Factors associated with ocular adverse event after immune checkpoint inhibitor treatment

Abstract

Ocular adverse events (OAEs) including vision-threatening intraocular inflammation after immune checkpoint inhibitor (ICI) treatment have been increasingly reported; however, the risk factors associated with OAEs remain elusive. Here, we determined the factors associated with OAEs after ICI treatment. We analyzed 40 consecutive patients who experienced OAEs after ICI treatments. The OAEs included anterior uveitis, chorioretinitis, papillitis, foveal interdigitation zone thickening/serous retinal detachment (IZT/SRD), retinal vascular occlusion, and strabismus and ptosis. Of 40 patients, 18 (45%) were treated with atezolizumab, 13 (33%) with pembrolizumab, 7 (18%) with nivolumab, 1 (3%) with ipilimumab/nivolumab, and the other 1 (3%) with durvalumab/tremelimumab. BRAF/MEK inhibitors were concurrently used in 19 (48%) patients. Occurrence of intraocular inflammation was significantly associated with previous ocular surgery and trauma history (P = 0.015) and pembrolizumab use (P = 0.031). Neuro-ophthalmic complications and IZT/SRD were associated with brain metastasis (P = 0.005) and treatment with BRAF/MEK inhibitor (P < 0.001), respectively. In extensive literature review for clinical cases, we identified seven cases with intraocular inflammation, which were not observed with ipilimumab treatment, that occurred after a change of the drug to pembrolizumab. Collectively, these findings provide better understandings of OAEs after ICI treatment.

Introduction

Since the remarkable effects of pembrolizumab on advanced melanoma and non-small cell lung cancer have been published, immune checkpoint inhibitors (ICIs) have become one of the mainstays of cancer treatment [1, 2]. Currently, six FDA-approved ICIs are widely used to treat various cancers. These are monoclonal antibodies that activate the immune system by targeting CTLA-4 [Ipilimumab (Yervoy®)], PD-1 [pembrolizumab (Keytruda®), nivolumab (Opdivo®)], and PD-L1 [avelumab (Bavencio®), durvalumab (Imfinzi®), and atezolizumab (Tecentriq)] [3]. CTLA-4 and PD-1 are receptors on the surface of activated T cells, while PD-L1 resides on cancer cells [4]. PD1/PD-L1 and CTLA4/B7-1 or B7-2 interactions suppress T-cell function, and ICIs counteract this inhibitory process, resulting in T-cell activation [5, 6].

By increasing T-cell activity, systemic inflammatory side effects associated with ICI treatment have been reported [3]. Possible mechanisms underlying immune-related adverse events include increasing T-cell activity against antigens that are present in tumors and healthy tissues, increasing levels of preexisting autoantibodies, increasing levels of inflammatory cytokines, and enhancing complement-mediated inflammation [7]. Since Robinson et al. described the uveitis developed during anti-CTLA-4 therapy in 2004, many ocular adverse events (OAEs) affecting orbit and ocular adnexa, ocular surface, optic nerve, uvea, and retina have also been reported [3, 8]. The clinical features of OAEs have been described in case reports and small case-series studies; however, the factors associated with OAEs remain elusive [9–35]. In the present study, we analyzed the characteristics and statistically associated factors of the development of OAEs after ICI treatment, and have comprehensively reviewed the literature reporting intraocular inflammation with posterior segment complications or Vogt–Koyanagi–Harada (VKH)-like features after ICI treatment.

Methods

Study population and approval

The medical records of consecutive patients treated with FDA-approved ICIs (ipilimumab, pembrolizumab, nivolumab, avelumab, durvalumab, and atezolizumab) and visited the ophthalmology department after ICI treatment between January 2011 and April 2019 were retrospectively reviewed. The patients who met the following criteria were included: (1) completed an ophthalmic examination, and (2) had newly developed ocular signs during ICI treatment. Patients with only mild dry eye/cataract or no newly developed ophthalmic abnormalities were excluded from the study. The recorded parameters included the primary tumor for ICI treatment, the use of other chemotherapeutic agents including BRAF/MEK inhibitors, and tumor metastasis. This research adhered to the tenets of the Declaration of Helsinki. The institutional Review Board/Ethics Committee approved this retrospective study (Severance Hospital, Yonsei University Health System, IRB no. 4-2019-1100).

Ophthalmic examinations

Each patient underwent a comprehensive ophthalmic examination including best-corrected visual acuity, slit-lamp biomicroscopy, tonometry, fundus photography, and a detailed fundus examination. Ancillary testing was performed with spectral-domain optical coherence tomography (Spectralis, Heidelberg Engineering, Heidelberg, Germany), fluorescein angiography, and indocyanine green angiography. Depending on the case, the visual field test, cover-uncover test, prism cover test, or measurement of marginal reflex distance were performed. At the initial visit, the patients were asked for detailed personal history including ocular trauma and surgery.

