Di Nan
Xiang Yin
Di Ma
Jiachun Feng- Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China
Posterior reversible encephalopathy syndrome (PRES) is a relatively rare clinical disease, characterized by reversible subcortical vasogenic edema. Here, we present the first reported case of PRES induced by anlotinib, a multi-target tyrosine kinase inhibitor. A 56-year-old female patient with lung adenocarcinoma and bone metastasis experienced hypertension and mental confusion when she received anti-angiogenesis treatment. PRES was diagnosed after magnetic resonance of the patient's brain revealed hyperintensities bilaterally around the cerebellum, pons, fronto-parieto-occipital areas, and corona radiate. Diffusion-weighted imaging showed hyperintensities bilaterally in the parieto-occipital cortical regions. Subsequently, the patient was diagnosed with PRES, and remission was achieved with anti-hypertensive drugs. Six cases of rare adverse effects induced by anlotinib were reviewed in the literature. Since anlotinib has been widely applied as a novel third-line treatment in patients with non-small-cell lung cancer, the association between PRES and anlotinib would benefit neurologists and oncologists in future diagnoses and treatment.
Background
Posterior reversible encephalopathy syndrome (PRES) was first reported by Hinchey et al. (1) in 1996 and is characterized by seizures, encephalopathy, confusion, headaches, and visual disturbances. Moreover, patients with severe hypertension, fluctuations in blood pressure, renal failure, immunosuppressant therapy, chemotherapy, eclampsia, and autoimmune disorder have an increased risk of developing this condition (2).
Anlotinib is a tyrosine kinase inhibitor inhibiting angiogenesis targeting vascular endothelial growth factor receptor (VEGF), fibroblast growth factor receptor, platelet-derived growth factor receptor, c-Kit, and c-MET (3). It has been approved by the China National Medical Products Administration (NMPA) in 2018 and has been widely used to treat patients with advanced non-small-cell lung cancer (NSCLC) who have undergone at least two lines of chemotherapy. A study reporting the phase I clinical trial outcomes for this drug found that the safety dosage is 12 mg/day (4) and that the most common adverse effects related to nervous system disorder was reported to be dizziness and headache in the ALTER0303 trial (5). In addition, there are a few rare adverse effects reported (6–10). Though there have been cases of PRES induced by other VEGF inhibitors, anlotinib has not been previously reported to be associated with PRES (11–13). Here, we present the case of a 56-year-old female patient with lung adenocarcinoma and bone metastasis who developed PRES after being treated with anlotinib.
Case Presentation
Five-years prior to the hospitalization for PRES, the patient was diagnosed with peripheral lung cancer and bone metastasis in 2013. Percutaneous puncture biopsy supported the diagnosis of adenocarcinoma and the patient was subsequently treated with icotinib for 3 years; however, it failed to limit the progression of the disease. Following this, her oncologists discontinued icotinib and switched to a combined therapy of Taxol plus platinum-based chemotherapy and Pemetrexed plus platinum-based chemotherapy in order to prevent the rapid progression of her cancer. After this course of treatment, she underwent a percutaneous puncture biopsy and genetic testing for EGFR and T90M mutations, which tested negative. Magnetic resonance imaging (MRI) of her brain was also performed and it did not reveal any abnormalities. In August 2018, the patient who had no history of hypertension began anlotinib treatment (12 mg/day) and developed several side-effects as a result of this treatment including poor appetite, fluctuating blood pressure, and headaches which persisted. However, her treating physician did not find any neurological deficits prior to her hospitalization in 2019.
