[Unexpected adverse events of immunotherapies in non-small cell lung cancer: About 2 cases]

G de Chabot1, G Justeau1, F Pinquié1

  • 1Service de pneumologie, CHU d'Angers, 4, rue Larrey, 49933 Angers, France.

Insights

Programmed death receptor 1 (PD1) inhibitors can cause rare immune toxicities like myositis and lupus. Early recognition and corticosteroid treatment are crucial for managing these nivolumab side effects.

Area of Science:

  • Oncology
  • Immunology
  • Neurology

Background:

  • Programmed death receptor 1 (PD1) inhibitors, like nivolumab, are vital immunotherapies for non-small cell lung cancer (NSCLC).
  • While known for toxicities such as colitis, endocrinopathies, and pneumonitis, rare immune-mediated adverse events are increasingly reported.
  • These toxicities can occur even in patients without a prior history of immune dysregulation.

Observation:

  • Two cases of rare nivolumab-associated toxicities are presented in patients without a history of immune disorders.
  • Case 1: A 79-year-old patient developed muscle weakness, diagnosed as myositis with elevated CPK and myasthenia symptoms after nivolumab treatment for large-cell carcinoma.
  • Case 2: An 82-year-old patient with EGFR-mutated bronchial adenocarcinoma experienced shoulder/hip pain and fatigue, diagnosed as systemic lupus erythematosus (SLE) under nivolumab therapy.

Findings:

  • Myositis, confirmed by biopsy, and myasthenia gravis symptoms were observed in one patient.
  • Systemic lupus erythematosus was diagnosed in the second patient.
  • Both patients' symptoms resolved after nivolumab discontinuation and initiation of systemic corticosteroid therapy.

Implications:

  • Clinicians should be vigilant for immune-mediated toxicities, including rare presentations like myositis and SLE, during PD1 inhibitor therapy.
  • Discontinuation of anti-PD1 therapy and prompt corticosteroid administration are essential for managing these adverse events.
  • Careful collegial discussion is needed regarding retreatment with PD1 inhibitors after symptom resolution, especially if alternative therapies are limited.

Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
2.0K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
9.0K
Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
10.2K
Drug Toxicity: Allergic Reactions01:30

Drug Toxicity: Allergic Reactions

Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial...
22