Statistical analysis

All statistical analyses were performed using SPSS statistical software for Windows, version 25.0 (SPSS, Chicago, IL, USA). The Kruskal–Wallis test and Pearson’s chi-square test were used to study the differences in clinical characteristics and features of OAEs among ICIs. Binomial logistic regression analysis was performed to identify factors associated with different types of OAEs. The odds ratios of the factors detected in the univariate and multivariate analyses were calculated. P < 0.05 was considered to indicate statistical significance.

Literature review

A comprehensive search of the electronic database including PubMed and Embase was performed from inception to July 2019. The searches were conducted using the combination of the following keywords in the title or abstract of the article: “ipilimumab”, “pembrolizumab”, “nivolumab”, “atezolizumab”, “durvalumab”, “avelumab”, “immune checkpoint inhibitor”, “uveitis”, “ocular”, “eye”, “adverse event”, and “ophthalmology”. The case reports, case-series, and review articles addressing intraocular inflammation with posterior segment complications or VKH-like features after ICI treatment were reviewed. Bibliographies of the reviewed articles were checked manually to prevent missing potentially relevant studies.

Results

Study population

Forty patients met the inclusion criteria and were included in the analyses. Of 40 patients, 18 (45%) were treated with atezolizumab, 13 (33%) with pembrolizumab, 7 (18%) with nivolumab, 1 (3%) with ipilimumab/nivolumab, and the other 1 (3%) with durvalumab/tremelimumab. The most common primary tumor for ICI treatment was lung cancer (15 patients), followed by skin melanoma (7 patients). Notably, 19 (48%) patients were treated with BRAF/MEK inhibitors during the ICI treatments. The details of the demographic characteristics are presented and summarized in Table 1.

Table 1.

Demography and clinical features of patients with ocular adverse events after immune checkpoint inhibitor treatment

