Prospective, Controlled and Monocentric Study to Evaluate the Effects of Topical 3% Diclofenac in 2.5% Hyaluronic Acid Gel on Tumor Metabolism in the Treatment of Actinic Keratoses in Immunocompetent and Immunocompromised Patients
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 38
- 试验地点
- 1
- 主要终点
- Lactate level in skin biopsies of actinic keratoses
研究概览
简要总结
The rationale of this study is to investigate the effects of topical diclofenac on tumor metabolism in the treatment of actinic keratoses in immunocompetent and immunocompromised patients.
Study hypothesis is that topical diclofenac lowers lactate level in skin biopsies of actinic keratoses. Planned number of patients is 38.
This study is a monocenter study investigating the effects of 3% diclofenac in 2.5% hyaluronic acid gel on tumor metabolism in the treatment of actinic keratoses. Treatment duration is 3 months. Skin biopsies will be obtained before treatment, at the end of the treatment and four weeks after the treatment. Control biopsies at visit 1 and 3 are performed in healthy, sun damaged and untreated skin. Evaluation of efficacy will be performed at the end of the treatment and four weeks after the treatment.
Duration of treatment is 3 months (±4 weeks). Approximately 0,5g Solaraze® 3% gel is applied on a 5cm x 5cm lesion. Solaraze® 3% gel is applied twice daily on the study lesions.
详细描述
Neoplastic cells show an increased glucose metabolism and glycolysis which is associated with high lactate concentrations. There is also data for several tumor entities that high levels of lactate in the tumor are associated with tumor progression, metastasis and poor clinical outcome. Kreutz et al. demonstrated that diclofenac inhibits tumor cell proliferation in vitro and tumor growth in vivo via COX-independent effects on glucose metabolism. Diclofenac is taken up by tumor cells and inhibits tumor cell proliferation through inhibition of the oncogene MYC and subsequently glycolysis and block of lactate transport. MYC regulates genes involved in glycolysis and is upregulated in neoplastic cells, which is in line with the metabolic switch to glycolysis, the so called "Warburg effect", that cancer cells show. Although these results were found in vitro using human melanoma cells and in vivo in a mouse model, a similar mechanism of action is assumed to be relevant for the treatment of actinic keratoses with topical diclofenac. However tumor metabolism in diclofenac-treated actinic keratoses has never been investigated. To investigate the mechanism of action of diclofenac in the treatment of actinic keratoses, a clinical study analyzing particularly lactate levels, glycolysis and inflammatory infiltrate is needed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Written informed consent has been signed prior to or at Screening Visit
- •Caucasian male and female patients
- •Age > 18 years
- •Negative pregnancy test in women of childbearing age
- •Clinical diagnosis of actinic keratosis (AK)
- •A minimum of three AK lesions
- •Exclusion Criteria in immunocompromised patients :
- •Concomitant UV-phototherapy
- •Pregnancy or lactation
- •Women in child-bearing age who do not use highly efficient contraceptive methods (<1% failure rate per year)
- •Skin diseases that might interfere with response evaluation of study treatment
- •Topical pretreatment of the AK study lesions with photodynamic therapy, Solaraze® 3% gel, Aldara®, 5-FU, or polyphenon E during the 8 weeks preceding study treatment
- •Radiation therapy performed in the treatment area during the 3 months preceding study therapy
- •Systemic treatment with diclofenac
- •Known intolerance to diclofenac or to any other ingredient of Solaraze® 3% gel
- •Conditions that might interfere with the ability to understand the study and thus give written informed consent
- •Simultaneous participation in another clinical study or participation in another clinical study in the 30 days directly preceding inclusion
- •Suspected lack of compliance
- •Exclusion criteria in immunocompetent patients:
- •Concomitant UV-phototherapy
- •Pregnancy or lactation
- •Women in child-bearing age who do not use highly efficient contraceptive methods (<1% failure rate per year)
- •Patients with clinically relevant suppression of the immune system (e.g. drug induced, infection)
- •Skin diseases that might interfere with response evaluation of study treatment
- •Topical pretreatment of the AK study lesions with photodynamic therapy, Aldara®, Solaraze® 3% gel , 5-FU, or polyphenon E during the 8 weeks preceding study treatment
- •Systemic treatment with cytostatic drugs or radiation therapy performed in the treatment area during the 3 months preceding study therapy
- •Systemic treatment with diclofenac
- •Known intolerance to diclofenac or to any other ingredient of Solaraze® 3% gel
- •Conditions that might interfere with the ability to understand the study and thus give written informed consent
- •Simultaneous participation in another clinical study or participation in another clinical study in participation in another clinical study in the 30 days directly preceding inclusion
- •Suspected lack of compliance
排除标准
- 未提供
研究组 & 干预措施
Diclofenac
3 % diclofenac in 2.5% hyaluronic acid gel (Solaraze® 3% gel) is applied twice daily in the treatment area. 3 % diclofenac in 2.5% hyaluronic acid gel (Solaraze® 3% gel) is to be applied 1cm beyond the single AK.
干预措施: 3% diclofenac in 2.5% hyaluronic acid gel (Drug)
结局指标
主要结局
Lactate level in skin biopsies of actinic keratoses
时间窗: 4 weeks after the treatment
Assessment of the effects of topical 3% diclofenac in 2.5% hyaluronic acid gel on lactate level in skin biopsies of actinic keratoses. Skin biopsies of actinic keratoses are obtained prior to treatment and 4 weeks after the treatment.
次要结局
- Metabolic changes (e.g. glucose, amino acids)(at the end of the tretment and 4 weeks after the treatment)
- Lactate level in skin biopsies of healthy skin in a subpopulation(Before treatment and 4 weeks after the treatment)
- Glycolysis-relevant proteins evaluated using PCR and Westernblot techniques(at the end of the treatment and 4 weeks after the treatment)
研究者
Professor Dr. Sigrid Karrer
Professor Dr.
University Hospital Regensburg