Refractory Chronic Lymphocytic Leukemia with Central Nervous System Involvement: A Case Report with Literature Review.

There have been few reports on central nervous system (CNS) involvement in chronic lymphocytic leukemia (CLL). This is an extremely rare disease with poor prognosis, owing to resistance to various treatments. We describe a 33-year-old man with intractable CLL with CNS involvement. He was diagnosed with CLL, with diplopia as the first manifestation. Magnetic resonance imaging revealed a contrast-enhancing tumor in the right temporal lobe, which was diagnosed as CNS involvement in CLL on brain biopsy. High-dose methotrexate therapy was ineffective for this lesion, which was also resistant to subsequent whole-brain irradiation, treatment with fludarabine-cyclophosphamide-rituximab chemoimmunotherapy, and ibrutinib administration. Because no standard protocol exists for CLL with CNS involvement, it is important to accumulate case data to verify the choice of new drugs for administration at an early stage. Therefore, we also conducted a literature review of 50 case reports of CNS lesions in the last 10 years to consider the pathophysiology, diagnosis, and treatment of CNS involvement in CLL. The possibility of new therapeutic agents, eg, ibrutinib and venetoclax, or a combination of these agents and methotrexate, can be envisioned as a treatment strategy for CLL with CNS involvement.

Introduction

Chronic lymphocytic leukemia (CLL) is the most frequent adult leukemia in the US and Europe, but is a rare disease in Japan, with a frequency 10% that in theUS.1 The disease typically occurs in older patients, and the median age at diagnosis is 72 years.2 Generally, CLL progresses slowly, but some cases progress rapidly and aggressively.3 Furthermore, CLL has a highly variable clinical course, and neurological complications arising from direct leukemic involvement in the central nervous system (CNS) are reported in only 1% of patients with CLL.4,5 Here, we present a rare case of a young CLL patient with CNS involvement that was resistant to various therapies. CLL treatment has improved considerably in the last decade; however, it remains unclear which the best treatment for CNS involvement in CLL is. Therefore, in this case report, we also conducted a comprehensive literature review of 50 case reports with CNS involvement in the last 10 years in which the clinical course was described.

Case Presentation

A 33-year-old man with diplopia was referred to our hospital. He had a 9 month history of asymptomatic revised Rai low– and Binet A–stage CLL that had been diagnosed owing to an increase in lymphocyte count at a medical checkup, but he had not come to the hospital at his own discretion. Thereafter, he developed diplopia and was referred to neurosurgery by an ophthalmologist. Except for double vision and intracranial hypertension–related headaches, the neurological examination was unremarkable, and he had no other symptoms or lymph-node swelling. Magnetic resonance imaging (MRI) revealed a 5×3.5 cm nonuniformly contrasted mass in the right temporal lobe that appeared hypointense on T1-weighted and hyperintense on T2-weighted images (Figure 1A). In this case, because there was a risk of cerebral hernia owing to a bulky CNS lesion, lumbar puncture could not be performed.

Figure 1

Magnetic resonance imaging (MRI) showing 5×3.5 cm abnormal nonuniformly contrasted mass with hypointensity on T1-weighted image (left) and with hyperintensity on T2-weighted image (right) in the right temporal lobe. (A) MRI at first consultation; (B) MRI after MPV administration (at day 17 after admission); (C) MRI after FCR administration (at day 34 after admission); (D) MRI after Ibr administration (at day 54 after admission).

A diagnostic cranioscopic biopsy was performed, which revealed infiltration of small monoclonal lymphocytes with expression of CD5, CD20 (Figure 2), and CD79A, but without CD10, CD23, cyclin D1, or evidence of transformation. Similarly, his blood showed CLL-cell clonality, with expression of CD5, CD19, CD20 (dim), CD22, and cell-surface Ig, but no expression of CD10, CD23, or IgH-BCL1 on fluorescence in situ hybridization. Bone marrow (BM) specimens revealed 96.6% of lymphocytes had the same flow-cytometry appearance as peripheral blood (PB). BM lymphocytes had a normal karyotype without poor prognostic factors, deletion 17p, deletion 11q, or transformation (Figure 3), which was compatible with a diagnosis of CLL. These findings were indicative of leukemic involvement in the CNS, and the patient was eventually transferred to hematology. In this case, Richter’s syndrome was initially suspected from the symptoms and course, but CNS-infiltrating cells were small lymphoid cells similar to those of PB and BM, and transformation to a diffuse large-cell type was ruled out by brain biopsy. Therefore, we diagnosed CNS involvement in CLL.

