Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab

被引:2
|
作者
Mizutani, Kosuke [1 ]
Ito, Toshiki [2 ]
Takahara, Kiyoshi [3 ]
Ando, Ryosuke [4 ]
Ishihara, Takuma [5 ]
Yasui, Takahiro [4 ]
Shiroki, Ryoichi [3 ]
Miyake, Hideaki [2 ]
Koie, Takuya [1 ]
机构
[1] Gifu Univ, Dept Urol, Grad Sch Med, 1-1 Yanagido, Gifu, Gifu 5011194, Japan
[2] Hamamatsu Univ Sch Med, Dept Urol, Hamamatsu, Shizuoka, Japan
[3] Fujita Hlth Univ, Dept Urol, Sch Med, Toyoake, Aichi, Japan
[4] Nagoya City Univ, Grad Sch Med Sci, Dept Nephro Urol, Nagoya, Aichi, Japan
[5] Gifu Univ Hosp, Innovat & Clin Res Promot Ctr, Gifu, Japan
关键词
immune-related adverse event; nivolumab; renal cell carcinoma; targeted therapy; INHIBITORS; EFFICACY; SAFETY; ASSOCIATION;
D O I
10.1097/MD.0000000000025402
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nivolumab has shown good prognosis in renal cell carcinoma (RCC) patients previously treated with targeted therapy. We aimed to study irAE (immune-related adverse event) due to nivolumab and numbers of previous treatment lines in RCC patients. Between October 2016 and November 2019, 114 patients were treated with nivolumab as second- and later-line therapy. Among them, 110 patients with complete data were evaluated in this retrospective observational study. The primary endpoint was the relation between irAE and numbers of previous targeted therapies. Secondary endpoints were the relation of irAE with the duration of nivolumab treatment and with best overall response. For the primary analysis, proportional odds logistic regression was used to assess the effect of the number of prior therapies on the grade of any irAE as the ordinal variable. For the secondary analysis, binomial logistic regression models adjusted for the covariates were prepared to confirm the association between the incidence of irAE and the number of courses, number of nivolumab treatments and best overall response. Overall, 69, 66, 33, 13, 9 and 9 patients were treated with sunitinib, axitinib, pazopanib, sorafenib, temsirolimus and everolimus, respectively, prior to nivolumab. In total, 60 adverse events (Grade 1, 21; Grade 2, 21; Grade 3, 14; Grade 4, 2; not evaluated, 2) were identified in the patients treated with nivolumab. Ordered logistic regression analysis showed that the adjusted odds ratios of numbers of prior treatment for grade of irAE were 1.12 (numbers of prior treatment: 2 to 1) and 1.31 (3 to 1). Odds ratios of the numbers of nivolumab treatments and best overall response for the incidence of irAE were not significant. No statistically significant relations were found between grade of irAE and numbers of treatments prior to nivolumab. Patients treated with nivolumab should be closely monitored for irAE regardless number of previous therapies.
引用
收藏
页数:6
相关论文
共 50 条
  • [41] Cutaneous immune-related adverse events in patients with melanoma treated with checkpoint inhibitors
    Gault, A.
    Anderson, A. E.
    Plummer, R.
    Stewart, C.
    Pratt, A. G.
    Rajan, N.
    BRITISH JOURNAL OF DERMATOLOGY, 2021, 185 (02) : 263 - 271
  • [42] Immune-related adverse events correlate with clinical outcomes in NSCLC patients treated with nivolumab: The Italian NSCLC expanded access program
    Baldini, Editta
    Lunghi, Alice
    Cortesi, Enrico
    Turci, Daniele
    Signorelli, Diego
    Stati, Valeria
    Melotti, Barbara
    Ricciuti, Biagio
    Frassoldati, Antonio
    Romano, Giampiero
    Ceresoli, Giovanni Luca
    Illiano, Alfonso
    Verderame, Francesco
    Fasola, Gianpiero
    Ricevuto, Enrico
    Marchetti, Paolo
    Pinto, Carmine
    Carteni, Giacomo
    Scotti, Vieri
    Tibaldi, Carmelo
    Fioretto, Luisa
    Giannarelli, Diana
    LUNG CANCER, 2020, 140 : 59 - 64
  • [43] Impact of Immune-Related Adverse Events on Survival in Patients with Advanced Non-Small Cell Lung Cancer Treated with Nivolumab
    Ricciuti, B.
    Genova, C.
    De Giglio, A.
    Brambilla, M.
    Bassanelli, M.
    Dal Bello, M. G.
    Baglivo, S.
    Metro, G.
    Grossi, F.
    Chiari, R.
    JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (10) : S390 - S391
  • [44] Prevalence of immune-related adverse reactions in patients treated with nivolumab at Puerto Real University Hospital
    Bello Bello, L.
    Raffo Nogueira, J. B.
    Fernandez-Pujol Marzo, M.
    Pacheco Rodriguez, M. E.
    Pedrosa Martinez, M. J.
    Dodero Anillo, J. M.
    BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2024, 135 : 31 - 31
  • [45] Severe immune-related adverse events (irAE) induced by nivolumab at our institution
    Hasegawa, Yoshikazu
    Tsukuda, Hiroshi
    Ota, Takayo
    Miyatake, Nozomi
    Matsui, Kaoru
    Fukuoka, Masahiro
    ANNALS OF ONCOLOGY, 2017, 28
  • [46] Evaluation of emergency department visits and immune-related adverse effects (irAEs) in patients treated with nivolumab
    Kudu, Emre
    Akdag, Goncagul
    Yildirim, Mahmut Emre
    SUPPORTIVE CARE IN CANCER, 2024, 32 (10)
  • [47] Immune-Related Adverse Events-A Novel Prediction of Nivolumab Efficacy? Reply
    Haratani, Koji
    Hayashi, Hidetoshi
    Nakagawa, Kazuhiko
    JAMA ONCOLOGY, 2018, 4 (07) : 1017 - 1018
  • [48] Ipilimumab and nivolumab induced immune-related adverse events in metastatic mucosal melanoma
    Cao, Yenong
    Afzal, Muhammad Zubair
    Shirai, Keisuke
    BMJ CASE REPORTS, 2021, 14 (08)
  • [49] Treatment Outcomes of Immune-Related Cutaneous Adverse Events
    Phillips, Gregory S.
    Wu, Jennifer
    Hellmann, Matthew D.
    Postow, Michael A.
    Rizvi, Naiyer A.
    Freites-Martinez, Azael
    Chan, Donald
    Dusza, Stephen
    Motzer, Robert J.
    Rosenberg, Jonathan E.
    Callahan, Margaret K.
    Chapman, Paul B.
    Geskin, Larisa
    Lopez, Adriana T.
    Reed, Vanessa A.
    Fabbrocini, Gabriella
    Annunziata, Maria Carmela
    Kukoyi, Oluwaseun
    Pabani, Aliyah
    Yang, Chih-Hsun
    Chung, Wen-Hung
    Markova, Alina
    Lacouture, Mario E.
    JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (30) : 2746 - +
  • [50] Analysis of immune-related adverse events in gastrointestinal malignancy patients treated with immune checkpoint inhibitors
    Niu, Chengu
    Zhu, Kaiwen
    Zhang, Jing
    Joshi, Utsav
    Liu, Hongli
    Zahid, Salman
    Jadhav, Nagesh
    Okolo, Patrick I.
    INTERNATIONAL JOURNAL OF CANCER, 2024, 154 (07) : 1261 - 1271