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Adverse Events of Novel Therapies for Hematologic Malignancies: What Emergency Physicians Should Know
Mohsin Shah1, Eva Rajha1, Courtney DiNardo2
1Department of Emergency Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
Abstract:
In the past decade, rapid advances in therapeutic target discovery in hematologic malignancies have led to many clinical studies demonstrating efficacy of novel agents. Between 2014 and 2018, Food and Drug Administration approvals of new drugs and agents have increased, with greater than 2 dozen novel agents. Rapidly identifying the risk profiles of these cancer therapeutics that may present with acute toxicities and understanding the timing, sequence, duration, and treatment of disease processes are the most important challenges faced by practitioners in emergency medicine, even in nononcologic centers. The emergency medicine literature lags behind rapid advances in oncology, and guidelines for rapid recognition and management of these emerging entities are not familiar. In this Review Article, we discuss the most recent and clinically relevant developments in the arena of hematologic malignancies, further expanding on drug toxicities and their clinical presentations and offering suggestions for management. Specifically, we discuss immune-related adverse events after immune checkpoint inhibitor therapy (including myocarditis and hemophagocytic lymphohistiocytosis), chimeric antigen receptor-T cell therapy, cytokine release syndrome, chimeric antigen receptor-T cell-related encephalopathy syndrome, differentiation syndrome, sinusoid occlusion syndrome, QT-interval prolongation, and tumor lysis syndrome. Rapid advances in hematology and oncology will bring many new challenges for emergency health care providers in the near future; thus, the urgency to raise awareness among this community.
Insights
Emergency physicians face challenges managing novel cancer drug toxicities in hematologic malignancies. This review covers immune-related adverse events and other acute toxicities, offering management guidance for these emerging oncologic emergencies.
Area of Science:
- Hematology and Oncology
- Emergency Medicine
- Pharmacology
Background:
- Significant advancements in hematologic malignancy therapeutics have occurred in the last decade.
- The Food and Drug Administration approved over two dozen novel agents between 2014 and 2018.
- Emergency medicine literature and guidelines have not kept pace with rapid oncology advances.
Purpose of the Study:
- To review recent, clinically relevant developments in hematologic malignancies.
- To expand on drug toxicities, their clinical presentations, and management strategies.
- To raise awareness among emergency health care providers regarding novel cancer therapeutic toxicities.
Main Methods:
- Review of recent literature on novel agents and their toxicities in hematologic malignancies.
- Discussion of specific immune-related adverse events and other acute toxicities.
- Provision of suggestions for the recognition and management of these conditions.
Main Results:
- Novel cancer therapeutics present unique and acute toxicities requiring prompt recognition.
- Specific toxicities discussed include immune-related adverse events (myocarditis, hemophagocytic lymphohistiocytosis), cytokine release syndrome, CAR T-cell-related encephalopathy syndrome, differentiation syndrome, sinusoid occlusion syndrome, QT-interval prolongation, and tumor lysis syndrome.
- Management strategies for these emerging oncologic emergencies are presented.
Conclusions:
- Rapid advancements in hematology and oncology pose significant challenges for emergency care.
- Familiarity with novel drug toxicities and their management is crucial for emergency physicians.
- Proactive awareness and education are essential to address the growing complexities of cancer therapeutics in emergency settings.
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