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Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis

BACKGROUND: A growing body of evidence suggests that non-viral hepatocellular carcinoma (HCC) might benefit less from immunotherapy. MATERIALS AND METHODS: We carried out a retrospective analysis of prospectively collected data from consecutive patients with non-viral advanced HCC, treated with atez...

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Autores principales: Rimini, M., Rimassa, L., Ueshima, K., Burgio, V., Shigeo, S., Tada, T., Suda, G., Yoo, C., Cheon, J., Pinato, D.J., Lonardi, S., Scartozzi, M., Iavarone, M., Di Costanzo, G.G., Marra, F., Soldà, C., Tamburini, E., Piscaglia, F., Masi, G., Cabibbo, G., Foschi, F.G., Silletta, M., Pressiani, T., Nishida, N., Iwamoto, H., Sakamoto, N., Ryoo, B.-Y., Chon, H.J., Claudia, F., Niizeki, T., Sho, T., Kang, B., D’Alessio, A., Kumada, T., Hiraoka, A., Hirooka, M., Kariyama, K., Tani, J., Atsukawa, M., Takaguchi, K., Itobayashi, E., Fukunishi, S., Tsuji, K., Ishikawa, T., Tajiri, K., Ochi, H., Yasuda, S., Toyoda, H., Ogawa, C., Nishimur, T., Hatanaka, T., Kakizaki, S., Shimada, N., Kawata, K., Tanaka, T., Ohama, H., Nouso, K., Morishita, A., Tsutsui, A., Nagano, T., Itokawa, N., Okubo, T., Arai, T., Imai, M., Naganuma, A., Koizumi, Y., Nakamura, S., Joko, K., Iijima, H., Hiasa, Y., Pedica, F., De Cobelli, F., Ratti, F., Aldrighetti, L., Kudo, M., Cascinu, S., Casadei-Gardini, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808460/
https://www.ncbi.nlm.nih.gov/pubmed/36208496
http://dx.doi.org/10.1016/j.esmoop.2022.100591
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author Rimini, M.
Rimassa, L.
Ueshima, K.
Burgio, V.
Shigeo, S.
Tada, T.
Suda, G.
Yoo, C.
Cheon, J.
Pinato, D.J.
Lonardi, S.
Scartozzi, M.
Iavarone, M.
Di Costanzo, G.G.
Marra, F.
Soldà, C.
Tamburini, E.
Piscaglia, F.
Masi, G.
Cabibbo, G.
Foschi, F.G.
Silletta, M.
Pressiani, T.
Nishida, N.
Iwamoto, H.
Sakamoto, N.
Ryoo, B.-Y.
Chon, H.J.
Claudia, F.
Niizeki, T.
Sho, T.
Kang, B.
D’Alessio, A.
Kumada, T.
Hiraoka, A.
Hirooka, M.
Kariyama, K.
Tani, J.
Atsukawa, M.
Takaguchi, K.
Itobayashi, E.
Fukunishi, S.
Tsuji, K.
Ishikawa, T.
Tajiri, K.
Ochi, H.
Yasuda, S.
Toyoda, H.
Ogawa, C.
Nishimur, T.
Hatanaka, T.
Kakizaki, S.
Shimada, N.
Kawata, K.
Tanaka, T.
Ohama, H.
Nouso, K.
Morishita, A.
Tsutsui, A.
Nagano, T.
Itokawa, N.
Okubo, T.
Arai, T.
Imai, M.
Naganuma, A.
Koizumi, Y.
Nakamura, S.
Joko, K.
Iijima, H.
Hiasa, Y.
Pedica, F.
De Cobelli, F.
Ratti, F.
Aldrighetti, L.
Kudo, M.
Cascinu, S.
Casadei-Gardini, A.
author_facet Rimini, M.
Rimassa, L.
Ueshima, K.
Burgio, V.
Shigeo, S.
Tada, T.
Suda, G.
Yoo, C.
Cheon, J.
Pinato, D.J.
Lonardi, S.
Scartozzi, M.
Iavarone, M.
Di Costanzo, G.G.
Marra, F.
Soldà, C.
Tamburini, E.
Piscaglia, F.
Masi, G.
Cabibbo, G.
Foschi, F.G.
Silletta, M.
Pressiani, T.
Nishida, N.
Iwamoto, H.
Sakamoto, N.
Ryoo, B.-Y.
Chon, H.J.
Claudia, F.
Niizeki, T.
Sho, T.
Kang, B.
D’Alessio, A.
Kumada, T.
Hiraoka, A.
Hirooka, M.
Kariyama, K.
Tani, J.
Atsukawa, M.
Takaguchi, K.
