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Case report and literature review of severe adverse reactions following pucotenlimab treatmentNew drug treatment linked to severe neurological reactions

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Note the potential for severe neurological complications and multiple organ dysfunction following pucotenlimab.

This publication consists of a case report and a literature review focusing on severe adverse reactions associated with pucoten 10limab. The authors present a case involving a patient with advanced breast cancer who experienced progressive neurological symptoms and subsequent death following treatment.

The report details the development of anti-aquaporin 4 antibody (AQP4-Ab)-positive neuromyelitis optica spectrum disorder (NMOSD). The clinical course included severe adverse reactions, multiple organ dysfunction syndrome, and death. The authors describe these events as occurring subsequent to treatment with pucotenlimab.

Clinical management of high-grade N-irAEs is noted as extremely challenging and potentially life-threatening. The authors highlight that diagnosis remains difficult because of nonspecific manifestations and an extensive range of differential diagnoses.

Because this is a single case report and literature review, the findings are limited to the reported instance and existing literature. The evidence does not establish a definitive causal link, but it underscores the need for vigilance regarding neurological complications in patients receiving this therapy.

When we test new medicines, we are often looking for ways to fight advanced diseases like breast cancer. However, sometimes these treatments can trigger unexpected and dangerous reactions in the body.

In a recent case report, a patient with advanced breast cancer received a drug called pucotenlimab. Following the treatment, the patient developed severe neurological symptoms. This reaction was linked to neuromyelitis optica spectrum disorder, which is a rare condition that attacks the central nervous system.

The situation became even more critical as the patient developed multiple organ dysfunction syndrome, a state where several organs fail at once. Sadly, the patient passed away after these severe adverse reactions.

Because this report focuses on just one person, we cannot say for certain if this will happen to others. However, it highlights how difficult it is for doctors to manage high-grade immune-related side effects, which can be life-threatening and hard to diagnose.

What this means for you:
A single case report shows severe, life-threatening neurological reactions following treatment with pucotenlimab.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Immune checkpoint inhibitors (ICIs) have been widely utilized in patients with cancer and established as a standard therapeutic modality for various solid tumors. Although generally well tolerated, ICIs can induce unique immune-related adverse events (irAEs) affecting systemic systems and organs, posing a significant challenge in clinical oncology practice. Neurological immune-related adverse events (N-irAEs) are relatively rare, but the clinical management of high-grade N-irAEs is extremely challenging and potentially life-threatening. Concurrently, the nonspecific manifestations and extensive differential diagnoses of N-irAEs render their diagnosis highly difficult, which may result in suboptimal clinical management. Herein, we report on a case of a patient with advanced breast cancer who developed severe adverse reactions subsequent to treatment with pucotenlimab and was diagnosed with anti-aquaporin 4 antibody (AQP4-Ab)-positive neuromyelitis optica spectrum disorder (NMOSD) following multidisciplinary discussion. Despite prompt administration of high-dose methylprednisolone and plasma exchange therapy, the patient’s neurological symptoms progressively worsened, leading to multiple organ dysfunction syndrome and subsequent death. A literature review on N-irAEs is also presented.
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