Palliative Care Center, Cancer Center, Kindai University Hospital, 377-2 Ohno-higashi, Osakasayama City, Osaka, 589-8511, Japan.
Department of Psychosomatic Medicine, Kindai University Faculty of Medicine, 377-2 Ohno-higashi, Osakasayama City, Osaka, 589-8511, Japan.
BMC Cancer. 2017 Oct 6;17(1):674. doi: 10.1186/s12885-017-3664-z.
Cancer patients experience pain that has physiological, sensory, affective, cognitive, behavioral, and sociocultural dimensions. Opioids are used in treatment of pain in patients with various types of cancer. We previously showed that the catechol-O-methyltransferase (COMT) genotype is related to the plasma level of morphine and the required dose of morphine in an exploratory prospective study. The findings showed that a group of patients with a GG single nucleotide polymorphism (SNP) rs4680 in COMT required a significantly higher dose of morphine than a non-GG group. A biomarker for selection of opioids for cancer pain relief would be particularly useful clinically, and therefore we have planned a randomized comparative study of morphine and oxycodone, using the COMT rs4680 SNP as a biomarker. This study is aimed at verifying the assumption that patients in the GG group require an increased morphine dose for pain relief.
The RELIEF study is a randomized, multi-institutional, open-label trial with a primary endpoint of the proportion of subjects requiring high-dose opioids, as calculated from the dose of a rescue preparation administered on day 0. Secondary endpoints include the Hospital Anxiety and Depression Scale, Short form McGill Pain Questionnaire-2, European Organization for Research and Treatment of Cancer QLQ-C15-PAL, Pain Catastrophizing Scale, and adverse events, Eligibility criteria are patients with advanced carcinoma with non-daily use of opioids in initial screening for registration; and cancer pain targeted for daily opioid treatment, NSAIDs or acetaminophen, NRS ≥3(average over 24 h), opioid-treatment naive within 30 h, no chemotherapy, radiotherapy, or bisphosphonate administration newly started within 2 weeks, and written informed consent at the time of second registration. Between November 2014 and June 2017, an estimated 110 patients from two sites in Japan were randomized (1:1) to morphine or oxycodone in GG and non-GG groups.
A method for selection of appropriate opioids in cancer patients is a high unmet medical need. This study was designed to evaluate the efficacy of different opioids in patients with cancer based on gene polymorphism, as the first potential multi-institutional registration trial to be conducted in cancer patients with pain.
UMIN000015579 Date of registration: 4 November 2014. It is updated once every six months, the latest update is 30 June 2017. Trial status. The enrollment started in November 2014. At the time of manuscript submission (July 2017), Three-quarters of patients have participated. We thus expect to complete the recruitment by March 2018.
癌症患者经历的疼痛具有生理、感觉、情感、认知、行为和社会文化等多个维度。阿片类药物被用于治疗各种类型癌症患者的疼痛。我们之前的研究表明,儿茶酚-O-甲基转移酶(COMT)基因型与吗啡的血浆水平和吗啡的所需剂量有关。研究结果表明,一组 COMT 基因中的 GG 单核苷酸多态性(SNP)rs4680 的患者需要比非-GG 组更高剂量的吗啡。用于癌症疼痛缓解的阿片类药物的生物标志物在临床上将非常有用,因此,我们计划使用 COMT rs4680 SNP 作为生物标志物,进行吗啡和羟考酮的随机对照研究。本研究旨在验证以下假设:GG 组患者需要更高剂量的吗啡来缓解疼痛。
RELIEF 研究是一项随机、多机构、开放性试验,主要终点是根据第 0 天给予的抢救制剂剂量计算需要高剂量阿片类药物的受试者比例。次要终点包括医院焦虑和抑郁量表、简短形式 McGill 疼痛问卷-2、欧洲癌症研究与治疗组织 EORTC QLQ-C15-PAL、疼痛灾难化量表和不良事件。入选标准为:在初始登记时患有晚期癌症,未每日使用阿片类药物;登记时癌症疼痛需要每日阿片类药物治疗、非甾体抗炎药或对乙酰氨基酚治疗,NRS≥3(平均 24 小时),阿片类药物治疗 30 小时内未接受治疗,2 周内未新开始化疗、放疗或双膦酸盐治疗,且在第二次登记时获得书面知情同意。2014 年 11 月至 2017 年 6 月,来自日本两个地点的估计 110 名患者被随机分配(1:1)至 GG 和非-GG 组接受吗啡或羟考酮治疗。
为癌症患者选择合适阿片类药物的方法是一项高度未满足的医疗需求。本研究旨在评估基于基因多态性的不同阿片类药物在癌症患者中的疗效,这是第一个针对癌症疼痛患者进行的潜在多机构注册试验。
UMIN000015579 注册日期:2014 年 11 月 4 日。每六个月更新一次,最新更新日期为 2017 年 6 月 30 日。试验状态。2014 年 11 月开始入组。在提交手稿时(2017 年 7 月),已有四分之三的患者参与。因此,我们预计将在 2018 年 3 月前完成招募。