Patient No	Dermography (at initial presentation)					Primary tumor	Chemotherapeutic agent		Ocular adverse event		Treatment
	Age (y)	Sex	Eye	Ocular history	BCVA (R/L)		ICI	Other	Manifestation	Time from ICI (days)
1	63	M	B	Blunt trauma	0.2/0.5	Skin melanoma	Ipilimumab Nivolumab	None	Ant. uveitis	351	PSTI Topical steroid
2	58	F	B	None	None	Renal cancer	Pembrolizumab	Lenvatinib	Panuveitis	47	ICI d/c PSTI Topical steroid
3	54	F	R N/A	Enucleation	0.5/NA	Uveal melanoma	Pembrolizumab	None	Panuveitis	51	ICI d/c Systemic steroid
4	66	M	B	PRK	0.9/0.3	Lung cancer Esophageal cancer	Pembrolizumab	None	Neuroretinitis	174	ICI d/c Systemic steroid
5	78	M	L N/A	Eyeball rupture Phthisis bulbi	NLP/CF	Lung cancer	Pembrolizumab	None	Panuveitis Uveal effusion	39	ICI d/c Systemic steroid
6	69	M	R	None	0.9/0.7	Lung cancer	Pembrolizumab	None	Rt. INO	31	Observation
7	62	M	B	None	0.6/1.0	Skin melanoma	Pembrolizumab	None	Papilledema	11	Observation
8	68	F	L	Glaucoma	1.0/LP	Skin melanoma	Pembrolizumab	None	Ptosis 3rd nerve palsy	37	Observation
9	60	F	B	None	1.0/0.9	Lung cancer	Pembrolizumab	None	Exotropia	35	Observation
10	65	M	B	None	0.8/0.4	Lung cancer	Pembrolizumab	Carboplatin	Ptosis	78	Observation
11	69	M	B	None	0.9/0.8	Skin melanoma	Nivolumab	None	Exotropia	710	Observation
12	71	M	B	None	0.5/0.06	Lung cancer	Nivolumab	None	NAION	95	Systemic steroid
13	57	M	B	None	0.9/1.0	Gastric cancer	Nivolumab	None	Exotropia VFD	47	Observation
14	59	M	B	None	1.0/1.0	Renal cancer	Atezolizumab	Cobimetinib	Exotropia	45	Observation
15	66	F	B	None	0.3/1.0	Skin melanoma	Pembrolizumab	Dabrafenib Trametinib	Foveal SRD	70	Observation
16	61	F	B	PDR, PRP	0.7/0.6	Gastric cancer	Nivolumab	None	Foveal SRD	50	ICI d/c IVB
17	67	M	B	None	1.0/1.0	Rectal cancer	Atezolizumab	Cobimetinib	Foveal EZT	28	Observation
18	66	M	B	None	1.0/1.0	Skin melanoma	Atezolizumab	Cobimetinib Vemurafenib	Foveal EZT	25	Observation
19	40	F	B	None	1.0/1.0	Breast cancer	Atezolizumab	Cobimetinib Paclitaxel	Foveal EZT	29	Observation
20	60	M	B	ARMD	1.0/1.0	Lung cancer	Atezolizumab	Cobimetinib	Foveal EZT Foveal SRD	31	Observation
21	50	M	B	Trabeculectomy Cataract surgery	0.5/1.0	Rectal cancer	Atezolizumab	Cobimetinib	Foveal SRD	14	ICI d/c Cobimetinib d/c
22	69	M	B	None	1.0/1.0	Colon cancer	Atezolizumab	Cobimetinib	Foveal EZT	42	Observation
23	58	M	B	None	1.0/1.0	Colon cancer	Atezolizumab	Cobimetinib	Foveal EZT	14	Observation
24	66	M	B	None	1.0/1.0	Colon cancer	Atezolizumab	Cobimetinib	Foveal SRD	11	ICI d/c
25	73	M	B	Cataract surgery	1.0/1.0	Ureter cancer	Atezolizumab	Cobimetinib	Foveal SRD	40	Observation
26	74	F	B	Cataract surgery	0.5/1.0	Ureter cancer	Atezolizumab	Cobimetinib	Foveal EZT	48	Observation
27	49	F	B	None	1.0/1.0	Renal cancer Bladder cancer	Atezolizumab	Cobimetinib	Foveal EZT	26	Observation
28	80	M	B	None	0.5/0.5	Skin melanoma	Atezolizumab	Cobimetinib	Foveal SRD	9	Observation
29	62	F	B	None	1.0/1.0	Breast cancer	Atezolizumab	Cobimetinib Paclitaxel	Foveal EZT	421	Observation
30	54	M	B	None	1.0/1.0	Lung cancer	Atezolizumab	Cobimetinib	Foveal EZT Foveal SRD	162	ICI d/c Cobimetinib d/c
31	57	M	B	None	1.0/1.0	Lung cancer	Atezolizumab	Cobimetinib	Foveal EZT Foveal SRD	42	Observation
32	66	M	B	None	1.0/0.9	Lung cancer	Atezolizumab	Cobimetinib	Foveal EZT	27	Observation
33	59	F	B	None	1.0/1.0	Breast cancer	Pembrolizumab	Doxorubicin Cyclophosphamide	EZ disruption CWS	117	Observation
34	67	M	R	None	0.2/0.8	Cholangiocarcinoma	Pembrolizumab	None	Preseptal cellulitis	13	Systemic antibiotics
35	52	F	B	None	1.0/1.0	Lung cancer	Pembrolizumab	None	Preseptal cellulitis	28	Systemic antibiotics
36	70	F	L	Cataract surgery	0.5/HM	Lung cancer	Nivolumab	None	RRD	407	PPV
37	66	F	B	PDR, PPV Cataract surgery	0.2/0.15	Lung cancer	Nivolumab	None	Neurotropic keratitis	160	Auto-serum
38	76	M	R	Cataract surgery	CF/0.6	Gastric cancer	Nivolumab	None	CRVO	31	IVB
39	58	M	L	None	0.9/0.3	Lung cancer	Atezolizumab	Cobimetinib	BRVO PED	119	Observation
40	66	M	L	None	0.8/CF	Lung cancer	Durvalumab Tremelimumab	None	CRVO	308	IVB

No. = number; M = male; F = female; B = both; R = right; L = left; NA = not applicable; ARMD = age-related macular degeneration; PDF = proliferative diabetic retinopathy; PPV = pars plana vitrectomy; PRK = photorefractive keratectomy; LP = light perception; CF = counting finger; HM = hand motion; NLP = no light perception; ICI = immune checkpoint inhibitor; INO = internuclear ophthalmoplegia; EZT = ellipsoid zone thickening; SRD = serous retinal detachment; EZ = ellipsoid zone; CWS = cotton wool spot; CRVO = central retinal vein occlusion; RRD = rhegmatogenous retinal detachment; NAION = non-arteritic anterior ischemic optic neuropathy; BRVO = branch retinal vein occlusion; PED = pigment epithelial detachment; VFD = visual field defect; PSTI = posterior subtenone triamcinolone injection; d/c = discontinuation; IVB = intravitreal bevacizumab injection; Time from ICI = Time from initial immune checkpoint inhibitor infusion

Ocular adverse events associated with ICIs

The details of the OAEs are presented in Table 1. The median time between the OAE and initial ICI treatment was 42.0 days [interquartile range (IQR), 28.0–111.5 days]. The median observation period after the OAE was 157.0 days (IQR, 47.0–265.5 days). Twenty-nine patients (73%) developed OAEs within 60 days of the initial ICI infusion. Notably, all patients treated with atezolizumab were treated with BRAF/MEK inhibitors.