On February 2019, the 56-year-old female patient was admitted to emergency department after complaining of headaches and vomiting. On admittance, she presented with elevated blood pressure (217/120 mmHg) which had reportedly persisted for 7 days prior to admission. She also presented with mental confusion which progressed over the course of the day. Upon neurological examination, her speech was unclear. She presented with normal muscle strength in her extremities, her reflexes were normal. A routine blood test including renal function, liver function, D-dimer, and ion were unremarkable. However, her C-reactive protein (CRP) level was slightly elevated. A computed tomography (CT) scan of her brain showed hypodense signals bilaterally in her subcortical and cortical occipital regions. Gadopentetate dimeglumine (Gd)-enhanced MRI identified T2 and fluid-attenuated inversion recovery (FLAIR) hyperintensities as well as T1 hypointensities bilaterally in the cerebellum, pons, fronto-parieto-occipital areas, and corona radiate. Apparent Diffusion Coefficient (ADC) showed hyperintensities bilaterally in the parieto-occipital cortical regions (Figure 1). No enhancement was observed.
Figure 1. MRI findings in this case of posterior reversible encephalopathy syndrome. T2 and Flair image showed hyperintensity in the area of the cerebellum, pons, fronto-parieto-occipital areas, and corona radiate [white arrows in panels (A,B)]; bilateral parieto-occipital cortical regions showed hyperintensity in ADC [white arrows in panel (C)].
The first day after admission, a diagnosis of PRES was made based on the patient's clinical presentation, her recent patient history, and by the results of the imaging studies. In response to this diagnosis, anlotinib was discontinued on the recommendation of the consulting oncologists and the patient received intravenous urapidil and mannitol to reduce her blood pressure and prevent vasogenic edemas. Her blood pressure was maintained at 130–140/80–90 mmHg and her neurological symptoms significantly improved after 5 days. However, the patient appeared to show signs of distress from her medical episode and as a result, she refused to undergo any follow-up imaging and she decided to prematurely end her stay in the hospital. The patient was prescribed a treatment course of Nifedipine GITS (30 mg/day) and daily monitoring of blood pressure. No further oncological treatments were administered.
Three months following her discharge from the hospital, the patient experienced dyspnea due to malignant pleural effusion and was subsequently re-hospitalized. She did not present with any neurological deficits and did not present with hypertension. A brain MRI scan was performed and revealed that the PRES had completely resolved from her previous hospital admission (Figure 2). Further symptomatic treatment was conducted in the oncology department. Graphical abstract of diseases courses is available in Supplementary Data 1.
Figure 2. T2 and Flair scans showed full regression from last attack, while no specific lesion was observed around the pons, cerebellum, frontal lobe, parietal lobe, and occipital lobe (A,B).
Literature Review
Rare adverse effects induced by anlotinib was searched in PubMed between 2018 and 2020, using the terms “Posterior reversible encephalopathy syndrome and anlotinib” and “PRES and anlotinib.” We found six cases of PRES induced by anlotinib in five papers. Clinical details are summarized in Table 1.
Table 1. Summary of rare adverse effects induced by anlotinib.
All those cases were coming from Chinese patients. Those six cases included four men and two women with the mean age of 55.33 year-old (ranging from 48 to 69 years). All those patients were diagnosed with severe carcinoma reached stage II and above. Adverse effect happened after the mean time of 117 days treatment with anlotinib (ranging from 42 days to 12 months). Those adverse effects include aortic dissection (1 case), acute myocardial infarction (1 case), hypertensive retinopathy (1 case), bronchopleural fistula (1 case), and esophago-tracheobronchial fistula (2 cases). Blood pressure monitoring was performed in first three cases. These three cases, who had no history of hypertension, simultaneously exhibited increased blood pressure during the adverse effects diseases course. The other three cases who diagnosed with bronchopleural fistula and esophago-tracheobronchial fistula had no description about blood pressure. The treatment duration of anlotinib was different in two groups. The former group takes 3–12 months to induce the vascular dysfunction, while the latter group only takes nearly 1 month to induce erosion of adjacent tissue. Although the adverse reactions were treated in time in all six cases, four cases were died of primary disease in the following months, except the case of acute myocardial infarction and hypertension retinopathy.
