Atezolizumab plus Bevacizumab in Unresectable Hepatocellular Carcinoma

被引:5354
作者
Finn, Richard S. [1 ]
Qin, Shukui [5 ]
Ikeda, Masafumi [8 ]
Galle, Peter R. [10 ]
Ducreux, Michel [11 ]
Kim, Tae-You [13 ]
Kudo, Masatoshi [9 ]
Breder, Valeriy [15 ]
Merle, Philippe [12 ]
Kaseb, Ahmed O. [16 ]
Li, Daneng [2 ,3 ]
Verret, Wendy [4 ]
Xu, Derek-Zhen [6 ]
Hernandez, Sairy [4 ]
Liu, Juan [6 ]
Huang, Chen [6 ]
Mulla, Sohail [17 ]
Wang, Yulei [4 ]
Lim, Ho Yeong [14 ]
Zhu, Andrew X. [7 ,18 ]
Cheng, Ann-Lii [19 ,20 ]
机构
[1] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Geffen Sch Med, Los Angeles, CA 90024 USA
[2] City Hope Comprehens Canc Ctr, Duarte, CA USA
[3] Beckman Res Inst, Duarte, CA USA
[4] Genentech Inc, San Francisco, CA 94080 USA
[5] Jinling Hosp, Peoples Liberat Army Canc Ctr, Nanjing, Peoples R China
[6] Jiahui Hlth, Roche Prod Dev, Shanghai, Peoples R China
[7] Jiahui Hlth, Jiahui Int Canc Ctr, Shanghai, Peoples R China
[8] Natl Canc Ctr Hosp East, Kashiwa, Chiba, Japan
[9] Kindai Univ, Fac Med, Osaka, Japan
[10] Univ Med Ctr Mainz, Mainz, Germany
[11] Paris Saclay Univ, Gustave Roussy Canc Ctr, Villejuif, France
[12] Univ Hosp La Croix Rousse, Lyon, France
[13] Seoul Natl Univ, Coll Med, Seoul, South Korea
[14] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Seoul, South Korea
[15] NN Blokhin Russian Canc Res Ctr, Moscow, Russia
[16] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[17] Hoffmann La Roche, Mississauga, ON, Canada
[18] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02115 USA
[19] Natl Taiwan Univ, Ctr Canc, Taipei, Taiwan
[20] Natl Taiwan Univ Hosp, Taipei, Taiwan
关键词
ENDOTHELIAL GROWTH-FACTOR; MONOCLONAL-ANTIBODY; PATIENTS PTS; PHASE-III; ANGIOGENESIS; SORAFENIB; VEGF; EXPRESSION; EFFICACY; THERAPY;
D O I
10.1056/NEJMoa1915745
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundThe combination of atezolizumab and bevacizumab showed encouraging antitumor activity and safety in a phase 1b trial involving patients with unresectable hepatocellular carcinoma. MethodsIn a global, open-label, phase 3 trial, patients with unresectable hepatocellular carcinoma who had not previously received systemic treatment were randomly assigned in a 2:1 ratio to receive either atezolizumab plus bevacizumab or sorafenib until unacceptable toxic effects occurred or there was a loss of clinical benefit. The coprimary end points were overall survival and progression-free survival in the intention-to-treat population, as assessed at an independent review facility according to Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST 1.1). ResultsThe intention-to-treat population included 336 patients in the atezolizumab-bevacizumab group and 165 patients in the sorafenib group. At the time of the primary analysis (August 29, 2019), the hazard ratio for death with atezolizumab-bevacizumab as compared with sorafenib was 0.58 (95% confidence interval [CI], 0.42 to 0.79; P<0.001). Overall survival at 12 months was 67.2% (95% CI, 61.3 to 73.1) with atezolizumab-bevacizumab and 54.6% (95% CI, 45.2 to 64.0) with sorafenib. Median progression-free survival was 6.8 months (95% CI, 5.7 to 8.3) and 4.3 months (95% CI, 4.0 to 5.6) in the respective groups (hazard ratio for disease progression or death, 0.59; 95% CI, 0.47 to 0.76; P<0.001). Grade 3 or 4 adverse events occurred in 56.5% of 329 patients who received at least one dose of atezolizumab-bevacizumab and in 55.1% of 156 patients who received at least one dose of sorafenib. Grade 3 or 4 hypertension occurred in 15.2% of patients in the atezolizumab-bevacizumab group; however, other high-grade toxic effects were infrequent. ConclusionsIn patients with unresectable hepatocellular carcinoma, atezolizumab combined with bevacizumab resulted in better overall and progression-free survival outcomes than sorafenib. (Funded by F. Hoffmann-La Roche/Genentech; ClinicalTrials.gov number, NCT03434379.) In patients with unresectable hepatocellular carcinoma, the combination of atezolizumab and bevacizumab was associated with better progression-free and overall survival outcomes, response rate, and preservation of quality of life than sorafenib. Serious toxic effects were noted in 38% of patients, similar to that seen in previous studies of these agents.
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收藏
页码:1894 / 1905
页数:12
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