Medical Oncology Unit, Laikon General Hospital, Athens University School of Medicine, Athens, Greece.
Clin Drug Investig. 2004;24(11):661-70. doi: 10.2165/00044011-200424110-00005.
To investigate the efficacy and toxicity of gemcitabine administration followed by the combination of fluorouracil (5-FU) modulated by folinic acid in patients with advanced, symptomatic pancreatic cancer. The main objective was to estimate tumour response and any improvement in patients' quality of life.
The study included 48 evaluable patients with metastatic disease with no prior chemotherapy. The study duration was 3 years.
Gemcitabine 1000 mg/m(2) intravenously was given on days 1 and 8 followed by fluorouracil 350 mg/m(2) intravenously as a bolus biologically modulated by folinic acid 350 mg/m(2) intravenously given on days 1, 2, 8 and 9 in order to develop the conditions for any potential drug synergism. The regimen was administered every 3 weeks for 1 year or until disease progression.
Objective partial responses were documented in ten (21%) patients (95% CI 10.5, 35). Twenty-two (46%) patients had stable disease while 16 (33%) patients had progressive disease. The median response duration was 8 months (range 4-20). The median time to progression was 6 months (range 2-24), while the median survival of the group was 7 months (range 3-36) and the probability of surviving beyond 12 months was 20%. Of the 44 patients with tumour-related symptoms who were considered evaluable for clinical-benefit response, 28 (70%) patients had pain improvement, 25 (52%) patients had improvement of their performance status, and nine (28%) patients experienced weight gain during treatment. Serum concentrations of cancer antigen (Ca-19-9) were decreased by more than 50% in 14 (37%) of the 38 assessable patients. Chemotherapy was well tolerated, with mild myelotoxicity. Gastrointestinal toxicity was moderate with mild mucositis.
The regimen of gemcitabine and fluorouracil administered in this study was well tolerated and showed a moderate antitumour activity and a significant palliative effect on tumour-related symptoms. Because fluorouracil is a low toxicity combination agent for gemcitabine, other forms of the two-drug combination warrant further investigation.
研究吉西他滨联合氟尿嘧啶(5-FU),并用亚叶酸钙调整在晚期、有症状的胰腺癌患者中的疗效和毒性。主要目标是评估肿瘤反应以及患者生活质量的任何改善。
该研究纳入了 48 例可评估的转移性疾病患者,这些患者既往未接受过化疗。研究持续 3 年。
吉西他滨 1000mg/m²静脉内给药,第 1 天和第 8 天;随后静脉内给予氟尿嘧啶 350mg/m²,作为氟尿嘧啶的生物调节剂,亚叶酸钙 350mg/m²静脉内给药,第 1、2、8 和 9 天,以产生任何潜在的药物协同作用的条件。该方案每 3 周给药 1 年,或直至疾病进展。
记录到 10 例(21%)患者(95%CI10.5,35)有客观部分缓解。22 例(46%)患者疾病稳定,16 例(33%)患者疾病进展。中位缓解持续时间为 8 个月(范围 4-20)。中位进展时间为 6 个月(范围 2-24),而该组的中位生存期为 7 个月(范围 3-36),12 个月后存活率为 20%。在 44 例有肿瘤相关症状的可评估患者中,28 例(70%)患者疼痛缓解,25 例(52%)患者体能状态改善,9 例(28%)患者在治疗期间体重增加。在可评估的 38 例患者中,14 例(37%)患者的癌抗原(Ca-19-9)血清浓度降低超过 50%。化疗耐受性良好,骨髓抑制轻微。胃肠道毒性为中度,轻度黏膜炎。
在本研究中,吉西他滨联合氟尿嘧啶的方案耐受性良好,显示出对肿瘤相关症状有中等程度的抗肿瘤活性和显著的姑息作用。因为氟尿嘧啶是吉西他滨的低毒性联合药物,其他形式的两药联合值得进一步研究。