Relapse of aseptic meningitis induced by ipilimumab and nivolumab therapy for metastatic renal cell carcinoma: A case report

Introduction

In recent years, combination therapy with nivolumab, a programmed death 1 (PD-1) immune checkpoint inhibitor antibody, and ipilimumab, an anti-cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) antibody, have demonstrated clinical efficacy in the treatment of metastatic RCC (mRCC) patients (1). These results led to the United State Food and Drug Administration approving the combination of ipilimumab and nivolumab in treatment-naïve patients with intermediate- or poor-risk disease according to the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) criteria in April 2018 (2,3). In Japan, this combination therapy has also been approved since August 2018. However, it is often associated with a wide variety of immune-related adverse events (irAEs) that can affect almost any organ site (1,4).

We herein report a patient with metastatic renal cell carcinoma who developed the uncommon irAE of aseptic meningitis as well as isolated ACTH deficiency and liver dysfunction during ipilimumab and nivolumab therapy.

Case report

A 70-year-old Japanese woman was referred to our institution for the evaluation of a right renal tumor that had been detected by abdominal ultrasonography at a screening examination in July 2018. She had a history of hypertension. She was diagnosed with right renal cell carcinoma (cT1bN0M0) by computed tomography (CT) and underwent right nephrectomy in the same month. Two months later, multiple lung metastases were observed by CT (Fig. 1A). Therefore, she was diagnosed as ‘intermediate risk’ according to the IMDC criteria [she had one prognostic factor (<1 year since the diagnosis)].

Figure 1. Chest CT. (A) Chest CT revealed metastatic lung tumors in the bilateral lobe prior to ipilimumab and nivolumab combinational therapy (white arrow). (B) Following the 3rd course of therapy, CT images revealed that the lung metastasis had disappeared.

Combination therapy (once every 3 weeks, intravenously) of ipilimumab (1 mg/kg) and nivolumab (240 mg/body) was administered as the first-line therapy in September 2018. On the 14th day of the 2nd course, she complained of nonspecific clinical symptoms, such as headaches, dizziness and nausea, and was admitted to our hospital. However, she did not complain of or develop any other specific clinical features pertaining to the central nervous system. She also did not report any neck stiffness. Brain magnetic resonance imaging (MRI) was preformed, but there were no brain metastases or any findings suggestive of encephalitis or meningitis (Fig. 2A). However, meningitis could not be ruled out clinically, so a cerebrospinal fluid (CSF) test was performed.

Figure 2. Brain MRI. (A) A sagittal section of a contrast-enhanced T1-weighted brain MRI scan revealed no abnormality. (B) A sagittal section of a contrast-enhanced T1-weighted brain MRI scan presented mild diffuse enlargement of the pituitary (white arrow).

The examination of the CSF revealed normal glucose levels but an elevated protein level at 195 mg/dl and a significantly elevated white blood cell (WBC) count of 830/mm3 (lymphocytes 825/mm3, neutrophils 5/mm3; Table I). In addition, CSF cytology showed no malignant cells, and the CSF analysis was negative for bacteria and viruses (cytomegalovirus, herpes simplex virus, varicella-zoster virus and human herpes virus type 6). Based on these results, she was diagnosed with aseptic meningitis induced by ipilimumab and nivolumab therapy, and prednisolone (1 mg/kg/day) was started intravenously. After a few days, her clinical symptoms improved rapidly, as did the CSF analysis findings, so prednisolone was tapered gradually. On the 49th day of the 2nd course, she had no recurrence of clinical symptoms on maintenance oral steroid treatment (prednisolone 10 mg/day), and a CSF analysis showed that the WBC count had dropped to 44/mm3 (only lymphocytes; Table I). After delivering a sufficient explanation of the risks and benefits to the patient, the 3rd course of the combination therapy was readministered the next day.

Table I. CSF analysis and blood glucose data of the case study.

Table I.

CSF analysis and blood glucose data of the case study.

CSF examination	Reference value	C2D14	C2D23	C2D49	C3D10	C3D25
Glucose, mg/dl	45-80	46	74	67	66	66
Protein, mg/dl	<45	195	97	41	52	48
WBC, n/mm3	<5	830	217	44	34	53
Lymphocyte, n/mm3	0	825	215	44	34	53
Neutrophil, n/mm3	0	5	2	0	0	0
Blood glucose, mg/dl	73-109	106	–	–	148	141
Blood to CSF glucose ratio		0.43	–	–	0.45	0.47

[i] CSF, cerebrospinal fluid; C, course; D, day; WBC, white blood cell.