Itobayashi, E.
Fukunishi, S.
Tsuji, K.
Ishikawa, T.
Tajiri, K.
Ochi, H.
Yasuda, S.
Toyoda, H.
Ogawa, C.
Nishimur, T.
Hatanaka, T.
Kakizaki, S.
Shimada, N.
Kawata, K.
Tanaka, T.
Ohama, H.
Nouso, K.
Morishita, A.
Tsutsui, A.
Nagano, T.
Itokawa, N.
Okubo, T.
Arai, T.
Imai, M.
Naganuma, A.
Koizumi, Y.
Nakamura, S.
Joko, K.
Iijima, H.
Hiasa, Y.
Pedica, F.
De Cobelli, F.
Ratti, F.
Aldrighetti, L.
Kudo, M.
Cascinu, S.
Casadei-Gardini, A.
author_sort Rimini, M.
collection PubMed
description BACKGROUND: A growing body of evidence suggests that non-viral hepatocellular carcinoma (HCC) might benefit less from immunotherapy. MATERIALS AND METHODS: We carried out a retrospective analysis of prospectively collected data from consecutive patients with non-viral advanced HCC, treated with atezolizumab plus bevacizumab, lenvatinib, or sorafenib, in 36 centers in 4 countries (Italy, Japan, Republic of Korea, and UK). The primary endpoint was overall survival (OS) with atezolizumab plus bevacizumab versus lenvatinib. Secondary endpoints were progression-free survival (PFS) with atezolizumab plus bevacizumab versus lenvatinib, and OS and PFS with atezolizumab plus bevacizumab versus sorafenib. For the primary and secondary endpoints, we carried out the analysis on the whole population first, and then we divided the cohort into two groups: non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH) population and non-NAFLD/NASH population. RESULTS: One hundred and ninety patients received atezolizumab plus bevacizumab, 569 patients received lenvatinib, and 210 patients received sorafenib. In the whole population, multivariate analysis showed that treatment with lenvatinib was associated with a longer OS [hazard ratio (HR) 0.65; 95% confidence interval (CI) 0.44-0.95; P = 0.0268] and PFS (HR 0.67; 95% CI 0.51-0.86; P = 0.002) compared to atezolizumab plus bevacizumab. In the NAFLD/NASH population, multivariate analysis confirmed that lenvatinib treatment was associated with a longer OS (HR 0.46; 95% CI 0.26-0.84; P = 0.0110) and PFS (HR 0.55; 95% CI 0.38-0.82; P = 0.031) compared to atezolizumab plus bevacizumab. In the subgroup of non-NAFLD/NASH patients, no difference in OS or PFS was observed between patients treated with lenvatinib and those treated with atezolizumab plus bevacizumab. All these results were confirmed following propensity score matching analysis. By comparing patients receiving atezolizumab plus bevacizumab versus sorafenib, no statistically significant difference in survival was observed. CONCLUSIONS: The present analysis conducted on a large number of advanced non-viral HCC patients showed for the first time that treatment with lenvatinib is associated with a significant survival benefit compared to atezolizumab plus bevacizumab, in particular in patients with NAFLD/NASH-related HCC.
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spelling pubmed-98084602023-01-04 Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis Rimini, M. Rimassa, L. Ueshima, K. Burgio, V. Shigeo, S. Tada, T. Suda, G. Yoo, C. Cheon, J. Pinato, D.J. Lonardi, S. Scartozzi, M. Iavarone, M. Di Costanzo, G.G. Marra, F. Soldà, C. Tamburini, E. Piscaglia, F. Masi, G. Cabibbo, G. Foschi, F.G. Silletta, M. Pressiani, T. Nishida, N. Iwamoto, H. Sakamoto, N. Ryoo, B.-Y. Chon, H.J. Claudia, F. Niizeki, T. Sho, T. Kang, B. D’Alessio, A. Kumada, T. Hiraoka, A. Hirooka, M. Kariyama, K. Tani, J. Atsukawa, M. Takaguchi, K. Itobayashi, E. Fukunishi, S. Tsuji, K. Ishikawa, T. Tajiri, K. Ochi, H. Yasuda, S. Toyoda, H. Ogawa, C. Nishimur, T. Hatanaka, T. Kakizaki, S. Shimada, N. Kawata, K. Tanaka, T. Ohama, H. Nouso, K. Morishita, A. Tsutsui, A. Nagano, T. Itokawa, N. Okubo, T. Arai, T. Imai, M. Naganuma, A. Koizumi, Y. Nakamura, S. Joko, K. Iijima, H. Hiasa, Y. Pedica, F. De Cobelli, F. Ratti, F. Aldrighetti, L. Kudo, M. Cascinu, S. Casadei-Gardini, A. ESMO Open Original Research BACKGROUND: A growing body of evidence suggests that non-viral hepatocellular carcinoma (HCC) might benefit less from immunotherapy. MATERIALS