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Meningioma WHO I with involvement of the optical structures—does proton therapy lead to changes in quality of life with regard to subjective visual performance?

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Abstract

Background

In addition to local tumor control, the aim of any curative radio-oncological treatment is to maintain quality of life. In the treatment of patients with meningioma with a close relationship to optical structures, the preservation of visual performance is a particular challenge. Use of proton therapy can reduce the dose burden to organs at risk immediately adjacent to the tumor. The aim of this study was to score the subjective assessment of visual performance in patients with meningioma involving the optical structures before and after proton therapy.

Methods

All proton-treated patients with meningioma WHO I whose planning target volumes (PTV) included parts of the optic nerve and/or chiasm were included in this study. Subjective assessment of visual performance was evaluated using the Visual Disorder Scale (VDS) of the EORTC QLQ-BN20 questionnaire. This scale includes values from 0 to 100, whereby high values reflect a high degree of subjective symptom burden and thus subjective visual impairment. The visual acuity in externally performed eye tests at baseline and follow-ups (FU) was also evaluated. The timepoints for testing were before the start of radiotherapy, at the end of treatment, and 3, 6, 12, and 24 months in FU (times t1–t6). All patients with at least the first annual postradiation FU at the time of the evaluation were included. The correlation between VDS changes and potential influencing factors such as previous therapies, dosimetric data, initial tumor volume, and tumor shrinkage 1 year after treatment was assessed.

Results

A total of 56 patients (45 female/11 male) aged 24–82 years (mean ± SD = 53.9 ± 13.3) treated between March 2017 and September 2019 were included in the analysis. The prescription dose was 54.0 Gy (RBE) with active scanned proton therapy. The mean/D2% dose ± SD for the optic chiasm and ipsilateral optic nerve was 43.4 ± 8.9 Gy (RBE)/49.9 ± 7.1 Gy (RBE) and 35.6 ± 11.7 Gy (RBE)/51.7 ± 4.8 Gy (RBE); the mean/D2% dose ± SD of the contralateral optic nerve was 18.8 ± 12.1 Gy (RBE)/42.4 ± 14.6 Gy (RBE), respectively. A total of 302 data collections were available (t1/t2/t3/t4/t5/t6: n = 56/56/48/56/52/34). Median observation time was 23.6 months. Mean symptom burden decreased over time (mean VDS: t1 29.8 ± 27.9; t2 25.0 ± 27.9; t3 21.8 ± 26.0; t4 22.2 ± 26.0; t5 21.4 ± 26.2; t6 17.3 ± 23.6) with statistically significant improvement at 3‑ and 6‑month FU as well as 1 year after proton therapy (p = 0.0205; p = 0.0187; p = 0.0054). Objective eye tests available in 41/52 patients confirm the trend towards improved visual acuity (97.5% stable/improved until 24-month FU). However, no potential predictor for VDS changes was revealed.

Conclusion

Proton treatment of patients with meningioma WHO I with involvement of optical structures does not impair subjective visual performance. After treatment, there is a significant improvement in perceived visual performance.

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References

  1. Ostrom QT, Patil N, Cioffi G, Waite K, Kruchko C, Barnholtz-Sloan JS (2020) CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2013–2017. Neuro Oncol 22(12 Suppl 2):iv1–iv96

    Article  PubMed  PubMed Central  Google Scholar 

  2. Nayeni M, Dang A, Mao AJ, Malvankar-Mehta MS (2021) Quality of life of low vision patients: a systematic review and meta-analysis. Can J Ophthalmol 56(3):151–157. https://doi.org/10.1016/j.jcjo.2020.10.014

    Article  PubMed  Google Scholar 

  3. Karsy M, Jensen MR, Guan J, Ravindra VM, Bisson EF, Couldwell WT (2019) EQ-5D quality-of-life analysis and cost-effectiveness after skull base meningioma resection. Neurosurgery 85(3):E543–E552. https://doi.org/10.1093/neuros/nyz040

