首页> 外文期刊>Endocrine-related cancer >Gemcitabine plus metronomic 5-fluorouracil or capecitabine as a second-/third-line chemotherapy in advanced adrenocortical carcinoma: a multicenter phase II study
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Gemcitabine plus metronomic 5-fluorouracil or capecitabine as a second-/third-line chemotherapy in advanced adrenocortical carcinoma: a multicenter phase II study

机译:吉西他滨联合节律性5-氟尿嘧啶或卡培他滨作为晚期肾上腺皮质癌的二线/三线化疗:一项多中心II期研究

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摘要

Adrenocortical carcinoma (ACC) is a rare neoplasm characterized by poor prognosis. First-line systemic treatments in advanced disease include mitotane, either alone or in combination with chemotherapy. Studies evaluating second-line therapy options have obtained disappointing results. This trial assessed the activity and toxicity of gemcitabine plus metronomic fluoropyrimidines in heavily pretreated advanced ACC patients. From 1998 to 2008, 28 patients with advanced ACC progressing after mitotane plus one or two systemic chemotherapy lines were enrolled. They received a combination of i.v. gemcitabine (800?mg/m2, on days 1 and 8, every 21 days) and i.v. 5-fluorouracil protracted infusion (200?mg/m2/daily without interruption until progression) in the first six patients, or oral capecitabine (1500?mg/daily) in the subsequent patients. Mitotane administration was maintained in all cases. The rate of non-progressing patients after 4 months of treatment was 46.3%. A complete response was observed in 1 patient (3.5%); 1 patient (3.5%) obtained a partial regression, 11 patients (39.3%) obtained a disease stabilization and 15 patients (53.7%) progressed. Treatment was well tolerated, with grade III and IV toxicities consisting of leukopenia in six patients (21.4%), thrombocytopenia in one patient (3.5%), and mucositis in one patient (3.5%). Median time to progression and overall survival in the patient population were 5.3 (range: 1–43) and 9.8 months (range: 3–73) respectively. Gemcitabine plus metronomic fluoropyrimidines is a well-tolerated and moderately active regimen in heavily pretreated ACC patients.
机译:肾上腺皮质癌(ACC)是一种以预后较差为特征的罕见肿瘤。晚期疾病的一线全身性治疗包括单独或与化学疗法联合使用的米诺坦。评估二线治疗方案的研究获得了令人失望的结果。该试验评估了吉西他滨加节律型氟嘧啶在经过大量治疗的晚期ACC患者中的活性和毒性。从1998年至2008年,纳入了28例行米多烷治疗后进展为晚期ACC的患者,加上一或两个全身化疗方案。他们获得了i.v.吉西他滨(800 mg / m2,在第1天和第8天,每21天)和静脉注射前六名患者长期使用5-氟尿嘧啶输注(200?mg / m2 /天,直到进展不间断),随后的患者口服口服卡培他滨(1500?mg /天)。在所有情况下均维持线粒体给药。治疗4个月后非进展患者的比例为46.3%。 1名患者(3.5%)观察到完全缓解; 1例患者(3.5%)获得了部分消退,11例患者(39.3%)获得了疾病稳定,15例患者(53.7%)进展。治疗耐受性良好,三级和四级毒性包括白细胞减少症6例(21.4%),血小板减少症1例(3.5%)和黏膜炎1例(3.5%)。患者群体的中位进展时间和总生存时间分别为5.3(范围:1-43)和9.8个月(范围:3-73)。在经过大量预处理的ACC患者中,吉西他滨加节律性氟嘧啶是一种耐受良好的中等活性方案。

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