Discussion
To the best of our knowledge, we have reported the very first case of PRES induced by Anlotinib. Given the development of novel Cancer immunotherapy has progressed considerably and new techniques for treatment have been introduced (14, 15). The new epoch of highly effective cancer immunotherapeutic options carry risks of probably rare, but severe, adverse effects (16). We believe that this novel case report of anlotinib-induced PRES and review of rare adverse effect have significant implications for cancer patients and prescribing physicians who are seeking to use this novel therapy.
In a phase III clinical trial by China NMPA consisting of 437 patients, anlotinib was found to be attributed to several commonly occurring side-effects including hypertension (67.4%), hand-foot syndrome (43.9%), hemoptysis (14.0%), thyroid stimulation hormone (TSH) elevation (46.6%), and corrected QT interval prolongation (26.2%) (5). Similar adverse effects were reported in a phase II study (3). However, no anlotinib-induced PRES case was reported. While, several studies have found that other anti-VEGF drugs can induce PRES. For example, one study found that anti-VEGF drugs including bevacizumab, sunitinib, sorafenib, aflibercept, pazopanib, and axitinib caused episodes of PRES 9.8-weeks following treatment (17). In alignment with this, these anti-VEGF drugs were also found to be associated with the onset of hypertension (92.3%), headaches (53.8%), seizures (46.1%), and visual impairment (46.1%) (17).
The underlying mechanism of PRES is still unclear. Hypertension is thought to be the main contributing factors, while endothelial dysfunction could play a role in drug-induced PRES, given that 15–20% of patients with normal blood pressure develop PRES (18). Anlotinib, as a VEGF inhibitor could induced endothelial dysfunction in central nervous system, leading to blood brain barrier (BBB) dysfunction and vascular edema. Additionally, hypertension, which is the most commonly seen adverse effect of anlotinib, could also induce PRES. Hence, anlotinib induced endothelial dysfunction and hypertension in our patient, who had no history of hypertension, may both contributed to PRES. Accordingly, in reviewed cases, we found that anlotinib occasionally increase blood pressure in those who had no history of hypertension, which simultaneously happened with vascular involved adverse effects (6, 8, 10). Discontinuation of anlotinib and anti-hypertensive drug could control increased blood pressure. This suggests that BP monitoring and anti-hypertensive drugs may be used to prevent the onset of PRES well before neurological symptoms become apparent with the treatment of anlotinib. It is important to note that anlotinib is metabolized by CYP3A4 (19) and therefore the use of verapamil and diltiazem, which are both CYP3A4 inhibitors, should be avoided.
According to the National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0, the dosage for anlotinib should be reduced to 8–10 mg per day for patients experiencing adverse effects (4, 20). If adverse events continue at 8 mg, then anlotinib should be discontinued. When considering whether a patient may react unfavorably to anlotinib treatment, a study by Liu et al., have shown that decreased CD31-labeled endothelial cells may predict the efficacy of anlotinib treatment. Thus, this may help weigh the risk-benefit of using this drug (21). Moreover, it is important to note that it is feasible to continue treating a patient with anlotinib even after a PRES episode given that the re-administration of anti-VEGF drugs following PRES has been shown not to cause an occurrence of neurological symptoms (22, 23).
The clinical symptoms of PRES are usually sustained for 2–8 days and fully recovered with significant remission as observed on MRI. However, if the pathogenesis is not managed promptly, PRES may induce severe disabilities, including hemiparesis, epilepsy, visual impairment, or death, thereby resulting in permanent neurological disabilities.
Conclusions
Our case report and review suggest that anlotinib may be damaging to the central nervous system and may cause potentially permanent neurological damage if left untreated. To mitigate this possibility, early prophylactic treatment and dose management should be considered when prescribing anlotinib. Moreover, our study shows that diagnosing anlotinib-induced PRES early may mitigate lasting neurological damage.
Ethics Statement
Written informed consent was obtained from the individual(s) for the publication of this case report, including any potentially identifiable images or data included in this article.
