Yang J, Wang Y, Tong XM. Sintilimab-induced autoimmune diabetes: A case report and review of the literature. World J Clin Cases 2022; 10(4): 1263-1277 [PMID: 35211559 DOI: 10.12998/wjcc.v10.i4.1263]
Corresponding Author of This Article
Xiang-Min Tong, MD, PhD, Chief Physician, Department of Hematology, Clinical Trial Institute, Zhejiang Provincial People’s Hospital, No. 158 Shangtang Road, Hangzhou 310014, Zhejiang Province, China. tongxiangmin@163.com
Research Domain of This Article
Oncology
Article-Type of This Article
Case Report
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Yang J, Wang Y, Tong XM. Sintilimab-induced autoimmune diabetes: A case report and review of the literature. World J Clin Cases 2022; 10(4): 1263-1277 [PMID: 35211559 DOI: 10.12998/wjcc.v10.i4.1263]
Author contributions: Yang J contributed to data curation; Tong XM and Wang Y contributed to project administration and resources; Yang J wrote the first draft; Tong XM reviewed and edited the manuscript.
Supported byKey Research and Development Project of Science and Technology Department of Zhejiang Province, No. 2019C03038.
Informed consent statement: Informed written consent was obtained from the patient for publication of this report and any accompanying images.
Conflict-of-interest statement: The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Corresponding author: Xiang-Min Tong, MD, PhD, Chief Physician, Department of Hematology, Clinical Trial Institute, Zhejiang Provincial People’s Hospital, No. 158 Shangtang Road, Hangzhou 310014, Zhejiang Province, China. tongxiangmin@163.com
Received: April 15, 2021 Peer-review started: April 15, 2021 First decision: July 6, 2021 Revised: July 8, 2021 Accepted: September 8, 2021 Article in press: September 8, 2021 Published online: February 6, 2022 Processing time: 283 Days and 16.9 Hours
Abstract
BACKGROUND
With the widespread application of immune checkpoint inhibitor (ICI) therapy, the number of immune-related adverse effects (irAEs) has increased over the years. Autoimmune diabetes mellitus (DM) is a rare irAEs of ICIs and can be troublesome and life threatening.
CASE SUMMARY
We report a 78-year-old woman with no history of diabetes who presented with hyperglycemia up to 23.4 mmol/L (random blood glucose level) after 14 courses of sintilimab. Hemoglobin A1c was 8.2%, fasting insulin was 0.29 mIU/mL, and fasting C-peptide was decreased to a level with negative autoantibodies. Combing her medical history and laboratory examination, she was diagnosed with programmed cell death (PD)-1-inhibitor-induced, new-onset autoimmune DM. After controlling her blood glucose, she was treated with daily insulin by subcutaneous injection. She was allowed to continue anti-PD-1 therapy and she still obtained some therapeutic efficacy. We also reviewed some published cases (n = 36) of PD-1/PD-ligand 1 (PD-L1) inhibitor-induced DM. We also discuss potential pathogenic mechanisms, clinical features, prognostic markers (β cell antibodies, human leukocyte antigen type, PD-L1 Level) of this rare adverse effect.
CONCLUSION
It is important for all clinicians to be aware of DM as an irAEs of ICIs.
Core tip: We report a case of programmed cell death (PD)-1-inhibitor-induced autoimmune diabetes mellitus (DM) after treatment of small cell lung cancer, and reviewed some published cases (n = 36) of PD-1/PD-ligand 1 inhibitor-induced DM. Plasma glucose monitoring is significant for preventing the occurrence of diabetic ketoacidosis.
Citation: Yang J, Wang Y, Tong XM. Sintilimab-induced autoimmune diabetes: A case report and review of the literature. World J Clin Cases 2022; 10(4): 1263-1277
Core tip: We report a case of programmed cell death (PD)-1-inhibitor-induced autoimmune diabetes mellitus (DM) after treatment of small cell lung cancer, and reviewed some published cases (n = 36) of PD-1/PD-ligand 1 inhibitor-induced DM. Plasma glucose monitoring is significant for preventing the occurrence of diabetic ketoacidosis.
