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. 2015 Oct 20;18(4):575–581. doi: 10.1093/neuonc/nov253

Table 1.

Management of patients with disease recurrence and subsequent outcomes

Pt CR1 Duration, mo Site of First Progression Second-line Rx Resp Third-line Rx Resp ASCT Outcome
1 41 Vitreous R-HD-MTX, i.t. MTX, intravitreal R CR R-BEAM PD ASCT +8 mo (vitreous) treated with intravitreal R, i.t. R/MTX → CR in remission at 32 mo from 2nd relapse
2 10 Vitreous Intravitreal MTX PD I.t. + intravitreal R CR GemBuMel PD ASCT +11 mo (cerebellum) treated with R-i.t. AC + i.t. R → PD; WBRT 30.6 Gy; posterior fossa boost +9 Gy → CR in remission +33 mo from 2nd relapse
3 5 Vitreous, optic nerve R-MPV ×3 PD Died from PD
5 35 Frontal lobe R-HD-MTX ×3 PD Died from septic shock/multi-organ failure
6 40 Temporoparietal lobe R-MPV × 5 CR Thiotepa, carmustine, R In remission ASCT +4 mo
10 10 Leptomeningeal R-HDAC ×2 + i.t. MTX PD R-temozolomide + i.t. MTX CR R-BEAM In remission ASCT +6 mo
11 9 Cerebelluma R-HD-MTX ×4 CR In remission HD-MTX +1 mo

Abbreviations: Pt, patient; Rx, treatment; MTX, methotrexate; HD, high-dose; R, rituximab; resp, response; PD, progressive disease; BEAM, carmustine, etoposide, cytarabine, melphalan; GemBuMel, gemcitabine, busulfan, melphalan; AC, cytarabine; WBRT, whole brain radiotherapy.

a

Not biopsy proven, as the site of suspected involvement was deemed unsafe for stereotactic biopsy and CSF negative.