跳至主要内容
临床试验/NCT05893654
NCT05893654Enrolling By Invitation1 期

Melphalan Intra-arterial Chemotherapy for Choroidal Melanoma Chemoreduction - a Phase I Clinical Trial

Hospital das Clínicas de Ribeirão Preto1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2021年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
Enrolling By Invitation
发起方
入组人数
10
试验地点
1
主要终点
Determination of treatment safety through electroretinography (ERG)

研究概览

简要总结

The goal of this clinical trial is to investigate a new approach for treating large uveal melanomas, a type of eye cancer. The study aims to determine the effectiveness of using intra-arterial melphalan, a chemotherapy drug, to reduce tumor thickness, allowing for subsequent radiation therapy using a Ru-106 plaque.

The main questions this trial seeks to answer are:

  • Can intra-arterial melphalan effectively reduce the thickness of large uveal melanomas?
  • Is the combination of intra-arterial melphalan and brachytherapy a safe and effective treatment option for these tumors?

Participants enrolled in the trial have clinically diagnosed choroidal melanoma with tumor thickness equal to or greater than 8.00 mm. They will undergo a procedure where the chemotherapy drug is injected directly into the blood vessels that supply the tumor. After a few weeks, they will receive the radiation treatment using a small device placed on the eye. Throughout the trial, participants will have different tests to monitor the tumor and their vision, such as ultrasound scans, pictures of the inside of the eye, and a test called electroretinography (ERG) to check the function of the retina. These tests will be done at the start of the trial and at 1, 3, and 6 months later to track the progress of the treatment.

详细描述

INTRODUCTION Choroidal melanoma is the most common primary intraocular malignancy in adults, thus being the focus of extensive research. The primary treatment goals of this disease consist in controlling local disease, reducing the risk of distant metastases, and avoiding enucleation whenever possible.

Plaque brachytherapy is currently the standard treatment for small and medium-sized uveal melanomas. In clinical practice, ruthenium (Ru-106) or iodine (I-125) are the most commonly employed radioisotopes. Ruthenium is the most utilized radioisotope in Europe and South America due to its availability and good clinical outcomes. It is currently the only available option in Brazil's public health system (SUS). However, its use for large tumors (greater than 10 mm in thickness and/or 22 mm in diameter) is limited by the inability of delivering an adequate therapeutic dose of radiation without causing further damage to the surrounding retinal tissue.

For this reason, researchers in medical physics have been investigating new treatment options in the last decades, including external beam radiotherapy (EBRT), radiosurgery (gamma knife or linear accelerator), and proton beam therapy. Although gamma knife radiosurgery and proton beam therapy are effective treatments with reliable tumor control rates, they are associated with poor visual outcomes, inadequate globe retention, and their use is reportedly limited in public health systems of low- or middle-income countries. EBRT carries potential side effects related to a broader radiation field, with an increased risk for complications in ocular and periocular structures, such as eyelids, sclera, lens, and retina. Finally, enucleation is an effective management for very large tumors, but it is usually a last resource.

Considering the above-mentioned treatment limitations for large choroidal melanomas, our group explored an alternative approach using intra-arterial melphalan for tumor chemoreduction, aiming to reduce thickness and allow subsequent brachytherapy using a Ru-106 plaque.

Intra-arterial chemotherapy (IAC) with melphalan has been used to treat multiple cancers, including liver metastases from uveal and skin melanomas, but it has never been described as a primary tumor treatment. Previous studies have demonstrated a reasonable safety profile of the therapy when used for the treatment of other tumors.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
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

入选标准

  • Age equal to or higher than 18 years
  • Diagnosis of choroidal melanoma with a thickness equal to or higher than 8 mm on ultrasound evaluation
  • Comprehension and signature of the informed consent
  • Adequate pupil dilation and sufficient cooperation to carry out the complementary exams

排除标准

  • Choroidal melanomas with a greatest basal diameter higher than 18mm
  • Any clinical condition that impairs fundus documentation or patient follow-up
  • Medical or psychological conditions that prevent comprehension and signature of the informed consent
  • Pregnancy, breastfeeding, or plans of getting pregnant in the next year
  • Past medical history of allergic reactions or hypersensitivity to melphalan

研究组 & 干预措施

Single Arm

Experimental

Participants will undergo intra-arterial catheterization of the ophthalmic artery, with administration of 7.5mg of melphalan. After 4±1 weeks, they will receive Ru-106 plaque brachytherapy, which will be performed using a 24-mm notched plaque. Due to tumor thickness and the previous IAC, the target dose to the tumor apex shall be as close as possible to 80 Gy, respecting the safety limits regarding the risk of excessive dosage to the tumor base and scleral melting.

干预措施: Melphalan Injection (Drug)

Single Arm

Experimental

Participants will undergo intra-arterial catheterization of the ophthalmic artery, with administration of 7.5mg of melphalan. After 4±1 weeks, they will receive Ru-106 plaque brachytherapy, which will be performed using a 24-mm notched plaque. Due to tumor thickness and the previous IAC, the target dose to the tumor apex shall be as close as possible to 80 Gy, respecting the safety limits regarding the risk of excessive dosage to the tumor base and scleral melting.

干预措施: Plaque brachytherapy (Radiation)

结局指标

主要结局

Determination of treatment safety through electroretinography (ERG)

时间窗: 6 months

Participants will undergo ERG exams at baseline, 1, 3, and 6 months after the first intervention. The researchers will assess the patterns of ERG waves to determine whether there are signs of retinal toxicity.

次要结局

  • Best Corrected Visual Acuity (BCVA)(6 months)
  • Reduction of Tumor Size(6 months)
  • Signs of intraocular inflammation(6 months)
  • Treatment-related adverse events(6 months)
  • Globe salvage(12 months)

研究者

发起方
Hospital das Clínicas de Ribeirão Preto
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验