TY - JOUR
T1 - Atezolizumab plus bevacizumab treatment for unresectable hepatocellular carcinoma progressing after molecular targeted therapy
T2 - A multicenter prospective observational study
AU - Sugimoto, Rie
AU - Satoh, Takeaki
AU - Ueda, Akihiro
AU - Senju, Takeshi
AU - Tanaka, Yuki
AU - Yamashita, Shinsaku
AU - Koyanagi, Toshimasa
AU - Kurashige, Tomoyuki
AU - Higuchi, Nobito
AU - Nakamura, Tsukasa
AU - Tanaka, Masatake
AU - Azuma, Yuuki
AU - Ohno, Akari
AU - Ooho, Aritsune
AU - Ooe, Mari
AU - Mutsuki, Taiji
AU - Uchimura, Koutarou
AU - Kuniyoshi, Masami
AU - Tada, Seiya
AU - Aratake, Yoshifusa
AU - Yoshimoto, Tsuyoshi
AU - Yamashita, Naoki
AU - Harada, Shigeru
AU - Nakamuta, Makoto
AU - Motomura, Kenta
AU - Kohjima, Motoyuki
N1 - Funding Information:
We used the official funds of Kyushu Cancer Center to fund the proofreading and submission of the paper.
Publisher Copyright:
© 2022 the Author(s). Published by Wolters Kluwer Health, Inc.
PY - 2022/10/7
Y1 - 2022/10/7
N2 - To evaluate the efficacy of atezolizumab plus bevacizumab treatment in patients with hepatocellular carcinoma (HCC) previously treated with molecular targeted agents (MTAs). Thirty-one patients treated with atezolizumab plus bevacizumab for unresectable HCC and previously treated with MTAs were enrolled in this study. The treatment lines ranged from second to sixth lines. The treatment effect on HCC differed from that during first-line treatment. The treatment effect was determined using the Response Evaluation Criteria in Solid Tumors (RECIST) and modified RECIST. The treatment response was different for each MTA immediately prior to atezolizumab + bevacizumab treatment. Tumors treated with lenvatinib followed by atezolizumab + bevacizumab showed rapid growth for a short period of time followed by shrinkage. However, patients who received ramucirumab, sorafenib, and regorafenib did not show such changes. This was likely because of differences in the mechanism of action of the MTA administered immediately beforehand. The side-effect profile differed from that observed in the IMbrave150 phase 3 study of atezolizumab plus bevacizumab, which showed more adverse events related to hepatic reserve. Patients treated with the combination of atezolizumab and bevacizumab after lenvatinib therapy may experience rapid tumor growth and subsequent shrinkage.
AB - To evaluate the efficacy of atezolizumab plus bevacizumab treatment in patients with hepatocellular carcinoma (HCC) previously treated with molecular targeted agents (MTAs). Thirty-one patients treated with atezolizumab plus bevacizumab for unresectable HCC and previously treated with MTAs were enrolled in this study. The treatment lines ranged from second to sixth lines. The treatment effect on HCC differed from that during first-line treatment. The treatment effect was determined using the Response Evaluation Criteria in Solid Tumors (RECIST) and modified RECIST. The treatment response was different for each MTA immediately prior to atezolizumab + bevacizumab treatment. Tumors treated with lenvatinib followed by atezolizumab + bevacizumab showed rapid growth for a short period of time followed by shrinkage. However, patients who received ramucirumab, sorafenib, and regorafenib did not show such changes. This was likely because of differences in the mechanism of action of the MTA administered immediately beforehand. The side-effect profile differed from that observed in the IMbrave150 phase 3 study of atezolizumab plus bevacizumab, which showed more adverse events related to hepatic reserve. Patients treated with the combination of atezolizumab and bevacizumab after lenvatinib therapy may experience rapid tumor growth and subsequent shrinkage.
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U2 - 10.1097/MD.0000000000030871
DO - 10.1097/MD.0000000000030871
M3 - Article
C2 - 36221372
AN - SCOPUS:85139691826
SN - 0025-7974
VL - 101
SP - E30871
JO - Medicine (United States)
JF - Medicine (United States)
IS - 40
ER -