Trans-arterial chemoembolization with degradable starch microspheres (DSM-TACE) versus selective internal radiation therapy (SIRT) in multifocal hepatocellular carcinoma

被引:13
作者
Auer, Timo A. [1 ]
Jonczyk, Martin [1 ]
Collettini, Federico [1 ]
Marth, Adrian [1 ]
Wieners, Gero [1 ]
Hamm, Bernd [1 ]
Gebauer, Bernhard [1 ]
机构
[1] Charite Univ Med Berlin, Dept Radiol, Berlin, Germany
关键词
Hepatocellular carcinoma; trans-arterial chemoembolization; degradable starch microspheres; selective internal radiation therapy; multifocal hepatocellular carcinoma; BRACHYTHERAPY CT-HDRBT; TRANSARTERIAL CHEMOEMBOLIZATION; SORAFENIB; SAFETY; EMBOLIZATION; MULTICENTER; EFFICACY; TRIAL; CM;
D O I
10.1177/0284185120926474
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background To date there is no therapy consensus in patients with multifocal hepatocellular carcinoma (mHCC). Purpose To compare outcome of trans-arterial chemoembolization (TACE) with degradable starch microspheres (DSM-TACE) versus selective internal radiation therapy (SIRT) in mHCC. Material and Methods In this single-center study, 36 patients without portal vein invasion, treated between May 2014 and May 2018, were enrolled retrospectively. Eighteen consecutive patients received DSM-TACE and were matched by age, gender, BCLC stage, Child-Pugh status, and tumor volume and 18 patients underwent SIRT. Overall survival (OS), progression-free survival (PFS), and local tumor control (LTC) were evaluated. Toxicity profiles for both therapies were also evaluated and compared. Results In the entire collective, median OS was 9.5, PFS 5.0, and LTC 5.5 months. Subgroup analysis revealed an OS of 9.5 months in both groups (P = 0.621). PFS was 6 months for the SIRT and 4 months for the DSM-TACE cohort (P = 0.065). Although not significantly, LTC was lower (4 months) in the SIRT compared to the DSM-TACE cohort (7 months; P = 0.391). When DSM-TACE was performed >= 3 times (n = 11), OS increased, however without statistical difference compared to SIRT, to 11 months, PFS to 7 months, and LTC to 7 months. When DSM-TACE was performed <3 times (n = 7), OS, PFS, and LTC decreased (5 months, P = 0.333; 2 months, P = 0.047; 2 months, P = 0.47). Toxicity profiles and adverse event analysis only revealed a significant difference for nausea and vomiting (more frequent in the SIRT cohort, P = 0.015), while no other parameter showed a significant difference (P > 0.05). Conclusion DSM-TACE might be an alternative to SIRT in multifocal HCC patients as OS, PFS, and LTC did not differ significantly and toxicity profiles seem to be comparable.
引用
收藏
页码:313 / 321
页数:9
相关论文
共 36 条
[1]   Phase II study of sorafenib in patients with advanced hepatocellular carcinoma [J].
Abou-Alfa, Ghassan K. ;
Schwartz, Lawrence ;
Ricci, Sergio ;
Amadori, Dino ;
Santoro, Armando ;
Figer, Arie ;
De Greve, Jacques ;
Douillard, Jean-Yves ;
Lathia, Chetan ;
Schwartz, Brian ;
Taylor, Ian ;
Moscovici, Marius ;
Saltz, Leonard B. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (26) :4293-4300
[2]   Heterogeneity of Patients with Intermediate (BCLC B) Hepatocellular Carcinoma: Proposal for a Subclassification to Facilitate Treatment Decisions [J].
Bolondi, Luigi ;
Burroughs, Andrew ;
Dufour, Jean-Francois ;
Galle, Peter R. ;
Mazzaferro, Vincenzo ;
Piscaglia, Fabio ;
Raoul, Jean Luc ;
Sangro, Bruno .