We divided the OAEs into four categories: (1) intraocular inflammation, (2) neuro-ophthalmic complications without intraocular inflammation, (3) foveal interdigitation zone thickening/serous retinal detachment (IZT/SRD) without visible intraocular inflammation, and (4) others. Intraocular inflammation developed in five patients. One patient who had nivolumab and ipilimumab combination treatment developed bilateral anterior uveitis. Panuveitis or neuroretinitis developed in four patients who had pembrolizumab treatment (Fig. 1a–d). In these four patients, pembrolizumab was discontinued, and periocular/systemic steroid was used to control inflammation. Neuro-ophthalmic complications included one bilateral nonarteritic anterior ischemic optic neuropathy, one ptosis, one papilledema, one internuclear ophthalmoplegia, one third nerve palsy, and four exotropia. Eight (89%) out of nine patients with neuro-ophthalmic complications had brain metastasis of the primary tumor. Brain magnetic resonance imaging (MRI) of one patient (Patient 13) without brain metastasis revealed posterior cerebral artery territory infarction. Foveal IZT/SRDs were observed in 18 patients (Fig. 1e–j). Comprehensive and ancillary ophthalmic examinations did not reveal any intraocular inflammation in most patients; one patient, however, differed markedly from the rest. Patient 15 had unilateral anterior uveitis refractory to steroid treatment, but aqueous humor cytology showed many skin melanoma cells, suggesting metastasis. Other OAEs included central retinal vein occlusion, branch retinal vein occlusion, newly developed ellipsoid zone disruption and cotton wool spots, rhegmatogenous retinal detachment, neurotrophic keratitis, and preseptal cellulitis.

Fig. 1.

Representative enhanced depth imaging optical coherence tomography images of patients with ellipsoid zone thickening/serous retinal detachment or chorioretinitis after immune checkpoint inhibitor therapy. a, b A 58-year-old female (Patient 2) presented with bilateral chorioretinitis/papillitis 47 days after pembrolizumab therapy. c, d, A 54-year-old female (Patient 3) presented with chorioretinitis/papillitis 51 days after pembrolizumab therapy (c). Undulating retinal pigment epithelium, subretinal fluid, and thickened was resolved after posterior subtenon triamcinolone injection and systemic steroid treatment (d). e–h A 54-year-old man (Patient 30) presented with bilateral ellipsoid zone thickening (e, f) 13 days after atezolizumab/cobimetinib therapy. Serous retinal detachment developed after five cycles of atezolizumab/cobimetinib therapy (g, h). i, j A 66-year-old woman (Patient 15) presented with bilateral ellipsoid zone thickening and serous retinal detachment 4 days after pembrolizumab/trametinib therapy. No abnormality was detected during pembrolizumab monotherapy in this patient

Factors associated with the types of ocular adverse events

The details of factors associated with different types of OAE are presented in Table 2. Using multivariate analysis, ocular trauma/surgery (P = 0.001) and pembrolizumab (P = 0.001) were associated with intraocular inflammation. Only brain metastasis (P = 0.005) and the treatment with BRAF/MEK inhibitor (P = 0.021) were associated with neuro-ophthalmic complications and foveal IZT/SRD, respectively. Atezolizumab was significantly associated with foveal IZT/SRD using univariate binomial logistic regression, but not using multivariate analysis.

Table 2.

Factors associated with intraocular inflammation, neuro-ophthalmic complications, and foveal interdigitation zone thickening/serous retinal detachment without intraocular inflammation after immune checkpoint inhibitor treatment

