Choroidal melanoma

脉络膜黑色素瘤
  • 文章类型: Review
    目的:本指南更新的目的是重新评估和更新2016年以前指南中关于葡萄膜黑色素瘤患者适当管理的建议。
    方法:2021年,来自省皮肤肿瘤小组的多学科工作组,艾伯塔省癌症护理,艾伯塔省卫生服务部召开会议以更新指南。对PubMed中的新研究证据以及来自著名肿瘤学小组的新临床实践指南的全面审查为更新提供了信息。方法的改进包括增加证据水平和建议强度。更新后的指南已分发给省皮肤癌小组的所有成员进行审查和认可。
    结果:新的和修改的建议满足了提供者的培训要求,用于检测转移的诊断成像,新辅助摘除前放疗,玻璃体内抗血管内皮生长因子治疗放射性视网膜病变,基因预后检测,在确定的局部治疗后进行监测,转移性葡萄膜黑色素瘤患者的全身治疗。
    结论:这些建议代表了一个大型多学科医疗专业人员小组同意的基于证据的护理标准。
    The purpose of this guideline update is to reassess and update recommendations in the prior guideline from 2016 on the appropriate management of patients with uveal melanoma.
    In 2021, a multidisciplinary working group from the Provincial Cutaneous Tumour Team, Cancer Care Alberta, Alberta Health Services was convened to update the guideline. A comprehensive review of new research evidence in PubMed as well as new clinical practice guidelines from prominent oncology groups informed the update. An enhancement in methodology included adding levels of evidence and strength of recommendations. The updated guideline was circulated to all members of the Provincial Cutaneous Tumour Team for review and endorsement.
    New and modified recommendations address provider training requirements, diagnostic imaging for the detection of metastases, neo-adjuvant pre-enucleation radiotherapy, intravitreal anti-vascular endothelial growth factor agents for radiation retinopathy, genetic prognostic testing, surveillance following definitive local therapy, and systemic therapy for patients with metastatic uveal melanoma.
    The recommendations represent evidence-based standards of care agreed to by a large multidisciplinary group of healthcare professionals.
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  • 文章类型: Journal Article
    评估碘-125上巩膜近距离放射治疗后中小脉络膜黑色素瘤(身高小于5.0mm)的预后。
    包括接受碘125近距离放射治疗的中小脉络膜黑色素瘤患者,根尖高度为1.0mm至5.0mm,最大基底直径≤16.0mm。从原始剂量测定计划中提取数据,以确定处方点到顶端高度的视力关键结构的剂量(实际剂量,ABS指南)和,模拟后,处方点高度为5.0毫米(模拟剂量,COMS协议)。视敏度(VA)结果与实际剂量和预测与模拟剂量一起估计局部复发,眼存活率,和5年生存。
    共纳入339例患者,平均年龄为61.5岁,平均随访时间为43.4个月。晶状体的平均剂量减少,光盘,中央凹占34%,39.4%,和41.4%,分别与实际剂量与模拟剂量进行比较。对于实际剂量和模拟剂量,Kaplan-Meier估计3年无事件VA率为20/50或更高分别为56%和31%。分别。仅观察到3例局部复发事件(摘除),产生5年局部控制和98%的眼生存率。5年总生存率(OS)和无转移生存率(MFS)分别为95%和87.5%,分别。
    根据ABS治疗的小型和中型脉络膜黑色素瘤具有优异的结果。与COMS方案相比,使用ABS指南的近距离放射治疗计划可能与较低的放射毒性和视力丧失率相关。
    To assess outcomes of small and medium choroidal melanoma (less than 5.0 mm in height) following Iodine-125 episcleral brachytherapy.
    Patients with small and medium choroidal melanoma that underwent Iodine-125 brachytherapy with apical height of 1.0 mm to 5.0 mm and largest basal diameter of ≤16.0 mm were included. Data were extracted from the original dosimetry plans to determine doses to vision critical structures with the prescription point to the apical height (actual dose, ABS guidelines) and, after simulation, with the prescription point to the height of 5.0 mm (simulated dose, COMS protocol). Visual acuity (VA) outcomes with actual dose and that predicted with the simulated dose were estimated along with local recurrence, ocular survival, and survival at 5 years.