Figure 2

Brain specimens (cranioscopic biopsy) showing infiltration of small monoclonal lymphocytes with expression of CD5 and CD20 (upper left, H&E ×40; upper right, H&E ×100; lowerleft CD5 ×100; lower right, CD20 ×100).

Figure 3

CLL cells from peripheral blood at first consultation and admission and BM at admission showed mature small monoclonal lymphocytes with narrow cytoplasm, concentrated nuclei, and partially aggregated chromatin without transformation to a large cell type (H&E ×40 and ×200).

Laboratory data (Table 1) were significant for a white blood–cell count of 464,200/μL (98.5% lymphocytes and 1.5% neutrophils). Hemoglobin level and platelet count were 11.7 g/dL and 305,000/μL, respectively. Lactate dehydrogenase was 262 IU/L (normal range 112–230 IU/L) and soluble IL2R 11,000 IU/L (normal range 124–466 IU/dL). β2-microglobulin was 2.1 mg/L. Evaluation with thoracoabdominal computed tomography (CT) revealed splenomegaly and mild systemic lymphadenopathy.

Table 1

Hematologic Assessment of Patient

White blood Cells/μL	464,200/μL	Na	141 mEq/L
Neutrophils	1.5%	K	4.2 mEq/L
Basophils	0	Cl	103 mEq/L
Eosinophils	0	BUN	12 mg/dL
Lymphocytes	98.5%	Cr	0.83 mg/dL
Monocytes	0	TP	6.5 g/dL
Others	0	Alb	4.1 g/dL
Plt	30.5×104/μL	AST	26 U/L
RBC	449×104/μL	ALT	37 U/L
Hb	11.7 g/dL	T-Bil	0.4 mg/dL
Ht	42.1%	D-Bil	0 mg/dL
MCV	93.8 fL	ALP	544 U/L
MCH	26.1 pg	γGTP	87 U/L
MCHC	27.8 g/dL	LDH	262 U/L
APTT	25.7 seconds	CRP	0.072 mg/dL
PT	107.4%
FBG	241 mg/dL	IgG	955 mg/dL
AT-III	109%	IgA	83 mg/dL
HBs-Ag	—	IgM	29 mg/dL
HCV-Ab	—	sIL2R	11,000 U/mL
HTLV-1	—	BMG	2.1 mg/L
HIV	—	ANA	—

Treatment with 2 mg betamethasone for 7 days transiently improved the diplopia and headaches, but tumor size evaluated by CT/MRI remained unchanged. No standard protocol exists for CLL with CNS involvement, because it is an extremely rare disease condition. Therefore, according to the treatment strategy of primary CNS lymphoma, MPV chemotherapy (methotrexate 3.5 mg/m2 on day 1, vincristine 1.4 mg/m2 [max 2.8 mg on day 1], and procarbazine 100 mg/m2 per day on days 1–7) was started. Ten days after treatment, intracranial hypertension–related symptoms, such as diplopia and headaches, recurred and performance status was decreased. MRI showed that the tumor size remained unchanged (Figure 1B) and PB-lymphocyte reduction was poor (Figure 4), indicating resistance to the MPV treatment. Therefore, rituximab (Rtx) 375 mg/m2 and subsequent whole-brain radiotherapy (30 Gy/15 fr) plus simultaneous in-field boost (10 Gy/5 fr) were administered.

Figure 4

Clinical course of WBC and lymphocyte counts after treatment.

After Rtx administration, the diplopia and headaches improved and lymphocyte reduction was observed. Therefore, treatment with one cycle of FCR chemotherapy (fludarabine 25 mg/m2 per day and cyclophosphamide 250 mg/m2 per day for the first 3 days, with addition of Rtx 375 mg/m2) was started. Although the PB lymphocytes decreased steadily (Figure 4) without recurrence of intracranial hypertension–related symptoms, no reductive effect on the intracranial tumor was observed on contrast-enhanced MRI (Figure 1C). Because the effects of ibrutinib (Ibr) on the CNS have been reported in CLL and mantle-cell lymphoma,6 we next selected Ibr 420 mg/day for treatment. However, 2 weeks later, contrast-enhanced MRI revealed no reductive effect, and diplopia and headaches had recurred (Figure 1D). Finally, the patient refused subsequent treatment and was self-discharged from the hospital. He died at home 9 weeks after the onset of initial symptoms (48 weeks after the diagnosis of CLL).

