Advanced Drug Delivery 5 - Antibody-Drug-Conjugates Flashcards

1
Q

Define Antibody-Drug Conjugates (ADC) for cancer therapy

A

Drug delivery technology in which mabs are covalently conjugated to cytotoxic agents

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2
Q

Rationale for ADC

A
  • Most mabs have little anti tumour activity (exceptions are anti-HER2 and anti-CD20)
  • However, they do have specificity to the target

Conjugating mab to the effector molecules:

  • The Mab ensures specific targeting
  • The effector molecule ensures anticancer effect.
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3
Q

Structure of ADC

A

3 main components:
- mab which acts as carrier and ensures specific targeting
- multiple drug molecules - cytotoxic drug which kills cancer cells
- linker: attaches antibody to drug

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4
Q

Considerations of ADC

A
  1. Target expression: tumour specific and target internalisation
  2. Linker
  3. Conjugation
  4. Choice of drug
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5
Q
  1. Tumour specific
A
  • tumour cells
  • cells associated with tumour cells e.g. tumour endothelial cells
  • antigens present in tumour microenvironment
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6
Q
  1. Target internalisation
A
  • Complex between target and ADC gets internalised by cell
  • Need to know the internalisation pathway to ensure correct activity of the drug.
  • Need to know cellular pharmacokinetics of the complex
  • Ensure it is compatible with position of effector drug to ensure ADC system works
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7
Q
  1. Considerations of linker
A
  • Needs to be stable in circulation and released at target
  • Ensure appropriate bonds e.g. disulphides, dipeptides, hydrazone linkages
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8
Q
  1. Considerations of choice of drug
A
  • How many drug molecules
  • Drug loading stoichiometry
  • Molecular homogeneity
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9
Q
  1. How much drug molecules
A

Too many:

  • could interfere with recognition of mab+antigen
  • impair binding

Too little:

  • Could decrease potency of ADC system
  • Need to balance both out to get good potency without compromising interaction
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10
Q
  1. Drug loading stoichiometry
A

Ratio between antibody and drug

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11
Q

Molecular homogeneity

A
  • Should have ADC that are as homogenous as possible
  • e.g. if 3 drug molecules, then try having all attached in same point as other AD
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12
Q
  1. Toxicity considerations: ADC compared to parent drug
A
  • ADC expected to be less toxic than parent drug
  • May have similar type of toxicity just to a lesser extent (e.g. lot more needed to produce same toxicity)
  • Need to consider potential toxicity coming from other components, not just the drug
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13
Q

Brentuximab vedotin

A
  • First ADC approved by FDA
  • Used for CD30+ Hodkin’s Lymphoma
  • Active drug works by disrupting microtubules
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14
Q

Ado-trastuzumab emtansine

A
  • IV administration
  • HER2+ metastatic breast cancer
  • Trastuzumab: mab that recognises and attaches to HER2 expressed on cancer cells, activating immune response that kills them
  • DM1: toxic substance that binds to tubulin in cancer cells, preventing mitosis and thus preventing growth and division of cancer cells
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