TY - JOUR
T1 - Survival benefit of hepatic arterial infusion chemotherapy over sorafenib in the treatment of locally progressed hepatocellular carcinoma
AU - New FP Study Group
AU - Kurume Liver Cancer Study Group of Japan
AU - Iwamoto, Hideki
AU - Niizeki, Takashi
AU - Nagamatsu, Hiroaki
AU - Ueshima, Kazuomi
AU - Nomura, Takako
AU - Kuzuya, Teiji
AU - Kasai, Kazuhiro
AU - Kooka, Yohei
AU - Hiraoka, Atsushi
AU - Sugimoto, Rie
AU - Yonezawa, Takehiro
AU - Ishihara, Akio
AU - Deguchi, Akihiro
AU - Arai, Hirotaka
AU - Shimose, Shigeo
AU - Shirono, Tomotake
AU - Nakano, Masahito
AU - Okamura, Shusuke
AU - Noda, Yu
AU - Kamachi, Naoki
AU - Sakai, Miwa
AU - Suzuki, Hiroyuki
AU - Aino, Hajime
AU - Matsukuma, Norito
AU - Matsugaki, Satoru
AU - Ogata, Kei
AU - Yano, Yoichi
AU - Ueno, Takato
AU - Kajiwara, Masahiko
AU - Itano, Satoshi
AU - Fukuizumi, Kunitaka
AU - Kawano, Hiroshi
AU - Noguchi, Kazunori
AU - Tanaka, Masatoshi
AU - Yamaguchi, Taizo
AU - Kuromatsu, Ryoko
AU - Kawaguchi, Atsushi
AU - Koga, Hironori
AU - Torimura, Takuji
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/2/2
Y1 - 2021/2/2
N2 - BACKROUND: Not all patients with hepatocellular carcinoma (HCC) benefit from treatment with molecular targeted agents such as sorafenib. We investigated whether New-FP (fine-powder cisplatin and 5-fluorouracil), a hepatic arterial infusion chemotherapy regimen, is more favorable than sorafenib as an initial treatment for locally progressed HCC. METHODS: To avoid selection bias, we corrected the data from different facilities that did or did not perform New-FP therapy. In total, 1709 consecutive patients with HCC initially treated with New-FP or sorafenib; 1624 (New-FP, n = 644; sorafenib n = 980) were assessed. After propensity score matching (PSM), overall survival (OS) and prognostic factors were assessed (n = 344 each). Additionally, the patients were categorized into four groups: cohort-1 [(without macrovascular invasion (MVI) and extrahepatic spread (EHS)], cohort-2 (with MVI), cohort-3 (with EHS), and cohort-4 (with MVI and EHS) to clarify the efficacy of each treatment. RESULTS: New-FP prolonged OS than sorafenib after PSM (New-FP, 12 months; sorafenib, 7.9 months; p < 0.001). Sorafenib treatment, and severe MVI and EHS were poor prognostic factors. In the subgroup analyses, the OS was significantly longer the New-FP group in cohort-2. CONCLUSIONS: Local treatment using New-FP is a potentially superior initial treatment compared with sorafenib as a multidisciplinary treatment in locally progressed HCC without EHS.
AB - BACKROUND: Not all patients with hepatocellular carcinoma (HCC) benefit from treatment with molecular targeted agents such as sorafenib. We investigated whether New-FP (fine-powder cisplatin and 5-fluorouracil), a hepatic arterial infusion chemotherapy regimen, is more favorable than sorafenib as an initial treatment for locally progressed HCC. METHODS: To avoid selection bias, we corrected the data from different facilities that did or did not perform New-FP therapy. In total, 1709 consecutive patients with HCC initially treated with New-FP or sorafenib; 1624 (New-FP, n = 644; sorafenib n = 980) were assessed. After propensity score matching (PSM), overall survival (OS) and prognostic factors were assessed (n = 344 each). Additionally, the patients were categorized into four groups: cohort-1 [(without macrovascular invasion (MVI) and extrahepatic spread (EHS)], cohort-2 (with MVI), cohort-3 (with EHS), and cohort-4 (with MVI and EHS) to clarify the efficacy of each treatment. RESULTS: New-FP prolonged OS than sorafenib after PSM (New-FP, 12 months; sorafenib, 7.9 months; p < 0.001). Sorafenib treatment, and severe MVI and EHS were poor prognostic factors. In the subgroup analyses, the OS was significantly longer the New-FP group in cohort-2. CONCLUSIONS: Local treatment using New-FP is a potentially superior initial treatment compared with sorafenib as a multidisciplinary treatment in locally progressed HCC without EHS.
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U2 - 10.3390/cancers13040646
DO - 10.3390/cancers13040646
M3 - Article
AN - SCOPUS:85100463020
SN - 2072-6694
VL - 13
SP - 1
EP - 14
JO - Cancers
JF - Cancers
IS - 4
M1 - 646
ER -