Target hepatic artery regional chemotherapy and bevacizumab perfusion in liver metastatic colorectal cancer after failure of first-line or second-line systemic chemotherapy

被引:12
作者
Chen, Hui [1 ]
Zhang, Ji [2 ]
Cao, Guang [1 ]
Liu, Peng [1 ]
Xu, Haifeng [1 ]
Wang, Xiaodong [1 ]
Zhu, Xu [1 ]
Gao, Song [1 ]
Guo, Jianhai [1 ]
Zhu, Linzhong [1 ]
Zhang, Pengjun [1 ]
机构
[1] Peking Univ, Canc Hosp, Key Lab Carcinogenesis & Translat Res, Dept Intervent Therapy,Minist Educ, Beijing 100142, Peoples R China
[2] Peking Univ, Canc Hosp, Dept Surg Gastroenterol, Beijing 100142, Peoples R China
关键词
bevacizumab; colorectal cancer; target vessel regional chemotherapy; hepatic artery; hepatic metastasis; SINUSOIDAL OBSTRUCTION SYNDROME; PHASE-III TRIAL; OXALIPLATIN-BASED CHEMOTHERAPY; CETUXIMAB PLUS IRINOTECAN; RANDOMIZED-TRIAL; ONCOLOGY-GROUP; FLUOROURACIL; LEUCOVORIN; THERAPY; COMBINATION;
D O I
10.1097/CAD.0000000000000290
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Colorectal cancer liver metastasis (CRLM) is a refractory disease after failure of first-line or second-line chemotherapy. Bevacizumab is recommended as first-line therapy for advanced colorectal cancer, but is unproven in CRLM through the hepatic artery. We report favorable outcomes with targeted vessel regional chemotherapy (TVRC) for liver metastatic gastric cancer. TVRC with FOLFOX and bevacizumab perfusion through the hepatic artery was attempted for CRLM for efficacy and safety evaluation. In a single-institution retrospective observational study, 246 patients with CRLM after at least first-line or second-line failure of systemic chemotherapy received TVRC with FOLFOX (i.e. oxaliplatin, leucovorin, and 5-fluorouracil). Of 246 patients, 63 were enrolled into two groups: group 1 (n=30) received bevacizumab and TVRC following tumor progression during previous TVRC treatments; group 2 (n=33) received TVRC plus bevacizumab for CRLM on initiating TVRC. There were no significant differences in the median survival time (14.7 vs. 13.2 months, P=0.367), although the median time to progression was significant (3.3 vs. 5.5 months, P=0.026) between groups. No severe adverse events related to TVRC plus bevacizumab perfusion occurred. Target vessel regional chemotherapy with FOLFOX plus bevacizumab perfusion through the hepatic artery was effective and safe in CRLM. The optimal combination of TVRC and bevacizumab needs further confirmation in future phase II-III clinical trials.
引用
收藏
页码:118 / 126
页数:9
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