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原发性肝癌雌激素受体表达及内分泌治疗 被引量:2

Estrogen receptor expression in hepatocellular carcinoma and tamoxifen endocrine therapy
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摘要 目的研究原发性肝癌雌激素受体(ER)的表达及内分泌治疗的临床价值.方法应用Lee氏荧光配体细胞化学法检测41例手术病理确诊的原发性肝癌ER的表达.本组男38例,女3例,年龄25岁~72岁.同时检测肝癌的组织类型、分化程度、肿瘤大小、血清AFP及CEA.6例ER阳性者采用他莫昔芬治疗(每次20mg,2次/d,长期服用)并观察疗效.结果肝癌组织ER阳性20/41例,阳性率488%.ER阳性率与患者年龄、性别、AFP、CEA含量及组织类型(梁状型ER阳性450%,腺样型333%,实体型714%,硬化型667%,透明细胞型250%;P>005)无明显关系,与肿瘤体积(≥10cm,ER阳性率750%;<10cm,ER阳性238%;P<001)和分化程度(分化好26例,ER阳性346%;分化差15例,ER阳性733%;P<005)有显著关系.本组ER阳性病例中6例经他莫昔芬内分泌治疗有效5/6(833%),其中4例AFP下降. AIM To study the expression of estrogen receptor (ER) and the clinical effectiveness of endocrine therapy in hepatocellular carcinoma (HCC). METHODS The estrogen receptor of 41 patients with hepatocellular carcinoma was assayed by the Lee′s fluorescein_labeled ligand cytochemical method. The patients included 38 men and 3 women, aged 25~72 years. Histologic types of the tumor, degree of differentiation, tumor size and serum levels of α_fetoprotein (AFP) or carcinoembryonic antigen (CEA) were assayed at the same time. Six of them with positive ER were treated constantly with tamoxifen (20mg bid) and the therapeutic effect was observed. RESULTS Twenty of 41 patients (48 78%) had positive ER, which was not significantly related to sex, age, AFP or CEA levels and histopathologic types of the tumor (trabecular pattern accounts for 45 0%, adenoid pattern 33 3%, solid pattern 71 4% cirrhotic pattern 66 7%, clear cell pattern 25 0%; P >0 05), but related to tumor size (≥10cm, ER positive 75%, <10cm, 23 8%; P <0 01) and degree of differentiation (26 well_differentiatied, ER positive 34 6%; 15 poor_differentiatied, ER positive 73 3%, P <0 05). Tamoxifen endocrine therapy was effective in 5/6 ER positive patients, AFP decreased in 4 of them. CONCLUSION Tamoxifen endocrine therapy was effective for the ER positive patients with HCC.
机构地区 四川省肿瘤医院
出处 《新消化病学杂志》 1997年第9期571-572,共2页
关键词 肝癌 原发性 雌激素受体 内分泌 治疗 liver neoplasms/metabolism carcinoma, hepatocellular/metabolism receptors, estrogen/metabolism tamoxifen/therapeutic use
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