Author/Authors :
Endo Masahiro نويسنده , Moriguchi Michihisa نويسنده Division of Interventional Radiology, Shizuoka Cancer
Center , Aramaki Takeshi نويسنده Division of Interventional Radiology, Shizuoka Cancer
Center , Yoza Kiichiro نويسنده Division of Interventional Radiology, Shizuoka Cancer
Center , Iwai Kenji نويسنده Division of Interventional Radiology, Shizuoka Cancer
Center , Sato Rui نويسنده Division of Interventional Radiology, Shizuoka Cancer
Center , Asakura Koiku نويسنده Division of Diagnostic Radiology, Shizuoka Cancer
Center , Furuta Mitsuhiro نويسنده Molecular Gastroenterology and Hepatology, Kyoto
Prefectural University of Medicine, Graduate School of Medical
Science , Seko Yuya نويسنده Molecular Gastroenterology and Hepatology, Kyoto
Prefectural University of Medicine, Graduate School of Medical
Science , Itoh Yoshito نويسنده Molecular Gastroenterology and Hepatology, Kyoto
Prefectural University of Medicine, Graduate School of Medical
Science
Abstract :
Background This study aimed to retrospectively assess the safety
and usefulness of hepatic arterial infusion chemotherapy (HAIC) with
cisplatin in patients with hepatocellular carcinoma (HCC) and Child-Pugh
(C-P) score ≥ 8, who were refractory to or ineligible for transcatheter
arterial chemoembolization (TACE). Methods In this study, 28
cisplatin-naïve patients with HCC, C-P score ≥ 8, and no evidence of
extrahepatic lesions were treated using HAIC with cisplatin between July
2004 and July 2013. Results Of 28 patients, 10 were refractory to TACE
and 18 ineligible for TACE. In terms of C-P score, 17 patients had a
score of 8, 6 a score of 9, and 5 a score of 10. The injected dose of
cisplatin was reduced in 64.3% of cases. The overall response rate was
10.7%, with a disease control rate of 35.7%. Overall, median survival
time (MST) and progression-free survival were 186 and 80 days,
respectively. In patients with macroscopic vascular invasion
(MVI-positive; n = 9), these values decreased to 161 and 72 days,
respectively; while they increased to 341 and 87 days, respectively, in
MVI-negative patients (n = 19). Patients achieving partial response (PR)
and stable disease (SD) status as well as those achieving SD status
showed significantly better survival than patients with progressive
disease (PD status): PR + SD vs. PD: MST = 447 vs. 123 days, P <
0.001; SD vs. PD: MST = 447 vs. 123 days, P = 0.001). No serious adverse
event or treatment-related death occurred. Conclusions HAIC with
cisplatin can be safely administered in patients with HCC and C-P score
≥ 8, who are TACE-refractory or -ineligible. An extended survival time
is expected when the treatment outcome is either SD or more favorable.