	All cases	Intraocular inflammation			Neuro-ophthalmic complication			Foveal IZT/SRD
	Total N = 40	Total N = 5	Odds ratio (95% CI)	P value	Total N = 9	Odds ratio (95% CI)	P value	Total N = 18	Odds ratio (95% CI)	P value
Sex (male)	26 (65%)	3 (60%)	0.783 (0.115–5.341)	0.99	7 (78%)	2.211 (0.392–12.47)	0.45	12 (67%)	1.143 (0.309–4.234)	0.99
Ocular surgery/trauma	11 (28%)	4 (80%)	16.00 (1.537–166.5)	0.015†	0 (0%)	0.690 (0.540–0.880)	0.043	4 (22%)	0.612 (0.147–2.554)	0.72
Pembrolizumab	13 (33%)	4 (80%)	11.56 (1.137–117.4)	0.031†	5 (56%)	3.594 (0.769–16.79)	0.23	1 (6%)	0.049 (0.006–0.436)	0.002
Nivolumab	8 (20%)	1 (20%)	1.000 (0.096–10.41)	0.99	3 (33%)	2.600 (0.483–14.01)	0.35	1 (6%)	0.126 (0.014–1.146)	0.05
Atezolizumab	18 (45%)	0 (0%)	0.773 (0.616–0.969)	0.05	1 (11%)	0.103 (0.011–0.925)	0.027	16 (89%)	80.00 (10.12–632.3)	< 0.001
BRAF/MEK inhibitor	19 (48%)	0 (0%)	0.762 (0.600–0.968)	0.049	1 (11%)	0.090 (0.010–0.813)	0.021	17 (94%)	170.0 (14.15–2042)	< 0.001†
Brain metastasis	17 (43%)	1 (20%)	0.297 (0.030–2.932)	0.37	8 (89%)	19.56 (2.126–179.8)	0.005†	5 (28%)	0.321 (0.085–1.211)	0.12
Presence of systemic IrAE	4 (10%)	1 (20%)	2.670 (0.221–32.18)	0.99	1 (11%)	1.167 (0.106–12.81)	0.99	2 (11%)	1.250 (0.158–9.879)	0.99

IZT/SRD = interdigitation zone thickening/serous retinal detachment; IrAE = Immune related adverse event

^† Statistically significant in multivariate analysis

Literature review for clinical cases presenting intraocular inflammation with posterior segment complications or VKH-like features associated with immune checkpoint inhibitors

Intraocular inflammation with posterior segment complications or VKH-like features has been considered as immune-related sight-threatening OAEs. We reviewed the literature and found 48 cases from 28 studies, including the present study. The clinical features of the cases are summarized and presented in Table 3. The most common primary tumor was skin melanoma (38 cases, 79%), followed by lung cancer (5 cases, 10%), and choroidal melanoma (3 cases, 6%). Four (8%) cases presented unilaterally. Eighteen (44%), fourteen (23%), eight (17%), six, and one case were treated with pembrolizumab, ipilimumab, nivolumab, nivolumab/ipilimumab, and pembrolizumab/ipilimumab infusion, respectively. Notably, only one case (Case 20) developed unilateral uveal effusion and SRD accompanied by shallow anterior chamber and closed angle after atezolizumab infusion. Nine patients had a history of ocular surgery, and one patient had metastatic choroidal melanoma. Nineteen patients showed co-occurring adverse events such as poliosis/vitiligo, preceding headache, hypophysitis, aseptic meningitis, and hearing abnormalities. ICI treatments were discontinued in 31 (65%) cases. In seven cases (Case 8, 9, 35, 36, 37, 41, and 42), the OAEs were not observed in the previous ipilimumab treatments, which occurred after pembrolizumab infusions. In case 42, bilateral panuveitis developed 1 week after unilateral cataract surgery during pembrolizumab treatment. Panuveitis recurred after reinfusion of pembrolizumab in this case.

Table 3.

Characteristics and clinical data in the literature of 48 patients experienced intraocular inflammation with posterior segment complications or Vogt–Koyanagi–Harada-like features after immune checkpoint inhibitor treatment