    A total of 339 patients with a mean age of 61.5 years with a mean follow up duration of 43.4 months were included. The mean dose reduction for lens, optic disc, and fovea was 34%, 39.4%, and 41.4%, respectively with actual dose when compared with simulated dose. The Kaplan-Meier estimations for 3 year event free rate of VA of 20/50 or better were 56% and 31% for actual dose and simulated dose, respectively. Only 3 events of local recurrence were observed (enucleated) yielding 5 year local control and ocular survival rate of 98%. Overall survival (OS) and metastasis free survival (MFS) were 95% and 87.5% at 5 years, respectively.
    Small and medium choroidal melanoma treated according to ABS has excellent outcomes. Brachytherapy planning using ABS guidelines as compared to COMS protocol may be associated with lower rates of radiation toxicity and vision loss.
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  • 文章类型: Journal Article
    Eye plaque brachytherapy represents a safe and effective therapeutic approach for choroidal melanoma, combining clinical outcomes with an eye and visual preservation. As it represents a complex procedure, a specific quality assurance program is strongly suggested to improve patients and operators safety, and to reduce possible complications linked to surgical procedure and radiation exposure. The aim of this paper is to describe the INTERACTS (Interventional Radiotherapy Active Teaching School) guidelines for quality assurance in choroidal melanoma interventional radiotherapy (brachytherapy) used in our institution.
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  • 文章类型: Journal Article
    背景:自1970年代初以来,葡萄膜黑色素瘤的生存率一直保持不变。因为结果与肿瘤的大小高度相关,及时准确的诊断可以增加治愈的机会。
    方法:制定了基于共识的指南以告知从业人员。搜索PubMed与此主题相关的出版物。手工搜索了关键出版物的参考列表。搜索了国家准则交换所和各个准则组织,以获取相关准则。一组来自医学的内容专家进行了共识讨论,辐射,和外科肿瘤学被用来制定建议。
    结果:八十四份出版物,包括五项现有准则,形成了证据基础。
    结论:主要建议强调,对于葡萄膜黑色素瘤及其在葡萄膜中不确定的黑素细胞病变,管理是复杂的,需要有经验的专家在眼科肿瘤培训。分期检查包括血清和放射学检查。大的病变仍然最常采用摘除术治疗,然而,放射治疗是最常见的治疗有资格的肿瘤。辅助治疗在降低转移风险方面尚未证明有效。没有全身治疗能明显改善转移性疾病的预后.如有,我们鼓励转移性疾病患者参加临床试验.高度选择的患者可能受益于肝转移的手术切除。
    BACKGROUND: Survival in uveal melanoma has remained unchanged since the early 1970s. Because outcomes are highly related to the size of the tumour, timely and accurate diagnosis can increase the chance for cure.
    METHODS: A consensus-based guideline was developed to inform practitioners. PubMed was searched for publications related to this topic. Reference lists of key publications were hand-searched. The National Guidelines Clearinghouse and individual guideline organizations were searched for relevant guidelines. Consensus discussions by a group of content experts from medical, radiation, and surgical oncology were used to formulate the recommendations.
    RESULTS: Eighty-four publications, including five existing guidelines, formed the evidence base.
    CONCLUSIONS: Key recommendations highlight that, for uveal melanoma and its indeterminate melanocytic lesions in the uveal tract, management is complex and requires experienced specialists with training in ophthalmologic oncology. Staging examinations include serum and radiologic investigations. Large lesions are still most often treated with enucleation, and yet radiotherapy is the most common treatment for tumours that qualify. Adjuvant therapy has yet to demonstrate efficacy in reducing the risk of metastasis, and no systemic therapy clearly improves outcomes in metastatic disease. Where available, enrolment in clinical trials is encouraged for patients with metastatic disease. Highly selected patients might benefit from surgical resection of liver metastases.
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