Two weeks later, she complained of nausea, anorexia and fatigue. A relapse of meningitis was suspected, but the CSF showed that the WBC count was not marked elevated compared to before (Table I). Although CT was performed to investigate the cause, no abnormal findings were found. However, all multiple lung metastases had disappeared, and a complete response was considered to have been achieved (Fig. 1B). The MRI of the brain showed mild diffuse enlargement of the pituitary (Fig. 2B). Her laboratory data showed a low sodium value (122 mmol/l). Based on the clinical symptoms, examination values and MRI findings, adrenocorticotropic hormone (ACTH) deficiency was suspected, and the administration of oral hydrocortisone 20 mg/day (Cortril®; morning 15 mg, evening 5 mg) was started after stopping prednisolone.

Two days later, her symptoms dramatically improved. The results of the endocrine system tests revealed that her ACTH (2.0 pg/ml) and cortisol (1.12 µg/dl) levels were lower than normal. The levels of other anterior pituitary hormones (prolactin, luteinizing hormone, follicle-stimulating hormone, thyroid-stimulating hormone) were not low (Table II). Based on these findings, the diagnosis was isolated ACTH deficiency induced by combination therapy of ipilimumab and nivolumab.

Table II. Patient laboratory data.

Table II.

Patient laboratory data.

Laboratory data	Reference value	C3D10	C3D15	C3D25	C3D27	C3D29	C3D50
WBC, n	3,300-8,600/µl	11,000	9,000	9,170	8,850	19,030	16,920
Eosino (%)	0.4–8.6	0.5	1.3	0.3	0.6	0.1	0.2
AST, U/l	13-30	35	50	131	155	69	20
ALT, U/l	10-42	41	57	204	244	176	44
Na, mmol/l	138-145	133	122	127	131	134	–
CRP, mg/dl	0-0.14	3.12	6.45	0.36	0.27	<0.07	–
ACTH, pg/ml	7.2–63.3	15.7	2	<1.5	–	–	–
Cortisol, µg/dl	6.24–18.0	3.18	1.12	38.1	–	–	–
TSH, µIU/ml	0.49–4.67	–	0.31	2.5	–	–	–
F-T4, ng/ml	0.71–1.85	–	0.91	0.89	–	–	–
PRL, ng/ml	4.29–13.69	–	60.5	–	–	–	–
LH, mIU/ml	0.79–5.72	–	8.08	–	–	–	–
FSH, mIU/l	2.00–8.30	–	30.54	–	–	–	–

[i] Certain data are not provided, as these parameters did not require follow-up at these stages. WBC, white blood cell; Eosino, eosinophil ratio; AST, aspartate aminotransferase; ALT, alanine aminotransferase; CRP, C-reactive protein; ACTH, adrenocorticotropic hormone; TSH, thyroid-stimulating hormone; F-T4, thyroxine; PRL, prolactin; LH, luteinizing hormone; FSH, follicle-stimulating hormone; C, course; D, day.

On the 25th day of the 3rd course, she complained of headache and anorexia. The CSF examination showed that the WBC count had increased again (53/mm3, only lymphocytes), and her laboratory data showed hepatic dysfunction and elevated aspartate aminotransferase at 155 U/l and alanine aminotransferase at 244 U/l (Tables I and II). She had no history of infection with hepatitis B and C virus, and abdominal echography showed no remarkable findings in her liver. She was diagnosed with liver dysfunction and relapse of aseptic meningitis induced by combination therapy of ipilimumab and nivolumab.

While continuing the administration of oral hydrocortisone 20 mg/day, the administration of intravenous prednisolone (total 1 mg/kg/day) was started additionally. The liver dysfunction and aseptic meningitis gradually improved (Table II). Three months later, CT showed that the multiple lung metastases had not reappeared. However, she had been taking oral hydrocortisone 20 mg/day for isolated ACTH deficiency and prednisolone 2.5 mg/day for liver dysfunction. Therefore, the immunotherapy was not restarted.

Discussion

Anti-CTLA-4 antibody and anti-PD-1 antibody have different working points and mechanisms of activity, and their combination brings about a synergetic effect on the tumor reduction effect and overall survival (1,5). However, the frequency and severity of irAEs is also synergistically affected. Although the patient backgrounds differed between these studies, grade 3 or 4 treatment-related AEs occurred in 18.7% of patients treated with nivolumab alone for mRCC (6), whereas such AEs occurred in 45.7% of patients treated with nivolumab plus ipilimumab for mRCC (1). The most frequently reported irAEs in the RCC population are skin events (59.6% of patients), endocrine events (40.4% of patients), gastrointestinal events (44.7% of patients), hepatic events (27.7%), renal events (12.8%) and pulmonary events (10.6 %) (7). Neurologic side-effects are rare but include cases of immune polyneuropathies, Guillain Barré syndrome, myasthenia gravis, posterior reversible encephalopathy syndrome, aseptic meningitis, enteric neuropathy, transverse myelitis as well as immune encephalitis (8). In a pooled analysis of nearly 1,500 patients with melanoma treated with ipilimumab, the incidence of neurologic irAEs was 0.1% (9,10).