Case No	Age	Sex	Eyes	Primary tumor	ICI	BRAF/MEK inhibitor	Ocular adverse event	Ocular history and Co-occurring condition	Treatment	Reference
1	58	F	B	Renal cancer	P	None	Panuveitis, papillitis	Headache, Tinnitus	ICI d/c, PSTI, topical steroid	This study (Patient 2)
2	54	F	N/A	Choroidal melanoma	P	None	Panuveitis, papillitis	Enucleation due to choroidal melanoma (L)	ICI d/c, Systemic steroid	This study (Patient 3)
3	66	M	B	Lung cancer	P	None	Neuroretinitis	Photorefractive keratectomy	ICI d/c, Systemic steroid	This study (Patient 4)
4	78	M	N/A	Lung cancer	P	None	Panuveitis, papillitis, uveal effusion	Phthisis bulbi after intraocular surgery (R)	ICI d/c, Systemic steroid	This study (Patient 5)
5	44	M	B	Skin melanoma	I	Not described	Panuveitis, Papillitis	Systemic IrAE including rash, diarrhea, fever	ICI d/c, Systemic steroid	#9
6	53	M	B	Skin melanoma	I	Sorafenib	Optic neuritis, No chorioretinal lesion	Systemic IrAE including rash, diarrhea, Accompanied by ophthalmic artery occlusion, aseptic meningitis, and hypophysitis	ICI d/c	#10
7	82	M	B	Skin melanoma	P	Not described	Optic neuritis, Ant. uveitis	Hypophysitis Hearing loss	ICI d/c, Systemic steroid	#11
8a	78	F	B	Skin melanoma	P	Not described	Panuveitis, Choroidal effusion	Hearing loss Bilateral vestibular hypofunction	ICI d/c, Systemic steroid, PSTI	#12
9a	61	F	B	Skin melanoma	P	Previous dabrafenib	Panuveitis	History of uveitis after dabrafenib irAE including colitis	ICI d/c, Systemic steroid	#13
10b	70 s	F	B	Skin melanoma	I	Not described	Bilateral multifocal SRD, choroiditis	None	ICI d/c, Temozolomide Topical steroid	#14
11b	47	M	B	Skin melanoma	I	Not described	Neuroretinitis with SRD,	None	ICI d/c	#15
12	60 s	M	B	Skin melanoma	I + N	Not described	Choroidal effusion with posterior subretinal fluid, undulating RPE, absence of leakage on FAG	Hyperopia (+ 5 D)	ICI d/c, Systemic steroid	#16
13	43	F	B	Skin melanoma	I	Not described	Panuveitis	Preceded by mild headache, accompanied by vitiligo and poliosis,	Systemic steroid	#17
14	55	M	B	Skin melanoma	N	Not described	Ant. Uveitis	VKH-like eruption, Allopecia areata, vitiligo, Poliosis	Topical steroid	#18
15	60	F	B	Skin melanoma	N	Vemurafenib	Chorioretinitis (early VKH-like)	Cataract surgery (R), Poliosis	Systemic steroid, Topical steroid	#19
16	56	M	B	Skin melanoma	N + I	Not described	Panuveitis	Panuveitis	ICI d/c, Systemic steroid, Topical steroid	#20
17b	62	F	L	Choroidal melanoma	N + I	Not described	VKH-like	Metastatic choroidal melanoma	Systemic steroid	#20
18	63	M	L	Skin melanoma	P	Not described	Unilateral VKH-like	Not described	Topical steroid	#20
19	30	F	B	Skin melanoma	I	Not described	VKH-like	Recurrent bilateral uveitis, systemic IrAE including transaminitis, diarrhea	Systemic steroid, Topical Steroid	#20
20	68	M	L	Lung cancer	A	Not described	Uveal effusion, conjunctival hyperemia, Ant. uveitis, Uveal effusion, CWS	Not described	ICI d/c, No other description	#21
21	52	M	B	Skin melanoma	N	Not described	Uveal effusion, Increased IOP, Shallow A/C, Ant. uveitis, Choroidal detachment	Not described	ICI d/c, peripheral iridotomy, topical steroid, IOP-lowering agent, topical atropine	#21
22	85	M	L	Skin melanoma	P	Not described	Uveal effusion, conjunctival chemosis	Not described	ICI d/c, no other description	#21
23	56	F	B	Skin melanoma	I	Not described	Ant. uveitis, papillitis	Not described	Retrobulbar steroid	#22
24	43	F	B	Skin melanoma	I	Not described	Post. Uveitis	Not described	ICI d/c, Systemic steroid	#22
25	61	F	B	Skin melanoma	I	Not described	Panuveitis	Not described	Topical steroid	#22
26	66	M	B	Skin melanoma	I	Not described	Panuveitis	Not described	ICI d/c, Systemic steroid	#22
27b	52	M	B	Skin melanoma	N + I	Not described	Panuveitis, subretinal fluid	Not described	ICI d/c, Topical steroid	#22
28	47	M	B	Skin melanoma	N	Not described	Panuveitis, papilledema	Not described	Systemic steroid, Topical steroid	#22
29	45	M	N/A	Skin melanoma	P	Not described	Panuveitis, subretinal fluid, papillitis	Not described	Systemic steroid, Topical steroid	#22
30	68	F	B	Skin melanoma	P	Not described	Panuveitis, papillitis	Not described	PSTI	#22
31	43	M	N/A	Skin melanoma	P	Previous Dabrafenib/ trametinib	Optic neuritis	Not described	Not described	#22
32	64	F	B	Lung cancer Renal cancer	N	Not described	Panuveitis, papillitis	Not described	ICI d/c, Systemic steroid	#23
33	77	M	B	Skin melanoma	P + I	Not described	Choroidal effusion	POAG, Cataract surgery	ICI d/t, Systemic steroid	#24
34	61	M	B	Lung cancer	P	Not described	Panuveitis, papillitis	Hearing loss Aseptic meningitis	ICI d/c, Systemic steroid	#25
35a	73	M	B	Skin melanoma	P	Not described	Panuveitis, choroidal effusion	Phacovitrectomy for RD, poliosis	ICI d/c, Systemic steroid, Phacovitrectomy with SO tamponade	#26
36a	55	F	B	Skin melanoma Breast cancer	P	Vemurafenib Dabrafenb	Subretinal fluid, no leaks on FAG	Not described	Systemic steroid, Change dabrafenib to trametinib	#27
37a	59	M	B	Skin melanoma	P	Not described	Chorioretinitis, exudative RD, papillitis	HLA-DR4/DRB1*04, vitiligo/Poliosis, aseptic meningitis	ICI d/c, Systemic steroid	#28
38	65	F	B	Skin melanoma	N + I	Not described	Neuroretinitis	Antiretinal autoantibody, diarrhea	IVB, PSTI	#29
39	63	F	B	Skin melanoma	N	Previous Vemurafenib	Panuveitis, papillitis	Headache, Poliosis	ICI d/c, Topical steroid	#30
40	54	F	B	Skin melanoma	I	Not described	Ant. uveitis, mydriasis, choroiditis, SRD	6-Melanoma Helper peptide vaccine, LASIK	ICI d/c, Systemic steroid	#31
41a	54	F	N/A	Choroidal melanoma	P	Not described	Panuveitis, papillitis	Enucleation due to uveal melanoma in right eye	Dexamethasone (Ozurdex®)	#32
42a,c	60	M	B	Skin melanoma	P	Not described but BRAF-WT Tumor	Panuveitis	Cataract surgery (R)	ICI d/c, Systemic steroid	#33
43	60 s	F	B	Skin melanoma	P	Vemurafenib Dabrafenib Trametinib	Panuveitis	Not described	PSTI	#34
44	57	M	B	Skin melanoma	P	Not described	Posterior uveitis	Not described	ICI d/c Systemic steroid	#35
45	78	F	B	Skin melanoma	P	Not described	Posterior uveitis	Hearing loss, Skin rash	ICI d/c Systemic steroid	#35
46	71	F	B	Skin melanoma	N + I	Not described	Panuveitis	Headache, arthralgias, myalgias	ICI d/c Systemic steroid	#35
47	52	M	B	Skin melanoma	N	Not described	Panuveitis	Skin depigmentation	Systemic steroid	#35
48	57	M	B	Lung cancer	N	Not described	Panuveitis	Not described	Topical steroid	#35