INTRODUCTION
Immune checkpoint inhibitors (ICIs) have been used widely in the treatment of various advanced malignances. Programmed cell death (PD)-1 (also known as CD279) is one of the best-known ICs, and is expressed on T cells, B cells, activated monocytes, dendritic cells (DCs) and natural killer cells[1]. Its ligand PD-L1 (B7-H1, CD274) is expressed on antigen-presenting cells, macrophagocytes, nonhematopoietic cells and parenchymatous organs such as heart, lungs, placenta and liver. When PD-1 binds to PD-L1 (B7-H1, CD274)/PD-L2 (B7-DC, CD273), a signal that inhibits the proinflammatory ability of T cells and attenuates the function of cytotoxic T cells is delivered. T cell tolerance protects human tissues from immune-mediated tissue damage[2]. However, PD-1 and PD-L1 pathways are also seized by tumors, which impairs tumor immunity and facilitates tumor survival. PD-1/PD-L1 inhibitors remove the inhibitory signals of T cells, enhance cytotoxicity and increase cytokine production. Thus, ICIs can enhance the antitumor effect, but they also increase the chance of inflammatory injury (Figure 1).
Figure 1 Mechanism of action of PD-1/PD-L1 immune checkpoint inhibitors.
PD-1: Programmed death-1; PD-L1: Programmed death-ligand 1.
According to recent research, ICIs induce immune-related adverse events (irAEs) that involve the whole body, including skin (46%–62%), gastrointestinal tract (22%–48%), autoimmune hepatitis (7%–33%), endocrine system (12%–34%), respiratory system (3%–8%) and urinary system (1%–7%)[3]. PD-1/PD-L1-inhibitor-associated autoimmune diabetes mellitus (DM) is rare, with an incidence rate of 0.1% in clinical trials[4]. ICI-induced DM (ICI-DM) is an irreversible event that can be life-threatening if not promptly recognized. Its incidence has increased with the widespread use of immunotherapy. Therefore, it is important for clinicians to fully understand the pathogenic mechanisms of these treatments and their potential irAEs.
Sintilimab is a PD-1 inhibitor that was newly approved in China for treatment of relapsed or refractory Hodgkin’s lymphoma in February 2019[5], and it is now also a feasible treatment for a variety of solid tumors, including non-small cell lung cancer and esophageal cancer. Small cell lung cancer (SCLC) is a malignant tumor with rapid metastasis and poor prognosis. Treatment of SCLC with sintilimab alone or combined with other chemotherapeutic drugs is rare and there are no reports published to describe its clinical effects. Here, we present the first case of new-onset autoimmune DM in a patient with SCLC during treatment with sintilimab, along with marked antitumor efficacy. We also provide a review of case reports of ICI-DM.
This study was conducted according to the advice of the Ethics Center of Zhejiang Provincial People’s Hospital. The patient’s written informed consent was obtained for publication of this case and any images or information that may identify the patient.
CASE PRESENTATION
Chief complaints
A 78-year-old Chinese woman was diagnosed with SCLC 1 year ago with no history of DM who presented with hyperglycemia up to 23.4 mmol/L (random blood glucose level) after 14 courses of sintilimab. The plasma glucose line shown in Figure 2.
Figure 2 Changes of fasting plasma glucose level after initiation of sintilimab.
History of present illness
The patient initially developed polyuria and polydipsia and her blood glucose level showed a mild increase after 12 cycles of sintilimab, but the treatment was continued. Two months later, the patient presented with hyperglycemia up to 23.4 mmol/L (random blood glucose level) with strong positive uric sugar (++++) and hemoglobin A1c of 8.2%.
History of past illness
The patient was diagnosed with SCLC on October 29, 2019 in the First Affiliated Hospital of Zhejiang University. She underwent endobronchial ultrasound-guided transbronchial needle aspiration, and the results were suggestive of poorly differentiated cell carcinoma, considered to be SCLC. Immunohistochemical staining demonstrated CKpan(+), P40(), P63(+), Ki67 (50%+), TTF-1(+), CgA(+), Syn(+), CD56(+) and CD45(). The patient immediately underwent concurrent chemotherapy and immunotherapy for SCLC (extensive). She received her first treatment, etoposide 82 mg, days 1–3; cisplatin 20 mg, days 1–3; and sintilimab 200 mg, day 1; EP plan) on October 30, 2019. The patient came to our hospital to continue treatment. After we assessed her condition, she continued the EP treatment plan, but we reformulated the doses as follows: etoposide 240 mg, days 1–3; cisplatin 250 mg, days 1–3; and sintilimab 200 mg, day 1. This therapy did control her disease well, with decreased tumor markers and no metastases found on imaging. In the following days, she came to our hospital monthly for evaluation. Her blood glucose level was normal after treatment. After five cycles with the EP plan, we changed to sintilimab 200 mg and anlotinib 8 mg q.d. because of severe gastrointestinal adverse reactions. After three cycles of the new treatment, the patient developed lower urinary tract infection, such as urinary frequency, difficulty urinating, pain with urination, and hematuria. Therefore, we had to stop anlotinib and used levofloxacin to treat the infection. Hence, we used sintilimab monotherapy, and imaging showed good antitumor effects (Figure 2). During the treatment, the patient only had mild gastrointestinal symptoms such as nausea and poor appetite.