    Article  PubMed  Google Scholar 

  4. Haider S, Taphoorn MJB, Drummond KJ, Walbert T (2021) Health-related quality of life in meningioma. Neuro Oncol Adv 3(1):vdab89. https://doi.org/10.1093/noajnl/vdab089

    Article  Google Scholar 

  5. Fabian A, Domschikowski J, Greiner W, Bockelmann G, Karsten E, Rühle A, Nicolay NH, Grosu AL, Dunst J, Krug D (2022) Financial toxicity in cancer patients treated with radiotherapy in Germany—a cross-sectional study. Strahlenther Onkol. https://doi.org/10.1007/s00066-022-01936-z

    Article  PubMed  PubMed Central  Google Scholar 

  6. Sindou M, Nebbal M, Guclu B (2015) Cavernous sinus meningiomas: imaging and surgical strategy. Adv Tech Stand Neurosurg 42:103–121. https://doi.org/10.1007/978-3-319-09066-5_6

    Article  PubMed  Google Scholar 

  7. Noel G, Gondi V (2016) Proton therapy for tumors of the base of the skull. Chin Clin Oncol 5(4):51. https://doi.org/10.21037/cco.2016.07.05

    Article  PubMed  Google Scholar 

  8. Combs SE (2017) Does proton therapy have a future in CNS tumors? Curr Treat Options Neurol 19(3):12. https://doi.org/10.1007/s11940-017-0447-4

    Article  PubMed  Google Scholar 

  9. Albrecht F, Wolters H, Ziert Y, Timmermann B, Kortmann RD, Matuschek C, Rübe C, Martini C, Christiansen H, Eich HT, Willich N, Steinmann D (2021) Evaluation of treatment-associated eye toxicity after irradiation in childhood and adolescence-results from the registry of the evaluation of side effects after radiotherapy in childhood and adolescence (RiSK). Strahlenther Onkol 197(8):700–710. https://doi.org/10.1007/s00066-021-01793-2

    Article  PubMed  PubMed Central  Google Scholar 

  10. Ahmed KA, Demetriou SK, McDonald M, Johnstone PA (2016) Clinical benefits of proton beam therapy for tumors of the skull base. Cancer Control 23(3):213–219. https://doi.org/10.1177/107327481602300304

    Article  PubMed  Google Scholar 

  11. Margolis MK, Coyne K, Kennedy-Martin T, Baker T, Schein O, Revicki DA (2002) Vision-specific instruments for the assessment of health-related quality of life and visual functioning: a literature review. PharmacoEconomics 20(12):791–812. https://doi.org/10.2165/00019053-200220120-00001

    Article  PubMed  Google Scholar 

  12. Taphoorn MJ, Claassens L, Aaronson NK, Coens C, Mauer M, Osoba D, Stupp R, Mirimanoff RO, van den Bent MJ, Bottomley A (2010) An international validation study of the EORTC brain cancer module (EORTC QLQ-BN20) for assessing health-related quality of life and symptoms in brain cancer patients. Eur J Cancer 46(6):1033–1040. https://doi.org/10.1016/j.ejca .2010.01.012

    Article  PubMed  Google Scholar 

  13. Maringwa J, Quinten C, King M, Ringash J, Osoba D, Coens C, Martinelli F, Reeve BB, Gotay C, Greimel E, Flechtner H, Cleeland CS, Schmucker-Von Koch J, Weis J, Van Den Bent MJ, Stupp R, Taphoorn MJ, Bottomley A (2011) Minimal clinically meaningful differences for the EORTC QLQ-C30 and EORTC QLQ-BN20 scales in brain cancer patients. Ann Oncol 22(9):2107–2112. https://doi.org/10.1093/annonc/mdq726

    Article  CAS  PubMed  Google Scholar 

  14. Osoba D, Rodrigues G, Myles J, Zee B, Pater J (1998) Interpreting the significance of changes in health-related quality-of-life scores. J Clin Oncol 16(1):139–144. https://doi.org/10.1200/JCO.1998.16.1.139