Discussion

Diagnostic cranioscopic biopsy was performed in our case, but many cases were diagnosed by cerebrospinal fluid (CSF) analysis in a retrospective cohort of 30 CLL patients with CNS involvement.7 In that cohort, biopsies were performed in only five cases, of which only one was diagnosed by brain biopsy.7 Our review of the literature revealed diagnostic biopsies had been performed in 12 of 50 cases (not including surgical resection). Ten of the 50 cases were diagnosed as Richter’s syndrome, and 11.3% of Richter’s transformation with intracranial involvement was found in an old literature review of CLL (before 2011).8 By contrast, there were no cases of Richter’s syndrome in the 30 cases of the retrospective cohort.7 It has been reported that Richter’s transformation occurs in approximately 5%–10% of the CLL population;9 therefore, it is still difficult to conclude whether there is an intimate correlation between CNS involvement and Richter’s transformation.

The 50 reported cases of CNS involvement in CLL had diverse and uncharacteristic symptoms, such as headaches, convulsions, diplopia, ataxia, facial paralysis, and cognitive dysfunction (Table 2). It is difficult to identify the risk factors for CNS involvement in CLL.10,11 Our literature review confirmed this, because we could not find a common feature in cases of CNS involvement. There are cases in which CNS involvement develops when the stage is not necessarily progressive (on Rai or Binet staging) or without high-risk chromosomal abnormality, such as del17p or del11q. This suggests clinical and pathophysiological heterogeneity of CNS involvement in CLL.7