Personal and family history
The patient denied any other specific personal history. But she has family history of cancer, her grandmother died of lung cancer, whereas her father died of colorectal cancer.
Physical examination
Height: 151 cm; weight: 40.4 kg; body mass index: 17.71 kg/m2. Physical examination was no positive signs.
Laboratory examinations
Other laboratory evaluation (Table 1) showed that urinary ketones were negative and blood pH was normal and the hypothalamic–pituitary–gonadal axis and hypothalamic–pituitary–adrenocortical axis were negative; but antithyroid autoantibodies were 17.80 IU/mL (normal< 4.0 IU/mL) and antithyroid peroxidase autoantibodies were 10.0 IU/mL (normal < 9.0 IU/mL). The islets antibodies tests were all negative, including anti-glutamic acid decarboxylase 65 (GADA) antibody, anti-islet cell antibody, and anti-insulin antibody tests were all negative. Moreover, zinc transporter 8 antibody levels were unavailable in our hospital. Human leukocyte antigen (HLA) class I and II, which was shown in Table 2, including HLA-A, B, C, DRB1, DQB1 and DPB1, were tested by polymerase chain reaction-sequence based typing (PCR-SBT).
According to the computed tomography scanning of the patient’s chest (Figure 3B), the tumor was shrinking, which indicated that anti-PD-1 therapy was effective.
Figure 3 Course of treatment of patients with diabetes induced by immune checkpoint inhibitors.
A: Changes of gastrin-releasing peptide precursor level during each period; B: Contrast-enhanced chest computed tomography during each period. Red arrows indicate the tumors.
FINAL DIAGNOSIS
The patient had no history of DM or autoimmune disease before treatment, and there was no medication, infection, thromboembolic event, or other factor that could cause hyperglycemia; according to the laboratory evaluation, thus, sintilimab-induced, new-onset autoimmune DM was diagnosed.
TREATMENT
Intravenous fluid infusion, continuous subcutaneous insulin infusion (insulin infusion pump therapy) and other supportive treatments were administered. After 10 d of insulin infusion pump therapy, the patient’s plasma glucose returned to normal levels. We performed a simple oral glucose tolerance test that revealed that the fasting and 0–2-h insulin levels were 0.29 and 2.50 IU/mL; fasting and 0–2-h C-peptide levels were 0.22 and 0.52 ng/mL, which indicated an insufficient function of pancreatic islet β cells. Subsequently, she was switched to once-daily basal insulin detemir (long-acting insulin, 10 U) plus thrice-daily premeal insulin aspart (fast acting insulin, 11 U, respectively 3U, 4U, 3U three meals) subcutaneous injection for long-term treatment.
OUTCOME AND FOLLOW-UP
By the time the manuscript was completed, the patient was without evidence of SCLC recurrence with no further treatment since sintilimab (Figure 3). Other endocrine adverse effects such as thyroiditis and hypophysitis did not occur. We retrieved 36 relevant case reports from 2016 to 2020 in PubMed to determine the common features of ICI-DM (Table 3)[6-37]. Table 4 summarizes the key features.
Table 3 Reported cases of diabetes induced by immune checkpoint inhibitors.
Sintilimab is a fully humanized IgG4 monoclonal antibody that binds to PD-1, then interferes with the interaction of PD-1 and its ligands (PD-L1 and PD-L2), thus activating and restoring the function of T cells, which contributes to an obvious antitumor effect. Accordingly, some normal tissues have been damaged in this process by the increase of cytokines. ICI-DM has rarely been reported as an irAEs of anti-PD1/PD-L1 therapy, and primarily in case reports.
