Evaluation of Nivolumab for Ototoxic Effects: An Animal Study in Rats

被引:4
作者
Guler, Ismail [1 ]
Kuzucu, Ihsan [2 ]
Baklaci, Deniz [3 ]
Kum, Rauf Oguzhan [4 ]
Ucaryilmaz, Esra Ozhamam [5 ]
Ozcan, Muge [4 ]
机构
[1] Ankara Medipol Univ, Dept Otorhinolaryngol, Sch Med, Ankara, Turkey
[2] Aksaray Univ, Dept Otorhinolaryngol, Sch Med, Aksaray, Turkey
[3] Kahramankazan State Hosp, Clin Otorhinolaryngol, Ankara, Turkey
[4] Ankara City Hosp, Clin Otorhinolaryngol, Ankara, Turkey
[5] Ankara City Hosp, Clin Pathol, Ankara, Turkey
关键词
Ototoxicity; nivolumab; immunotherapy; animal study; SENSORINEURAL HEARING-LOSS; ADVANCED MELANOMA; TUMOR RESPONSE; IPILIMUMAB; ANTI-PD-1; PEMBROLIZUMAB; MONOTHERAPY; MULTICENTER; SURVIVAL; SAFETY;
D O I
10.5152/iao.2020.7123
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
OBJECTIVES: The aim of this study was to assess whether nivolumab is ototoxic in rats and whether this ototoxicity is dose-dependent. MATERIALS and METHODS: Twelve rats were divided into two groups: Group 1 (control group, 6 rats, 12 ears) received intraperitoneal saline for 14 days. Group 2 (study group, 6 rats, 12 ears) and received two doses of 3 mg/kg intraperitoneal nivolumab within 14 days. Auditory brainstem responses (ABRs) were performed preoperatively and 4 and 8 weeks postoperatively. We compared between the groups, morphologic appearance of spiral ganglion cells and organ of Corti and density of spiral ganglion cells (measured with conventional light microscope connected to a personal computer). RESULTS: In our control group, both spiral ganglion and organ of corti had a normal morphological appearance. In our study group, spiral ganglion cells had a normal morphological appearance. However, some sections showed possibly mild degenerative changes in the organ of corti. Of 12 samples in the study group, four had a significant loss of density of spiral ganglion cells compared to the control group. The baseline ABR thresholds did not significantly differ between the groups (p=0.713). There was no statistically significant difference between the groups regarding ABR thresholds at week 4 (p=0.347). However, a statistically significant difference was observed in the ABR thresholds at week 8 (p=.0.045). CONCLUSION: The results of our study showed that nivolumab treatment has ototoxic effects. Based on our results, we recommend monitoring the changes in the hearing ability of chemotherapy patients.
引用
收藏
页码:218 / 221
页数:4
相关论文
共 16 条
[1]   Irreversible sensorineural hearing loss due to Imatinib [J].
Attili, Venkata Satya Suresh ;
Bapsy, P. P. ;
Anupama, G. ;
Lokanatha, D. .
LEUKEMIA RESEARCH, 2008, 32 (06) :991-992
[2]   Acute heart failure due to autoimmune myocarditis under pembrolizumab treatment for metastatic melanoma [J].
Laeubli, Heinz ;
Balmelli, Cathrin ;
Bossard, Matthias ;
Pfister, Otmar ;
Glatz, Kathrin ;
Zippelius, Alfred .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2015, 3
[3]   Emerging biomarkers for PD-1 pathway cancer therapy [J].
Lim, Joline S. J. ;
Sundar, Raghav ;
Chenard-Poirier, Maxime ;
Lopez, Juanita ;
Yap, Timothy A. .
BIOMARKERS IN MEDICINE, 2017, 11 (01) :53-67
[4]   Sensorineural Hearing Loss following Imatinib (Gleevec) Administration [J].
Lin, Harrison W. ;
Roberts, Daniel S. ;
Kay, Jonathan ;
Stankovic, Konstantina M. .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2012, 146 (02) :335-337
[5]   Anti-PD1 Following Ipilimumab for Mucosal Melanoma: Durable Tumor Response Associated with Severe Hypothyroidism and Rhabdomyolysis [J].
Min, Le ;
Hodi, F. Stephen .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (01) :15-18
[6]   Toxicities of the anti-PD-1 and anti-PD-L1 immune checkpoint antibodies [J].
Naidoo, J. ;
Page, D. B. ;
Li, B. T. ;
Connell, L. C. ;
Schindler, K. ;
Lacouture, M. E. ;
Postow, M. A. ;
Wolchok, J. D. .
ANNALS OF ONCOLOGY, 2015, 26 (12) :2375-2391
[7]   Adenovirus-mediated expression of brain-derived neurotrophic factor protects spiral ganglion neurons from ototoxic damage [J].
Nakaizumi, T ;
Kawamoto, K ;
Minoda, R ;
Raphael, Y .
AUDIOLOGY AND NEURO-OTOLOGY, 2004, 9 (03) :135-143
[8]   Efficacy and safety of ipilimumab monotherapy in patients with pretreated advanced melanoma: a multicenter single-arm phase II study [J].
O'Day, S. J. ;
Maio, M. ;
Chiarion-Sileni, V. ;
Gajewski, T. F. ;
Pehamberger, H. ;
Bondarenko, I. N. ;
Queirolo, P. ;
Lundgren, L. ;
Mikhailov, S. ;
Roman, L. ;
Verschraegen, C. ;
Humphrey, R. ;
Ibrahim, R. ;
de Pril, V. ;
Hoos, A. ;
Wolchok, J. D. .
ANNALS OF ONCOLOGY, 2010, 21 (08) :1712-1717
[9]   Association of Pembrolizumab With Tumor Response and Survival Among Patients With Advanced Melanoma [J].
Ribas, Antoni ;
Hamid, Omid ;
Daud, Adil ;
Hodi, F. Stephen ;
Wolchok, Jedd D. ;
Kefford, Richard ;
Joshua, Anthony M. ;
Patnaik, Amita ;
Hwu, Wen-Jen ;
Weber, Jeffrey S. ;
Gangadhar, Tara C. ;
Hersey, Peter ;
Dronca, Roxana ;
Joseph, Richard W. ;
Zarour, Hassane ;
Chmielowski, Bartosz ;
Lawrence, Donald P. ;
Algazi, Alain ;
Rizvi, Naiyer A. ;
Hoffner, Brianna ;
Mateus, Christine ;
Gergich, Kevin ;
Lindia, Jill A. ;
Giannotti, Maxine ;
Li, Xiaoyun Nicole ;
Ebbinghaus, Scot ;
Kang, S. Peter ;
Robert, Caroline .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 315 (15) :1600-1609
[10]   Tumor Immunotherapy Directed at PD-1 [J].
Ribas, Antoni .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (26) :2517-2519