Author Contributions
JF and DM conceptualized and designed the study. DN and XY performed literature research, drafted the manuscript. BW helped with the image. XJ revised it critically. All authors have read and approved the final version of the manuscript.
Funding
This study was supported in part by the National Natural Science Foundation of China (grant no. 81771257), the National Natural Science Foundation for Young Scientists of China (grant no.81701158). The science and technology planning project of Jilin Province (grant nos. 20180101161JC, 20180520134JH) and Innovative Research Team (grant no. 2017TD-30).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We thank the patient and the families for their participation in this study. We would like to thank Editage (www.editage.cn) for English language editing.
Supplementary Material
The Graphical Abstract of the Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fneur.2021.546481/full#supplementary-material
References
1. Hinchey J, Chaves C, Appignani B, Breen J, Pao L, Wang A, et al. A reversible posterior leukoencephalopathy syndrome. N Engl J Med. (1996) 334:494–500. doi: 10.1056/NEJM199602223340803
2. Fugate JE, Rabinstein AA. Posterior reversible encephalopathy syndrome: clinical and radiological manifestations, pathophysiology, and outstanding questions. Lancet Neurol. (2015) 14:914–25. doi: 10.1016/S1474-4422(15)00111-8
3. Han B, Li K, Zhao Y, Li B, Cheng Y, Zhou J, et al. Anlotinib as a third-line therapy in patients with refractory advanced non-small-cell lung cancer: a multicentre, randomised phase II trial (ALTER0302). Br J Cancer. (2018) 118:654–61. doi: 10.1038/bjc.2017.478
4. Sun Y, Niu W, Du F, Du C, Li S, Wang J, et al. Safety, pharmacokinetics, and antitumor properties of anlotinib, an oral multi-target tyrosine kinase inhibitor, in patients with advanced refractory solid tumors. J Hematol Oncol. (2016) 9:105. doi: 10.1186/s13045-016-0332-8
5. Zhou M, Chen X, Zhang H, Xia L, Tong X, Zou L, et al. China National Medical Products Administration approval summary: anlotinib for the treatment of advanced non-small cell lung cancer after two lines of chemotherapy. Cancer Commun. (2019) 39:36. doi: 10.1186/s40880-019-0383-7
6. Jiang B, Li J, Chen J, Xiang X, Xiong J, Deng J. Aortic dissection in a patient treated with anlotinib for metastatic lung squamous cell carcinoma. Thorac Cancer. (2020) 11:461–4. doi: 10.1111/1759-7714.13288
7. Li D, Wei G, Li L, Ma J, Huang X, Qin F, et al. Bronchopleural fistula in squamous cell lung cancer following anlotinib treatment: a case report. Mol Clin Oncol. (2019) 11:595–8. doi: 10.3892/mco.2019.1939
8. Liu G, Chen T, Ding Z. Anlotinib-induced acute myocardial infarction: a case report and literature review. Exp Med Ther. (2020) 20:3203–7. doi: 10.3892/etm.2020.9041
9. Zhang PL, Liu ZJ. Esophago-tracheobronchial fistula following treatment of anlotinib in advanced squamous cell lung cancer: two case reports. Medicine (Baltimore). (2019) 98:e17700. doi: 10.1097/MD.0000000000017700
10. Zhang X, Peng L, Xie Q, Wu Q, Sheng X. Hypertensive retinopathy secondary to anlotinib treatment. Front Pharmacol. (2020) 11:843. doi: 10.3389/fphar.2020.00843
11. Saraceno L, Ricigliano VAG, Cavalli M, Meola G. Posterior reversible encephalopathy syndrome after long-term treatment with low-dose sunitinib: a case report. Neurol Sci. (2017) 38:1119–21. doi: 10.1007/s10072-017-2851-7
