Optimal timing of combining sorafenib with trans-arterial chemoembolization in patients with hepatocellular carcinoma: A meta-analysis.

Hepatocellular carcinoma Meta-analysis Safety Sorafenib Survival Trans-arterial chemoembolization

Journal

Translational oncology
ISSN: 1936-5233
Titre abrégé: Transl Oncol
Pays: United States
ID NLM: 101472619

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 26 08 2021
revised: 30 09 2021
accepted: 02 10 2021
pubmed: 11 10 2021
medline: 11 10 2021
entrez: 10 10 2021
Statut: ppublish

Résumé

The combination therapy of trans-arterial chemoembolization (TACE) and sorafenib were proved to be one of the effective methods for intermediate and advanced hepatocellular carcinoma (HCC). Although it has been confirmed that the combination therapy can prolong survival for advanced HCC effectively, the therapeutic efficacy and safety are still controversial and the clinical value has not been determined. This meta-analysis aims to evaluate the efficacy and safety of combination therapy and discuss the optimal timing of combination for better clinical benefits. PubMed, EMBASE, the Cochrane Library, MEDLINE, and Web of Science were systematically reviewed to search for relevant studies published before May 15, 2021. Studies comparing the efficacy and safety of TACE + sorafenib with TACE + placebo / alone were adopted. Two reviewers independently extracted study outcomes. The data were analyzed through fixed/random-effect meta-analysis models with Review Manager (Version 5. 3) software. 7 randomized controlled trials (RCTs) were included with 1464 patients with unresectable HCC (734 in TACE + sorafenib group and 730 in TACE + placebo or alone group). Meta-analysis showed that objective response rate (ORR) and disease control rate (DCR) were slightly improved in TACE + sorafenib group (ORR: risk ratio = 1.24; 95% confidence interval: 1.08-1.42; P = 0.002; DCR: risk ratio = 1.09; 95% confidence interval: 1.01-1.18; P = 0.02). The combination therapy obviously improved time to progression (TTP) (hazard ratio: 0.73; 95% confidence interval: 0.55-0.96; P = 0.03) and progression-free survival (PFS) (hazard ratio 0.62; 95% confidence interval: 0.52-0.73, P < 0.00001) but not overall survival (OS) (hazard ratio: 0.93; 95% confidence interval: 0.59-1.46; P = 0.75) or time to untreatable progression (TTUP) (hazard ratio: 0.76; 95% confidence interval: 0.31-1.89; P = 0.56). In addition, the incidence of adverse reactions (AEs) in combination group were higher than TACE + placebo / alone group. Furthermore, the subgroup analysis showed that the heterogeneity of TTP was notably decreased (pre-TACE: P = 0.12, I The combination of TACE and sorafenib significantly can improve TTP and PFS, and reduce the level of risk of adverse reactions of unresectable HCC, especially in the combination before TACE.

Sections du résumé

BACKGROUND BACKGROUND
The combination therapy of trans-arterial chemoembolization (TACE) and sorafenib were proved to be one of the effective methods for intermediate and advanced hepatocellular carcinoma (HCC). Although it has been confirmed that the combination therapy can prolong survival for advanced HCC effectively, the therapeutic efficacy and safety are still controversial and the clinical value has not been determined. This meta-analysis aims to evaluate the efficacy and safety of combination therapy and discuss the optimal timing of combination for better clinical benefits.
DATA SOURCES METHODS
PubMed, EMBASE, the Cochrane Library, MEDLINE, and Web of Science were systematically reviewed to search for relevant studies published before May 15, 2021. Studies comparing the efficacy and safety of TACE + sorafenib with TACE + placebo / alone were adopted. Two reviewers independently extracted study outcomes. The data were analyzed through fixed/random-effect meta-analysis models with Review Manager (Version 5. 3) software.
RESULTS RESULTS
7 randomized controlled trials (RCTs) were included with 1464 patients with unresectable HCC (734 in TACE + sorafenib group and 730 in TACE + placebo or alone group). Meta-analysis showed that objective response rate (ORR) and disease control rate (DCR) were slightly improved in TACE + sorafenib group (ORR: risk ratio = 1.24; 95% confidence interval: 1.08-1.42; P = 0.002; DCR: risk ratio = 1.09; 95% confidence interval: 1.01-1.18; P = 0.02). The combination therapy obviously improved time to progression (TTP) (hazard ratio: 0.73; 95% confidence interval: 0.55-0.96; P = 0.03) and progression-free survival (PFS) (hazard ratio 0.62; 95% confidence interval: 0.52-0.73, P < 0.00001) but not overall survival (OS) (hazard ratio: 0.93; 95% confidence interval: 0.59-1.46; P = 0.75) or time to untreatable progression (TTUP) (hazard ratio: 0.76; 95% confidence interval: 0.31-1.89; P = 0.56). In addition, the incidence of adverse reactions (AEs) in combination group were higher than TACE + placebo / alone group. Furthermore, the subgroup analysis showed that the heterogeneity of TTP was notably decreased (pre-TACE: P = 0.12, I
CONCLUSION CONCLUSIONS
The combination of TACE and sorafenib significantly can improve TTP and PFS, and reduce the level of risk of adverse reactions of unresectable HCC, especially in the combination before TACE.

