Skip to main content

Advertisement

Log in

Predictive risk factors for radiation retinopathy and optic neuropathy after proton beam therapy for uveal melanoma

  • Oncology
  • Published:
Graefe's Archive for Clinical and Experimental Ophthalmology Aims and scope Submit manuscript

Abstract

Purpose

This study was performed in order to evaluate the incidence of radiation retinopathy and optic neuropathy occurring after proton beam therapy for uveal melanoma.

Methods

Included in this study were all patients who had been treated with primary proton beam therapy for uveal melanoma at the oncology service between May 1998 and June 2014 with a minimum follow-up of 12 months. Excluded were all patients who underwent re-irradiation, or vitrectomy due to exudative retinal detachment or for tumor-resection.

Results

During this period, 1127 patients matched the inclusion criteria, of whom 768 (68.1 %) and 463 (41.0 %) developed radiation retinopathy and optic neuropathy after a median time of 18.9 months (2.0–99.84 months) and 19.8 months (0.2–170.4 months), respectively. Mean follow-up was 53.4 months (12–170.4 months). Included were 558 men (49.5 %) and 569 women (50.5 %). Mean age was 61 years (16–89 years). Visual acuity slightly decreased from initial levels of 0.3 logMAR–0.4 logMAR in patients without developing any radiation-induced complication but severely decreased to 1.0 logMAR or 1.5 logMAR in the case of developing radiation retinopathy only or optic neuropathy, respectively. Independent risk factors for radiation retinopathy were a centrally (<2.5 mm from sensitive structures) located tumor or a thick tumor located more than 2.5 mm from sensitive structures, while those for radiation optic neuropathy comprised a short distance and applied dose to the optic disk.

Conclusion

The risk for radiation retinopathy is higher in central uveal melanoma.

Mid-/peripheral tumors are at high risk for radiation retinopathy and maculopathy if presenting with increased thickness.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Denker A, Cordini D, Heufelder J et al (2007) On accelerator applications in medicine and cultural heritage. Nucl Inst Methods Phys Res A 580:457–461

    Article  CAS  Google Scholar 

  2. Goitein M, Miller T (1983) Planning proton therapy of the eye. Med Phys 10(3):275–83

    Article  CAS  PubMed  Google Scholar 

  3. Dobler B, Bendl R (2002) Precise modelling of the eye for proton therapy of intra-ocular tumours. Phys Med Biol. 21;47(4):593–613

  4. Brown GC, Shields JA, Sanborn G et al (1982) Radiation retinopathy. Ophthalmology 89:1489–1493

    Article  CAS  PubMed  Google Scholar 

  5. Gündüz K, Shields CL, Shields JA et al (1999) Radiation retinopathy following plaque radiotherapy for posterior uveal melanoma. Arch Ophthalmol 117:609–614

    Article  PubMed  Google Scholar 

  6. Bechrakis NE, Foerster MH (2006) Neoadjuvant proton beam radiotherapy combined with subsequent endoresection of choroidal melanomas. Int Ophthalmol Clin 46:95–107

    Article  PubMed  Google Scholar 

  7. Seibel I, Cordini D, Willerding G et al (2015) Endodrainage, tumor photocoagulation, and silicone oil tamponade for primary exudative retinal detachment due to choroidal melanoma persisting after proton beam therapy. Ocul Oncol Pathol 1:24–33

    Article  Google Scholar 

  8. Riechardt AI, Cordini D, Willerding GD et al (2014) Proton beam therapy of parapapilllary choroidal melanoma. Am J Ophthalmol 157:1258–1265

    Article  PubMed  Google Scholar 

  9. Sagoo MS, Shields CL, Emrich J et al (2014) Plaque radiotherapy for juxtapapillary choroidal melanoma: treatment complications and visual outcomes in 650 consecutive cases. JAMA Ophthalmol 132:697–702

    Article  PubMed  Google Scholar 

  10. Finger PT (2000) Tumour location affects the incidence of cataract and retinopathy after ophthalmic plaque radiation therapy. Br J Ophthalmol 84:1068–1070

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Egbert PR, Fajardo LF, Donaldson SS et al (1980) Posterior ocular abnormalities after irradiation for retinoblastoma: a histopathological study. Br J Ophthalmol 64:660–665

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Archer D Doyne Lecture (1993) response of retinal and choroidal vessels to ionizing radiation. Eye 71–113

  13. Kinyoun JL (2008) Long-term visual acuity results of treated and untreated radiation retinopathy (an AOS thesis). Trans Am Ophthalmol Soc 106:325–335

    PubMed  PubMed Central  Google Scholar 

  14. Kim IK, Lane AM, Egan KM et al (2010) Natural history of radiation papillopathy after proton beam irradiation of parapapillary melanoma. Ophthalmology 117:1617–22

    Article  PubMed  Google Scholar 

  15. Finger PT, Chin KJ, Yu GP et al (2010) Palladium-103 for Choroidal Melanoma Study G, Risk factors for radiation maculopathy after ophthalmic plaque radiation for choroidal melanoma. Am J Ophthalmol 149:608–615

    Article  PubMed  Google Scholar 

  16. Damato BE (2012) Local resection of uveal melanoma. Dev Ophthalmol 49:66–80. doi:10.1159/000328261.Epub2011

    Article  PubMed  Google Scholar 

  17. Jager MJ, Desjardins L, Kivelä T et al (2012) Current Concepts in Uveal Melanoma. Dev Ophthalmol Basel, Karger 49:41–57

    Google Scholar 

  18. Schönfeld S, Cordini D, Riechardt AI et al (2014) Proton beam therapy leads to excellent local control rates in choroidal melanoma in the intermediate fundus zone. Am J Ophthalmol 158:1184–91

    Article  PubMed  Google Scholar 

  19. Gragoudas ES, Li W, Lane AM et al (1999) Risk factors for radiation maculopathy and papillopathy after intraocular irradiation. Ophthalmology 106:1572–1578

    Article  Google Scholar 

  20. Hayreh SS (2015) Ocular vascular occlusive disorders. Blood supply of the optic nerve head, vol 5. Springer International Publishing, Switzerland, pp 103–110

    Google Scholar 

Download references

Acknowledgments

Statistical analysis was performed by Dr. Ulrich Gauger, medical statistician, Berlin, Germany

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ira Seibel.

Ethics declarations

Funding

No funding was received for this research

Conflict of interest statement

Prof. A. Joussen and Dr. M. Rehak report personal fees from Bayer, personal fees from Novartis, and personal fees from Allergan, outside the submitted work. All other authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. For this type of study formal consent is not required.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Seibel, I., Cordini, D., Hager, A. et al. Predictive risk factors for radiation retinopathy and optic neuropathy after proton beam therapy for uveal melanoma. Graefes Arch Clin Exp Ophthalmol 254, 1787–1792 (2016). https://doi.org/10.1007/s00417-016-3429-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00417-016-3429-4

Keywords

Navigation