In case 43, Birdshot-like chorioretinopathy developed 2 years after the initiation of pembrolizumab treatment

No. number, M male, F female, B both, R right, L left, N/A not applicable, ICI immune checkpoint inhibitor, P pembrolizumab, N nivolumab, I ipilimumab, A atezolizumab, WT wild-type, SRD serous retinal detachment, FAG fluorescein angiography, RPE retinal pigment epithelium, VKH Vogt–Koyanagi–Harada, CWS cotton wool spot, A/C anterior chamber, Ant. Anterior, Post. Posterior, RD retinal detachment, IOP intraocular pressure, irAE immune-related adverse event, LASIK laser-assisted in situ keratomileusis, D diopter, d/c discontinuation, PSTI posterior subtenon triamcinolone injection, IVB intravitreal bevacizumab injection, SO silicone oil, IVT intravitreal steroid

^aNo ocular adverse event with previous ipilimumab therapy

^bSimilar to ocular adverse event associated with BRAF/MEK inhibitor as determined by representative OCT images

^cBilateral panuveitis developed within a week after elective unilateral cataract surgery during pembrolizumab therapy

Discussion

The use of ICIs has led to great advances in cancer therapy. They reverse the immune evasion of cancer cell by blocking the innate immune inhibitory process of T cells [1, 2, 5, 6]. Enhanced T-cell activity has been known to induce various immune responses in other parts of the body, called immune-related complications [7]. These adverse events have also been found in the eye. Intraocular inflammation (uveitis) and dry eye are common, and Graves’s ophthalmopathy is known to occur [3, 36]. In the present study, intraocular inflammation, foveal IZT/SRD, neuro-ophthalmic complications, and retinal vein occlusion were observed.

Foveal IZT/SRD was associated with the use of atezolizumab, but multivariate analysis suggested that it was due to BRAF/MEK inhibitors that were concurrently used. Serous retinal detachments after ICI therapy have been mostly reported in skin melanomas and lung cancers. In these tumors, gain-of-function mutations in members of the MAPK pathway were common [37, 38]. BRAF/MEK inhibitors have been known to cause foveal IZT/SRD without inflammation; thus, it is likely due to BRAF/MEK inhibitors rather than ICIs in the present study [39–41]. Likewise, regarding neuro-ophthalmic complications, all patients presenting with strabismus or ptosis had brain metastases or infarctions in the present study. Foveal IZT/SRD and neuro-ophthalmic complications have been reported after ICI therapy [3]. Our findings suggest that the use of concurrent BRAF/MEK inhibitors and the evaluation of brain lesions should be carefully considered when determining the association between the use of ICIs and OAEs.

