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Various clinical presentations of uveitis associated with durvalumab treatment Cover

Various clinical presentations of uveitis associated with durvalumab treatment

Open Access
|Apr 2022

Figures & Tables

Figure 1

Case I. Fundoscopy, at presentation, on one-week and five-week follow-up. Follow-up images show diminishment of vitreous haze and regression of optic disc swelling.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)
Case I. Fundoscopy, at presentation, on one-week and five-week follow-up. Follow-up images show diminishment of vitreous haze and regression of optic disc swelling.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)

Figure 2

Case I. Optical coherence tomography (OCT) of optic discs. Optic disc drusen at presentation and on a five-week follow-up. No alteration in optic disc drusen size is visible. Up images show diminishment of vitreous haze and regression of optic disc swelling.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)
Case I. Optical coherence tomography (OCT) of optic discs. Optic disc drusen at presentation and on a five-week follow-up. No alteration in optic disc drusen size is visible. Up images show diminishment of vitreous haze and regression of optic disc swelling.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)

Figure 3

Case I. Fluorescein angiography at presentation. Early and late frames. Contrast blockage in the upper temporal part of the right optic disc (white arrow), corresponding to a peripapillary haemorrhage. Hypofluorescent dots (black arrow) corresponded to hyperreflective spots on optical coherence tomography (OCT). Fluorescein angiography five weeks on methylprednisolone treatment. Early and late frames. Diminishment of the contrast blockage in the upper temporal part of the right optic disc (white arrow) corresponding to a peripapillary haemorrhage. Hypofluorescent dots (black arrow) are less prominent.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)
Case I. Fluorescein angiography at presentation. Early and late frames. Contrast blockage in the upper temporal part of the right optic disc (white arrow), corresponding to a peripapillary haemorrhage. Hypofluorescent dots (black arrow) corresponded to hyperreflective spots on optical coherence tomography (OCT). Fluorescein angiography five weeks on methylprednisolone treatment. Early and late frames. Diminishment of the contrast blockage in the upper temporal part of the right optic disc (white arrow) corresponding to a peripapillary haemorrhage. Hypofluorescent dots (black arrow) are less prominent.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)

Figure 4

Case I. Optical coherence tomography (OCT) of optic discs, at presentation, one week on methylprednisolone treatment, five weeks on methylprednisolone treatment. Follow-up shows regression of optic disc swelling.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)
Case I. Optical coherence tomography (OCT) of optic discs, at presentation, one week on methylprednisolone treatment, five weeks on methylprednisolone treatment. Follow-up shows regression of optic disc swelling.OD(R) = oculus dexter (right); OS(L) = oculus sinister (left)

Figure 5

Case II. (A) Fundoscopy, prior to non-small cell lung cancer diagnosis in 2013: posterior pole and peripheral retinal changes. (B) Colour fundus photography at presentation in March 2021: multiple flat, grey-white lesions (black arrows) are visible at presentation. (C) Three weeks on methylprednisolone treatment in April 2021: a diminishment of lesions (white arrows) is observed.OD = oculus dexter; OS(L) = oculus sinister
Case II. (A) Fundoscopy, prior to non-small cell lung cancer diagnosis in 2013: posterior pole and peripheral retinal changes. (B) Colour fundus photography at presentation in March 2021: multiple flat, grey-white lesions (black arrows) are visible at presentation. (C) Three weeks on methylprednisolone treatment in April 2021: a diminishment of lesions (white arrows) is observed.OD = oculus dexter; OS(L) = oculus sinister

Figure 6

Case II. (A) Macular optical coherence tomography (OCT) presentation and (B) two weeks on methylprednisolone treatment. Loss of ellipsoid zone and hyperreflective haze in outer plexiform and outer nuclear layers is evident at presentation. Indocyanine angiography at presentation shows hypofluorescent lesions corresponding to ellipsoid zone disruptions (white arrows). Two weeks on methylprednisolone treatment ellipsoid zone appears granular.OD = oculus dexter; OS(L) = oculus sinister
Case II. (A) Macular optical coherence tomography (OCT) presentation and (B) two weeks on methylprednisolone treatment. Loss of ellipsoid zone and hyperreflective haze in outer plexiform and outer nuclear layers is evident at presentation. Indocyanine angiography at presentation shows hypofluorescent lesions corresponding to ellipsoid zone disruptions (white arrows). Two weeks on methylprednisolone treatment ellipsoid zone appears granular.OD = oculus dexter; OS(L) = oculus sinister

Figure 7

Case II. Fluorescein angiography at presentation, early and late frames. Note surface capillary net dilatation and late staining of the papilla and hypofluorescent areas on the posterior pole and periphery. Indocyanine angiography at presentation showing hypofluorescent lesions.OD = oculus dexter; OS(L) = oculus sinister
Case II. Fluorescein angiography at presentation, early and late frames. Note surface capillary net dilatation and late staining of the papilla and hypofluorescent areas on the posterior pole and periphery. Indocyanine angiography at presentation showing hypofluorescent lesions.OD = oculus dexter; OS(L) = oculus sinister

Figure 8

Case II. Fundus autofluorescence images at presentation show no pathologic changes. Hyperautofluorescent spots are visible three weeks on methylprednisolone treatment.AF = fundus autofluorescence; OD = oculus dexter; OS(L) = oculus sinister
Case II. Fundus autofluorescence images at presentation show no pathologic changes. Hyperautofluorescent spots are visible three weeks on methylprednisolone treatment.AF = fundus autofluorescence; OD = oculus dexter; OS(L) = oculus sinister