In our review of case reports, the main tumor types were melanoma (13/36, 36.1%) and non-SCLC (8/36, 22.2%). The different treatment regimens included monotherapy with anti-PD-1 (19/ 36, 52.7%) anti-PD-L1 (8/36, 22.2%) or a combination of anti-CTLA-4 with anti-PD-1 (9/36, 25.0%). Diabetic ketoacidosis (DKA) was the first sign of diabetes in 29 of 36 (80.5%) case reports, which is similar to 85.7% in another study[38], and the average time from initiation of anti-PD-1/PD-L1 therapy to diagnosis of ICI-DM was 14.6 wk (range 2–48 wk). Low C-peptide levels were present at diagnosis in 82% (23/28) of cases. In addition, 26 of 36 patients presented with a median glycated hemoglobin level of 7.6% (average: 7.8%; range: 6.4%–10.9%), which is the same as in other studies[39,40]. Most of the patients did not have relevant autoimmune history, which was only seen in 18.3% of our reviewed cases. These case reports have different definitions for ICI-DM. Since the syndrome has similarities with classic type 1 (T1)DM, most reports simply classified ICI-DM as T1DM, but ICI-DM has its own features. We found several significant features of ICI-DM: (1) Abrupt onset of hyperglycemia, and low to absent insulin C-peptide levels; (2) Rapid destruction of islets β cells, leading to endogenous insulin deficiency; and (3) High risk of DKA[39]. In addition to the above features, ICI-DM does not have a “honeymoon period” like juvenile T1DM, nor does it have GADA as in latent autoimmune DM in adults[41].
Similar to a previous study[39], our autoantibody analysis was positive in 50% of patients for GADA. Some studies have demonstrated that GADA-positive patients developed ICI-DM in the first 2 mo after initiation of therapy, and GADA-negative patients developed ICI-DM after 2 mo of treatment[42]. Patients with any positive diabetes autoantibodies at the time of presentation of ICI-DM have fewer cycles than those with negative autoantibodies. Our results showed that GADA-positive patients had ICI-DM onset at an average of 8 wk after immunotherapy compared with 22.8 wk in GADA-negative patients. It has been demonstrated that the interval from initiation of anti-PD-1/PD-L1 therapy and onset of ICI-DM is related to the presence/absence of GADA. Serological examination of GADA prior to anti-PD-1/PD-L1 therapy might be helpful for predicting the development of ICI-DM. In addition, several major histocompatibility complex and HLA molecules are associated with increased susceptibility to T1DM, especially HLA-DRB1, -DQB1 and –DQA1[43]. Different combinations of DRB1, DQB1 and DQA1 determine the extent of haplotypic risk. The most susceptible HLA haplotypes are DRB1*0405–DQA1*0301–DQB1*0302, followed by DRB1*0401–DQA1*0301–DQB*0302, DRB1*0301–DQA1*0501–DQB1*0201, and DRB1*0402–DQA1*0301–DQB1*0302. Subsequently, DQB1*0302 allele is the key susceptibility allele[44]. However, another study confirmed that DPB1*0301 and DPB1*0202 are also susceptible haplotypes for T1DM. Hence, the HLA typing of our patient (Table 2) showed a high risk of T1DM. Based on this evidence, there were seven patients with high-risk genes for T1DM among 13 patients tested. Accordingly, understanding the association between HLA and the development of ICI-DM by anti-PD-1/PD-L1 therapy is significant in predicting susceptible patients. When clinical features are discordant with the results of autoantibody testing, genetic risk score (GRS) could be an important addition to diagnosis of ICI-DM. This GRS summarizes risk-associated variation across the genome of T1DM[45]. One limitation of our case was the lack of information before sintilimab, such as autoimmune antibodies and genetic factors like HLA genotypes that may predispose to endocrine irAEs.
Multiple studies have indicated both the PD-1 and CTLA-4 pathways in the pathogenesis of T1DM and suggest a synergistic effect between these two negative regulatory receptors to enhance autoimmune disorders. Furthermore, the incidence of ICI-induced endocrine irAEs is significantly higher in patients treated with combination immunotherapy compared with single immunotherapy. The incidence of thyroid dysfunction is high in patients treated with single PD-1 antibodies. In contrast, the incidence of hypophysitis is highest in patients treated with ipilimumab[46]. Similarly, our review also found that combination of PD-1 inhibitor and anti-CTLA-4 therapy causes endocrine dysfunction. The most common combination was nivolumab and ipilimumab. An animal study found that single CTLA-4 blockers in nonobese diabetic (NOD) mice only induced diabetes in baby mice, while PD-1 blocked secondary diabetes in NOD mice at any age[47]. A recent case reported that ipilimumab induced T1DM. The mechanism by which single anti-CTLA-4 therapy induced ICI-DM was unclear and needs further study[48]. However, a randomized, double-blind, phase 3 study suggested that combination of immunotherapy significantly increases progression-free survival more than monotherapy does[49]. Therefore, it is important for clinicians to consider whether to continue to use combination therapy when endocrine irAEs appear.
