Fufang BanmaoCapsule, a Traditional Chinese Medicinal Formulation, Enhances the Survival of Patients with Hepatocellular Carcinoma and Vp3-4 Portal Vein Tumor Thrombosis Undergoing Supportive Treatment

被引:15
作者
Liu, Yao [1 ]
Li, Yuxin [1 ]
Wang, Xiaojing [1 ]
Huang, Yunyi [2 ]
Zhang, Qun [1 ]
Shi, Ke [2 ]
Ran, Chongping [1 ]
Hou, Jie [2 ]
Wang, Xianbo [1 ]
机构
[1] Capital Med Univ, Beijing Ditan Hosp, Ctr Integrat Med, 8 Jing Shun East St, Beijing 100015, Peoples R China
[2] Beijing Univ Chinese Med, Dongzhimen Hosp, Dept Gastroenterol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Traditional Chinese Medicinal formulation; hepatocellular carcinoma; portal vein tumor thrombosis; integrative therapy; survival; HISTORY;
D O I
10.1089/acm.2019.0334
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objectives:Fufang Banmao(FFBM) capsule, a type of Chinese medicinal formulation, has decades of history in treating hepatocellular carcinoma (HCC). This retrospective study aimed to observe the effect of FFBM capsules on the 6-month survival of patients with advanced HCC and Vp3-4 portal vein tumor thrombosis (PVTT) who received supportive therapy alone. Design:In total, 320 HCC/Vp3-4 PVTT patients underwent treatment with supportive therapy, of whom 95 took FFBM capsules and were treated with supportive therapy (FFBM group) and 225 received supportive therapy alone (control group). Comparisons of the 6-month overall survival (OS) rate of the two groups were performed. Propensity score matching (PSM) was used to match the characteristics between individuals in the two groups. A nomogram was built based on independent predictive factors for OS. Results:Cox multivariate analysis revealed that hepatic encephalopathy, aspartate transaminase (AST) and gamma-glutamyl transpeptidase levels, Child-Pugh class, prothrombin time, alpha-fetoprotein level, largest tumor diameter, and use of FFBM capsules were independent predictive factors of OS. Variceal bleeding, alanine transaminase, AST, total bilirubin, and Barcelona Clinic for Liver Cancer stage were different at baseline in the FFBM and control groups. Analysis revealed no significant adverse effects or toxicities relevant to the medications. After PSM (1:1), 95 patient pairs were analyzed as FFBM versus control. The OS probability was remarkably higher for patients in the FFBM group than in those in the control group at 6 months (p < 0.0001). The median survival time was 4 months in the FFBM group and 2.2 months in the control group. Kaplan-Meier analysis showed significant statistical differences in the 6-month OS rates in the patients with total nomogram scores >= 84 (p < 0.0001). Conclusions:Given the satisfying survival outcomes, the results suggested that FFBM capsules should be administered to patients with HCC/Vp3-4 PVTT in the high-risk group (score >= 84). FFBM capsules have the potential for improving patient survival time in those with advanced HCC and Vp3-4 PVTT who receive supportive therapy alone, especially those in the high-risk group (score >= 84).
引用
收藏
页码:956 / 965
页数:10
相关论文
共 27 条
[1]   The Burden of Primary Liver Cancer and Underlying Etiologies From 1990 to 2015 at the Global, Regional, and National Level Results From the Global Burden of Disease Study 2015 [J].
