Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies
Abstract Background The efficacy of bevacizumab combined with erlotinib (B + E) for the treatment of advanced hepatocellular carcinoma, especially for sorafenib-refractory patients, has been observed and evaluated in several trials. We conducted this single arm meta-analysis to generally assess the...
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doaj-5daa2604ab1d4846a4ed4ff54c8fffae2020-11-25T02:07:48ZengBMCBMC Cancer1471-24072019-03-0119111310.1186/s12885-019-5487-6Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studiesLiyun He0Huan Deng1Jun Lei2Fengming Yi3Jine Li4Xiu De Fan5Yiping Wei6Jianjun Xu7Wenxiong Zhang8Department of Thoracic Surgery, The Second Affiliated Hospital of Nanchang UniversityDepartment of Thoracic Surgery, The Second Affiliated Hospital of Nanchang UniversityDepartment of Hepatobiliary Surgery, The Second Affiliated Hospital of Nanchang UniversityDepartment of Oncology, The Second Affiliated Hospital of Nanchang UniversityJiangxi Medical College, Nanchang UniversityDepartment of Infectious Diseases, The First Affiliated Hospital of Xi’an Jiaotong UniversityDepartment of Thoracic Surgery, The Second Affiliated Hospital of Nanchang UniversityDepartment of Thoracic Surgery, The Second Affiliated Hospital of Nanchang UniversityDepartment of Thoracic Surgery, The Second Affiliated Hospital of Nanchang UniversityAbstract Background The efficacy of bevacizumab combined with erlotinib (B + E) for the treatment of advanced hepatocellular carcinoma, especially for sorafenib-refractory patients, has been observed and evaluated in several trials. We conducted this single arm meta-analysis to generally assess the benefit and risk with B + E for advanced hepatocellular carcinoma. Methods The PubMed, Cochrane Library, Embase, ScienceDirect, Web of Science and Scopus databases were searched for related studies. The main outcomes were objective response rate (ORR), disease control rate (DCR), overall survival (OS), progression-free survival (PFS) and adverse effects (AEs). Results Eight phase II clinical trials including 342 hepatocellular carcinoma patients were analyzed. The pooled ORR was 12.6% (95% CI: 6.3–19.0%), and the pooled DCR was 54.5% (95% CI: 48.9–66.8%). The 16-week PFS rate was 50.2% (95% CI: 38.2–62.2%). The 6- and 12-month OS rates were 77.8% (95% CI: 71.3–84.2%) and 44.9% (95% CI: 36.8–53.0%). The main grade 3–4 AEs were fatigue (11.9%), diarrhea (9.0%), hypertension (6.7%), acne (5.8%) and hemorrhage (5.3%). The only RCT showed that the B + E regimen had a consistent response and equable median OS but fewer toxicities (grade 3–4 AEs: 19% vs. 27%) than sorafenib. Subgroup analysis showed that as a second-line treatment, the B + E regimen had substantial value with a favorable PFS-16w (P = 0.012), OS-12 m (P = 0.048) and a favorable tendency of ORR (P = 0.089), but obvious toxicities in the second-line setting could not be neglected. Conclusion Bevacizumab combined with erlotinib is effective for treating hepatocellular carcinoma patients, especially sorafenib-refractory patients. More well-designed and large-scale RCTs are warranted to prove our findings.http://link.springer.com/article/10.1186/s12885-019-5487-6Meta-analysisBevacizumabErlotinibHepatocellular carcinomaSorafenib |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Liyun He Huan Deng Jun Lei Fengming Yi Jine Li Xiu De Fan Yiping Wei Jianjun Xu Wenxiong Zhang |
spellingShingle |
Liyun He Huan Deng Jun Lei Fengming Yi Jine Li Xiu De Fan Yiping Wei Jianjun Xu Wenxiong Zhang Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies BMC Cancer Meta-analysis Bevacizumab Erlotinib Hepatocellular carcinoma Sorafenib |
author_facet |
Liyun He Huan Deng Jun Lei Fengming Yi Jine Li Xiu De Fan Yiping Wei Jianjun Xu Wenxiong Zhang |
author_sort |
Liyun He |
title |
Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies |
title_short |
Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies |
title_full |
Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies |
title_fullStr |
Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies |
title_full_unstemmed |
Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies |
title_sort |
efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies |
publisher |
BMC |
series |
BMC Cancer |
issn |
1471-2407 |
publishDate |
2019-03-01 |
description |
Abstract Background The efficacy of bevacizumab combined with erlotinib (B + E) for the treatment of advanced hepatocellular carcinoma, especially for sorafenib-refractory patients, has been observed and evaluated in several trials. We conducted this single arm meta-analysis to generally assess the benefit and risk with B + E for advanced hepatocellular carcinoma. Methods The PubMed, Cochrane Library, Embase, ScienceDirect, Web of Science and Scopus databases were searched for related studies. The main outcomes were objective response rate (ORR), disease control rate (DCR), overall survival (OS), progression-free survival (PFS) and adverse effects (AEs). Results Eight phase II clinical trials including 342 hepatocellular carcinoma patients were analyzed. The pooled ORR was 12.6% (95% CI: 6.3–19.0%), and the pooled DCR was 54.5% (95% CI: 48.9–66.8%). The 16-week PFS rate was 50.2% (95% CI: 38.2–62.2%). The 6- and 12-month OS rates were 77.8% (95% CI: 71.3–84.2%) and 44.9% (95% CI: 36.8–53.0%). The main grade 3–4 AEs were fatigue (11.9%), diarrhea (9.0%), hypertension (6.7%), acne (5.8%) and hemorrhage (5.3%). The only RCT showed that the B + E regimen had a consistent response and equable median OS but fewer toxicities (grade 3–4 AEs: 19% vs. 27%) than sorafenib. Subgroup analysis showed that as a second-line treatment, the B + E regimen had substantial value with a favorable PFS-16w (P = 0.012), OS-12 m (P = 0.048) and a favorable tendency of ORR (P = 0.089), but obvious toxicities in the second-line setting could not be neglected. Conclusion Bevacizumab combined with erlotinib is effective for treating hepatocellular carcinoma patients, especially sorafenib-refractory patients. More well-designed and large-scale RCTs are warranted to prove our findings. |
topic |
Meta-analysis Bevacizumab Erlotinib Hepatocellular carcinoma Sorafenib |
url |
http://link.springer.com/article/10.1186/s12885-019-5487-6 |
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