MCO Molecular and Clinical Oncology 2049-9450 2049-9469 D.A. Spandidos MCO-0-0-02206 10.3892/mco.2021.2206 Articles Absence of meaningful neurocognitive recovery in comatose patients with primary central nervous system lymphoma despite an effective response to chemotherapy: Case reports LimRyan Mao Heng 1 ChanJason Yongsheng 2 3 4 5 Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Republic of Singapore Division of Medical Oncology, National Cancer Centre Singapore, Singapore 169610, Republic of Singapore SingHealth Duke-NUS Blood Cancer Centre, Singapore 169857, Republic of Singapore Duke-NUS Medical School, Singapore 169857, Republic of Singapore Cancer Science Institute of Singapore, National University of Singapore, Singapore 117599, Republic of Singapore Correspondence to: Dr Jason Yongsheng Chan, Division of Medical Oncology, National Cancer Centre Singapore, 11 Hospital Drive, Singapore 169610, Republic of Singapore jason.chan.y.s@nccs.com.sg

Abbreviations: PCNSL, primary CNS lymphoma; MMSE, mini-mental state examination; WBRT, whole-brain radiotherapy; GCS, Glasgow Coma Scale; DLBCL, diffuse large B-cell lymphoma; GCB, germinal centre B-cell like

 03 2021 13 01 2021 14 3 44 07 09 2020 23 12 2020 Copyright: © Lim et al. 2020 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Primary central nervous system lymphoma (PCNSL) is a rare type of non-Hodgkin's lymphoma that occurs in patients who are elderly and immunocompromised. The most common treatment for PCNSL is high-dose methotrexate-based chemotherapy. Studies have suggested that the radiological response to high-dose methotrexate-based chemotherapy is associated with improved neurocognitive ability that remains stable upon follow-up. However, no study involving patients with an extremely poor neurological status before chemotherapy initiation has been reported, and the neurological prognosis of this group of patients remains unknown. The current case study described 3 patients with PCNSL diagnosed via biopsy who had comatose neurological states due to disease progression prior to treatment. All patients were treated with high-dose methotrexate-based chemotherapy. However, although effective radiological responses to treatment were achieved, no meaningful neurological or cognitive recovery was documented. Patients with PCNSL exhibiting a baseline comatose state have a poor neurological prognosis even with an effective tumour response to chemotherapy. Therefore, rapid detection and prompt treatment are crucial in patients with this disease.

 primary central nervous system lymphoma chemotherapy Glasgow Coma Scale neurocognition prognosis case report Introduction

Primary central nervous system lymphoma (PCNSL) is a rare form of non-Hodgkin's lymphoma that is usually confined to the brain, leptomeninges, spine, cerebrospinal fluid and eyes without evidence of systemic spread (1). PCNSL represents approximately 4% of all newly diagnosed central nervous system (CNS) tumours (2,3), and most seem to be of late or post-germinal centre B-cell origin (4,5). Immunodeficiency due to congenital immunodeficiency syndromes such as ataxia-telangiectasia and Wiskott-Aldrich syndrome, as well as secondary causes such as acquired immunodeficiency syndrome and iatrogenic immunosuppression for transplant procedures, has been implicated in the development of PCNSL (6).

The prognosis of PCNSL has improved substantially in recent years, particularly in immunocompetent patients (7). However, treatment of PCSNL may cause neurotoxicity and compromise health-related quality of life. Studies have suggested that patients treated with combined high-dose methotrexate chemotherapy and consolidation whole-brain radiotherapy (WBRT) in the treatment of PCNSL develop worse neurotoxicity and cognitive dysfunction than those treated with chemotherapy alone (8-12). Thus, consolidation WBRT is often withheld unless necessary, particularly in elderly patients (13). Conversely, cognition, as measured by mini-mental state examination (MMSE) scores, frequently improves following the successful treatment of PCNSL with chemotherapy with or without immunotherapy (rituximab) and remains stable on follow-up (10,14-16). However, currently, no study has described the neurological prognosis of PCNSL patients with a very poor neurocognitive function at baseline.

In this study, we reviewed the cases of 3 patients with neuroimaging- and biopsy-proven PCNSL who had baseline comatose neurological states at presentation (Table I). All 3 were treated with high-dose methotrexate-based chemotherapy only without WBRT and achieved either a partial or complete response to treatment, as assessed using International PCNSL Collaborative Group criteria (17).