Akinyemiju, Tomi ;
Abera, Semaw ;
Ahmed, Muktar ;
Alam, Noore ;
Alemayohu, Mulubirhan Assefa ;
Allen, Christine ;
Al-Raddadi, Rajaa ;
Alvis-Guzman, Nelson ;
Amoako, Yaw ;
Artaman, Al ;
Ayele, Tadesse Awoke ;
Barac, Aleksandra ;
Bensenor, Isabela ;
Berhane, Adugnaw ;
Bhutta, Zulfiqar ;
Castillo-Rivas, Jacqueline ;
Chitheer, Abdulaal ;
Choi, Jee-Young ;
Cowie, Benjamin ;
Dandona, Lalit ;
Dandona, Rakhi ;
Dey, Subhojit ;
Dicker, Daniel ;
Phuc, Huyen ;
Ekwueme, Donatus U. ;
Zaki, Maysaa El Sayed ;
Fischer, Florian ;
Furst, Thomas ;
Hancock, Jamie ;
Hay, Simon I. ;
Hotez, Peter ;
Jee, Sun Ha ;
Kasaeian, Amir ;
Khader, Yousef ;
Khang, Young-Ho ;
Kumar, G. Anil ;
Kutz, Michael ;
Larson, Heidi ;
Lopez, Alan ;
Lunevicius, Raimundas ;
Malekzadeh, Reza ;
McAlinden, Colm ;
Meier, Toni ;
Mendoza, Walter ;
Mokdad, Ali ;
Moradi-Lakeh, Maziar ;
Nagel, Gabriele ;
Nguyen, Quyen ;
Nguyen, Grant ;
Ogbo, Felix .
JAMA ONCOLOGY, 2017, 3 (12) :1683-1691
[2]   Hepatic arterial infusion chemotherapy for advanced hepatocellular carcinoma with portal vein tumor thrombosis - Analysis of 48 cases [J].
Ando, E ;
Tanaka, M ;
Yamashita, F ;
Kuromatsu, R ;
Yutani, S ;
Fukumori, K ;
Sumie, S ;
Yano, Y ;
Okuda, K ;
Sata, M .
CANCER, 2002, 95 (03) :588-595
[3]   Efficacy of a Hepatectomy and a Tumor Thrombectomy for Hepatocellular Carcinoma with Tumor Thrombus Extending to the Main Portal Vein [J].
Ban, Daisuke ;
Shimada, Kazuaki ;
Yamamoto, Yusuke ;
Nara, Satoshi ;
Esaki, Minoru ;
Sakamoto, Yoshihiro ;
Kosuge, Tomoo .
JOURNAL OF GASTROINTESTINAL SURGERY, 2009, 13 (11) :1921-1928
[4]   Tumor and liver determinants of prognosis in unresectable hepatocellular carcinoma: a large case cohort study [J].
Carr, Brian I. ;
Pancoska, Petr ;
Branch, Robert A. .
HEPATOLOGY INTERNATIONAL, 2010, 4 (01) :396-405
[5]   Effect of Paeonol on Antioxidant and Immune Regulatory Activity in Hepatocellular Carcinoma Rats [J].
Chen, Bendong ;
Ning, Mingliang ;
Yang, Guangshun .
MOLECULES, 2012, 17 (04) :4672-4683
[6]   Cancer Statistics in China, 2015 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Baade, Peter D. ;
Zhang, Siwei ;
Zeng, Hongmei ;
Bray, Freddie ;
Jemal, Ahmedin ;
Yu, Xue Qin ;
He, Jie .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) :115-132
[7]   HEPATOCELLULAR-CARCINOMA AND PORTAL-VEIN INVASION - RESULTS OF TREATMENT WITH TRANSCATHETER OILY CHEMOEMBOLIZATION [J].
CHUNG, JW ;
PARK, JH ;
HAN, JK ;
CHOI, BI ;
HAN, MC .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1995, 165 (02) :315-321
[8]  
European Assoc Study Liver, 2012, EUR J CANCER, V48, P599, DOI [10.1016/j.ejca.2011.12.021, 10.1016/j.jhep.2011.12.001]
[9]   Cantharidic acid induces apoptosis through the p38 MAPK signaling pathway in human hepatocellular carcinoma [J].
Feng, I-Che ;
Hsieh, Ming-Ju ;
Chen, Pei-Ni ;
Hsieh, Yi-Hsien ;
Ho, Hsin-Yu ;
Yang, Shun-Fa ;
Yeh, Chao-Bin .
ENVIRONMENTAL TOXICOLOGY, 2018, 33 (03) :261-268
[10]   Hepatocellular carcinoma [J].
Forner, Alejandro ;
Llovet, Josep M. ;
Bruix, Jordi .
LANCET, 2012, 379 (9822) :1245-1255