Table 2

Literature on CNS Involvement in CLL

Reference	Age(years), sex	Symptoms	Interval from diagnosis of CLLto first CNS symptoms	Rai/Binet	Lymphocyte count	FISH(G-band)	Method of diagnosis	Transformation to Richter’s syndrome	Treatment(treatment prior to diagnosis of CNS involvement)	Response
Clin Case Rep. 2020.8.269.17	71M	Epilepticseizures	12 years	NA	NA	11q deletion	CSF–Clinical diagnosis		WW/FCR/Rtx–bendamustine–IbrHD MtxRtxVenetoclax	VenetoclaxPR
Mult Scler Relat Disord. 2020.37.10145519	50M	Fecal incontinence,tetraparesis	NA	NA	131,000(WBC)	NA	CSF+		Rtx and cyclophosphamideIVIg	CR
Can J Neurol Sci. 2019.46.640.20	53M	Neckpain, adenopathy, urinary retention,monocular vision loss in right eye	5 years	NA	NA	NA	CSF+		WWDex pulse⇢Rtx and cyclophosphamide	CR
Haematologica.2019.104. e222.18	58	NA	NA	NA	NA	Trisomy 12	CSF+		Six FCR courses, six Rtx–bendamustine cycles, and four Rtx–DHAP coursesIbrVenetoclax with IT chemotherapy(cytarabine plus methotrexate)	IbrPDVenetoclaxCR
Case Rep Hematol. 2019. 1,825,491;21	62M	Dysmetria, left upper–extremity paresis, apraxia, mild amnesia, and prosopagnosi	NA	NA	5,300(WBC)	del13q14(BM)	Craniotomy with resectionCSF–		FCR	CR
BMC Neurol. 2019 0.19. 200.22	45F	6-month history of headache	NA	NA	NA	NA	BiopsyCSF+		HD Mtx with IT Mtx and AraC	CR
BMC Neurol. 2019 0.19. 200.22	49M	Headache and dizziness for past 5 years	NA	NA	NA	NA	BiopsyCSF+		Rtx, HD Mtx, Dex, and vincristine with IT Mtx	CR
Neuropathology. 2019.39.54.23	61F	Mental disturbance	14 years	NA	3300(WBC)	Trisomy 12(lymph node)	BiopsyCSF+		CHOP/FCHD Mtx	PD
Cureus. 2018. 10. e2176.16	61F	Chronicheadaches	14 years	Rai I	NA	NA	CSF+		WW/FCRIbr 420 mg→560 mg	CR
Case Rep Hematol. 2018.7,817,918.24	65M	Headachecomplaints, photophobia, vertigo, and extensive pain(from the cervical spine down to the inferior limbs)	9 years	Rai 0Binet A	NA	13q deletion	CSF+		Chlorambucil monotherapyIT Mtx + liposomal AraC⇢Ibr 420 mg⇢HD Mtx⇢WBRT	CR
Adv Clin Exp Med. 2018.27. 1683.25	54M	Disturbances of consciousness	71 months	Rai II	NA	NA	CTAutopsy	Yes	CVP, CHOP, FC, F, ofatumumab + idelalisib vs no treatment	PD
Turk J Hematol 2018.35.147.26	71F	Expressive aphasia, memory problems, confusion, and headache	12 years	Binet A	14,652	Normal	Biopsy rejectCSF–		WWRtxIbr 420 mg	PR
Annals of Hematology.2018.97.1627.27	81M	Paralysis of the left oculomotor nerveand left hemianopsia	20 months	Rai 0Binet A	35,600	NA	CSF+		WWRtx and chlorambucil with IT Mtx	PR
Annals of Hematology.2018.97.1627.27	77M	Apathy,urinary incontinence	9 years	Rai IIBinet B	44,500	NA	CSF+		Fludarabine and cyclophosphamideNo	PD
Medicine.2018. 97. e1270128	67F	Slurred speech, headache, and left-sided hemiparesis	NA	NA	14,500	p53+	Surgical resectionCSF(DLBCL)	Yes	HD MtxIT Mtxand AraC	PD
Cureus.2018.10. e366029	84F	Mild dysmetria in the upper-left extremity	NA	Rai 0	15,311,000	NA	Tumor resection	Yes	Temozolomide and WBRT	PD
Ann Indian Acad Neurol. 2018. 21.85.30	57M	Bradypsychia,headaches,nausea,vomiting	6 months	Rai III	85,500(WBC)	del17p	CSF+		WWHD Mtx	PD
Ann Indian Acad Neurol. 2018. 21.85.30	43M	Dysphasia,repeated unconsciousness,urinaryincontinence	62 months	Rai IV	23,000(WBC)	Normal	CSF+		FCFCR	SD?
Ann Indian Acad Neurol. 2018. 21.85.30	72M	Dyslexia,lack of fine motor control,diplopia	9 months	Rai IV	103,900(WBC)	13q14 nullisomy	CSF–		WWDHAP	PD
Ann Indian Acad Neurol. 2018. 21.85.30	49M	Diplopia,bilateral eyelid swelling, and tumors	63 months	Rai II	86,500(WBC)	NA	CSF+		CHOPDHAP	PD
Br J Haematol.2017.176.829.31	66M	Tightness, paresthesia, andneuropathic pain in the left hand and left arm	NA	Rai III	94,000	NA	CSF+		SteroidsIbr 420 mg	CR
BMC Hematol. 2017.17.332	60F	Progressive lower-extremity weaknessand urinary incontinence	NA	Rai 0	13,400	Normal	CSF+		FCR	PR→PD
J Neuroophthalmol. 2016.36.61.33	45M	Visual loss in the right eye	2 years	NA	2304	NA	Optic nerve–sheathbiopsyCSF+		Ibr with IT Mtx	CR
Blood.2016.127.235634	58M	Dysautonomy	NA	Binet C	NA	del17p	CSF+		Eight prior lines of therapy for CLLIbr 420 mg	CR
Blood.2016.127.235634	75M	Headaches and cognitivedisturbance	NA	Binet B	NA	del17p	CSF+		Four prior lines of therapy for CLLIbr 420 mg	CR