AND METHODS: We carried out a retrospective analysis of prospectively collected data from consecutive patients with non-viral advanced HCC, treated with atezolizumab plus bevacizumab, lenvatinib, or sorafenib, in 36 centers in 4 countries (Italy, Japan, Republic of Korea, and UK). The primary endpoint was overall survival (OS) with atezolizumab plus bevacizumab versus lenvatinib. Secondary endpoints were progression-free survival (PFS) with atezolizumab plus bevacizumab versus lenvatinib, and OS and PFS with atezolizumab plus bevacizumab versus sorafenib. For the primary and secondary endpoints, we carried out the analysis on the whole population first, and then we divided the cohort into two groups: non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH) population and non-NAFLD/NASH population. RESULTS: One hundred and ninety patients received atezolizumab plus bevacizumab, 569 patients received lenvatinib, and 210 patients received sorafenib. In the whole population, multivariate analysis showed that treatment with lenvatinib was associated with a longer OS [hazard ratio (HR) 0.65; 95% confidence interval (CI) 0.44-0.95; P = 0.0268] and PFS (HR 0.67; 95% CI 0.51-0.86; P = 0.002) compared to atezolizumab plus bevacizumab. In the NAFLD/NASH population, multivariate analysis confirmed that lenvatinib treatment was associated with a longer OS (HR 0.46; 95% CI 0.26-0.84; P = 0.0110) and PFS (HR 0.55; 95% CI 0.38-0.82; P = 0.031) compared to atezolizumab plus bevacizumab. In the subgroup of non-NAFLD/NASH patients, no difference in OS or PFS was observed between patients treated with lenvatinib and those treated with atezolizumab plus bevacizumab. All these results were confirmed following propensity score matching analysis. By comparing patients receiving atezolizumab plus bevacizumab versus sorafenib, no statistically significant difference in survival was observed. CONCLUSIONS: The present analysis conducted on a large number of advanced non-viral HCC patients showed for the first time that treatment with lenvatinib is associated with a significant survival benefit compared to atezolizumab plus bevacizumab, in particular in patients with NAFLD/NASH-related HCC. Elsevier 2022-10-06 /pmc/articles/PMC9808460/ /pubmed/36208496 http://dx.doi.org/10.1016/j.esmoop.2022.100591 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Rimini, M.
Rimassa, L.
Ueshima, K.
Burgio, V.
Shigeo, S.
Tada, T.
Suda, G.
Yoo, C.
Cheon, J.
Pinato, D.J.
Lonardi, S.
Scartozzi, M.
Iavarone, M.
Di Costanzo, G.G.
Marra, F.
Soldà, C.
Tamburini, E.
Piscaglia, F.
Masi, G.
Cabibbo, G.
Foschi, F.G.
Silletta, M.
Pressiani, T.
Nishida, N.
Iwamoto, H.
Sakamoto, N.
Ryoo, B.-Y.
Chon, H.J.
Claudia, F.
Niizeki, T.
Sho, T.
Kang, B.
D’Alessio, A.
Kumada, T.
Hiraoka, A.
Hirooka, M.
Kariyama, K.
Tani, J.
Atsukawa, M.
Takaguchi, K.
Itobayashi, E.
Fukunishi, S.
Tsuji, K.
Ishikawa, T.
Tajiri, K.
Ochi, H.
Yasuda, S.
Toyoda, H.
Ogawa, C.
Nishimur, T.
Hatanaka, T.
Kakizaki, S.
Shimada, N.
Kawata, K.
Tanaka, T.
Ohama, H.
Nouso, K.
Morishita, A.
Tsutsui, A.
Nagano, T.
Itokawa, N.
Okubo, T.
Arai, T.
Imai, M.
Naganuma, A.
Koizumi, Y.
Nakamura, S.
Joko, K.
Iijima, H.
Hiasa, Y.
Pedica, F.
De Cobelli, F.
Ratti, F.
Aldrighetti, L.
Kudo, M.
Cascinu, S.
Casadei-Gardini, A.
Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
title Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
title_full Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
title_fullStr Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
title_full_unstemmed Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
title_short Atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
title_sort atezolizumab plus bevacizumab versus lenvatinib or sorafenib in non-viral unresectable hepatocellular carcinoma: an international propensity score matching analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808460/
https://www.ncbi.nlm.nih.gov/pubmed/36208496
http://dx.doi.org/10.1016/j.esmoop.2022.100591
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