Published cases reporting uveitis secondary to durvalumab (PD-L1 inhibitor) treatment

Author, yearNumber of cases reportedIndicationOcular inflammation specification (% eyes)TreatmentDiscontinuing immune checkpoint inhibitor
Dow et al. 202063n/aAnterior uveitis 80%Posterior uveitis 20%Local corticosteroidSystemic corticosteroidNo
Parikh et al., 202071Non-small cell lung cancerAnterior uveitisLocal corticosteroidYes
Andrade et al., 202081Non-small cell lung cancerRetinal vasculitisSystemic corticosteroidYes
Vrabic et al., 20212Small cell lung cancer, non-small cell lung cancerIntermediate uveitis, Posterior uveitisSystemic corticosteroidYes

Published cases reporting uveitis and optic disc oedema/papillitis secondary to other immune checkpoint inhibitors

Author, yearImmune checkpoint inhibitorTarget receptorCancer diagnosisClinical findings at presentationComplicationsInitial treatmentDiscontinuing immune checkpoint inhibitor
Hahn et al., 20169IpilimumabCTLA-4Malignant melanomaAC inflammation, keratic precipitatesPanuveitis, papillitis, intraretinal, subfoveal fluidTopical prednisolone acetate, brimonidine tartrate timolol maleate, oral prednisolone 20 mg/dayDiscontinued
Aaberg et al., 201710PembrolizumabPD-1Uveal melanomaAC inflammation, vitreous cells and hazeOptic disc oedema, posterior uveitis, retinal vasculitisIntraocular dexamethasone implantNo.
Wang et al., 201911NivolumabPD-1Renal carcinomaAC inflammation, keratoprecipitates, posterior synechiae, vitreous floatersPanuveitis, papillitis, serous retinal detachmentIntravenous methylprednisolone 500 mg/day, followed by oral prednisolone 30 mg/day tapered over 2 months; recurrence of uveitis managed with periocular methylprednisolone, and intraocular dexamethasone implantDiscontinued, resumed 6 weeks after discontinuation, recurrence of uveitis 2 weeks after resumption
Reid et al., 201812PembrolizumabPD-1Malignant melanomaAC vitreous inflammation, cells, choroidal thickening, posterior synechiaePanuveitis, optic disc oedema, hypotonyOral prednisolone 75 mg/day 7 days, tapered over 3 weeksDiscontinued after 12 months commenced on nivolumab therapy
Navarro- Perea et al., 201913PembrolizumabPD-1Malignant melanomaAC inflammation, irido-crystalline synechiaeOptic disc oedemaTopical dexamethasone, cyclopentolate, tropicamide, phenylephrine, oral prednisolone 40 mg/day tapered over 2 monthsDiscontinued, replaced by vemurafenib and cobimetinib
Sun et al., 20205NivolumabPD-1Malignant melanomaAC inflammation, vitreous cells, and hazeOptic disc oedema, ocular hypertensionTopical prednisolone acetate, oral prednisolone 60 mg/dayn/a
Sun 2020et 5 al.,PembrolizumabPD-1Malignant melanomaAC inflammationHypotony, PapillitisTopical difluprednate, subtenon triamcinolone acetoniden/a
Sun et al., 20205IpilimumabPD-1Malignant melanomaAC inflammation, vitreous cellsMacular oedema, PapillitisTiamcinolonetransseptal followed by retrobulbar)n/a
Kim et al., 202014PembrolizumabPD-1Renal carcinoman/aPanuveitis, papillitisTopical steroid, posterior subtenon triamcinolone injectionDiscontinued
Kim 2020et 14 al.,PembrolizumabPD-1Uveal melanoman/aPanuveitis, papillitisSystemic steroidDiscontinued
Kim 2020et 14 al.PembrolizumabPD-1Lung cancern/aPanuveitis, uveal effusion papillitis,Systemic steroidDiscontinued
Kikuchi et al. 202015NivolumabPD-1Hypopharyngeal cancerGranulomatous mutton-fat keratic precipitates, AC inflammation, posterior synechiaePanuveitis, papillitis, serous retinal detachment; Vogt- Koyanagi-Harada disease-like uveitisSub-tenon triamcinolone acetonide, followed by methylprednisolone 1000 mg/day 3 days, followed by oral methylprednisolone 50 mg/day tapered by 5 mg every weekDiscontinued due to the patient’s deteriorating health
Vrabic et al.durvalumabPDL-1NSCLCAC inflammation, vitreous cellsIntermediate uveitis, optic dics oedemaSystemic steroid 500 mg/day 3 days, followed by oral methylprednisolone 48 mg/day tapered over 6 weeksDiscontinued
DOI: https://doi.org/10.2478/raon-2022-0007 | Journal eISSN: 1581-3207 | Journal ISSN: 1318-2099
Language: English
Page range: 129 - 137
Submitted on: Nov 24, 2021
Accepted on: Jan 10, 2022
Published on: Apr 12, 2022
Published by: Association of Radiology and Oncology
In partnership with: Paradigm Publishing Services
Publication frequency: 4 times per year

© 2022 Nika Vrabic, Ana Fakin, Polona Jaki Mekjavic, Urska Janzic, Martina Vrankar, Natasa Vidovic Valentincic, published by Association of Radiology and Oncology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.