Efficacy and Safety of Bevacizumab for the Treatment of Advanced Hepatocellular Carcinoma: A Systematic Review of Phase II Trials

被引:85
作者
Fang, Ping [1 ]
Hu, Jin-hua [2 ]
Cheng, Zhi-gang [3 ]
Liu, Zhe-feng [1 ]
Wang, Jin-liang [1 ]
Jiao, Shun-chang [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Inst Canc, Dept Oncol, Beijing, Peoples R China
[2] Shandong Prov Hosp, Dept Digest, Jinan, Peoples R China
[3] Peoples Liberat Army Gen Hosp, Inst Canc, Dept Ultrasound Intervent, Beijing, Peoples R China
来源
PLOS ONE | 2012年 / 7卷 / 12期
关键词
PLUS ERLOTINIB; THERAPY; CANCER; COMBINATION; CHEMOTHERAPY; PERSPECTIVES; CHALLENGES; MANAGEMENT;
D O I
10.1371/journal.pone.0049717
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Hepatocellular carcinoma (HCC) is a common cancer associated with a poor prognosis. Bevacizumab is a monoclonal antibody that binds vascular endothelial growth factor, a mediator of tumor angiogenesis. Bevacizumab is currently under investigation as treatment for HCC. We performed a systematic review of the efficacy and safety of bevacizumab for the treatment of advanced HCC. Methods: PubMed, the Cochrane Library, and Google Scholar were searched using the terms "bevacizumab AND hepatocellular carcinoma AND (advanced OR unresectable)". Phase II trials of bevacizumab for the treatment of advanced HCC were included. Outcomes of interest included progression-free and overall survival (PFS and OS), tumor response, and toxicities. Results: A total of 26 records were identified. Of these, 18 were excluded. Hence, eight trials involving 300 patients were included. Bevacizumab was given as monotherapy (n = 1 trial) or in combination with erlotinib (n = 4 trials), capecitabine (n = 1 trial), capecitabine+oxaliplatin (n = 1 trial), or gemcitabine+oxaliplatin (n = 1 trial). Most trials (five of eight) reported median PFS and OS between 5.3 months and 9.0 months and 5.9 and 13.7 months, respectively. The disease control rate was consistent in five of eight trials, ranging from 51.1% to 76.9%. The response and partial response rates ranged from 0 to 23.7%, but were around 20% in four trials. Only one patient had a complete response. Frequently reported Grade 3/4 toxicities were increased aspartate transaminase/alanine transaminase (13%), fatigue (12%), hypertension (10%), diarrhea (8%), and neutropenia (5%). Thirty patients experienced gastrointestinal bleeding (grade 1/2 = 18, grade 3/4 = 12), typically due to esophageal varices. Conclusions: Bevacizumab shows promise as an effective and tolerable treatment for advanced HCC. The reported efficacy of bevacizumab appears to compare favorably with that of sorafenib, the only currently approved treatment for unresectable HCC. Phase III trials are warranted to comprehensively examine the efficacy and safety of bevacizumab for treatment of advanced HCC.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Clinical Efficacy and Safety of Bevacizumab, Apatinib, and Recombinant Human Endothelial Inhibitor in the Treatment of Advanced Gastric Cancer
    Wang, Liang
    Li, Wei
    Liu, Ya-Gang
    Zhang, Cui
    Gao, Wei-Na
    Gao, Li-Fei
    JOURNAL OF ONCOLOGY, 2022, 2022
  • [42] A phase II study of pegylated liposomal doxorubicin for treatment of advanced hepatocellular carcinoma
    Halm, U
    Etzrodt, G
    Schiefke, I
    Schmidt, F
    Witzigmann, H
    Mössner, J
    Berr, F
    ANNALS OF ONCOLOGY, 2000, 11 (01) : 113 - 114
  • [43] Safety and efficacy of sorafenib in patients with advanced thyroid carcinoma: a phase II study (NCT02084732)
    Fierro-Maya, Luis Felipe
    Gonzalez, Gloria Garavito
    Melo, Leonardo Javier Rojas
    Cuellar, Andres Arturo Cuellar
    Carreno, Alexander
    Cordoba, Claudia
    ARCHIVES OF ENDOCRINOLOGY METABOLISM, 2021, 65 (04): : 404 - 410
  • [44] Efficacy and safety of sorafenib in elderly patients with advanced hepatocellular carcinoma
    Marta, Guilherme Nader
    da Fonseca, Leonardo G.
