Transarterial chemoembolization in pancreatic adenocarcinoma with liver metastases: MR-based tumor response evaluation, apparent diffusion coefficient (ADC) patterns, and survival rates

医学 实体瘤疗效评价标准 吉西他滨 有效扩散系数 胰腺癌 内科学 完全响应 进行性疾病 腺癌 胃肠病学 肿瘤科 癌症 化疗 放射科 磁共振成像
作者
Thomas J. Vogl,Sherif A. Mohamed,Moritz H. Albrecht,Tatjana Gruber-Roh,Han Lin,Nour-Eldin A. Nour-Eldin,Iliana Bednarova,N Naguib,Bita Panahi
出处
期刊:Pancreatology [Elsevier]
卷期号:18 (1): 94-99 被引量:23
标识
DOI:10.1016/j.pan.2017.11.014
摘要

To retrospectively investigate the effectiveness of triple drug combination transarterial chemoembolization (TACE) on local tumor response and survival in patients with liver metastases from pancreatic cancer. Also, this study will evaluate the variances in response regarding the number of metastases, assess the correlation between tumor response and the changes in the apparent diffusion coefficients (ADC) in diffusion weighted (DW) MRI.One hundred and twelve patients (58 men and 54 women; mean age 57) with malignant liver metastases from pancreatic adenocarcinoma underwent at least one session of TACE with a chemotherapeutic combination of mitomycin C, cisplatin, and gemcitabine. A size-based evaluation of tumor response (response evaluation criteria in solid tumors (RECIST)) was conducted, along with ADC values, and survival indices as related to treatment pattern.Four weeks following the end of the treatment, 78.26% of patients showed stable disease and 11.59% showed partial response. The median survival time was 19 months and for the stable disease group, 26 months. Low pretreatment ADC values showed no significant correlation to poor response to treatment (r = 0.347,p = 0.146).The triple drug TACE technique showed improvements in median survival times in patients with hepatic metastases from pancreatic carcinoma and helped control disease progression, whereas the number of hepatic lesions was not a statistically significant factor in patients' response to TACE. The data suggest that pre-treatment ADC values in DW-MRI have no statistical correlation with tumor response.
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