Intraocular inflammation, an immune-related OAE, occurs in approximately 1% of patients treated with ICIs [3, 42]. Most intraocular inflammation is known to present as anterior uveitis, but vision-threatening posterior segment complications have been reported [18, 19, 25, 28, 30]. In our study, patients with intraocular inflammation were associated with a history of intraocular trauma/surgery. Furthermore, of 48 cases in our literature review, 27 (56%) cases exhibited a history of ocular surgery or co-occurring systemic immune-related adverse event. These findings suggest that in patients vulnerable to the development of autoimmune disease or sensitized to intraocular antigen, the risk of ICI-related, vision-threatening posterior uveitis is high. Notably, there were several cases to support this possibility. Case 40 had a six-melanoma helper peptide vaccine before developing panuveitis [31]. Case 42 had severe bilateral panuveitis after elective unilateral cataract surgery during pembrolizumab treatment [33].

Distinguishing ICI-related severe uveitis from VKH is often difficult, because the inflammation also exhibit chorioretinitis, exudative retinal detachment, choroidal thickening, poliosis/vitiligo/hypophysitis, and sensorineural hearing loss. The difficulty is aggravated by similarity in responses to steroid treatment. However, in cases of ICI-related complications, the previous reports indicate that discontinuation of the drug often resolves and re-initiation of the drug re-induces the inflammatory response. Thus, the evaluation of underlying medical conditions and evaluation of the prescription will be valuable in distinguishing inflammation from VKH. Considering that VKH is common among Asian population and that it is associated with HLA-DR4, further studies are also needed on racial differences and the role of HLA subtype in intraocular inflammation following ICI treatment.

Recent reports indicate that intravitreous metastasis is an important differential diagnosis to consider in patients suspected to have uveitis following ICI infusion [43, 44]. The reported cases so far are those patients with skin melanoma; similarly, the masquerading uveitis observed in Patient 15 of our study also had underlying skin melanoma. Our study results suggest that in cases of intraocular inflammation after ICI infusion that do not respond to treatment, further investigations such as cytology are needed to verify the presence of vitreoretinal metastasis.

In the present study, all cases involving posterior uveitis occurred after treatment with pembrolizumab, a PD-1 inhibitor. While systemic immune-related adverse events appear to be more common with ipilimumab, a CTLA-4 inhibitor, than with other ICIs, most published cases with serous chorioretinitis/papillitis were associated with the use of PD-1 inhibitors [7]. A recent study involving patients with melanoma reported that PD-1 inhibitors could be safely used after severe ipilimumab-related systemic adverse events [45]. In contrast, we found seven cases with intraocular complications, which were not observed with ipilimumab treatment, that occurred after a change of the drug to pembrolizumab [12, 13, 26–28, 32, 33]. Collectively, these findings suggested that the use of PD-1 inhibitors may increase the chance of severe intraocular inflammation when compared with the use of CTLA-4 or PD-L1 inhibitors. Serious posterior uveitis associated with PD-L1 inhibitors have been rarely reported, which is likely to be because PD-L1 is expressed on the surface of cancer cells, unlike PD-1 or CTLA-4. Since PD-1 is expressed on T cells, activated T cells following PD-1 inhibition may theoretically be involved with ‘off-target’ inflammation more frequently. In most cases with intraocular inflammation with posterior segment complication or VKH-like features, ICI was discontinued, but visual sequelae remained. We think that the discontinuation of ICI treatment should be carefully determined over benefits therapeutic responses and costs of systemic immune-related adverse events.

The use of ICIs is already one of the mainstays of cancer treatment, and their use is increasing. Clinicians should be aware that severe intraocular inflammation can developed after ICI treatment, particularly in patients who have undergone ocular surgery/trauma. The use of BRAF/MEK inhibitors and the presence of brain metastasis should be also examined in patients with OAEs.

Abbreviations

ICI

Immune checkpoint inhibitor

IQR

Interquartile range

IZT

Interdigitation zone thickening

OAE

Ocular adverse event

SRD

Serous retinal detachment

Author contributions

YJK, SCL, and CSL conceived the study. Clinical data collection and interpretation were done by YJK, JSL, JL, SCL, TK, SHB, and CSL. YJK and CSL wrote the manuscript.

Funding

This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) under grant funded by the Korea government (Ministry of Science and ICT) (NRF-2019R1A2C2002393). The funding organization had no role in the design or conduct of this research.

Compliance with ethical standards

Conflict of interest

The authors declare no potential conflicts of interest.

Ethics approval

This study was reviewed and approved by the Institutional Review Board of Severance Hospital, Seoul Korea (approval number: 4-2019-1100).

Informed consent

The requirement for informed consent for the retrospective study was waived by the Institutional Review Board.