    Braghiroli, Maria Ignez
    Moura, Fernando
    Hoff, Paulo M.
    Sabbaga, Jorge
    CLINICS, 2021, 76 : 1 - 6
  • [45] Treatment of advanced hepatocellular carcinoma
    Forner, Alejandro
    Rodriguez De Lope, Carlos
    Reig, Maria
    Bruix, Jordi
    GASTROENTEROLOGIA Y HEPATOLOGIA, 2010, 33 (06): : 461 - 468
  • [46] Comparing the clinical efficacy and safety of second-line targeted therapy and immunotherapy in patients with mid- to advanced stages of hepatocellular carcinoma - A systematic review and meta-analysis of randomized clinical trials
    Li, J. -F.
    Fu, Y. -X.
    Zhang, H. -C.
    Ma, H.
    Yuan, G. -J.
    Tan, Y.
    EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2023, 27 (22) : 11156 - 11168
  • [47] Efficacy, Safety, and Potential Biomarkers of Sunitinib and Transarterial Chemoembolization (TACE) Combination in Advanced Hepatocellular Carcinoma (HCC): Phase II Trial
    Pokuri, Venkata K.
    Tomaszewski, Garin M.
    Ait-Oudhia, Sihem
    Groman, Adrienne
    Khushalani, Nikhil I.
    Lugade, Amit A.
    Thanavala, Yasmin
    Ashton, Edward A.
    Grande, Catherine
    Fetterly, Gerald J.
    Iyer, Renuka
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2018, 41 (04): : 332 - 338
  • [48] A Phase I/Randomized Phase II Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of Nintedanib versus Sorafenib in Asian Patients with Advanced Hepatocellular Carcinoma
    Yen, Chia-Jui
    Kim, Tae-You
    Feng, Yin-Hsun
    Chao, Yee
    Lin, Deng-Yn
    Ryoo, Baek-Yeol
    Huang, Dennis Chin-Lun
    Schnell, David
    Hocke, Julia
    Loembe, Arsene-Bienvenu
    Cheng, Ann-Lii
    LIVER CANCER, 2018, 7 (02) : 165 - 178
  • [49] Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies
    He, Liyun
    Deng, Huan
    Lei, Jun
    Yi, Fengming
    Li, Jine
    Fan, Xiu De
    Wei, Yiping
    Xu, Jianjun
    Zhang, Wenxiong
    BMC CANCER, 2019, 19 (1)
  • [50] A Phase II and Biomarker Study of Sorafenib Combined with Modified FOLFOX in Patients with Advanced Hepatocellular Carcinoma
    Goyal, Lipika
    Zheng, Hui
    Abrams, Thomas A.
    Miksad, Rebecca
    Bullock, Andrea J.
    Allen, Jill N.
    Yurgelun, Matthew B.
    Clark, Jeffrey W.
    Kambadakone, Avinash
    Muzikansky, Alona
    Knowles, Michelle
    Galway, Aralee
    Afflitto, Anthony J.
    Dinicola, Caroline F.
    Regan, Eileen
    Hato, Tai
    Mamessier, Emilie
    Shigeta, Kohei
    Jain, Rakesh K.
    Duda, Dan G.
    Zhu, Andrew X.
    CLINICAL CANCER RESEARCH, 2019, 25 (01) : 80 - 89