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肺癌眼葡萄膜转移:194 例患者的临床特征、治疗和转归。

Uveal metastasis from lung cancer: clinical features, treatment, and outcome in 194 patients.

机构信息

Ocular Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pennsylvania.

Ocular Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pennsylvania.

出版信息

Ophthalmology. 2014 Jan;121(1):352-357. doi: 10.1016/j.ophtha.2013.07.014. Epub 2013 Aug 26.

Abstract

PURPOSE

To evaluate the clinical features, treatment, and prognosis of patients with uveal metastasis from lung cancer.

DESIGN

Retrospective chart review.

PARTICIPANTS

There were 194 patients with a diagnosis of uveal metastasis from lung cancer.

INTERVENTION

Radiotherapy, chemotherapy, enucleation, or observation.

MAIN OUTCOME MEASURES

Ocular tumor control, final visual acuity, and tumor-related death.

RESULTS

There were 374 uveal metastatic tumors originating from primary lung cancer in 229 eyes of 194 patients. Tumor location included choroid (88%), ciliary body (2%), and iris (10%), with bilateral involvement in 18%. Diagnosis of uveal metastasis preceded the diagnosis of primary lung cancer in 44% of patients. The choroidal metastatic focus had a mean basal diameter of 8 mm and mean thickness of 3 mm, and were mostly located posterior to the equator (91%). The choroidal metastasis commonly had yellow or orange color (98%), had plateau (61%) or dome (38%) configuration, and displayed associated subretinal fluid (85%). Choroidal tumors were multifocal in 49 cases (23%). Ciliary body tumors were commonly dome shaped (75%) with an episcleral sentinel vessel (75%). Iris tumors were multifocal in 2 cases (13%), had visible intrinsic vessels (97%), and were associated with tumor seeding in the angle (38%) or on the iris stroma (25%). The uveal metastases were treated with teletherapy (31%), chemotherapy (18%), brachytherapy (9%), chemotherapy combined with teletherapy or brachytherapy (14%), enucleation (3%), or observation (21%). At last visit, eyes with follow-up showed tumor regression (66%), stability (12%), growth (14%), recurrence (3%), or new metastasis (5%). Visual acuity improved or remained stable in 59% eyes. One-year mortality from the time of detection of uveal metastasis was 54%.

CONCLUSIONS

Of 194 patients with uveal metastasis from lung cancer, 44% did not have a history of known lung cancer. Current methods of ocular treatment allow globe salvage in 92% of patients and improved/stable vision in 59% of patients. Systemic prognosis remains poor with tumor-related death in 54% of patients at 1 year.

摘要

目的

评估肺癌眼转移患者的临床特征、治疗方法和预后。

设计

回顾性病例分析。

参与者

共 194 例肺癌眼转移患者。

干预措施

放疗、化疗、眼球摘除术或观察。

主要观察指标

眼内肿瘤控制、最终视力和肿瘤相关死亡。

结果

194 例患者的 229 只眼中共有 374 个源于原发性肺癌的眼转移瘤。肿瘤位置包括脉络膜(88%)、睫状体(2%)和虹膜(10%),18%的患者为双眼受累。在 44%的患者中,眼转移瘤的诊断先于原发性肺癌的诊断。脉络膜转移灶的基底直径平均为 8mm,厚度平均为 3mm,多位于赤道后(91%)。脉络膜转移瘤多呈黄色或橙色(98%),呈盘状(61%)或丘状(38%),伴有视网膜下积液(85%)。49 例(23%)脉络膜肿瘤为多灶性。睫状体肿瘤多为丘状(75%),伴巩膜哨兵血管(75%)。虹膜肿瘤有 2 例(13%)为多灶性,可见固有血管(97%),并伴有角部(38%)或虹膜基质(25%)肿瘤播散。眼内转移瘤采用远距离放射治疗(31%)、化疗(18%)、近距离放射治疗(9%)、化疗联合远距离放射治疗或近距离放射治疗(14%)、眼球摘除术(3%)或观察(21%)。末次随访时,有随访记录的眼内肿瘤消退(66%)、稳定(12%)、进展(14%)、复发(3%)或新发转移(5%)。视力提高或保持稳定的占 59%。从发现眼转移瘤到死亡的 1 年生存率为 54%。

结论

194 例肺癌眼转移患者中,44%的患者无已知肺癌病史。目前的眼部治疗方法可使 92%的患者保留眼球,并使 59%的患者视力提高或保持稳定。但患者的全身预后仍较差,1 年时肿瘤相关死亡率为 54%。

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