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射波刀治疗晚期肝细胞癌

Cyberknife treatment for advanced or terminal stage hepatocellular carcinoma.

作者信息

Kato Hiroyuki, Yoshida Hideo, Taniguch Hiroyoshi, Nomura Ryutaro, Sato Kengo, Suzuki Ichiro, Nakata Ryo

机构信息

Hiroyuki Kato, Hideo Yoshida, Hiroyoshi Taniguch, Ryo Nakata, Department of Gastroenterology, Japanese Red Cross Medical Center, Tokyo 150-8935, Japan.

出版信息

World J Gastroenterol. 2015 Dec 14;21(46):13101-12. doi: 10.3748/wjg.v21.i46.13101.

Abstract

AIM

To investigate the safety and efficacy of the Cyberknife treatment for patients with advanced or terminal stage hepatocellular carcinoma (HCC).

METHODS

Patients with HCC with extrahepatic metastasis or vascular or bile duct invasion were enrolled between May 2011 and June 2015. The Cyberknife was used to treat each lesion. Treatment response scores were based on Response Evaluation Criteria in Solid Tumors v1.1. The trends of tumor markers, including alpha fetoprotein (AFP) and proteins induced by vitamin K absence II (PIVKA II) were assessed. Prognostic factors for tumor response and tumor markers were evaluated with Fisher's exact test and a logistic regression model. Survival was evaluated with the Kaplan-Meier method and multivariate analysis was performed using the Cox proportional hazards model.

RESULTS

Sixty-five patients with 95 lesions were enrolled. Based on the Barcelona Clinic Liver Cancer classification, all patients were either in the advanced or terminal stage of the disease. The target lesions were as follows: 52 were bone metastasis; 9, lung metastasis; 7, brain metastasis; 9, portal vein invasion; 4, hepatic vein invasion; 4, bile duct invasion; and 10 other lesion types. The response rate and disease control rate were 34% and 53%, respectively. None of the clinical factors correlated significantly with tumor response. Fiducial marker implantation was associated with better control of both AFP (HR = 0.152; 95%CI: 0.026-0.887; P = 0.036) and PIVKA II (HR = 0.035; 95%CI: 0.003-0.342; P = 0.004). The median survival time was 9 mo (95%CI: 5-15 mo). Terminal stage disease (HR = 9.809; 95%CI: 2.589-37.17, P < 0.001) and an AFP of more than 400 ng/mL (HR = 2.548; 95%CI: 1.070-6.068, P = 0.035) were associated with worse survival. A radiation dose higher than 30 Gy (HR = 0.274; 95%CI: 0.093-0.7541, P = 0.012) was associated with better survival. In the 52 cases of bone metastasis, 36 patients (69%) achieved pain relief. One patient had cerebral bleeding and another patient had an esophageal ulcer after treatment.

CONCLUSION

The Cyberknife can be safely administered to patients with advanced or terminal stage HCC. High AFP levels were associated with worse survival, but a higher radiation dose improved the survival.

摘要

目的

探讨射波刀治疗晚期或终末期肝细胞癌(HCC)患者的安全性和有效性。

方法

纳入2011年5月至2015年6月期间出现肝外转移或血管或胆管侵犯的HCC患者。使用射波刀治疗每个病灶。治疗反应评分基于实体瘤疗效评价标准v1.1。评估肿瘤标志物的变化趋势,包括甲胎蛋白(AFP)和维生素K缺乏诱导蛋白II(PIVKA II)。采用Fisher精确检验和逻辑回归模型评估肿瘤反应和肿瘤标志物的预后因素。采用Kaplan-Meier法评估生存率,并使用Cox比例风险模型进行多因素分析。

结果

共纳入65例患者,95个病灶。根据巴塞罗那临床肝癌分类,所有患者均处于疾病的晚期或终末期。靶病灶如下:52个为骨转移;9个为肺转移;7个为脑转移;9个为门静脉侵犯;4个为肝静脉侵犯;4个为胆管侵犯;10个为其他病灶类型。有效率和疾病控制率分别为34%和53%。没有临床因素与肿瘤反应显著相关。植入基准标志物与更好地控制AFP(HR = 0.152;95%CI:0.026 - 0.887;P = 0.036)和PIVKA II(HR = 0.035;95%CI:0.003 - 0.342;P = 0.004)相关。中位生存时间为9个月(95%CI:5 - 15个月)。终末期疾病(HR = 9.809;95%CI:2.589 - 37.17,P < 0.001)和AFP大于400 ng/mL(HR = 2.548;95%CI:1.070 - 6.068,P = 0.035)与较差的生存率相关。辐射剂量高于30 Gy(HR = 0.274;95%CI:0.093 - 0.7541,P = 0.012)与较好的生存率相关。在52例骨转移患者中,36例(69%)疼痛缓解。治疗后1例患者发生脑出血,另1例患者发生食管溃疡。

结论

射波刀可安全用于晚期或终末期HCC患者。高AFP水平与较差的生存率相关,但较高的辐射剂量可改善生存率。

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