    Article  CAS  PubMed  Google Scholar 

  15. El Shafie RA, Czech M, Kessel KA, Habermehl D, Weber D, Rieken S, Bougatf N, Jäkel O, Debus J, Combs SE (2018) Clinical outcome after particle therapy for meningiomas of the skull base: toxicity and local control in patients treated with active rasterscanning. Radiat Oncol 13(1):54. https://doi.org/10.1186/s13014-018-1002-5

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Vernimmen FJ, Harris JK, Wilson JA, Melvill R, Smit BJ, Slabbert JP (2001) Stereotactic proton beam therapy of skull base meningiomas. Int J Radiat Oncol Biol Phys 49(1):99–105. https://doi.org/10.1016/S0360-3016(00)01457-7

    Article  CAS  PubMed  Google Scholar 

  17. Weber DC, Lomax AJ, Rutz HP, Stadelmann O, Egger E, Timmermann B, Pedroni ES, Verwey J, Miralbell R, Goitein G (2004) Spot-scanning proton radiation therapy for recurrent, residual or untreated intracranial meningiomas. Radiother Oncol 71(3):251–258. https://doi.org/10.1016/j.radonc.2004.02.011

    Article  PubMed  Google Scholar 

  18. Vaishnav YJ, Singh R, Didwania P, Lehrer EJ, Bakaeva T, Harris TJ, Migliori ME, Sheehan JP, Trifiletti DM (2022) Radiotherapy and radiosurgery in the management of optic nerve sheath meningiomas: an international systematic review and meta-analysis of twenty studies. World Neurosurg 164:e929–e944. https://doi.org/10.1016/j.wneu.2022.05.064

    Article  PubMed  Google Scholar 

  19. Marchetti M, Conti A, Beltramo G, Pinzi V, Pontoriero A, Tramacere I, Senger C, Pergolizzi S, Fariselli L (2019) Multisession radiosurgery for perioptic meningiomas: medium-to-long term results from a CyberKnife cooperative study. J Neurooncol 143(3):597–604. https://doi.org/10.1007/s11060-019-03196-x

    Article  PubMed  Google Scholar 

  20. Kheir V, Faouzi M, Borruat FX (2019) Visual outcomes of fractionated radiotherapy in optic nerve sheath meningioma: a retrospective study. Klin Monbl Augenheilkd 236(4):526–529. https://doi.org/10.1055/a-0828-7335

    Article  PubMed  Google Scholar 

  21. Combs SE, Adeberg S, Dittmar JO, Welzel T, Rieken S, Habermehl D, Huber PE, Debus J (2013) Skull base meningiomas: Long-term results and patient self-reported outcome in 507 patients treated with fractionated stereotactic radiotherapy (FSRT) or intensity modulated radiotherapy (IMRT). Radiother Oncol 106(2):186–191. https://doi.org/10.1016/j.radonc.2012.07.008

    Article  PubMed  Google Scholar 

  22. Castle-Kirszbaum M, Kam J, Dixon B, Goldschlager T, King J, Wang YY (2022) Surgical outcomes and longitudinal quality of life after endoscopic endonasal surgery for anterior skull base meningioma. J Neurosurg. https://doi.org/10.3171/2021.11.JNS212090

    Article  PubMed  Google Scholar 

  23. Pintea B, Boström A, Katsigiannis S, Gousias K, Pintea R, Baumert B, Boström J (2021) Prognostic factors for functional outcome of patients with optic nerve sheath meningiomas treated with stereotactic radiotherapy-evaluation of own and meta-analysis of published data. Cancers 13(3):522. https://doi.org/10.3390/cancers13030522

    Article  PubMed  PubMed Central  Google Scholar 

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Correspondence to Carola Lütgendorf-Caucig.

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B. Flechl, L. Konrath, E. Hug, P. Fossati, C. Lütgendorf-Caucig, M. Achtaewa, M. Pelak, and P. Georg declare that they have no competing interests.

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Flechl, B., Konrath, L., Hug, E. et al. Meningioma WHO I with involvement of the optical structures—does proton therapy lead to changes in quality of life with regard to subjective visual performance?. Strahlenther Onkol 199, 404–411 (2023). https://doi.org/10.1007/s00066-022-02024-y

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