We herein report a 70-year-old woman with mRCC receiving combination nivolumab and ipilimumab therapy who developed aseptic meningitis, isolated ACTH deficiency and hepatic dysfunction that were probably induced by an auto-immune related mechanism. As meningitis and encephalitis were suspected based on clinical symptoms, lumber puncture proved extremely helpful for making a diagnosis because there were no findings on brain MRI. CSF abnormalities with an elevated proteins level associated with lymphocytic pleocytosis supported the presence of inflammatory-mediated disease. General bacterial meningitis was initially excluded because of the lymphocyte-dominated findings on CSF. Tuberculous meningitis has also been reported to have lymphocyte-dominated findings. However, in modern Japan, tuberculosis infection itself is so rare that it was not considered as a differential diagnosis. A CSF analysis was the most useful examination for supporting the relationship between the aseptic meningitis status and the response to steroid treatment. Aseptic meningitis fortunately responded well to high-dose steroid therapy, and her irAEs also improved to Grade 1 promptly. The early improvement of the patient's symptoms and CSF analysis findings by steroid treatment ruled out tuberculous meningitis. There were no sequelae, and the prednisolone dose was able to be reduced to 10 mg/day within 1 month after the start of steroid therapy.

Whether or not to resume immune checkpoint inhibitor treatment after neurological recovery is a matter of debate, and a careful analysis of the risks and benefits should be done on a case by case basis. The therapeutic effect was a complete response after only 2 courses. However, the durability of the response to this combination therapy for mRCC still remains unclear and this combination immunotherapy is only allowed in the first-line setting for mRCC in Japan. Steroid treatment therapy for this irAE foutunately demonstrated a good response, so the combination therapy was re-administered after both the risks and benefits were sufficiently explained to the patient. However, isolated ACTH deficiency occurred with the oral administration of steroids. Furthermore, relapse of aseptic meningitis and liver dysfunction also occurred. An autopsy analysis of the pituitary glands of patients with cancer treated by CTLA-4 blockade described type II and IV hypersensitivity reactions and a strong CTLA-4 expression in the pituitary gland (11). Therefore, this hypophysitis with pituitary enlargement hypothetically could have been caused by type II hypersensitivity reactions, such as complement activation and infiltration with macrophages and phagocytosis, and type IV hypersensitivity reactions, such as infiltration with autoreactive T lymphocytes. Although the study was conducted in a melanoma population, it was reported that approximately 40% of patients with advanced melanoma who received nivolumab combined with ipilimumab in clinical trials discontinued treatment because of AEs. However, the efficacy outcomes seemed similar between patients who discontinued nivolumab plus ipilimumab treatment because of AEs during the induction phase and those who did not discontinue the treatment because of AEs (12). In the present case, re-administration of nivolumab and ipilimumab therapy occurred not only other irAEs but also relapse of aseptic meningitis. Therefore, we decided to resume immunotherapy when the disease progressed.

No standard treatment has yet been defined for neurological irAEs. A commonly used protocol is oral prednisone at roughly 1 mg/kg/day. A neurological irAE management algorithm has been proposed (5,8). However, further studies are necessary in order to establish the precise framework regarding the dose, timing of tapering and administration period of steroid treatment. In the present case, a longer tapering period for steroids might have been needed in order to prevent recurrent irAEs. Indeed, it was reported that neurological irAEs are not always reversible (13), highlighting the importance of optimizing treatment regimens.

With the increasing use of immune checkpoint inhibitors in cancer treatment, practicing oncologists need to be aware of the potential risks of neurologic irAEs and be able to provide prompt treatment for this uncommon but potentially serious class of AEs. Treatment algorithms for relatively frequent AEs have been established, and there are many case reports of relatively frequent AEs that can be referenced (14,15). The present case of aseptic meningitis is a rare AE, and the diagnosis and treatment of such events can be facilitated by the publication of detailed clinical case reports. Proper testing based on the careful observation of patients' clinical symptoms and intervention with steroids will enable the effective treatment at an earlier point in the clinical course.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

All data generated or analyzed during the present study are included in this published article.

Authors' contributions

DT, NF and TN participated, conceived and designed the present case report, analyzed and interpreted the data and wrote the manuscript. DT, KI, TI and KT evaluated the patient and participated in therapy. KI and MN evaluated radiological images. TN and MN supervised the study and critically reviewed the manuscript. All authors have read and approved the final version of the manuscript.

Ethics approval and consent to participate

The present case report was approved by the Institutional Review Board of National Hospital Organization Kyushu Cancer Center (approval no. 2014-99). Written informed consent was obtained from the patient.

Patient consent for publication

The patient provided written informed consent for the publication of any associated data and accompanying images.

Competing interests

The authors declare that they have no competing interests.

References