Clinical outcomes of systemic therapy in patients with unresectable or metastatic combined hepatocellular-cholangiocarcinoma

被引:34
|
作者
Kim, Eo Jin [1 ]
Yoo, Changhoon [1 ]
Kang, Hyo Jeong [2 ]
Kim, Kyu-Pyo [1 ]
Ryu, Min-Hee [1 ]
Park, Sook Ryun [1 ]
Lee, Danbi [3 ]
Choi, Jonggi [3 ]
Shim, Ju Hyun [3 ]
Kim, Kang Mo [3 ]
Lim, Young-Suk [3 ]
Lee, Han Chu [3 ]
Ryoo, Baek-Yeol [1 ]
机构
[1] Univ Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, 88 Olymp Ro,43 Gil, Seoul 05505, South Korea
[2] Univ Ulsan, Dept Pathol, Asan Med Ctr, Coll Med, Seoul, South Korea
[3] Univ Ulsan, Dept Gastroenterol, Asan Med Ctr, Coll Med, 88 Olymp Ro,43 Gil, Seoul 05505, South Korea
关键词
chemotherapy; combined hepatocellular‐ cholangiocarcinoma; sorafenib; BILIARY-TRACT CANCER; 1ST-LINE TREATMENT; DOUBLE-BLIND; MULTICENTER; GEMCITABINE; SORAFENIB; CARCINOMA; CHEMOTHERAPY; CISPLATIN;
D O I
10.1111/liv.14813
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims The optimal systemic chemotherapy for combined hepatocellular-cholangiocarcinoma (cHCC-CCA) has not yet been defined. The definition and classification of cHCC-CCA has changed recently in the 5th edition of WHO classification. We reviewed the pathological findings with the new classification and analysed the efficacy of systemic chemotherapy in patients with unresectable/metastatic cHCC-CCA. Methods Among 254 patients with histologically confirmed cHCC-CCA from 1999 to 2015 in Asan Medical Center, Seoul, Korea, 99 patients who received systemic chemotherapy for unresectable/metastatic disease were included. Overall response rate (ORR), progression-free survival (PFS) and overall survival (OS) were retrospectively evaluated. Results Sorafenib (n = 62) and cytotoxic chemotherapy (n = 37) were administered as first-line chemotherapies; the ORR was 14.1%, and the median PFS and OS were 3.8 and 10.6 months, respectively, with a median follow-up duration of 39.6 months. The efficacy outcomes were not significantly different between patients who received sorafenib and those who received cytotoxic chemotherapy (ORR, 9.7% vs 21.6%, P = .14; median PFS, 4.2 vs 2.9 months, P = .52; median OS, 10.7 vs 10.6 months, P = .34). In multivariate analysis, large intrahepatic tumour burden (>= 30% of liver volume), elevated serum bilirubin and non-platinum containing first-line chemotherapy remained as significant prognostic factors for poorer OS. Conclusions The efficacy outcomes according to first-line treatment were not significantly different between sorafenib and cytotoxic chemotherapy, and pathological findings were not found to help for determining appropriate therapeutic agent or assessing the prognosis. To overcome the poor treatment outcomes, further studies are needed to find proper treatment targets, biomarkers and the best treatment strategies.
引用
收藏
页码:1398 / 1408
页数:11
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