Suppr超能文献

姜黄素植物药复合物作为晚期胰腺癌的补充疗法,提高了吉西他滨的安全性和疗效:一项前瞻性 II 期试验的结果。

Phytosome complex of curcumin as complementary therapy of advanced pancreatic cancer improves safety and efficacy of gemcitabine: Results of a prospective phase II trial.

机构信息

Rare Tumors Unit, Veneto Institute of Oncology IOV - IRCCS, Via Gattamelata 64, 35128 Padua (PD), Italy; Department of Oncology, S. Maria del Prato Hospital, Via Bagnols sur Ceze 3, 3203 Feltre (BL), Italy.

Regional Center for Biomarkers, Department of Clinical Pathology and Transfusion Medicine, Azienda ULSS 3 Serenissima, Regional Hospital, Campo SS Giovanni e Paolo 6777, 30122 Venice (VE), Italy.

出版信息

Pharmacol Res. 2018 Jun;132:72-79. doi: 10.1016/j.phrs.2018.03.013. Epub 2018 Mar 31.

Abstract

A large body of biomedical evidence indicates that activation of Nrf2 by curcumin increases the nucleophilic tone and damps inflammation cumulatively supporting the malignant phenotype. Conversely, genetic analyses suggest a possible oncogenic nature of constitutive Nrf2 activation since an increased nucleophilic tone is alleged increasing chemoresistance of cancer cells. Aiming to contribute to solve this paradox, this study addressed the issue of safety and efficacy of curcumin as complementary therapy of gemcitabine on pancreatic cancer. This was a single centre, single arm prospective phase II trial. Patients received gemcitabine and Meriva, a patented preparation of curcumin complexed with phospholipids. Primary endpoint was response rate, secondary endpoints were progression free survival, overall survival, tolerability and quality of life. Analysis of inflammatory biomarkers was also carried out. Fifty-two consecutive patients were enrolled. Forty-four (13 locally advanced and 31 metastatic) were suitable for primary endpoint evaluation. Median age was 66 years (range 42-87); 42 patients had Eastern Cooperative Oncology Group performance status 0-1. The median number of treatment cycle was 4.5 (range 2-14). We observed 27.3% of response rate and 34.1% of cases with stable disease, totalizing a disease control rate of 61.4%. The median progression free survival and overall survival were 8.4 and 10.2 months, respectively. Higher IL-6 and sCD40L levels before treatment were associated to a worse overall survival (p < 0.01). Increases in sCD40L levels after 1 cycle of chemotherapy were associated with a reduced response to the therapy. Grade 3/4 toxicity was observed (neutropenia, 38.6%; anemia, 6.8%). There were no significant changes in quality of life during therapy. In conclusion, the complementary therapy to gemcitabine with phytosome complex of curcumin is not only safe but also efficiently translate in a good response rate in first line therapy of advanced pancreatic cancer.

摘要

大量的生物医学证据表明,姜黄素激活 Nrf2 会增加亲核性,并逐渐抑制炎症,从而支持恶性表型。相反,遗传分析表明,Nrf2 的组成性激活可能具有致癌性质,因为据称增加亲核性会增加癌细胞的化疗耐药性。为了解决这一矛盾,本研究探讨了姜黄素作为吉西他滨辅助治疗胰腺癌的安全性和有效性。这是一项单中心、单臂前瞻性 II 期临床试验。患者接受吉西他滨和 Meriva(一种姜黄素与磷脂复合的专利制剂)治疗。主要终点是缓解率,次要终点是无进展生存期、总生存期、耐受性和生活质量。还进行了炎症生物标志物的分析。共纳入 52 例连续患者。44 例(13 例局部晚期,31 例转移性)适合进行主要终点评估。中位年龄为 66 岁(范围 42-87);42 例患者的东部合作肿瘤学组表现状态为 0-1。中位治疗周期数为 4.5 个(范围 2-14)。我们观察到缓解率为 27.3%,稳定疾病的病例为 34.1%,总疾病控制率为 61.4%。中位无进展生存期和总生存期分别为 8.4 个月和 10.2 个月。治疗前较高的 IL-6 和 sCD40L 水平与总生存期较差相关(p<0.01)。化疗 1 周期后 sCD40L 水平升高与对治疗的反应降低相关。观察到 3/4 级毒性(中性粒细胞减少症,38.6%;贫血,6.8%)。治疗过程中生活质量无明显变化。总之,姜黄素植物素复合物与吉西他滨联合辅助治疗不仅安全,而且在晚期胰腺癌一线治疗中能有效转化为高缓解率。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验