Dipartimento di Scienze Cliniche e Biologiche Università di Torino, Orbassano, Italy.
Endocr Relat Cancer. 2010 Apr 21;17(2):445-53. doi: 10.1677/ERC-09-0281. Print 2010 Jun.
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/m(2), on days 1 and 8, every 21 days) and i.v. 5-fluorouracil protracted infusion (200 mg/m(2)/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.
肾上腺皮质癌 (ACC) 是一种预后不良的罕见肿瘤。晚期疾病的一线全身治疗包括米托坦,单独使用或与化疗联合使用。评估二线治疗选择的研究取得了令人失望的结果。本试验评估了吉西他滨联合节拍式氟嘧啶类药物在经大量预处理的晚期 ACC 患者中的疗效和毒性。1998 年至 2008 年,共招募了 28 例接受米托坦加一线或二线全身化疗后进展的晚期 ACC 患者。他们接受静脉注射吉西他滨(800mg/m2,第 1 和 8 天,每 21 天一次)和静脉注射 5-氟尿嘧啶持续输注(200mg/m2/天,无中断,直至进展),前 6 例患者接受此方案,随后的患者接受口服卡培他滨(1500mg/天)。所有患者均维持米托坦治疗。治疗 4 个月后无进展患者的比例为 46.3%。1 例患者(3.5%)达到完全缓解;1 例患者(3.5%)部分缓解,11 例患者(39.3%)疾病稳定,15 例患者(53.7%)进展。治疗耐受性良好,6 例患者(21.4%)出现 3 级和 4 级毒性,包括白细胞减少症,1 例患者(3.5%)血小板减少症,1 例患者(3.5%)黏膜炎。该患者人群的中位无进展生存期和总生存期分别为 5.3 个月(范围:1-43 个月)和 9.8 个月(范围:3-73 个月)。吉西他滨联合节拍式氟嘧啶类药物是一种在经大量预处理的 ACC 患者中耐受性良好且具有一定疗效的方案。