Literature DB >> 25985566

Combination of oxaliplatin and S-1 versus sorafenib alone in patients with advanced hepatocellular carcinoma.

Yufeng Lv, Rong Liang, Xiaohua Hu, Zhihui Liu, Xiaoli Liao, Yan Lin, Chunling Yuan, Sina Liao, Qian Li, Jinyan Zhang, Yongqiang Li.   

Abstract

Sorafenib and conventional systemic cytotoxicity chemotherapy are currently being used in parallel for the patients with advanced hepatocellular carcinoma (HCC). While sorafenib has been proven to improve the prognosis in patients with this malignant disease, however, the outcome of other newly developed systemic chemotherapeutic regimens remains controversial. We evaluated the outcome and safety of patients treated with the SOX regimen (oxaliplatin + S-1) and those treated with sorafenib in a single-center cohort. This retrospective study involved a total of 46 patients with advanced HCC, 22 of which were treated with SOX regimen (oxaliplatin [130 mg/m2] on day 1 and S-1 [80 mg/m2/day] on day 1-14, every 3 weeks), and 24 were daily treated with sorafenib (400 mg, b.i.d.). The median progression-free survival was 3.6 months (95% confidence interval [CI], 1.7 to 5.6) with SOX and 1.7 months (95% CI, 1.5 to 1.9) with sorafenib, respectively (P = 0.444). The median overall survival in SOX and sorafenib group was 7.6 months (95% CI, 4.3 to 10.9) and 4.7 months (95% CI, 2.7 to 7.3), respectively (P = 0.246). Response rate was 22.2% with SOX and 5.6% with sorafenib, respectively (P = 0.154). The frequent side effects in SOX-treated patients were thrombocytopenia, elevation of transaminase levels and neuropathy, whereas hand-foot syndrome, diarrhea and pruritus were common in sorafenib-treated patients. These preliminary results suggest that the SOX regimen may serve as an effective treatment for patients with advanced HCC, and the treatment-related toxicities were generally well-tolerated.

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Year:  2014        PMID: 25985566

Source DB:  PubMed          Journal:  Pharmazie        ISSN: 0031-7144            Impact factor:   1.267


  5 in total

1.  Hypoxia induces universal but differential drug resistance and impairs anticancer mechanisms of 5-fluorouracil in hepatoma cells.

Authors:  Jing-Qiu Li; Xian Wu; Lu Gan; Xiang-Liang Yang; Ze-Hong Miao
Journal:  Acta Pharmacol Sin       Date:  2017-07-10       Impact factor: 6.150

Review 2.  S-1 for treatment of advanced hepatocellular carcinoma: a systematic review of the literature.

Authors:  Wu-Kui Huang; Li-Na You; Shu-Fa Yang; Deng-Yao Liu; Mo Liu; Xi-Wen Fan
Journal:  Contemp Oncol (Pozn)       Date:  2017-03-22

3.  Transcatheter arterial chemoembolisation (TACE) plus S-1 for the treatment of BCLC stage B hepatocellular carcinoma refractory to TACE.

Authors:  Wu-Kui Huang; Shu-Fa Yang; Li-Na You; Mo Liu; Deng-Yao Liu; Peng Gu; Xi-Wen Fan
Journal:  Contemp Oncol (Pozn)       Date:  2017-01-12

4.  A phase II trial of S-1 and oxaliplatin in patients with advanced hepatocellular carcinoma.

Authors:  Dae-Won Lee; Kyung-Hun Lee; Hee-Jun Kim; Tae-Yong Kim; Jin-Soo Kim; Sae-Won Han; Do-Youn Oh; Jee Hyun Kim; Seock-Ah Im; Tae-You Kim
Journal:  BMC Cancer       Date:  2018-03-05       Impact factor: 4.430

5.  A twenty gene-based gene set variation score reflects the pathological progression from cirrhosis to hepatocellular carcinoma.

Authors:  Yan Lin; Rong Liang; Jiazhou Ye; Qian Li; Ziyu Liu; Xing Gao; Xuemin Piao; Rongyun Mai; Donghua Zou; Lianying Ge
Journal:  Aging (Albany NY)       Date:  2019-12-06       Impact factor: 5.682

  5 in total

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