Treatment strategies in primary vitreoretinal lymphoma: a 17-center European collaborative study

Publication date

2015-02

Authors

Riemens, AnjoISNI 0000000419547217
Bromberg, Jacoline
Touitou, Valerie
Sobolewska, Bianka
Missotten, Tom
Baarsma, Seerp
Hoyng, Carel
Cordero-Coma, Miguel
Tomkins-Netzer, Oren
Rozalski, Anna

Editors

Advisors

Supervisors

Document Type

Article

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License

taverne

Abstract

IMPORTANCE: The best treatment option for primary vitreoretinal lymphoma (PVRL) without signs of central nervous system lymphoma (CNSL) involvement determined on magnetic resonance imaging or in cerebrospinal fluid is unknown. OBJECTIVE: To evaluate the outcomes of treatment regimens used for PVRL in the prevention of subsequent CNSL. DESIGN, SETTING, AND PARTICIPANTS: A retrospective cohort study was conducted at 17 referral ophthalmologic centers in Europe. We reviewed clinical, laboratory, and imaging data on 78 patients with PVRL who did not have CNSL on presentation between January 1, 1991, and December 31, 2012, with a focus on the incidence of CNS manifestations during the follow-up period. INTERVENTIONS: The term extensive treatment was used for various combinations of systemic and intrathecal chemotherapy, whole-brain radiotherapy, and peripheral blood stem cell transplantation. Therapy to prevent CNSL included ocular radiotherapy and/or ocular chemotherapy (group A, 31 patients), extensive systemic treatment (group B, 21 patients), and a combination of ocular and extensive treatment (group C, 23 patients); 3 patients did not receive treatment. A total of 40 patients received systemic chemotherapy. MAIN OUTCOMES AND MEASURES: Development of CNSL following the diagnosis of PVRL relative to the use or nonuse of systemic chemotherapy and other treatment regimens. RESULTS: Overall, CNSL developed in 28 of 78 patients (36%) at a median follow-up of 49 months. Specifically, CNSL developed in 10 of 31 (32%) in group A, 9 of 21 (43%) in group B, and 9 of 23 (39%) in group C. The 5-year cumulative survival rate was lower in patients with CNSL (35% [95% CI, 50% to 86%]) than in patients without CNSL (68% [95% CI, 19% to 51%]; P = .003) and was similar among all treatment groups (P = .10). Adverse systemic effects occurred in 9 of 40 (23%) patients receiving systemic chemotherapy; the most common of these effects was acute renal failure. CONCLUSIONS AND RELEVANCE: In the present series of patients with isolated PVRL, the use of systemic chemotherapy was not proven to prevent CNSL and was associated with more severe adverse effects compared with local treatment.

Keywords

Adult, Aged, Aged, 80 and over, Biopsy, Cause of Death, Combined Modality Therapy, Disease-Free Survival, Europe, Female, Follow-Up Studies, Humans, Lymphoma, Non-Hodgkin, Male, Middle Aged, Practice Guidelines as Topic, Retinal Neoplasms, Retrospective Studies, Survival Rate, Time Factors, Treatment Outcome, Vitreous Body, Taverne, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't

Citation

Riemens, A, Bromberg, J, Touitou, V, Sobolewska, B, Missotten, T, Baarsma, S, Hoyng, C, Cordero-Coma, M, Tomkins-Netzer, O, Rozalski, A, Tugal-Tutkun, I, Guex-Crosier, Y, Los, L I, Bollemeijer, J G, Nolan, A, Pawade, J, Willermain, F, Bodaghi, B, ten Dam-van Loon, N, Dick, A, Zierhut, M, Lightman, S, Mackensen, F, Moulin, A, Erckens, R, Wensing, B, le Hoang, P, Lokhorst, H & Rothova, A 2015, 'Treatment strategies in primary vitreoretinal lymphoma : a 17-center European collaborative study', JAMA Ophthalmology, vol. 133, no. 2, pp. 191-197. https://doi.org/10.1001/jamaophthalmol.2014.4755