The purpose of this study is to measure the rate of complete response (CR and UCR) at the end of a course of immuno-chemotherapy: * before cerebral radiotherapy for PCL * after the course of immuno-chemotherapy for aggressive lymphomas with neuromeningeal involvement Toxicity of the protocol Overall survival Survival without relapse Long-term incidence of neurocognitive toxicity
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
375 mg/m2 D1
50 mg D3
ZNA Stuivenberg
Antwerp, Belgium
Hôpital Saint Joseph
Arlon, Belgium
A. Z. Sint-Jan
Bruges, Belgium
UCL- Saint Luc
Brussels, Belgium
CH Notre Dame
Charleroi, Belgium
AZ VUB
Jette, Belgium
Response to treatment (CR/PR)
Time frame: End of treatment - 5 months
Toxicity, Overall survival, Time to progression
Time frame: End of study - 5 years
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CHR de la Citadelle
Liège, Belgium
CHU Charleroi-Vésale
Montigny-le-Tilleul, Belgium
Clinique Saint Pierre
Ottignies, Belgium
Heilig Hart Ziekenhuis
Roeselare, Belgium
...and 36 more locations