TY - JOUR
T1 - Validation of the easy-to-use lenvatinib prognostic index to predict prognosis in advanced hepatocellular carcinoma patients treated with lenvatinib
AU - Rimini, Margherita
AU - Kang, Wonseok
AU - Burgio, Valentina
AU - Persano, Mara
AU - Aoki, Tamoko
AU - Shimose, Shigeo
AU - Tada, Toshifumi
AU - Kumada, Takashi
AU - Sho, Takuya
AU - Lai, Eleonora
AU - Celsa, Ciro
AU - Campani, Claudia
AU - Tonnini, Matteo
AU - Tamburini, Emiliano
AU - Hiraoka, Atsushi
AU - Takaguchi, Koichi
AU - Nishida, Naoshi
AU - Iwamoto, Hideki
AU - Itobayashi, Ei
AU - Tsuji, Kunihiko
AU - Sakamoto, Naoya
AU - Ishikawa, Toru
AU - Toyoda, Hidenori
AU - Kudo, Masatoshi
AU - Kawaguchi, Takumi
AU - Hatanaka, Takeshi
AU - Nouso, Kazugiro
AU - Suda, Goki
AU - Cabibbo, Giuseppe
AU - Marra, Fabio
AU - Della Corte, Angelo
AU - Ratti, Francesca
AU - Pedica, Federica
AU - De Cobelli, Francesco
AU - Aldrighetti, Luca
AU - Scartozzi, Mario
AU - Cascinu, Stefano
AU - Casadei-Gardini, Andrea
N1 - Publisher Copyright:
© 2022 The Authors. Hepatology Research published by John Wiley & Sons Australia, Ltd on behalf of Japan Society of Hepatology.
PY - 2022/12
Y1 - 2022/12
N2 - Aim: The identification of new prognostic factors able to stratify hepatocellular carcinoma patients candidate to first-line therapy is urgent. In the present work we validated the prognostic value of the lenvatinib prognostic index. Methods: Data of Eastern and Western patients treated with lenvatinib as first-line for Barcelona Clinic Liver Cancer stage B or C hepatocellular carcinoma were recollected. The lenvatinib prognostic index was composed by three classes of risk according with our previous study. The “low risk” group includes patients with prognostic nutritional index (PNI) >43.3 and with previous transarterial chemoembolization. The “medium risk” group includes patients with PNI >43.3, but without previous transarterial chemoembolization and patients with PNI <43.3, albumin-bilirubin grade 1 and Barcelona Clinic Liver Cancer stage B. The “high risk” group includes patients with PNI <43.3, albumin-bilirubin grade 2, and patients with PNI <43.3, albumin-bilirubin grade 1 and Barcelona Clinic Liver Cancer stage C. Results: A total of 717 patients were included. The median overall survival was 20.7 months (95% CI 16.1–51.6) in patients with low risk (n = 223), 16.7 months (95% CI 13.3–47.0) in patients with medium risk (n = 264), and 10.7 months (95% CI 9.3–12.2) in patients with high risk (n = 230; HR 1, 1.29, and 1.92, respectively; p < 0.0001). Median progression-free survival was 7.3 months (95% CI 6.3–46.5) in patients with low risk, 6.4 months (95% CI 5.3–8.0) in patients with medium risk, and 4.9 months (95% CI 4.3–5.5) in patients with high risk (HR 1, 1.07, 1.47 respectively; p = 0.0009). Conclusion: The lenvatinib prognostic index confirms its prognostic value on an external cohort of hepatocellular carcinoma patients treated with Lenvatinib.
AB - Aim: The identification of new prognostic factors able to stratify hepatocellular carcinoma patients candidate to first-line therapy is urgent. In the present work we validated the prognostic value of the lenvatinib prognostic index. Methods: Data of Eastern and Western patients treated with lenvatinib as first-line for Barcelona Clinic Liver Cancer stage B or C hepatocellular carcinoma were recollected. The lenvatinib prognostic index was composed by three classes of risk according with our previous study. The “low risk” group includes patients with prognostic nutritional index (PNI) >43.3 and with previous transarterial chemoembolization. The “medium risk” group includes patients with PNI >43.3, but without previous transarterial chemoembolization and patients with PNI <43.3, albumin-bilirubin grade 1 and Barcelona Clinic Liver Cancer stage B. The “high risk” group includes patients with PNI <43.3, albumin-bilirubin grade 2, and patients with PNI <43.3, albumin-bilirubin grade 1 and Barcelona Clinic Liver Cancer stage C. Results: A total of 717 patients were included. The median overall survival was 20.7 months (95% CI 16.1–51.6) in patients with low risk (n = 223), 16.7 months (95% CI 13.3–47.0) in patients with medium risk (n = 264), and 10.7 months (95% CI 9.3–12.2) in patients with high risk (n = 230; HR 1, 1.29, and 1.92, respectively; p < 0.0001). Median progression-free survival was 7.3 months (95% CI 6.3–46.5) in patients with low risk, 6.4 months (95% CI 5.3–8.0) in patients with medium risk, and 4.9 months (95% CI 4.3–5.5) in patients with high risk (HR 1, 1.07, 1.47 respectively; p = 0.0009). Conclusion: The lenvatinib prognostic index confirms its prognostic value on an external cohort of hepatocellular carcinoma patients treated with Lenvatinib.
KW - hepatocellular carcinoma
KW - lenvatinib
KW - prognostic factors
UR - https://www.scopus.com/pages/publications/85136600485
U2 - 10.1111/hepr.13824
DO - 10.1111/hepr.13824
M3 - Article
AN - SCOPUS:85136600485
SN - 1386-6346
VL - 52
SP - 1050
EP - 1059
JO - Hepatology Research
JF - Hepatology Research
IS - 12
ER -