Table 4

PFS, OS, and cumulative incidence of CNS progression according to test results for occult leptomeningeal dissemination

Crude
Adjusted*
HR95% CIHR95% CI
PFS 
    Test for occult leptomeningeal dissemination     
        Both negative   
        FCM+ and CC 1.28 0.56-2.94 1.2 0.49-2.94 
        Both positive 3.86 1.77-8.45 3.14 1.32-7.46 
    FCM test 
        Negative   
        Positive 2.00 1.11-3.6 1.8 0.93-3.5 
OS 
    Test for occult leptomeningeal dissemination     
        Both negative   
        FCM+ and CC 1.08 0.43-2.71 0.94 0.36-2.45 
        Both positive 4.49 2.03-9.92 3.51 1.43-8.66 
    FCM test 
        Negative   
        Positive 1.95 1.05-3.63 1.59 0.8-3.18 
Cumulative incidence of CNS progression     
    Test for occult leptomeningeal dissemination     
        Both negative    
        FCM+ and CC 8.16 1.45-46 49.59 1.94-1269.48 
        Both positive 6.00 0.68-53.28 14.94 1.4-159.27 
    FCM test     
        Negative    
        Positive 7.29 1.63-32.6 23.75 2.83-199.54 
Crude
Adjusted*
HR95% CIHR95% CI
PFS 
    Test for occult leptomeningeal dissemination     
        Both negative   
        FCM+ and CC 1.28 0.56-2.94 1.2 0.49-2.94 
        Both positive 3.86 1.77-8.45 3.14 1.32-7.46 
    FCM test 
        Negative   
        Positive 2.00 1.11-3.6 1.8 0.93-3.5 
OS 
    Test for occult leptomeningeal dissemination     
        Both negative   
        FCM+ and CC 1.08 0.43-2.71 0.94 0.36-2.45 
        Both positive 4.49 2.03-9.92 3.51 1.43-8.66 
    FCM test 
        Negative   
        Positive 1.95 1.05-3.63 1.59 0.8-3.18 
Cumulative incidence of CNS progression     
    Test for occult leptomeningeal dissemination     
        Both negative    
        FCM+ and CC 8.16 1.45-46 49.59 1.94-1269.48 
        Both positive 6.00 0.68-53.28 14.94 1.4-159.27 
    FCM test     
        Negative    
        Positive 7.29 1.63-32.6 23.75 2.83-199.54 
*

Effects on PFS and OS were adjusted for IPI, B symptoms, methotrexate treatment, and cytarabine treatment; effects on cumulative incidence of CNS progression were adjusted for methotrexate treatment and cytarabine treatment.

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