Diferencia entre revisiones de «Oncologic therapy related adverse events»

Sin resumen de edición
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===Panobinostat lactate (Farydak)===
===Panobinostat lactate (Farydak)===
A*dverse Events:
*Adverse Events:
**[[Cytopenia]]
**[[Cytopenia]]
**[[Diarrhea]]
**[[Diarrhea]]
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===Brentuximab vedotin (Adcetris)===
===Brentuximab vedotin (Adcetris)===
*[[Progressive multifocal leukoencephalopathy]]
*Adverse Events:
*[[Peripheral neuropathy]]
**[[Progressive multifocal leukoencephalopathy]]
*[[Bone marrow suppression]]
**[[Peripheral neuropathy]]
**[[Bone marrow suppression]]


==Immunotoxin==
==Immunotoxin==
===Moxetumomab pasudotox-tdfk (Lumoxiti)===
===Moxetumomab pasudotox-tdfk (Lumoxiti)===
*[[Hemolytic uremic syndrome]]
*Adverse Events:
*[[Capillary leak syndrome]]
**[[Hemolytic uremic syndrome]]
**[[Capillary leak syndrome]]


==Bispecific T-cell engager (Blincyto)==
==Bispecific T-cell engager (Blincyto)==
===Blinatumomab===
===Blinatumomab===
*[[CNS depression]]
*Adverse Events:
*[[Cytokine release syndrome]]
**[[CNS depression]]
**[[Cytokine release syndrome]]


==Disposition==
==Disposition==

Revisión del 18:33 6 mar 2020

Background

Many of the oncologic therapies currently employed involved immune system checkpoint inhibition which allow for improvement of T-cell activation towards cancer cells. This boost to the immune system can occur by many mechanisms that encompass the list of "novel" oncologic agents" described below.[1]

Clinical Features

  • Many novel oncologic therapies and Biologic immunomodulators adverse reactions may mimic common ED presentations such as sepsis.

Types of novel oncologic agents

  • Genetically engineered T cells
    • CD19–chimeric antigen receptor (CAR)-T cell therapy
  • Monoclonal Antibodies against PD-1 checkpoints
  • Small-molecule inhibitors
  • Monoclonal antibodies against cell surface antigens
  • Antibody-drug conjugates
  • Immunotoxins
  • Bispecific T-cell engagers

Differential Diagnosis


CAR-T cells medications

Tisagenlecleucel (Kymriah)

Axicabtagene ciloleucel (Yescarta)

PD1 Monoclonal Antibodies

Pembrolizumab (Keytruda)

  • A PD-1 humanized mouse mAb
  • Adverse events include:
    • Infusion reactions
    • Musculoskeletal pain
    • Dyspnea
    • Diarrhea
  • (Arrhythmias
  • (Myocardial infarctions
  • (Pericardial effusions

Nivolumab (OPDIVO)


Small molecule inhibitors

Enasidenib (IDHIFA)


Ivosidenib (Tibsovo)

Midostaurin (Rydapt)

Nilotinib (Tasigna)

Bosutinib (Bosulif)

Ibrutinib (Imbruvica)


Acalabrutinib (Calquence)

Duvelisib (Copiktra)

Copanlisib (Aliqopa)


Panobinostat lactate (Farydak)

Ixazomib citrate (Ninlaro)

Venetoclax (Venclexta)

Monoclonal antibodies against cell surface antigens

Ofatumumab (Arzerra)


Obinutuzumab (Gazyva)


Daratumumab (Darzalex)

Elotuzumab (Empliciti)

Empliciti (Poteligeo)

Antibody-drug conjugates

Inotuzumab ozogamicin (Besponsa)


Gemtuzumab ozogamicin (Mylotarg)


Brentuximab vedotin (Adcetris)

Immunotoxin

Moxetumomab pasudotox-tdfk (Lumoxiti)

Bispecific T-cell engager (Blincyto)

Blinatumomab

Disposition

See Also

External Links

References

  1. Shah, M., Rajha, E., DiNardo, C., Muckey, E., Wierda, W. G., & Yeung, S. C. J. (2020). Adverse Events of Novel Therapies for Hematologic Malignancies: What Emergency Physicians Should Know. Annals of Emergency Medicine, 75(2), 264–286. https://doi.org/10.1016/j.annemergmed.2019.07.015