Yang Tsai-Shen, Chang Hsien-Khun, Chen Jen-Shi, Lin Yung-Chang, Liau Chi-Ting, Chang Wen-Cheng
Division of Hematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, 199 Tung Hwa North Road, Taipei 105, Taiwan.
J Gastroenterol. 2004;39(4):362-9. doi: 10.1007/s00535-003-1303-8.
We evaluated the anti-tumor efficacy and toxicity of 5-fluorouracil (5-FU), mitoxantrone, and cisplatin (FMP) in patients with advanced hepatocellular carcinoma (HCC), and conducted an analysis of the prognostic factors for response to such therapy and patient survival.
Sixty-three patients suffering from unresectable and non-embolizable HCC and who had objectively measurable tumors, adequate liver and renal function, and adequate bone-marrow reserve were enrolled in this study. The therapeutic regimen consisted of cisplatin 80 mg/m(2) and mitoxantrone 6 mg/m(2) intravenously on day 1, and 5-FU 450 mg/m(2) per day continuous infusion for a period of 5 days. Univariate and multivariate analyses of patient and disease characteristics were used to identify factors predicting patient response and survival.
The objective response was 23.8% (95% confidence interval [CI], 13.0-34.6%). The median survival for all 63 patients was 4.9 months (95% CI, 3.2-6.6 months). The median time to progression was 2.5 months (95% CI, 1.7-3.3 months). Multivariate analysis identified only performance status ( P = 0.050) and liver tumor size ( P = 0.012) as being significantly related to patient objective response. Independent variables associated with a better patient survival included: the absence of ascites ( P = 0.003), a lower total bilirubin level ( P = 0.026), and the patient being a positive chemotherapy responder ( P = 0.009).
The response rate to an FMP regimen was still unsatisfactory, although a specific subgroup of patients (good performance status, smaller liver tumor mass, good liver reserve, and distant metastasis) may benefit from this regimen.We evaluated the anti-tumor efficacy and toxicity of 5-fluorouracil (5-FU), mitoxantrone, and cisplatin (FMP) in patients with advanced hepatocellular carcinoma (HCC), and conducted an analysis of the prognostic factors for response to such therapy and patient survival.
我们评估了5-氟尿嘧啶(5-FU)、米托蒽醌和顺铂(FMP)对晚期肝细胞癌(HCC)患者的抗肿瘤疗效和毒性,并分析了对此类治疗反应及患者生存的预后因素。
本研究纳入了63例患有无法切除且不可栓塞的HCC、具有客观可测量肿瘤、肝肾功能良好且骨髓储备充足的患者。治疗方案为第1天静脉注射顺铂80mg/m²和米托蒽醌6mg/m²,5-FU 450mg/m²每天持续输注5天。采用患者和疾病特征的单因素和多因素分析来确定预测患者反应和生存的因素。
客观缓解率为23.8%(95%置信区间[CI],13.0 - 34.6%)。63例患者的中位生存期为4.9个月(95%CI,3.2 - 6.6个月)。疾病进展的中位时间为2.5个月(95%CI,1.7 - 3.3个月)。多因素分析仅确定体能状态(P = 0.050)和肝肿瘤大小(P = 0.012)与患者客观反应显著相关。与患者更好生存相关的独立变量包括:无腹水(P = 0.003)、较低的总胆红素水平(P = 0.026)以及患者为化疗阳性反应者(P = 0.009)。
尽管特定亚组患者(体能状态良好、肝肿瘤肿块较小、肝脏储备良好且有远处转移)可能从此方案中获益,但FMP方案的缓解率仍不尽人意。我们评估了5-氟尿嘧啶(5-FU)、米托蒽醌和顺铂(FMP)对晚期肝细胞癌(HCC)患者的抗肿瘤疗效和毒性,并分析了对此类治疗反应及患者生存的预后因素。