SEMINARS IN LIVER DISEASE, 2012, 32 (04) :348-359
[3]   Randomized Trial of Hepatic Artery Embolization for Hepatocellular Carcinoma Using Doxorubicin-Eluting Microspheres Compared With Embolization With Microspheres Alone [J].
Brown, Karen T. ;
Do, Richard K. ;
Gonen, Mithat ;
Covey, Anne M. ;
Getrajdman, George I. ;
Sofocleous, Constantinos T. ;
Jarnagin, William R. ;
D'Angelica, Michael I. ;
Allen, Peter J. ;
Erinjeri, Joseph P. ;
Brody, Lynn A. ;
O'Neill, Gerald P. ;
Johnson, Kristian N. ;
Garcia, Alessandra R. ;
Beattie, Christopher ;
Zhao, Binsheng ;
Solomon, Stephen B. ;
Schwartz, Lawrence H. ;
DeMatteo, Ronald ;
Abou-Alfa, Ghassan K. .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (17) :2046-+
[4]  
CARR BI, 1997, SEMINARS ONCOLOGY S6, V24
[5]   Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial [J].
Cheng, Ann-Lii ;
Kang, Yoon-Koo ;
Chen, Zhendong ;
Tsao, Chao-Jung ;
Qin, Shukui ;
Kim, Jun Suk ;
Luo, Rongcheng ;
Feng, Jifeng ;
Ye, Shenglong ;
Yang, Tsai-Sheng ;
Xu, Jianming ;
Sun, Yan ;
Liang, Houjie ;
Liu, Jiwei ;
Wang, Jiejun ;
Tak, Won Young ;
Pan, Hongming ;
Burock, Karin ;
Zou, Jessie ;
Voliotis, Dimitris ;
Guan, Zhongzhen .
LANCET ONCOLOGY, 2009, 10 (01) :25-34
[6]   SIRveNIB: Selective Internal Radiation Therapy Versus Sorafenib in Asia-Pacific Patients With Hepatocellular Carcinoma [J].
Chow, Pierce K. H. ;
Gandhi, Mihir ;
Tan, Say-Beng ;
Khin, Maung Win ;
Khasbazar, Ariunaa ;
Ong, Janus ;
Choo, Su Pin ;
Cheow, Peng Chung ;
Chotipanich, Chanisa ;
Lim, Kieron ;
Lesmana, Laurentius A. ;
Manuaba, Tjakra W. ;
Yoong, Boon Koon ;
Raj, Aloysius ;
Law, Chiong Soon ;
Cua, Ian H. Y. ;
Lobo, Rolley R. ;
Teh, Catherine S. C. ;
Kim, Yun Hwan ;
Jong, Yun Won ;
Han, Ho-Seong ;
Bae, Si-Hyun ;
Yoon, Hyun-Ki ;
Lee, Rheun-Chuan ;
Hung, Chien-Fu ;
Peng, Cheng-Yuan ;
Liang, Po-Chin ;
Bartlett, Adam ;
Kok, Kenneth Y. Y. ;
Thng, Choon-Hua ;
Low, Albert Su-Chong ;
Goh, Anthony S. W. ;
Tay, Kiang Hiong ;
Lo, Richard H. G. ;
Goh, Brian K. P. ;
Ng, David C. E. ;
Lekurwale, Ganesh ;
Liew, Wei Ming ;
Gebski, Val ;
Mak, Kenneth S. W. ;
Soo, Khee Chee .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (19) :1913-+
[7]  
DAKHIL S, 1982, CANCER-AM CANCER SOC, V50, P631, DOI 10.1002/1097-0142(19820815)50:4<631::AID-CNCR2820500403>3.0.CO
[8]  
2-M
[9]  
European Assoc Study Liver, 2018, J HEPATOL, V69, P182, DOI 10.1016/j.jhep.2018.03.019
[10]   Treatment of intermediate-stage hepatocellular carcinoma [J].
Fomer, Alejandro ;
Gilabert, Marine ;
Bruix, Jordi ;
Raoul, Jean-Luc .
NATURE REVIEWS CLINICAL ONCOLOGY, 2014, 11 (09) :525-535