Blood.2016.127.2356–235834	63M	Cerebellar syndrome andaphasia, confusion	NA	Binet C	NA	NA	CSF+		Two prior lines of therapy for CLLIbr 420 mg	CR
Blood.2016.127.235634	68F	Visual loss	NA	Binet A	NA	del17p	CSF+		No prior lines of therapy for CLLIbr 420 mg	CR
BMC Res Notes. 2014.7.645.35	75F	Headache, otalgiain the right ear, fever, dizziness, and dysphagia	5 years	Rai 1	24,300(WBC)	NA	CSF+		Chlorambucil and prednisoneIT MtxFC	CR
Leukemia Lymphoma.2014. 55.193936	64M	Hypoesthesia	2 months	Binet B	251,000	Normal	CSF+		WWIT Mtx + AraCRtx–bendamustine	CR
BMJ Case Rep. 2014.Bcr-2013-202,051.37	45F	Seizures,headaches, and vomiting	NA	NA	NA	NA	Biopsy		Surgical excisionRT	Relapse
Clin Lymphoma Myeloma Leuk. 2013.13. 338.38	44F	Double vision	3 years	Rai 1	98,280	Trisomy 12 and 13q-	BiopsyCSF+		RtxmPSLIT AraCFCR	CR
Leuk Lymphoma. 2013.54.2070.39	67M	Gaitdisturbance, tremors, slurred speech, marked fatigue, intermittent confusion, and visualimpairment	10 years	Rai 1	2200 (WBC)	Diploid	CSF+	Yes	Chlorambucil–fludarabine–pentostatin, cyclophosphamide, and Rtx–ofatumumab–lenalidomideIT liposomal AraCIT RtxHD AraCWBRT	PD
J Clin Exp Hematop. 2013.53.15740	66F	Fatigue and difficulty walking	2 years	Rai 0	27,000	NA	Biopsy (CT-guided),non-GCB DLBCL	Yes	WW/cyclophosphamide + PSLIT DexRTRtx	Transient PR→relapse
J Clin Oncol. 2013.31e28041	75M	Right-eye pain associated with blurryvision, floaters, and bright halos	1 years	Rai 0	34,900	Trisomy12	CSF+		PSLRtx–fludarabine	CR
Acta Haematol. 2012;127.9342	56M	Seizures,psychomotoric deficits, and left-sided hemiparesis	1 month	Binet A	NA	NA	Stereotactic biopsyCSF–	Yes	Systemic and intraventricularpolychemotherapy regimenWBRTTopotecan	Transient CR→relapse
J Neurooncol 2012.106.1858	53F	Vision changes	4 years	Rai 1	16,000,000(WBC)	NA	CSF+		CVPRtx–fludarabineAlemtuzumabRtxIT MtxTemozolomideRT	PR
J Neurooncol 2012.106.1858	52M	Encephalopathy, dementia,seizures	3 years	Rai IV	14,000,000(WBC)	NA	CSF+		FludarabineNone	PD
J Neurooncol. 2012.109.21343	65F	Difficulty speaking,weakness in the right arm and leg	1 month	Rai IV	600,000(WBC)	13q14 deletion(biopsy)	Biopsy		Cyclophosphamide + steroidsFCRWBRTRtx–bendamustine	CR
Case Rep Hematol. 2012589,71844	66F	Bilateral hearing loss	NA	NA	104,000(WBC)	del(17p13.1) and del(13q34)	Tympanic membrane biopsyCSF+		Rtx-CVPRtxIT liposomal cytarabineCyclophosphamide, cladribine, and RtxHyperCVAD	PR
Am J Hematol. 2011.86.78345	73	Bilateral visual loss	NA	Rai IIBinet B	NA	NA	Ethmoidectomy		Fludarabine/FCRSteroidsRT	PD
J Neurol Neurosurg Psychiatry. 2011.82.94346	late60sM	Bilateral leg weakness, pain,and urinary retention	NA	Rai III	NA	Normal	Brain biopsy	Yes	WW/chlorambucil/FCR/CHOPHD Mtx	PD
J Clin Oncol. 2010.28.e3047	58M	Temporary seizures,poor memory,and progressive blindness	10 years	Rai III	36,000(WBC)	NA	Open-brain biopsyCSF–		MtxFluRT	PD6 months
Blood.2010.116.261748	68M	Paraparesis of bothlegs, urinary and stool incontinence, and central right-sided facialnerve palsy	NA	NA	NA	NA	CSF+		HD Mtx + ifosfamideHD AraC + Mit + IT MtxDasatinib	CR
Br J Haematol.2010.150.61849	52M	Headache, cognitivecomplaints: slowresponse andinattentiveness	61 months	Rai 1Binet A	NA	NA	CSF+		IT liposomal AraCRTRtx + VCR + HD Mtx+ PCBZ + HD AraCFCR	CR
Br J Haematol.2010.150.61849	68F	V cranial pair palsy	34 months	Rai IVBinet B	NA	NA	CSF+	Yes	IT liposomal AraCHD Mtx + HD AraC	Transient CR➙relapse
Br J Haematol.2010.150.61849	44M	Headache, chin andface dysesthesia,optic neuritis,blurred vision	25 months	Rai IVBinet C	NA	NA	CSF+		IT liposomal AraCChlorambucil	Transient CR➙relapse
Br J Haematol.2010.150.61849	81M	Headache, nausea,weakness,somnolence,lethargy, andconfusioned state	25 months	Rai 0Binet A	NA	NA	CSF+		IT liposomal AraCFCR	CR
Br J Haematol.2010.150.61849	64F	Headache anddiplopia	13 months	Rai IVBinet C	NA	NA	CSF+		IT liposomal AraCR-CHOP	CR
Br J Haematol.2010.150.61849	79M	Leg weakness,difficulty walking,upper-back pain, andVII cranial pair palsy	66 months	Rai IVBinet B	NA	NA	CSF+	Yes	IT Mtx and liposomal AraCHyperCVAD/MA	Transient CR➙relapse
Br J Haematol.2010.150.61849	68F	Headache	24 months	Rai IVBinet B	NA	NA	CSF+	Yes	IT Mtx and liposomal AraCAraC	CR