T1DM is caused by destruction of pancreatic β cells by virus infection, genetic factors and autoimmune disorders[32]. Accordingly, the main mechanism of ICI-DM may be islet cell damage. There is an active interaction between β cells and immune cells during insulitis. This kind of interaction usually has a largely negative effect on β cells. An animal study has shown that PD-1 deficiency accelerates the occurrence and frequency of T1DM in NOD mice, and infiltration of pancreatic islets by T cells with strong T helper 1 polarization[50]. In addition, animal and human experiments have shown that PD-L1 in insulin-positive cells of T1DM, but absent in nondiabetic individuals and type 2 DM, is mainly due to islet β cell expression[6]. The present data indicate that interferon (IFN)-α and IFN-γ are the main regulators of PD-L1 expression in human pancreatic β cells, especially IFN-γ. IFN-γ suppresses autoreactive T cells by upregulating PD-L1. In other words, PD-L1 protects islet β cells to delay progression of DM and even prevent its onset[50-52]. Yet, IFN-α and IFN-γ induce proinflammatory responses. For instance, HLA class I upregulation, cytokine production and endoplasmic reticulum stress are harmful to the human body, including the pancreas. Inhibition of signal transducer and activator of transcription 2 can prevent IFNα-induced HLA class I expression, and at the same time allow PD-L1 upregulation[53], but this lacks clinical validation. Therefore, the level of PD-L1 expression may serve as an additional criterion for irAEs after ICI treatment. PD-L1 expression can also be used as a prognostic marker of immunotherapy[54]. In our patient, in spite of tumor necrosis factor-α, IL-1β and IFN-γ, all of the cytokines were normal during treatment with sintilimab, which suggest the particular pathogenic mechanism of ICI-DM. However, the precise mechanism mediating ICI-DM is still unclear. Further studies are required to elucidate the pathogenesis and background factors for this form of DM.
CONCLUSION
This is the second case of sintilimab-induced autoimmune DM. The first one was a recently published case report of autoimmune DM diagnosed in a patient with hepatocellular carcinoma[37]. What makes our case different from others is that there was no DKA in the process of DM. This may be because patients were regularly monitored for plasma glucose level. This illustrates the importance of regular monitoring of glucose during immunotherapy for inhibiting progression of DM. Furthermore, based on the information collected in our review, we recommend measuring PD-L1 expression, HLA typing, islet cell antibody testing, C peptide measurement, or even determining T1DM-associated GRS for clinicians before or during immunotherapy. We can compare symptom severity and therapeutic efficacy in DM patients with or without a history of DM after treatment with PD-1/PD-L1 inhibitors in the future, so as to evaluate whether patients with potential risk of DM are suitable for treatment with PD-1/PD-L1 inhibitors.
Usui Y, Udagawa H, Matsumoto S, Imai K, Ohashi K, Ishibashi M, Kirita K, Umemura S, Yoh K, Niho S, Osame K, Goto K. Association of Serum Anti-GAD Antibody and HLA Haplotypes with Type 1 Diabetes Mellitus Triggered by Nivolumab in Patients with Non-Small Cell Lung Cancer.J Thorac Oncol. 2017;12:e41-e43.
[RCA] [PubMed] [DOI] [Full Text][Cited by in Crossref: 37][Cited by in RCA: 58][Article Influence: 5.8][Reference Citation Analysis (0)]
Erlich H, Valdes AM, Noble J, Carlson JA, Varney M, Concannon P, Mychaleckyj JC, Todd JA, Bonella P, Fear AL, Lavant E, Louey A, Moonsamy P; Type 1 Diabetes Genetics Consortium. HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium families.Diabetes. 2008;57:1084-1092.
[RCA] [PubMed] [DOI] [Full Text][Cited by in Crossref: 588][Cited by in RCA: 613][Article Influence: 34.1][Reference Citation Analysis (0)]
Colli ML, Hill JLE, Marroquí L, Chaffey J, Dos Santos RS, Leete P, Coomans de Brachène A, Paula FMM, Op de Beeck A, Castela A, Marselli L, Krogvold L, Dahl-Jorgensen K, Marchetti P, Morgan NG, Richardson SJ, Eizirik DL. PDL1 is expressed in the islets of people with type 1 diabetes and is up-regulated by interferons-α and-γ via IRF1 induction.EBioMedicine. 2018;36:367-375.
[RCA] [PubMed] [DOI] [Full Text] [Full Text (PDF)][Cited by in Crossref: 93][Cited by in RCA: 160][Article Influence: 20.0][Reference Citation Analysis (0)]
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
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