Diabetic ketoacidosis induced by nivolumab in invasive mucinous adenocarcinoma of the lung: a case report and review of the literature

被引:2
作者
Yan, Juan [1 ]
Xie, Zheng-Zheng [2 ,9 ]
Moran, Teresa [3 ,4 ,5 ,6 ]
Gridelli, Cesare [7 ]
Zheng, Mao-Dong [1 ]
Dai, Su-Juan [8 ]
机构
[1] Hebei North Univ, Dept Pharm, Affiliated Hosp 1, Zhangjiakou, Peoples R China
[2] Beijing Shijitan Hosp, Dept Pharm, Beijing, Peoples R China
[3] Hosp Universitari Germans Trias I Pujol, Catalan Inst Oncol Badalona, Med Oncol Dept, Barcelona, Spain
[4] Inst Germans Trias I Pujol, Barcelona, Spain
[5] Badalona Appl Res Grp Oncol, Barcelona, Spain
[6] Univ Autonoma Barcelona UAB, Dept Med, Campus Can Ruti, Barcelona, Spain
[7] SG Moscati Hosp, Div Med Oncol, Avellino, Italy
[8] Sun Yat sen Univ, Zengchen Dist Peoples Hosp Guangzhou, Dept Pharm, Boji Affiliated Hosp, Guangzhou, Peoples R China
[9] Beijing Shijitan Hosp, Dept Pharm, 10 Tieyi Rd, Beijing, Peoples R China
关键词
Diabetic ketoacidosis; immunotherapy adverse effects; nivolumab; programmed cell death receptor 1 inhibitor (PD-1 inhibitor); case report; IMMUNE-CHECKPOINT BLOCKADE; TYPE-1; MELLITUS; IMMUNOTHERAPY; PATIENT;
D O I
10.21037/atm-22-5211
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Nivolumab is the first programmed cell death receptor 1 (PD-1) inhibitor approved in China. Compared with chemotherapy, nivolumab has shown advantages of good efficacy and safety in the treatment of a variety of tumors. However, due to its short time of use in China and lack of safety experience, clinical understanding of its adverse reactions has not been sufficiently elucidated. In recent years, cases of diabetic ketoacidosis caused by nivolumab have been reported in the emergency department, which has aroused our concern. Case Description: Here we present a serious case of diabetic ketoacidosis in a 69-year-old woman with invasive mucinous adenocarcinoma of the lung, which occurred following therapy with the PD-1 inhibitor nivolumab and dendritic cell/cytokine-induced killer cell (DC/CIK) immunotherapy. She presented with diabetic ketoacidosis 5 days after the second cycle of nivolumab administration. The patient presented with dry mouth symptoms, a maximum blood glucose of 511.2 mg/dL, hemoglobin A1c (HbA1c) level of 7.4%, urine ketone body value of 3+, and extracellular fluid residual alkali level of -3.8 mmol/L. Normal saline and insulin was initiated. The patient had no history of obesity or family history of diabetes. She received a single dose of 3.75 mg of dexamethasone treatment during this period of time which resulted in cough improvement, but did not explain the onset of the diabetes. She was treated with insulin, sitagliptin phosphate tablets and acarbose tablets. Diabetic ketoacidosis was considered an immune-related toxicity caused by nivolumab, and consequently, treatment with nivolumab was suspended. Patient was maintained under insulin treatment with a blood glucose levels normalization. Conclusions: The incubation period of nivolumab-induced diabetic ketoacidosis is dispersive and the clinical risk is high. Patients need life-long insulin therapy. Blood glucose and HbA1c should be monitored routinely before and during nivolumab immunotherapy to avoid the occurrence of diabetic ketoacidosis. After the occurrence of diabetic ketoacidosis, insulin should be used to actively control blood glucose and do a good job in medication education to ensure long-term compliance of patients. Nivolumab should only be initiated if the patient has a clinical benefit under stable glucose control.
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页数:9
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共 43 条
  • [21] DIABETIC KETOACIDOSIS AS A DELAYED IMMUNE-RELATED EVENT AFTER DISCONTINUATION OF NIVOLUMAB
    Mae, Soichiro
    Kuriyama, Akira
    Tachibana, Hiromi
    [J]. JOURNAL OF EMERGENCY MEDICINE, 2020, 60 (03) : 342 - 344
  • [22] Diabetes and Blood Glucose Disorders Under Anti-PD1
    Magis, Quentin
    Gaudy-Marqueste, Caroline
    Basire, Agnes
    Loundou, Anderson
    Malissen, Nausicaa
    Troin, Laura
    Monestier, Sandrine
    Mallet, Stephanie
    Hesse, Sylvie
    Richard, Marie-Aleth
    Valero, Rene
    Beliard, Sophie
    Grob, Jean-Jacques
    [J]. JOURNAL OF IMMUNOTHERAPY, 2018, 41 (05) : 232 - 240
  • [23] The efficacy and safety of immune checkpoint inhibitor plus chemotherapy in patients with advanced non-small-cell lung cancer: a meta-analysis
    Meng, Li-Fang
    Huang, Jian-Feng
    Luo, Peng-Hui
    Huang, Shang-Xiao
    Wang, Han-Lei
    [J]. INVESTIGATIONAL NEW DRUGS, 2022, 40 (04) : 810 - 817
  • [24] Nivolumab for the treatment of esophageal cancer
    Mikuni, Hayato
    Yamamoto, Shun
    Kato, Ken
    [J]. EXPERT OPINION ON BIOLOGICAL THERAPY, 2021, 21 (06) : 697 - 703
  • [25] Nivolumab, an Anti-Programmed Cell Death-1 Antibody, Induces Fulminant Type 1 Diabetes
    Miyoshi, Yuka
    Ogawa, Osamu
    Oyama, Yu
    [J]. TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2016, 239 (02) : 155 - 158
  • [26] Immunogenetics of type 1 diabetes mellitus
    Morran, Michael P.
    Vonberg, Andrew
    Khadra, Anmar
    Pietropaolo, Massimo
    [J]. MOLECULAR ASPECTS OF MEDICINE, 2015, 42 : 42 - 60
  • [27] A METHOD FOR ESTIMATING THE PROBABILITY OF ADVERSE DRUG-REACTIONS
    NARANJO, CA
    BUSTO, U
    SELLERS, EM
    SANDOR, P
    RUIZ, I
    ROBERTS, EA
    JANECEK, E
    DOMECQ, C
    GREENBLATT, DJ
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1981, 30 (02) : 239 - 245
  • [28] Monitoring immune-checkpoint blockade: response evaluation and biomarker development
    Nishino, Mizuki
    Ramaiya, Nikhil H.
    Hatabu, Hiroto
    Hodi, F. Stephen
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2017, 14 (11) : 655 - 668
  • [29] Immunotherapy-induced endocrinopathies: assessment, management and monitoring
    Nogueira, Edson
    Newsom-Davis, Tom
    Morganstein, Daniel L.
    [J]. THERAPEUTIC ADVANCES IN ENDOCRINOLOGY AND METABOLISM, 2019, 10
  • [30] Fulminant type1 diabetes mellitus with anti-programmed cell death-1 therapy
    Okamoto, Masahide
    Okamoto, Mitsuhiro
    Gotoh, Koro
    Masaki, Takayuki
    Ozeki, Yoshinori
    Ando, Hisae
    Anai, Manabu
    Sato, Asami
    Yoshida, Yuichi
    Ueda, So
    Kakuma, Tetsuya
    Shibata, Hirotaka
    [J]. JOURNAL OF DIABETES INVESTIGATION, 2016, 7 (06) : 915 - 918