# Type I Diabetes—A Rare Adverse Event Described in Patients Receiving Immunotherapy Versus a Side Effect from SARS-CoV-2 Infection

**Authors:** Raluca-Ileana Pătru, Miruna Ghigeanu, Maria-Alexandra Barbu, Andreea Iuliana Ionescu, Antone-Iordache Ionuț-Lucian

PMC · DOI: 10.3390/reports8010031 · 2025-03-14

## TL;DR

This paper reports a rare case of type I diabetes in a lung cancer patient treated with immunotherapy and infected with SARS-CoV-2, suggesting a possible synergistic effect.

## Contribution

It presents a unique case linking immunotherapy, SARS-CoV-2 infection, and new-onset type 1 diabetes in an older adult.

## Key findings

- The patient developed type I diabetes after SARS-CoV-2 infection during immunotherapy.
- The patient showed complete remission of cancer after diabetes onset.
- The case highlights the unclear etiology of diabetes in older adults receiving immunotherapy.

## Abstract

Background and Clinical Significance: Lung cancer, a leading cause of global cancer diagnoses, maintains the highest mortality risk despite advances in treatment. Immunotherapy agents, such as anti-programmed death-1/programmed death ligand-1 (PD-1/PD-L1), have revolutionized care for non-small cell lung cancer (NSCLC). However, the success is tempered by the emergence of immune-mediated adverse reactions, including the rare onset of type I diabetes. The incidence of diabetes mellitus increased during the SARS-CoV-2 pandemic. While there are several cases of new-onset diabetes after COVID-19 and COVID-19 vaccination, no case of new-onset type 1 diabetes after COVID-19 was described in an immune checkpoint inhibitor (ICI)-treated patient. Case Presentation: A 57-year-old male with stage IV NSCLC (brain and liver metastases) who had been treated with nivolumab for 4 years appeared positive for SARS-CoV-2 infection at a routine check. After two weeks, he was admitted to our clinic with severe fatigue, hyperglycemia, hyponatremia, and hyperkalemia. HbA1c level was normal and serum peptide C was undetectable. Nivolumab treatment was ceased, and the patient became fully dependent on basal–bolus insulin. After 3 months, the patient showed a complete imagistic remission. Conclusions: The case presented significant challenges due to the unclear etiology of newly onset diabetes and the uncommon age at which type 1 diabetes is developed. The outcome suggests that anti-PD-1 and SARS-CoV-2 infection can act synergistically.

## Linked entities

- **Diseases:** type I diabetes (MONDO:0005147), lung cancer (MONDO:0005138), non-small cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** hyponatremia (MESH:D007010), hyperkalemia (MESH:D006947), COVID-19 (MESH:D000086382), NSCLC (MESH:D002289), metastases (MESH:D009362), Type I Diabetes (MESH:D003922), hyperglycemia (MESH:D006943), fatigue (MESH:D005221), diabetes (MESH:D003920), Lung cancer (MESH:D008175), cancer (MESH:D009369)
- **Chemicals:** insulin (MESH:D007328), Nivolumab (MESH:D000077594), immune checkpoint (-), peptide C (MESH:C050632)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12199958/full.md

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Source: https://tomesphere.com/paper/PMC12199958