Identifiants

pubmed: 34628285
pii: S1936-5233(21)00230-8
doi: 10.1016/j.tranon.2021.101238
pmc: PMC8515486
pii:
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101238

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Références

Oncology. 2014;87(6):330-41
pubmed: 25227534
Medicine (Baltimore). 2020 Jul 17;99(29):e20962
pubmed: 32702836
Recent Results Cancer Res. 2014;193:75-95
pubmed: 24008294
Ann Intern Med. 2009 Aug 18;151(4):W65-94
pubmed: 19622512
J Hepatol. 2021 Aug 27;:
pubmed: 34454995
Onco Targets Ther. 2020 Dec 04;13:12477-12487
pubmed: 33311988
BMC Gastroenterol. 2018 Sep 4;18(1):138
pubmed: 30180810
J Clin Oncol. 2011 Oct 20;29(30):3960-7
pubmed: 21911714
Clin Adv Hematol Oncol. 2016 Aug;14(8):585-7
pubmed: 27487101
Clin Radiol. 2014 Dec;69(12):e553-61
pubmed: 25304928
Clin Cancer Res. 2018 Apr 1;24(7):1518-1524
pubmed: 29138342
Clin Mol Hepatol. 2020 Apr;26(2):155-162
pubmed: 31937081
Cancers (Basel). 2019 Jul 31;11(8):
pubmed: 31370248
Surg Oncol Clin N Am. 2019 Oct;28(4):695-715
pubmed: 31472914
Gut. 2020 Aug;69(8):1492-1501
pubmed: 31801872
Clin Res Hepatol Gastroenterol. 2016 Dec;40(6):688-697
pubmed: 27339594
J Gastrointest Oncol. 2017 Apr;8(2):215-228
pubmed: 28480062
Aliment Pharmacol Ther. 2011 Jul;34(2):205-13
pubmed: 21605146
Immunotherapy. 2021 Jun;13(8):637-644
pubmed: 33820447
Eur J Cancer. 2011 Sep;47(14):2117-27
pubmed: 21664811
Hepatology. 2003 Feb;37(2):429-42
pubmed: 12540794
J BUON. 2020 Mar-Apr;25(2):945-951
pubmed: 32521890
J Hepatol. 2016 May;64(5):1090-1098
pubmed: 26809111
Future Oncol. 2021 Mar;17(7):755-757
pubmed: 33508960
Hepatology. 2021 Jan;73 Suppl 1:4-13
pubmed: 32319693
Lancet Gastroenterol Hepatol. 2017 Aug;2(8):565-575
pubmed: 28648803
Int J Cancer. 2015 Mar 15;136(6):1458-67
pubmed: 25099027
Oncologist. 2012;17(3):359-66
pubmed: 22334456
Clin Drug Investig. 2015 Nov;35(11):751-9
pubmed: 26446004
Jpn J Clin Oncol. 2018 Dec 1;48(12):1058-1069
pubmed: 30272196
Am J Cancer Res. 2019 Jun 01;9(6):1254-1265
pubmed: 31285957
BMC Cancer. 2015 May 11;15:392
pubmed: 25957784

Auteurs

Yanmei Dai (Y)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China.

Huijie Jiang (H)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China. Electronic address: jianghuijie@hrbmu.edu.cn.

Hao Jiang (H)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China.

Sheng Zhao (S)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China.

Xu Zeng (X)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China.

Ran Sun (R)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China.

Ruoshui Zheng (R)

Department of Radiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province 150086, China.

Classifications MeSH