A Phase II Trial of Flouro-Gem as a First Line Treatment of Metastatic Adenocarcinoma of the Pancreas (GEFLUPAN trial)

Ahmed Sohaib, R. Abdelaziz, Faten Younis, Amira Hegazy
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Abstract

Background: Gemcitabine and 5 FU+folinic acid have both proved efficacy in treating patients with advanced pancreatic cancer. Objective: In our study, we combined the two most active agents against pancreatic cancer; gemcitabine and 5FU that were given every 2 weeks to gain the maximum benefit of both drugs and avoid the toxicity that occurs very frequently with FOLFIRINOX. Patients and Methods: This prospective phase II study included 42 patients of metastatic cancer pancreas who met the inclusion criteria Results: The median age at diagnosis was 55 years. Males were more common (59.5%) than females. The most common site of metastasis was the liver (57.1%). Toxicity profile showed that neutropenia and thrombocytopenia were the most common forms of toxicity being high grade in 11.9% of patients. Other forms of toxicity were minimal not exceeding 5%. The overall response rate (ORR) was 33.3% with no reported complete responses. There was a significant correlation between the change of tumor markers levels (CEA, and CA 19.9) and both response and quality of life (QOL). The changes of CEA and CA19.9 levels were found to be independent predictors of progression free survival (PFS). One year OS rate was 49%. The median OS was 11.3 months, while the median PFS was 8.8 months. Response was also found to be a surrogate marker for survival. Conclusions: Gemcitabine-5
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将 Flouro-Gem 作为胰腺转移性腺癌一线治疗方法的 II 期试验(GEFLUPAN 试验)
背景:吉西他滨和 5 FU+folinic acid 治疗晚期胰腺癌患者的疗效均已得到证实。研究目的在我们的研究中,我们将吉西他滨和 5FU 这两种对胰腺癌最有效的药物结合在一起,每两周给药一次,以获得两种药物的最大疗效,并避免 FOLFIRINOX 经常出现的毒性。患者和方法这项前瞻性 II 期研究纳入了 42 名符合纳入标准的胰腺癌转移患者:确诊时的中位年龄为 55 岁。男性(59.5%)多于女性。最常见的转移部位是肝脏(57.1%)。毒性概况显示,中性粒细胞减少和血小板减少是最常见的毒性形式,在11.9%的患者中为高度毒性。其他形式的毒性很小,不超过5%。总反应率(ORR)为 33.3%,无完全反应报告。肿瘤标志物水平(CEA和CA19.9)的变化与反应和生活质量(QOL)之间存在明显的相关性。研究发现,CEA和CA19.9水平的变化是无进展生存期(PFS)的独立预测因素。一年的OS率为49%。中位 OS 为 11.3 个月,中位 PFS 为 8.8 个月。研究还发现,反应也是生存期的替代指标。结论吉西他滨-5
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