12. Aanes SG, Nieder C, Prytz J, Odeh F. A man in his 50s with neurological symptoms during cancer treatment. Tidsskr Nor Laegeforen. (2018) 17:138. doi: 10.4045/tidsskr.18.0096
13. Hamid M, Ghani A, Micaily I, Sarwar U, Lashari B, Malik F. Posterior reversible encephalopathy syndrome (PRES) after bevacizumab therapy for metastatic colorectal cancer. J Commun Hosp Intern Med Perspect. (2018) 8:130–3. doi: 10.1080/20009666.2018.1478563
14. Mellman I, Coukos G, Dranoff G. Cancer immunotherapy comes of age. Nature. (2011) 480:480–9. doi: 10.1038/nature10673
15. Emens LA, Ascierto PA, Darcy PK, Demaria S, Eggermont AMM, Redmond WL, et al. Cancer immunotherapy: opportunities and challenges in the rapidly evolving clinical landscape. Eur J Cancer. (2017) 81:116–29. doi: 10.1016/j.ejca.2017.01.035
16. Singer S, Grommes C, Reiner AS, Rosenblum MK, DeAngelis LM. Posterior reversible encephalopathy syndrome in patients with cancer. Oncologist. (2015) 20:806–11. doi: 10.1634/theoncologist.2014-0149
17. Tlemsani C, Mir O, Boudou-Rouquette P, Huillard O, Maley K, Ropert S, et al. Posterior reversible encephalopathy syndrome induced by anti-VEGF agents. Target Oncol. (2011) 6:253–8. doi: 10.1007/s11523-011-0201-x
18. Rabinstein AA, Mandrekar J, Merrell R, Kozak OS, Durosaro O, Fugate JE. Blood pressure fluctuations in posterior reversible encephalopathy syndrome. J Stroke Cerebrovasc Dis. (2012) 21:254–8. doi: 10.1016/j.jstrokecerebrovasdis.2011.03.011
19. Si X, Zhang L, Wang H, Zhang X, Wang M, Han B, et al. Management of anlotinib-related adverse events in patients with advanced non-small cell lung cancer: experiences in ALTER-0303. Thorac Cancer. (2019) 10:551–6. doi: 10.1111/1759-7714.12977
20. Chi Y, Fang Z, Hong X, Yao Y, Sun P, Wang G, et al. Safety and efficacy of anlotinib, a multikinase angiogenesis inhibitor, in patients with refractory metastatic soft-tissue sarcoma. Clin Cancer Res. (2018) 24:5233–8. doi: 10.1158/1078-0432.CCR-17-3766
21. Liu Z, Wang J, Meng Z, Wang X, Zhang C, Qin T, et al. CD31-labeled circulating endothelial cells as predictor in anlotinib-treated non-small-cell lung cancer: analysis on ALTER-0303 study. Cancer Med. (2018) 7:3011–21. doi: 10.1002/cam4.1584
22. Lou E, Turner S, Sumrall A, Reardon DA, Desjardins A, Peters KB, et al. Bevacizumab-induced reversible posterior leukoencephalopathy syndrome and successful retreatment in a patient with glioblastoma. J Clin Oncol. (2011) 29:e739–42. doi: 10.1200/JCO.2011.36.1865
Keywords: posterior reversible encephalopathy syndrome, anlotinib, adverse effects, targeted therapy, case report
Citation: Nan D, Yin X, Ma D, Jiang X, Wu B and Feng J (2021) Posterior Reversible Encephalopathy Syndrome Associated With Anlotinib: A Case Report and Literature Review. Front. Neurol. 12:546481. doi: 10.3389/fneur.2021.546481
Received: 24 April 2020; Accepted: 08 April 2021;
Published: 06 May 2021.
Edited by:
Barak Bar, University of Wisconsin-Madison, United StatesReviewed by:
Minjee Kim, Northwestern University, United StatesRajaNandini Muralidharan, Winthrop University Hospital, United States
Copyright © 2021 Nan, Yin, Ma, Jiang, Wu and Feng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jiachun Feng, fengjcfrank2017@163.com