Young Chang, Soung Won Jeong, Jae Young Jang, Hyuksoo Eun, Young‑Sun Lee, Do Seon Song, Su Jong Yu, Sae Hwan Lee, Won Kim, Hyun Woong Lee, Sang Gyune Kim, Seongho Ryu, Suyeon Park
J Liver Cancer. 2022;22(2):167-177. Published online September 29, 2022
Background/Aim New biomarkers are urgently needed to aid in the diagnosis of early stage hepatocellular carcinoma (HCC). We performed a meta-analysis on the diagnostic utility of circulating tumor DNA (ctDNA) levels in patients with hepatitis B virus-induced HCC.
Methods We retrieved relevant articles from PubMed, Embase, and the Cochrane Library up to February 8, 2022. Two subgroups were defined; one subset of studies analyzed the ctDNA methylation status, and the other subset combined tumor markers and ctDNA assays. Pooled sensitivity (SEN), specificity (SPE), positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), and area under the summary receiver operating characteristic curve (AUC) were analyzed.
Results Nine articles including 2,161 participants were included. The overall SEN and SPE were 0.705 (95% confidence interval [CI], 0.629-0.771) and 0.833 (95% CI, 0.769-0.882), respectively. The DOR, PLR, and NLR were 11.759 (95% CI, 7.982-17.322), 4.285 (95% CI, 3.098- 5.925), and 0.336 (0.301-0.366), respectively. The ctDNA assay subset exhibited an AUC of 0.835. The AUC of the combined tumor marker and ctDNA assay was 0.848, with an SEN of 0.761 (95% CI, 0.659-0.839) and an SPE of 0.828 (95% CI, 0.692-0.911).
Conclusions Circulating tumor DNA has promising diagnostic potential for HCC. It can serve as an auxiliary tool for HCC screening and detection, especially when combined with tumor markers.
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There are various methods for treating advanced hepatocellular carcinoma with portal vein invasion, such as systemic chemotherapy, transarterial chemoembolization, transarterial radioembolization, and concurrent chemoradiotherapy. These methods have similar clinical efficacy but are designed with a palliative aim. Herein, we report a case that experienced complete remission through “associating liver partition and portal vein ligation for staged hepatectomy (ALPPS)” after concurrent chemoradiotherapy and hepatic artery infusion chemotherapy. In this patient, concurrent chemoradiotherapy and hepatic artery infusion chemotherapy induced substantial tumor shrinkage, and hypertrophy of the nontumor liver was sufficiently induced by portal vein ligation (stage 1 surgery) followed by curative resection (stage 2 surgery). Using this approach, long-term survival with no evidence of recurrence was achieved at 16 months. Therefore, the optimal use of ALPPS requires sufficient consideration in cases of significant hepatocellular carcinoma shrinkage for curative purposes.
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Is multidisciplinary treatment effective for hepatocellular carcinoma with portal vein tumor thrombus? Won Hyeok Choe Journal of Liver Cancer.2022; 22(1): 1. CrossRef
Young Joon Yoon, Ki Tae Yoon, Jun Yong Park, Hyun Woong Lee, Hwa Sook Kim, Jae Kyung Kim, Young Nyun Park, Kwang-Hyub Han, Chae Yoon Chon, Young Myung Moon, Mi-Suk Park, Sang Hoon Ahn
Journal of the Korean Liver Cancer Study Group. 2007;7(1):41-44. Published online June 30, 2007
Focal nodular hyperplasia (FNH) usually occurs in non-cirrhotic livers and was defined as a nodule composed
of benign appearing hepatocytes occurring in a liver that is otherwise histologically normal or nearly normal.
However, due to improvements in imaging techniques and pathological evaluation of explant livers, a focal lesion
that is very similar to the classic form of focal nodular hyperplasia that occurs in cirrhotic liver has been
described by several reports. Therefore, the term FNH-like nodules has been proposed. In this report, we report
a case of focal nodular hyperplasia-like nodules in cirrhosis. A 59 year old woman with known hepatitis B virus
infection visited our institution for routine check up. She was diagnosed as having liver cirrhosis and 3.5 cm sized
liver mass on abdomen ultrasonography (US). Because tumor marker was negative and US findings are not
compatible with hepatocellular carcinoma, other imaging modalities were performed. Magnetic resonance imaging
(MRI) documented a 3.5 cm sized hypervascular nodule with internal aberrant vascular structure and multiple
small sized nodules in remaining liver. Needle biopsy was targeted to the liver main mass. Microscopic finding
revealed FNH-like nodule and underlying liver cirrhosis.
Keun-Ho Lee, Ja Kyung Kim, Kwang-Hyub Han, Jong Tae Lee, Do Youn Lee, Jong Yoon Won, Hyun Woong Lee, Hwa Sook Kim, Ki Tae Yoon, Sang Hoon Ahn, Chae Yoon Chon, Young Myoung Moon
Journal of the Korean Liver Cancer Study Group. 2006;6(1):42-46. Published online June 30, 2006
There is no treatment of curative aim in advanced hepatocellular carcinoma (HCC) with portal vein thrombosis
(PVT), which is associated with poor prognosis. Albeit one of the treatment options is intra-arterial infusional
chemotherapy, its therapeutic efficacy was minimal. In this report, we present an unusual case of a patient with
favorable result after intra-arterial infusional chemotherapy. This patient was HBV carrier and diagnosed having
HCC of stage IVb (T4N0M1) with right PVT on February 1999. Direct right adrenal gland and right kidney
invasion and numerous intrahepatic metastases were also noted. The serum AFP level showed more than 60,000
ng/mL, and the Child-Pugh score was 5 (class A). The patient received three sessions of intra-arterial
5-fluorouracil (5-FU) and cisplatin combination chemotherapy and two additional sessions of systemic (5-FU)
chemotherapy combined with intra-arterial cisplatin infusion. After total 5 sessions of combination chemotherapy,
follow-up CT scan revealed grossly total necrosis of main HCC and numerous intrahepatic metastases, without
evidence of viable portion in July 1999. The AFP level decreased to 79.4 ng/mL. The latest CT scan taken in
November 2005 also showed no evidence of recurrence. It is noteworthy that the patient with advanced HCC with
PVT showed complete remission only after 5 sessions of intra-arterial chemotherapy and the status of complete
remission is maintained for more than 76 months.