Vascular co-option in lung cancer metastatic to the eye after treatment with bevacizumab
© The Author(s) 2010
Received: 23 September 2010
Accepted: 26 October 2010
Published: 17 November 2010
Chemotherapy with bevacizumab alters the angiogenic environment, and therefore, the growth and spread of metastases. We present a patient with metastatic lung adenocarcinoma to the eye with findings suggestive of retinal vascular co-option.
A 57-year-old male, receiving systemic bevacizumab for metastatic lung adenocarcinoma, presented with vitreous opacities and clumped deposits adherent to the retinal vessels. No choroidal metastases were present. Diagnostic vitrectomy yielded cellular evidence of adenocarcinoma, with thyroid transcription factor-1 staining confirming a lung primary.
The perivascular growth of small foci of metastatic vitreous cells suggests vascular co-option from the native retinal circulation. Similar modification of metastatic disease by bevacizumab has been observed in animal models and selected human cases.
Ocular metastases most commonly present as mass lesions in the choroid. Retinal metastases and diffuse metastases to the vitreous have been previously reported in cutaneous melanoma, and breast and lung adenocarcinoma without any recognizable angiocentric pattern. We present a patient with retinal and vitreous metastases from lung adenocarcinoma whose ocular findings suggest that bevacizumab treatment resulted in distinctive perivascular growth by fostering vascular co-option of the retinal vasculature by metastatic tumor cells.
We examined a 57-year-old male who presented to the Bascom Palmer Eye Institute in Oct 2009 with a 6-month history of floaters in his left eye (OS). He had reported flashes in the OS 3 months prior and had undergone laser retinopexy without resolution of symptoms and was now diagnosed as uveitis. Past medical history was significant for stage IV non-small cell carcinoma of the lung diagnosed in Aug 2005 and treated with left pneumonectomy. Within 1 year, brain metastases developed and were treated with whole brain irradiation, 6-thioguanine, temozolomide, and stereotactic radiosurgical treatment of some larger masses. In June 2009, recurrent brain metastases were detected. Cerebrospinal fluid was negative for malignant cells. Chemotherapy was resumed. Erlotinib was stopped 2 months prior to presentation, and a 6-week prior MRI of the brain showed no evidence of tumor. Treatment with bevacizumab, capecitabine, and camptosar was ongoing. He had an implantable venous access device in the right subclavian vein present for 4 years. The skin over the device was intact and uninflamed. He was afebrile.
Lung cancer is the most common origin of ocular metastases. Malignant cells can metastasize via the systemic circulation to the high-flow posterior ciliary circulation and seed the choroid. Retinal metastases can shed into the vitreous, or the vitreous can be seeded via the highly vascular ciliary processes of the ciliary body. In cases of central nervous system malignancy, it is hypothesized that cells may gain access to the vitreous via the optic nerve. A Medline search revealed two prior reports of lung cancer metastasizing to the vitreous that were confirmed by cytologic examination and cytokeratin staining. [1, 2] Specific TTF-1 immunocytochemical staining  provides an additional tool for diagnosis of vitreous metastasis from a lung primary.
Preoperative OCT examination confirmed preretinal localization of the cellular deposits. The striking finding at surgery was the adherence of individual cellular clumps to the retinal surface often lining up along the retinal arteries and veins. Settling of cells into areas of tight vitreous insertion around the optic nerve or along the large retinal vessels was unlikely, since the deposits did not change after inducing a posterior vitreous detachment. The deposits could be individually aspirated from the retinal surface and did not form a sheet as would occur if the cells were growing along the posterior hyaloid.
We propose that the retinal adherence and the predilection for growth along the retinal vessels represent vascular co-option by tumor cells in an anti-angiogenic milieu created by systemic bevacizumab. A solid tumor will not generally exceed a diameter of 0.4–1.0 mm without first establishing its own vasculature,  which increases proportionate to tumor size. Use of vascular endothelial growth factor (VEGF) inhibitors, such as bevacizumab, thus arrest tumor growth. For comparison, the width of the optic nerve is approximately 1.5 mm and the width of a large retinal vein about 0.150 μm. The large optic nerve deposit seen in March 2010 was roughly 1.0 mm in greatest dimension (Fig. 3), which may have grown to this extent only because of co-option of vascular supply from the oxygen-rich vessels on the nerve face; it may have been unable to increase further in size without angiogenesis.
Survival of tumor cells by vascular co-option in an anti-VEGF environment has been demonstrated in animal studies . In a study by Rubenstein et al. , G55 human glioblastoma cells were inoculated into the basal ganglia of athymic rats which were then treated with intraperitoneal anti-VEGF antibody. There was a statistically significant increase in survival in the anti-VEGF treated animals compared to untreated controls. Tumors in the untreated animals grew as well-circumscribed, focal lesions, whereas tumors in the anti-VEGF treated animals had an infiltrative and invasive pattern of growth. Ninety per cent of these small (10 μm) “satellites” were located along a blood vessel, which was attributed to vascular co-option in an anti-angiogenic environment. TUNEL staining indicated higher apoptosis indices in tumor cells remote from blood vessels compared to tumor cells co-opting the native circulation.
In humans, vascular co-option is also likely to exist. Two patients with non-small cell lung carcinoma on systemic bevacizumab developed atypical leptomeningeal carcinomatosis identified by both neuroradiological imaging and histopathology . Both cases demonstrated nodular micrometastases centered on small blood vessels suggesting co-option of the normal vasculature.
In summary, we have identified a 57-year-old male on systemic bevacizumab with vitreous metastasis of TTF-1 positive metastatic non-small cell lung adenocarcinoma with tumor cell clumping along the retinal vasculature. We believe that this distribution of cells demonstrates retinal vascular co-option in an anti-angiogenic environment similar to that shown in previous animal and human studies.
No grants or funds were used to support this study.
Conflict of interest
The authors have no proprietary interest in this report.
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