Portal vein embolization and its effect on tumour progression for colorectal cancer liver metastases

被引:52
作者
Simoneau, E. [1 ]
Hassanain, M. [2 ,4 ]
Shaheen, M. [1 ]
Aljiffry, M. [5 ]
Molla, N. [3 ]
Chaudhury, P. [1 ,2 ]
Anil, S. [4 ]
Khashper, A. [3 ]
Valenti, D. [3 ]
Metrakos, P. [1 ]
机构
[1] McGill Univ, Dept Surg, Div Hepatopancreatobiliary Surg, Montreal, PQ H3A 2T5, Canada
[2] McGill Univ, Dept Surg, Div Oncol, Montreal, PQ H3A 2T5, Canada
[3] McGill Univ, Dept Radiol, Montreal, PQ, Canada
[4] King Saud Univ, Dept Surg, Riyadh, Saudi Arabia
[5] King Abdulaziz Univ, Fac Med, Dept Surg, Jeddah 21413, Saudi Arabia
关键词
MAJOR HEPATECTOMY; HEPATIC METASTASES; 1ST-LINE TREATMENT; GROWTH-RATE; RESECTION; CHEMOTHERAPY; BEVACIZUMAB; RECURRENCE; RESECTABILITY; REGENERATION;
D O I
10.1002/bjs.9872
中图分类号
R61 [外科手术学];
学科分类号
摘要
BackgroundThe aim of this study was to evaluate the long-term outcomes of patients with colorectal cancer liver metastasis (CRCLM) exhibiting disease progression after portal vein embolization (PVE). MethodsPatients with CRCLM requiring PVE before hepatectomy between 2003 and 2014 were included. Clinical variables, and liver and tumour volumes determined by three-dimensional CT volumetry were assessed before and after PVE. Overall and disease-free survival data were obtained. Univariable and multivariable logistic regression analyses were performed to identify predictors of tumour progression after PVE. ResultsOf 141 patients who underwent PVE, 93 (660 per cent) had tumour progression and 17 (121 per cent) developed new contralateral lesions. Significantly fewer patients had resectable disease in the group with disease progression than among those with stable disease: 43 (46 per cent) of 93 versus 36 (75 per cent) of 48 respectively (P = 0001). Median survival was similar in patients with and without tumour growth after PVE: 225 versus 260months for patients with unresectable tumours (P = 0706) and 462 versus 522months for those with resectable disease (P = 0953). However, disease-free survival for patients with tumour progression after PVE was shorter than that for patients with stable disease (60 versus 202months; P = 0045). Response to neoadjuvant chemotherapy was the only significant factor associated with tumour progression in multivariable analysis. ConclusionTumour progression after PVE did not affect overall survival, but patients with resected tumours who had tumour growth after embolization experienced earlier recurrence. A borderline response to neoadjuvant chemotherapy seemed to be associated with tumour progression after PVE. Tumour progression after portal vein embolization has no effect on survival
引用
收藏
页码:1240 / 1249
页数:10
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