% CI) OS was 21.9 (14.8–29.0) months. The absence of PVT was associated with improved OS (p = 0.005) Disease control at 90-days was also associated with an OS benefit (p = 0.037). Conclusions Patients with unresectable HCC and marginal functional hepatic reserve treated with RE had favorable objective response and disease control rates, both predictive of overall survival.
AB - Purpose To evaluate the outcomes of radioembolization (RE) as a therapy for unresectable hepatocellular carcinoma (HCC) in patients with marginal functional hepatic reserve. Methods A retrospective review of 471 patients (1/2010–7/2015) treated with RE (Therasphere, BTG, UK) was performed. A total of 36 patients (mean age: 66.1 ± 9.3, male: 86.1%) underwent therapy for HCC with a MELD ≥ 15 (median: 16, range: 15–22). Baseline demographics of the study cohort were as follows: etiology (HCV: 26, 72.2%), cirrhosis (n = 32, 88.9%), ECOG 0 (n = 16, 44.4%), Child-Pugh class (A = 15, B = 19, C = 2), unilobar distribution (n = 27, 75%), AFP > 200 (n = 11, 30.6%), portal vein thrombosis (PVT, n = 7, 19.4%), metastasis (n = 3, 8.3%). Outcomes analyzed included CTCAEv4.03 laboratory toxicities (120-day), imaging response (mRECIST), progression-free survival (PFS), and overall survival (OS). Results A total of 42 treatments were performed with mean dose of 2.02 ± 1.23 GBq. The cumulative grade 3/4 toxicity was 28% overall and 21% for bilirubin at 120-days. The objective response and disease control rates were 48.3% (14/29) and 69% (20/29) respectively. The median (95% CI) PFS was 5.9 (4.4–7.7) months. Ten (27.8%) patients received additional locoregional therapy at a median (IQR) of 138 (102–243) days post RE. The mean (95% CI) OS was 21.9 (14.8–29.0) months. The absence of PVT was associated with improved OS (p = 0.005) Disease control at 90-days was also associated with an OS benefit (p = 0.037). Conclusions Patients with unresectable HCC and marginal functional hepatic reserve treated with RE had favorable objective response and disease control rates, both predictive of overall survival.
KW - Hepatocellular carcinoma treatment
KW - Interventional oncology
KW - Radioembolization
UR - http://www.scopus.com/inward/record.url?scp=85027707593&partnerID=8YFLogxK
U2 - 10.1016/j.clinimag.2017.07.011
DO - 10.1016/j.clinimag.2017.07.011
M3 - Article
C2 - 28834778
AN - SCOPUS:85027707593
VL - 47
SP - 34
EP - 40
JO - Clinical Imaging
JF - Clinical Imaging
SN - 0899-7071
ER -