Biological, clinical, and radiologic characteristics of patients at diagnosis of CNSi and outcome on ibrutinib
. | Patient 1 . | Patient 2 . | Patient 3 . | Patient 4 . |
---|---|---|---|---|
Age (y)/sex | 58/M | 75/M | 63/M | 68/F |
Prior lines of therapy for CLL | 8 | 4 | 2 | 0 |
Binet stage at CNSi | C | B | C | A |
Lymphocytosis at CNSi (G/L) | 20 | 0.9 | 245 | 5.5 |
Progressive disease at CNSi diagnosis | Yes | No | Yes | No |
Del17p | Yes | Yes | No | Yes |
Neurologic symptoms | Dysautonomy | Headache and cognitive disturbance | Cerebellar syndrome and aphasia confusion | Visual loss |
Last neuroimaging before ibrutinib initiation | Nodular enhancement of left parietal lobe with not specific periventricular T2 hyperintensities | Normal | NA | Thickening of optic nerves and chiasma. FLAIR hyperintensities |
with nodular lesion of internal occipito-temporal region | ||||
CSF cellularity (μ−1) | 22 | 231 | 176 | 52 |
CSF involvement | 93% monoclonal B cells | 78% monoclonal B cells | 96% monoclonal B cells | 0.7% CLL cells and 91% CD4+ T cells |
Red cells (μ−1) | 0 | 0 | 0 | 0 |
Proteinorachia (g/L) | 0.53 | 1.42 | 0.39 | 1.78 |
Delay between neurologic manifestations and CNSi diagnosis (mo) | 19 | 0 | 1 | 3 |
Intra-CSF chemotherapy In another line of treatment | ||||
Yes | Yes | Yes | No | |
Response to ibrutinib | ||||
CSF evaluation | CR | CR | CR | CR |
Neurologic symptoms | Not evaluable | CR | CR | CR |
Hematologic disease | PR with lymphocytosis | CR | CR | CR |
Neuroimaging | Normalization | — | — | Near normalization |
Follow up (mo) | 9 | 14 | 8 | 9 |
Status at last follow up | Dead in CR | Alive in CR | Alive in CR | Alive in CR |
(stroke) |
. | Patient 1 . | Patient 2 . | Patient 3 . | Patient 4 . |
---|---|---|---|---|
Age (y)/sex | 58/M | 75/M | 63/M | 68/F |
Prior lines of therapy for CLL | 8 | 4 | 2 | 0 |
Binet stage at CNSi | C | B | C | A |
Lymphocytosis at CNSi (G/L) | 20 | 0.9 | 245 | 5.5 |
Progressive disease at CNSi diagnosis | Yes | No | Yes | No |
Del17p | Yes | Yes | No | Yes |
Neurologic symptoms | Dysautonomy | Headache and cognitive disturbance | Cerebellar syndrome and aphasia confusion | Visual loss |
Last neuroimaging before ibrutinib initiation | Nodular enhancement of left parietal lobe with not specific periventricular T2 hyperintensities | Normal | NA | Thickening of optic nerves and chiasma. FLAIR hyperintensities |
with nodular lesion of internal occipito-temporal region | ||||
CSF cellularity (μ−1) | 22 | 231 | 176 | 52 |
CSF involvement | 93% monoclonal B cells | 78% monoclonal B cells | 96% monoclonal B cells | 0.7% CLL cells and 91% CD4+ T cells |
Red cells (μ−1) | 0 | 0 | 0 | 0 |
Proteinorachia (g/L) | 0.53 | 1.42 | 0.39 | 1.78 |
Delay between neurologic manifestations and CNSi diagnosis (mo) | 19 | 0 | 1 | 3 |
Intra-CSF chemotherapy In another line of treatment | ||||
Yes | Yes | Yes | No | |
Response to ibrutinib | ||||
CSF evaluation | CR | CR | CR | CR |
Neurologic symptoms | Not evaluable | CR | CR | CR |
Hematologic disease | PR with lymphocytosis | CR | CR | CR |
Neuroimaging | Normalization | — | — | Near normalization |
Follow up (mo) | 9 | 14 | 8 | 9 |
Status at last follow up | Dead in CR | Alive in CR | Alive in CR | Alive in CR |
(stroke) |
FLAIR, fluid attenuated inversion recover; NA, not available.