 Case reports <sec> <title>Case 1

A 73-year-old Chinese man presented with worsening lethargy and drowsiness, together with behavioural changes for 1 month. He had a medical history of hypertension, diabetes mellitus, hyperlipidaemia and ischaemic heart disease. During his initial admission, magnetic resonance imaging (MRI) of the brain revealed multiple foci of abnormal enhancement with low to heterogeneous T2 signals in a periventricular distribution, including the ependymal margins of both lateral ventricles, infundibular recess of the 3rd ventricle and pituitary stalk. These findings were highly suggestive of PCNSL. Despite these findings, the patient declined further work-up and was discharged against medical advice. He was subsequently re-admitted a month later for progressive drowsiness and fever. Neurological examination revealed a severely depressed level of consciousness with a Glasgow Coma Scale (GCS) of E3V1M1. Imaging of the brain showed interval disease progression and obstructive hydrocephalus. The patient subsequently underwent an external ventricular drain insertion, followed by stereotactic biopsy of the right caudate region two weeks later.

Histological evaluation confirmed diffuse large B-cell lymphoma (DLBCL), non-germinal centre B-cell like (non-GCB) subtype. He was administered dexamethasone, procarbazine, vincristine and high-dose methotrexate (2.5 g/m2) (18). At the point of treatment initiation, the GCS remained poor at E2V2M1. The time from the initial presentation to time of treatment initiation was 2 months. Because chemotherapy was complicated by repeated infective episodes, including pyelonephritis, colitis and pneumonia, only 4 cycles were administered (up to week 8). Brain MRI performed at the end of treatment showed no residual tumour or interval new tumour, indicating a complete response (Fig. 1A).

Despite the complete response of the lymphoma to chemotherapy, the patient's neurocognitive status did not improve and the GCS remained poor at E2V2M1. The patient eventually died of relapsed disease 8 months later.

 Case 2

A 42-year-old Bruneian man with no significant medical history initially presented with diplopia and was referred to the National Cancer Centre, Singapore, for suspected PCNSL on preliminary brain imaging. Physical examination revealed a GCS of E3V4M6, cranial nerve III, IV and VI palsy bilaterally, a fixed left pupil and extremely poor visual acuity with inability to visualize light bilaterally. Mild left hemiparesis was also evident. Brain MRI revealed homogeneously enhancing lesions in the optic chiasma, optic nerves and tract, midbrain and pons, and hypothalamus.

Stereotactic biopsy of the left suprasellar lesion confirmed DLBCL, non-GCB type. Unfortunately, the patient became progressively drowsier because of the interval enlargement of the known suprasellar mass associated with an increasing mass effect and worsening hydrocephalus. The patient subsequently underwent ventriculoperitoneal shunt insertion and tracheostomy, while his GCS continued to deteriorate to E1VTM1. He was administered high-dose methotrexate-based chemotherapy for 5 cycles based on the protocol by Shah et al (rituximab, vincristine, procarbazine and methotrexate 2.5 g/m2) (19). The time from the initial presentation to the start of treatment was 6 months. Post-treatment brain MRI showed a stable hypothalamus lesion and marked improvement in the lesions in the right temporal lobe, bilateral basal ganglia and brainstem, indicating an effective partial response to treatment (Fig. 1B).

Despite the overall response to treatment, the patient did not achieve significant improvement in cognition or physical function. His post-treatment GCS remained low at E2V1M1. Thereafter, he was managed with best supportive care alone at a hospice.

 Case 3

A 68-year-old Chinese man with a significant medical history of hypertension, hyperlipidaemia and stroke presented with an unsteady gait with frequent falls, impairment of semantic memory and slow speech. His physical examination was unremarkable, and he had no gross neurological deficits. His GCS was E4V4M6. Brain MRI showed lobulated semi-confluent enhancing lesions at the bilateral periventricular regions involving the corpus callosum and corona radiata.

Stereotactic biopsy of the left frontal periventricular region revealed DLBCL, GCB type. Post operatively, he was administered levetiracetam and dexamethasone because he had mild fasciculations of his right thigh and twitching of his left biceps suggestive of a provoked seizure. He was intubated when his GCS subsequently deteriorated to E1V1M1, following which a tracheostomy was performed. Subsequently, he was administered high-dose methotrexate-based chemotherapy for 5 cycles including rituximab, vincristine and methotrexate (2.5 g/m2) but not procarbazine. Post-treatment brain MRI revealed complete resolution of the lesions along the periventricular region and corpus callosum, indicating a complete response to treatment (Fig. 1C).

Similar to cases 1 and 2, despite an effective tumour response to chemotherapy, he remained in a comatose state with a GCS of 3 and died 8 months later.

 Discussion

We described the cases of 3 patients with extremely poor neurological statuses before treatment initiation. All 3 patients did not achieve meaningful neurological recovery despite an effective tumour response to chemotherapy, as evidenced by the low post-treatment GCS of 5, 4 and 3 for cases 1, 2 and 3, respectively. These findings contrast those of earlier studies that reported an improvement in cognitive function following the successful treatment of PCNSL (10,14-16). Although these cohorts generally comprise patients with grossly intact neurological and cognitive function (median MMSE range, 22-23), our study is novel because the 3 patients had extremely poor neurocognitive function at baseline with a GCS score of 5 or below before treatment initiation.

