Severe immune-related autoimmune hemolytic anemia induced by pembrolizumab: a case report with novel immunosuppressive strategy - Report - MDSpire

Severe immune-related autoimmune hemolytic anemia induced by pembrolizumab: a case report with novel immunosuppressive strategy

  • By

  • Qin Ye

  • Meng Li

  • Ping Zhou

  • Shan Huang

  • Ke Xie

  • May 8, 2026

  • 0 min

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Clinical Report: Severe Autoimmune Hemolytic Anemia Triggered by Pembrolizumab

Overview

This case report details a 52-year-old female with malignant melanoma who developed severe autoimmune hemolytic anemia (AIHA) following pembrolizumab treatment. An innovative immunosuppressive approach involving cyclophosphamide and fluorouracil was effective in managing her condition, allowing for safe rechallenge with pembrolizumab.

Background

Immune checkpoint inhibitors (ICIs) like pembrolizumab have significantly improved survival rates in melanoma patients, but they can cause severe immune-related adverse events (irAEs). Autoimmune hemolytic anemia (AIHA) is a rare but serious complication that can arise from ICI therapy, necessitating prompt recognition and management. Understanding the treatment options for AIHA is crucial for optimizing patient outcomes while continuing effective cancer therapies.

Data Highlights

No numerical data available in the article.

Key Findings

  • A 52-year-old female developed severe AIHA after one cycle of pembrolizumab.
  • Initial treatment with corticosteroids and IVIG was insufficient to control hemolysis.
  • Combination therapy with cyclophosphamide and fluorouracil alongside corticosteroids effectively managed the severe AIHA.
  • After three months, the patient was safely rechallenged with pembrolizumab, managing subsequent AIHA with corticosteroids alone.
  • This case highlights the need for innovative treatment strategies for severe AIHA associated with ICIs.
  • Further research is needed to validate the efficacy of this combined immunosuppressive approach in larger patient populations.

Clinical Implications

Clinicians should be vigilant for signs of AIHA in patients receiving ICIs, particularly when symptoms of anemia arise. The combination of cyclophosphamide and fluorouracil with corticosteroids may offer a viable treatment strategy for severe cases of AIHA, allowing for the continuation of effective cancer therapies.

Conclusion

This case underscores the importance of recognizing and managing severe AIHA as a potential complication of pembrolizumab therapy. With appropriate interventions, safe rechallenge with ICIs may be achievable in select patients.

Related Resources & Content

  1. The ASCO Post, 2019 -- What Causes Liver Injury During Treatment With Pembrolizumab
  2. Frontiers in Immunology, 2026 -- Severe neuromyelitis optica spectrum disorder induced by pucotenlimab: a case report and literature review
  3. The ASCO Post, 2020 -- Do HIV Positivity and Autoimmune Disease Preclude Treatment With Checkpoint Inhibitors?
  4. The ASCO Post, 2018 -- Early Data Suggest TLR9 Agonist May Combat PD-1 Resistance in Advanced Melanoma
  5. PubMed, 2023 -- Pembrolizumab versus ipilimumab for advanced melanoma: 10-year follow-up of the phase III KEYNOTE-006 study
  6. Frontiers, 2025 -- Immune hemolytic anemia associated with the use of immune checkpoint inhibitors: a scoping review
  7. PMC, 2021 -- Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immune checkpoint inhibitor-related adverse events
  8. Pembrolizumab versus ipilimumab for advanced melanoma: 10-year follow-up of the phase III KEYNOTE-006 study - PubMed
  9. Frontiers | Immune hemolytic anemia associated with the use of immune checkpoint inhibitors: a scoping review
  10. Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immune checkpoint inhibitor-related adverse events - PMC

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