Paroxysmal nocturnal hemoglobinuria: Review of the patient experience and treatment landscape

Anem Waheed, Jamile Shammo, David Dingli*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

1 Scopus citations

Abstract

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disorder caused by complement-mediated hemolysis and thrombosis through the alternative pathway. The most common symptom of PNH is fatigue due to chronic anemia, which can negatively impact quality of life (QoL) and affect overall well-being. The currently approved therapies for PNH significantly limit intravascular hemolysis (IVH) and reduce the risk of thrombosis; however, they are associated with an infusion schedule that can become burdensome, and not all patients experience complete disease control. Several new complement inhibitors are in development that address the need for convenient routes of administration and aim to provide better disease control. With the variety of new treatment options on the horizon, hematologic markers as well as QoL concerns, patient opinion, and lifestyle factors should be considered to choose the optimal PNH treatment for each specific patient.

Original languageEnglish (US)
Article number101158
JournalBlood Reviews
Volume64
DOIs
StatePublished - Mar 2024

Funding

Medical writing support of this manuscript was funded by Novartis Pharmaceuticals Corporation.Editorial and medical writing support was provided by Erika Tomei, PhD, of Nucleus Global, and was funded by Novartis. Medical writing support of this manuscript was funded by Novartis Pharmaceuticals Corporation .

Keywords

  • Breakthrough hemolysis
  • Complement inhibition
  • Extravascular hemolysis
  • Paroxysmal nocturnal hemoglobinuria
  • Quality of life
  • Residual anemia

ASJC Scopus subject areas

  • Hematology
  • Oncology

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