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IMbrave150: Efficacy and Safety of Atezolizumab Plus Bevacizumab vs Sorafenib in Patients With Barcelona Clinic Liver Cancer Stage B Unresectable Hepatocellular Carcinoma-An Exploratory Analysis of the Phase III Study
被引:15
|作者:
Kudo, Masatoshi
[1
]
Finn, Richard S. S.
[2
]
Galle, Peter R. R.
[3
]
Zhu, Andrew X. X.
[4
,5
]
Ducreux, Michel
[6
]
Cheng, Ann-Lii
[7
,8
]
Ikeda, Masafumi
[9
]
Tsuchiya, Kaoru
[10
]
Aoki, Ken-ichi
[11
]
Jia, Jing
[12
]
Lencioni, Riccardo
[13
]
机构:
[1] Kindai Univ, Fac Med, Dept Gastroenterol & Hepatol, 377-2 Ohno Higashi, Osaka, Osaka 5898511, Japan
[2] UCLA, David Geffen Sch Med, Dept Med, Div Hematol & Oncol,Jonsson Comprehens Canc Ctr, Los Angeles, CA USA
[3] Univ Med Ctr Mainz, Dept Internal Med, Mainz, Germany
[4] Massachusetts Gen Hosp, Canc Ctr, Harvard Med Sch, Boston, MA USA
[5] Jiahui Hlth, Jiahui Int Canc Ctr, Shanghai, Peoples R China
[6] Paris Saclay Univ, Gustave Roussy Canc Ctr, Dept Med Oncol, Inserm U1279, Villejuif, France
[7] Natl Taiwan Univ, Canc Ctr, Dept Oncol, Taipei, Taiwan
[8] Natl Taiwan Univ Hosp, Taipei, Taiwan
[9] Natl Canc Ctr Hosp East, Dept Hepatobiliary & Pancreat Oncol, Kashiwa, Japan
[10] Musashino Red Cross Hosp, Dept Gastroenterol & Hepatol, Tokyo, Japan
[11] Chugai Pharmaceut Ltd, Tokyo, Japan
[12] Hoffmann La Roche Ltd, Mississauga, ON, Canada
[13] Univ Pisa, Pisa, Italy
关键词:
SUBCLASSIFICATION;
HETEROGENEITY;
PROPOSAL;
D O I:
10.1159/000528272
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Introduction: The Phase III IMbrave150 study established atezolizumab + bevacizumab as standard of care in patients with unresectable hepatocellular carcinoma (HCC). This exploratory analysis reports efficacy and safety results in patients with baseline Barcelona Clinic Liver Cancer (BCLC) Stage B disease. Methods: Patients with systemic treatment-naive unresectable HCC and Child-Pugh Class A liver function were randomized 2:1 to receive 1200 mg of atezolizumab plus 15 mg/kg of bevacizumab or 400 mg of sorafenib. Co-primary endpoints were overall survival (OS) and progression-free survival (PFS) per independent review facility (IRF)-assessed Response Evaluation Criteria in Solid Tumours (RECIST) version 1.1 in the BCLC Stage B subgroup. Patients in this analysis had BCLC Stage B disease at baseline per electronic case report form. Secondary efficacy endpoints included objective response rate (ORR) and change in the sum of longest diameter (SLD) of target lesions from baseline per IRF RECIST 1.1 and modified RECIST (mRECIST) for HCC. Results: Of 501 enrolled patients, 74 (15%) had BCLC Stage B disease at baseline (atezolizumab + bevacizumab, n=49; sorafenib, n=24). For this group, median follow-up was 19.7 months. A trend toward improved OS and PFS per IRF RECIST 1.1 was observed with atezolizumab + bevacizumab vs sorafenib (OS: HR, 0.63; 95% CI: 0.29, 1.34; PFS: HR, 0.64; 95% CI: 0.36, 1.12). ORRs per IRF RECIST 1.1 and HCC mRECIST were 43% and 50% with atezolizumab + bevacizumab and 26% and 30% with sorafenib, respectively. Percentage change in SLD of target lesions from baseline per IRF RECIST 1.1 and HCC mRECIST showed durable responses with atezolizumab + bevacizumab treatment. Safety data were consistent with known profiles of atezolizumab and bevacizumab, as seen in the overall study population.Discussion/Conclusion: Efficacy benefits were observed with atezolizumab + bevacizumab in patients with baseline BCLC Stage B disease, consistent with the intention-to-treat population.
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页码:238 / 250
页数:13
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