The GCS decreased in all 3 patients in the short time frame between the initial presentation and start of treatment, ranging from 12 days to 6 months. In case 1, treatment was delayed because the patient had initially requested for discharge against medical advice, whereas the delay in case 2 was due to the patient being referred from an overseas hospital. In case 3, treatment was promptly commenced. Thus, PCNSL is an aggressive disease with an unpredictable clinical course. A sharp decrease in the GCS representing disease progression of PCNSL may indicate a poor neurological prognosis even if the tumour responds well to chemotherapy. In such a scenario, best supportive care focusing on the quality of life may be considered and weighed carefully against aggressive chemotherapy with curative intent.

Although cases 1 and 3 involved elderly Chinese patients older than 65 years, case 2 involved a young Bruneian man aged only 42 years at diagnosis. Despite the differences in both age and race, all 3 patients had similarly poor neurological outcomes at the end of chemotherapy treatment. This supports the hypothesis that a poor neurocognitive status before treatment is a poor prognostic indicator for the post-treatment neurological outcome across various demographical factors such and age and race.

In conclusion, the neurocognitive status of PCNSL patients can deteriorate quickly, indicating dismal outcomes. Patients with severe neurocognitive compromise may have a poor neurological prognosis despite an effective response to treatment. Further validation studies should be conducted to examine the neurological prognosis of PCNSL patients with poor neurological function at baseline who were treated successfully with chemotherapy, as well as to determine the possible causes of and prevent poor neurological status in these patients. Our study suggests that administering early treatment in PCNSL patients and avoiding unnecessary delays are necessary to achieve optimal neurocognitive recovery.

 Acknowledgements

Not applicable.

 Funding

This work was supported by the Singapore Ministry of Health's National Medical Research Council of Singapore (grant no. NMRC/FLWSHP/054/2017-00), SHF-Foundation (grant no. SHF/FG653P/2017) and SingHealth Duke-NUS Academic Medical Centre and Oncology ACP (grant no. 08-FY2017/P1/14-A28).

 Availability of data and materials

Data sharing is not applicable to this article, as no datasets were generated or analysed during the present study.

 Authors' contributions

RMHL and JYC conceptualized the study and wrote the manuscript. RMHL acquired, analysed and interpreted the data. JYC enrolled the study patients, obtained their consent and treated them. Both authors have confirmed the authenticity of all raw data, as well as read and approved the final manuscript.

 Ethics approval and consent to participate

The present study was approved by the Singhealth Centralised Institutional Review Board (CIRB 2018/3084). Written informed consent was obtained from all the participants and/or their legal guardians.

 Patient consent for publication

Written informed consent was obtained from the patients for the publication of this case report and any accompanying images.

 Competing interests

The authors declare that they have no competing interests.

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T1-weighted MRI images reveal the anatomical involvement of PCNSL at various junctures of treatment. (A) Complete responses to chemotherapy were observed in case 1, (B) partial response to chemotherapy was observed in case 2 and (C) complete responses to chemotherapy were observed in case 3. The red arrows indicate the initial sites of disease. PCNSL, primary CNS lymphoma.

Clinical characteristics and treatment outcomes of patients with PCNSL.

ID Age at diagnosis (years) Gender Significant comorbidities Presenting symptoms Histology Anatomical location Treatment regimen GCS (at presentation) GCS (before treatment) Time to treatment End of treatment responseb GCS (post- treatment)
1 73 Male Hypertension Diabetes mellitus Hyperlipidaemia Ischaemic heart disease Lethargy Drowsiness Behaviour change DLBCL, non-GCB Basal ganglia Thalamus Midbrain Periventricular Corpus callosum High-dose methotrexate based (2.5 g/m2) for 4 cycles E3V1M1a E2V2M1 2 months Complete response E2V2M1
2 42 Male Nil Diplopia Poor visual acuity DLBCL, non-GCB Optic chiasma, optic nerves and tract Midbrain and pons Hypothalamus High-dose metho trexate based (2.5 g/m2) for 5 cycles E3V4M6 E1VTM1 6 months Partial response E2V1M1
3 68 Male Hypertension Hyperlipidaemia Stroke Unsteady gait Memory impairment Slow speech DLBCL, GCB Periventricular Corpus callosum Corona radiata High-dose methotrexate based (2.5 g/m2) for 5 cycles E4V4M6 E1V1M1 12 days Complete response E1V1M1

aNon-purposeful movements observed;

bAssessed using International PCNSL Collaborative Group (IPCG) criteria [17]; PCNSL, primary CNS lymphoma; DLBCL, diffuse large B-cell lymphoma; GCB, germinal center B-cell; GCS, Glasgow Coma Scale.