| Literature DB >> 28045618 |
Kenya Kamimura1, Yuji Kobayashi1, Yoshifumi Takahashi1, Hiroyuki Abe1, Daisuke Kumaki1, Takeshi Yokoo1, Hiroteru Kamimura1, Norihiro Sakai1, Akira Sakamaki1, Satoshi Abe1, Masaaki Takamura1, Hirokazu Kawai1, Satoshi Yamagiwa1, Shuji Terai1.
Abstract
Intrahepatic lesions of hepatocellular carcinoma (HCC) have been controlled by significant advances in treatment using loco-regional therapies, including, surgery, ablative therapy, catheter-based chemotherapy, and embolization. Consequently, the number of patients with extrahepatic metastatic lesions has increased. Their prognosis remains poor with approximately <1 y of survival from the time of diagnosis. A molecularly targeted drug, sorafenib, have been used to treat extrahepatic lesions and shown the prolonged survival time. However, the therapeutic benefit for the brain metastasis remains unclear, since it causes intratumor bleeding leading to the severe brain damage. No guidelines for the brain metastasis of HCC have been developed to date due to the shortage of the experiences and evidences. Therefore, the development of standard therapy for brain metastasis following the early diagnosis is essential by accumulating the information of clinical courses and evidences. For this purpose, we reviewed cases of HCC brain metastasis reported to date and analyzed additional 8 cases from our hospital, reviewing 592 advanced HCC cases to estimate the possible metastatic lesions in the brain. With careful review of cases and literature, we suggest that the cases with lung metastasis with increase tendency of tumor markers within recent 3-6 months have higher risks of brain metastasis. Therefore, they should be carefully followed by imaging modalities. In addition, the loco-regional treatment, including surgical resection and radiation therapy should be performed for better prognosis by preventing re-bleeding from the tumors.Entities:
Keywords: AFP; Hepatocellular carcinoma; L3; brain metastasis; radiation; surgery; tumor marker
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Year: 2017 PMID: 28045618 PMCID: PMC5362986 DOI: 10.1080/15384047.2016.1276134
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742