Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panel
- PMID: 38642304
- DOI: 10.1007/s00277-024-05736-6
Expert consensus on the management of infusion-related reactions (IRRs) in patients with sickle cell disease (SCD) receiving crizanlizumab: a RAND/UCLA modified Delphi panel
Abstract
Crizanlizumab, a monoclonal antibody against P-selectin, has been shown to reduce vaso-occlusive crises (VOCs) compared to placebo in patients ≥ 16 years with sickle cell disease (SCD). However, there have been rare reports of patients experiencing severe pain and subsequent complications within 24 hours of crizanlizumab infusions. These events are defined as infusion-related reactions (IRRs). Informed by current literature and clinical experience, a group of content experts developed clinical guidelines for the management of IRRs in patients with SCD. We used the RAND/University of California, Los Angeles (UCLA) modified Delphi panel method, a valid, reproducible technique for achieving consensus. We present our recommendations for managing IRRs, which depend on patient characteristics including: prior history of IRRs to other monoclonal antibodies or medications, changes to crizanlizumab infusion rate and patient monitoring, pain severity relative to patient's typical SCD crises, and severe allergic symptoms. These recommendations outline how to evaluate and manage IRRs in patients receiving crizanlizumab. Future research should validate this guidance using clinical data and identify patients at risk for these IRRs.
Keywords: Allergy; Crizanlizumab; Hematology; Monoclonal antibody; Vaso-occlusive crises.
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Similar articles
-
Systematic Review of Crizanlizumab: A New Parenteral Option to Reduce Vaso-occlusive Pain Crises in Patients with Sickle Cell Disease.Pharmacotherapy. 2020 Jun;40(6):535-543. doi: 10.1002/phar.2409. Epub 2020 May 20. Pharmacotherapy. 2020. PMID: 32350885
-
Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease: final results from the phase II SOLACE-adults study.Ther Adv Hematol. 2024 Nov 3;15:20406207241292508. doi: 10.1177/20406207241292508. eCollection 2024. Ther Adv Hematol. 2024. PMID: 39497751 Free PMC article.
-
Real-World Evidence of Crizanlizumab Showing Reductions in Vaso-Occlusive Crises and Opioid Usage in Sickle Cell Disease.Eur J Haematol. 2025 Feb;114(2):293-302. doi: 10.1111/ejh.14323. Epub 2024 Oct 29. Eur J Haematol. 2025. PMID: 39473076 Free PMC article. Clinical Trial.
-
Crizanlizumab: First Approval.Drugs. 2020 Jan;80(1):79-84. doi: 10.1007/s40265-019-01254-2. Drugs. 2020. PMID: 31933169 Review.
-
Successful Treatment of SCD-Related Priapism With Crizanlizumab: A Case Series.J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231191873. doi: 10.1177/23247096231191873. J Investig Med High Impact Case Rep. 2023. PMID: 37731262 Free PMC article.
Cited by
-
Accelerated drug approvals and patient trust: impact of voxelotor and crizanlizumab for sickle cell disease.Blood Adv. 2025 Jun 10;9(11):2857-2862. doi: 10.1182/bloodadvances.2025015822. Blood Adv. 2025. PMID: 40085957 Free PMC article.
-
Fostering a healthier generation of children with sickle cell disease through advancements in care.Pediatr Res. 2025 Mar;97(4):1280-1289. doi: 10.1038/s41390-024-03566-w. Epub 2024 Sep 13. Pediatr Res. 2025. PMID: 39271903 Review.
References
-
- Brousseau DC, Panepinto JA, Nimmer M, Hoffmann RG (2009) The number of people with sickle cell disease in the United States: National and state estimates. Am J Hematol NA-NA. https://doi.org/10.1002/ajh.21570 - DOI
-
- Hassell KL (2010) Population estimates of Sickle Cell Disease in the U.S. Am J Prev Med 38:S512–S521. https://doi.org/10.1016/j.amepre.2009.12.022 - DOI - PubMed
-
- Quinn CT, Rogers ZR, McCavit TL, Buchanan GR (2010) Improved survival of children and adolescents with sickle cell disease. Blood 115:3447–3452. https://doi.org/10.1182/blood-2009-07-233700 - DOI - PubMed - PMC
-
- Wang Y, Liu G, Caggana M et al (2015) Mortality of New York children with sickle cell disease identified through newborn screening. Genet Med 17:452–459. https://doi.org/10.1038/gim.2014.123 - DOI - PubMed
-
- Nze C, Fortin B, Freedman R et al (2020) Sudden death in sickle cell disease: current experience. Br J Haematol 188:e43–e45. https://doi.org/10.1111/bjh.16314 - DOI - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical