首页> 外文期刊>World Journal of Gastroenterology >Evaluation of HCPTd(1), d(14)-double passaged intervening chemotherapy protocol for hepatocellular carcinoma.
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Evaluation of HCPTd(1), d(14)-double passaged intervening chemotherapy protocol for hepatocellular carcinoma.

机译:HCPTd(1),d(14)-双通道介入化疗方案对肝细胞癌的评估。

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AIM: To establish a kind of standardization of the clinical chemotherapeutic prototypes for unresectable hepatocellular carcinomas (HCC). METHODS: 10-Hydroxycamptothecin (HCPT) was applied through transcatheter arterial embolization (TAE) to HCC patients who were categorized into three groups: (1) test group: treatment with HCPT twice (HCPT d1 and 14) through TAE and portal venous embolization. (2) Control I: treatment with anticancer drugs without HCPT. (3) Control II: treatment with HCPT as a major component in anticancer drugs once (HCPT d1). A set of comparisons between test groups and control I and II groups were performed before and after the treatment to study the effectiveness of each treatment, in terms of tumor volumes, dynamic variations in serum alpha-fetoprotein (AFP), gamma-glutamyl transferase hepatoma-specific band (GGT-II), patient survival and adverse events. RESULTS: The general effectiveness rate of the test group reached 62.1% (72/116), remarkably higher than that of control I (32.1%, 40/124) and control II (54.7%, 47/56), (P<0.01 and P<0.05, respectively). Especially, the reduction rate or disappearance of the portal vein tumor emboli was as high as 88.4% (61/69) in the test group, in contrast with 13.9% (10/72) in control I and 35.9% (18/51) in control II (P<0.01 and P<0.01, respectively). After treatment, AFP decreased or turned to negative levels at 52.3% (34/65) in control I, 67.3% (35/52) in control II, and 96.8% (60/62) in the test group. Also GGT-II declined or became negative at 37.8% (28/74) in control I, 69.5% (57/82) in control II, and 94.7% (89/94) in test group (P<0.01 and P<0.05, respectively). CONCLUSION: We have designed a good protocol (test group) to treat HCC with excellent advantages of high efficiency, low cost, low toxicity and low adverse events and easy application. It could be recommended as one of the standardizations for HCC treatment in clinical practice.
机译:目的:建立一种不可切除肝细胞癌(HCC)临床化学治疗原型的标准化方法。方法:通过经导管动脉栓塞术(TAE)将10-羟基喜树碱(HCPT)应用于三类HCC患者:(1)测试组:通过TAE和门静脉栓塞两次进行HCPT治疗(HCPT d1和14)。 (2)对照I:用无HCPT的抗癌药治疗。 (3)对照II:一次以HCPT作为主要抗癌药物治疗(HCPT d1)。在治疗前后,在测试组与对照组I和II组之间进行了一组比较,以研究每种治疗的有效性,包括肿瘤体积,血清甲胎蛋白(AFP),γ-谷氨酰转移酶肝癌的动态变化特异性带(GGT-II),患者存活率和不良事件。结果:试验组总有效率达62.1%(72/116),明显高于对照组I(32.1%,40/124)和对照组II(54.7%,47/56),(P <0.01)和P <0.05)。尤其是,在测试组中,门静脉肿瘤栓塞的减少率或消失率高达88.4%(61/69),相比之下,对照I为13.9%(10/72),而对照组为35.9%(18/51)。在对照II中(分别为P <0.01和P <0.01)。治疗后,AFP下降或转为阴性,对照组I为52.3%(34/65),对照组II为67.3%(35/52),测试组为96.8%(60/62)。另外,对照组I的GGT-II下降或变为阴性,分别为37.8%(28/74),对照组II的69.5%(57/82)和试验组的94.7%(89/94)(P <0.01和P <0.05 , 分别)。结论:我们设计了一个好的方案(测试组)来治疗肝癌,具有高效,低成本,低毒性和低不良事件以及易于应用的优良优势。它可以被推荐为临床实践中HCC治疗的标准之一。

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