Department of Radiation Oncology, University Hospital, 2 rue de la Milétrie, 86000 Poitiers, France.
NCTeam, Strahlenklinik, University Hospital Essen, D-45122 Essen, Germany.
Cancer Treat Rev. 2014 Dec;40(10):1119-28. doi: 10.1016/j.ctrv.2014.09.006. Epub 2014 Oct 5.
Choroidal metastases (CM) are the most common malignant intraocular lesion observed in up to 4-12% of necropsy series of patients with solid cancer. The spectrum of presentations varies from prevalent CM in disseminated cancer to isolated CM. CM are responsible for visual deterioration. Depending on the primary cancer, estimated life expectancy, overall cancer presentation and ocular symptoms, the management of CM varies widely. We address the multidisciplinary management of CM and technical aspects of radiotherapy.
A systematic review of literature was performed from 1974 to 2014.
Choroidal metastases occur preferentially in breast and lung carcinomas but are reported in all cancer types. The standard treatment remains external beam radiotherapy, applying 30Gy in 10 fractions or 40Gy in 20 fractions. The reported complete response and improved visual acuity rates are 80% and 57% to 89%, respectively. Some chemotherapy or new targeted therapy regimens yield promising CM response rates.
Radiation therapy consistently shows rapid symptom alleviation, yield excellent local control and functional outcomes. However, there are only few reports on late toxicities after 6months given the unfavorable prognostic of CM patients. Selected patients may live more than two years, underlying the need to better assess mean and long term outcomes. Some authors have favored exclusive systemic strategies with omission of irradiation. The current literature suffers from the scarcity of prospective trials. Duration of tumor response following systemic therapy is rarely reported but appears less favorable as compared to radiotherapy. Systemic treatments may be proposed for pauci-symptomatic CM in a polymetastatic context while radiation therapy remains necessary in symptomatic CM either upfront or as an alternating treatment. Focalized radiation like brachytherapy and proton therapy may be proposed for isolated CM with long disease-free interval between primary and CM, as these techniques have the potential to yield better tumor and functional outcomes in patients with long life expectancy.
脉络膜转移(CM)是最常见的眼内恶性肿瘤,在 4-12%的实体瘤患者尸检中均可发现。临床表现从广泛转移癌中的CM 为主到孤立性 CM 均有出现。CM 可导致视力下降。根据原发肿瘤、预估预期寿命、全身癌症表现和眼部症状,CM 的治疗方法差异较大。我们探讨了 CM 的多学科治疗和放射治疗技术。
对 1974 年至 2014 年的文献进行了系统性回顾。
CM 多发生于乳腺癌和肺癌,但也见于所有癌症类型。标准治疗仍然是外照射放疗,应用 30Gy/10 次或 40Gy/20 次。报道的完全缓解率和视力改善率分别为 80%和 57%至 89%。一些化疗或新的靶向治疗方案也能获得较好的 CM 缓解率。
放疗能迅速缓解症状,提供良好的局部控制和功能预后。然而,由于 CM 患者预后不佳,仅少数报告对 6 个月后进行的迟发性毒性作用进行了评估。一些患者可生存超过 2 年,因此需要更好地评估平均和长期结果。一些作者更倾向于采用仅行全身治疗而不进行放疗的方案。目前的文献由于缺乏前瞻性试验而存在不足。全身治疗后肿瘤反应的持续时间很少有报道,但与放疗相比,似乎更差。全身治疗可用于多发性转移背景下的症状性 CM,但对于症状性 CM 仍需进行放疗,或作为交替治疗。对于原发肿瘤和 CM 之间有较长无病间期的孤立性 CM,可采用聚焦放疗,如近距离放疗和质子治疗,这些技术可能为预期寿命较长的患者提供更好的肿瘤和功能预后。