Abbreviations: NA, not available; FISH, fluorescence in situ hybridization; CSF, cerebrospinal fluid; Rtx, rituximab; FCR, fludarabine–cyclophosphamide–Rtx; MPV, methotrexate–procarbazine–vincristine; HD, high dose; Mtx, methotrexate; Mit, mitoxantrone; AraC, cytosine arabinoside (cytarabine); CVP, cyclophosphamide–vincristine–prednisone; IT, intrathecal; RT, radiotherapy; Ibr, ibrutinib; WBRT, whole-brain radiotherapy; hyperCVAD, cyclophosphamide–vincristine–adriamycin–dexamethasone; CHOP, cyclophosphamide–hydroxydaunorubicin (doxorubicin)–oncovin (vincristine)–prednisone; DHAP, dexamethasone–HD AraC (cytarabine)–platinol (cisplatin); WW, watch and wait.

A report summarizing the literature published before 2011 of CNS involvement in CLL8 showed average age 63.4 years, average latency between CLL diagnosis and first signs of CNS involvement 2.6 years, average overall survival (OS) from CLL diagnosis 3.8 years, and average OS from time of CNS onset 12 months. Our review of the 50 case reports revealed average age 62.2 years (in 49 cases) and average latency 4.9 years (in 32 cases. OS data could not be extracted. Our case showed a younger and more aggressive disease course of age 33 years, latency 9 months, OS 48 weeks, and OS from time of CNS onset 9 weeks. Our case was resistant to high-dose Mtx and whole-brain radiotherapy as standard treatments for primary CNS lymphoma. As the standard treatment for non–high risk CLL, FCR was effective in reducing the number of PB lymphocytes and improved intracranial hypertension-related symptoms; however, it had less effect on tumor shrinkage, indicating it was ineffective for the CNS lesion. Although the number of reports of CNS involvement in CLL is low, there were reports of successful treatment with FCR in some cases in our literature review (Table 2). However, in general, prognosis was poor, owing to resistance to various treatments, such as high-dose Mtx, intrathecal injection, whole-brain radiotherapy, and FCR. A similar result was obtained in our case

Ibr has been reported to be effective in CNS lesions of mantle-cell lymphoma6 and Waldenström macroglobulinemia.12 Effects of Ibr appear 1–2 weeks after administration.13 Nine successful cases of Ibr treatment for CNS involvement in CLL were found in 50 cases (complete response in eight cases, partial response in one) (Table 2); therefore, Ibr may be a promising drug for CNS involvement. However, this was not found in our case. It is possible that the effective concentration of Ibr in the CNS lesion had not reached sufficient levels in our case. Concentration in CSF was reported to be 2log lower than in the plasma of 18 patients with primary CNS lymphoma treated with Ibr.14 It has been reported that an increased dose of Ibr escalates CSF concentration without adverse events,15 and that increasing the dose of Ibr is effective for CNS lesions in CLL.16 It will be necessary in the future to verify the optimal dose of Ibr for CNS lesions. Bulky disease in CNS lesion might also cause treatment failure. Although ofatumumab and alemtuzumab are alternative treatment options, we did not select them, because they did not show superiority to Ibr in the data or in drug penetration of the CNS. In addition, there have been two reports showing the effectiveness of venetoclax against CNS lesions (Table 2).17,18 One of those was a case where venetoclax was effective after Ibr resistance, and thus it may be beneficial to test venetoclax against CNS involvement in CLL.

Conclusion

Patients with CNS lesions in lymphoid tumors have a poor prognosis, but the possibility of concomitant use of Mtx and Ibr or venetoclax can be envisioned. Accumulation of data from cases is important to verify the choice of new or combination drugs for administration from an early stage.