8/26- Common Cancer Drugs 2: Targeted Therapy Flashcards

(31 cards)

1
Q

How can corticosteroids be used for targeted cancer therapy (what are hormone interaction characteristics of tumors)?

A

Tumors that are steroid hormone-sensitive may be either:

  1. Hormone responsive -> tumor regresses following hormone treatment
  2. Hormone dependent -> removal causes tumor regression
  3. Hormone dependent -> antagonism can block & cause tumor regression
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2
Q

What is a corticosteroids that may be used?

A

Prednisone

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3
Q

What is Prednisone?

  • Characteristics
  • Uses
A

Potent, synthetic, anti-inflammatory corticosteroid

  • Used to induce remission in patients with ALL
  • Used to treat both Hodgkin and non-Hodgkin lymphomas

Prednisone has the ability to destroy (or severely limit) lymphocytes; leukemias that result from uncontrolled growth of lymphocytes respond to treatment.

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4
Q

What is the mechanism of Prednisone?

Resistance?

Pharmocokinetics?

A

Mechanism: binds to HREs and alters transcription

Resistance: receptor is absent or mutated to a low-affinity form

Pharmacokinetics: readily absorbed orally; binds to plasmin albumin and transcortin

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5
Q

What are the ASEs of Prednisone?

A
  • Immunosuppression
  • GI ulcers and pancreatitis
  • Cushing’s Syndrome
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6
Q

What are some sex hormone agonists and antagonists that may be used for targeted cancer treatment?

A
  • Estrogens
  • Tamoxifen
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7
Q

How is estrogen used for cancer treatment?

Uses?

Mechanism?

A
  • Estrogens such as ethinyl estradiol or diethylstilbestrol were used in the treatment of prostate cancer
  • Estrogens inhibit the growth of prostatic tissue by blocking the production of LH in the pituitary, thereby reducing androgen synthesis in the testis.

Not as big a role anymore

  • They have been largely replaced by the GnRH analogs because of fewer adverse effects
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8
Q

What is Tamoxifen?

  • Mechanism
  • Resistance
  • Uses
A

An estrogen antagonist

  • Classified as a SERM (selective estrogen-receptor modulator)
  • Currently approved for 5 yrs of prophylactic use for women at high risk of BC

Mechanism: interferes with the action of natural estrogens in ER+ breast cancers

  • Binds to the estrogen receptor, but the complex is not transcriptionally active

Resistance:

  • Fewer E receptors
  • Decreased affinity
  • Dysfunction

Uses:

  • First line therapy to treat estrogen receptor positive breast cancer!!
  • Weak estrogenic activity -> endometrial CA
  • 40-50% positive response in breast cancer and prophylactic therapy
  • New results: stopping treatment at 5 yrs (rather than 8 yrs) –> a small but significant benefit in DFS and a trend favoring overall survival
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9
Q

Details on Tamoxifen:

  • Pharmacokinetics
  • ASEs
A
  • Effective on oral administration

ASEs: similar to natural estrogens

  • Hot flashes, nausea, and fluid retention
  • 2x increase in endometrial CA
  • Thromboembolic risk
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10
Q

What is GnRH?

What are GnRH agonists and antagonists used for?

A

Normally secreted by the hypothalamus and stimulates the anterior pituitary to secrete LH and FSH which cause stimulation of gonadotropin secretion

  • Used for types of prostate cancer hormone therapy
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11
Q

How do GnRH agonists work? Antogonists?

A

Agonists -> chemical castration

  • Cause a huge, but brief, flare in testosterone production
  • Feedback of “flare levels” block further testosterone production

Antagonists -> blocks pituitary

  • Pituitary loses responsiveness to GnRH
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12
Q

What are some GnRH agonists?

A

Injected once daily:

  • Leuprolide
  • Histerelin

Nasal spray:

  • Nafarelin

Depot preparation:

  • Leuprolide
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13
Q

What is Leuprolide?

  • Mechanism
  • Uses
A

Analog of GnRH

  • Binds to GnRH receptor in the pituitary
  • Cause desensitization of…
  • Results in inhibition of release of FSH and LH
  • Both androgen and estrogen synthesis are reduced

Uses:

  • Response to leuprolide in prostatic cancer is equivalent to orchiectomy
  • Leuprolide has largely replaced estrogen in therapy for prostate cancer
  • Some benefit seen in premenopausal women with advanced breast cancer
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14
Q

What are some GnRH antagonists?

A
  • Abarelix
  • Triptorelin

(Peptide antagonists of the GnRH receptor)

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15
Q

What is Abarelix?

  • Unique
  • Mechanism
  • Uses
A

GnRH antagonist

  • Does not exhibit the “flare phenomenon” of GnRH agonists
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16
Q

What is Triptorelin?

  • Unique
  • Mechanism
  • Ueses
A

GnRH antagonist

  • Reduces the production of LH and causes testosterone levels to fall, but may exhibit a ‘flare phenomenon’
17
Q

What are aromatases?

A

Responsible for the extra-adrenal gland synthesis of estrogen from testosterone.

  • Found in: iver, fat, muscle, skin, and breast tissues
18
Q

What are classes of aromatase inhibitors? Agents?

A

Class:

  • Aminoglutethimide
  • Steroids
  • Imidazoles

Agents:

  • Anastrozole
  • Ietrozole
19
Q

What is the mechanism of aromatase inhibitors?

Adverse side effects?

A

Selective inhibition of aromatase results in less conversion of androgen to estrogen

ASEs:

  • Thromboembolism
  • Fractures
  • Cataracts
  • Endometrial CA
20
Q

Uses of aromatase inhibitors?

A

- Advanced ER+ and PR+ breast cancers

  • Breast cancer prevention trials
21
Q

What is Exemestane?

  • Mechanism
  • Absorption
  • ASEs
  • Contraindications
A
  • Irreversible inhibitor of aromatase
  • Steroidal
  • Well absorbed orally

- Toxicities include: nausea, fatigue and hot flashes

  • Metabolites excreted in urine, hence dosage must be lowered if patient is in renal failure
22
Q

What is Anastrozole?

  • Benefits
  • ASEs
A
  • Imidazole aromatase inhibitors
  • nonsteroidal
  • More potent
  • More selective
  • Hydrocortisone supplementation not needed
  • Do not predispose to endometrial cancer
  • Devoid of androgenic side effects
  • Second line in US; first line in other countries
23
Q

What is Imatinib (Gleevec)? Uses?

A

An inhibitor of a specific protein tyrosine kinases that was targeted to the platelet-derived growth factor receptor (PDGF-R).

  • It was found to inhibit the constitutively active fusion product arising from the Philadelphia (Ph) chromosome of chronic myelogenous leukemia (CML) and c-kit (CD117), which is overexpressed in GI stromal tumors.

Recently approved for:

  • CML refractory to interferon therapy
  • GI stromal cancers
24
Q

What are some ASEs of Imatinib?

A
  • fever, sore throat, and headache with a severe blistering, peeling, and red skin rash;
  • nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);
  • fever, chills, body aches, flu symptoms;
  • black, bloody, or tarry stools;
  • coughing up blood or vomit that looks like coffee grounds;
  • pale skin, easy bruising or bleeding, unusual weakness;
  • feeling short of breath, even with mild exertion;
  • swelling, rapid weight gain;
  • urinating more or less than usual, or not at all
  • sudden, severe headache or pain behind the eyes.

Less severe:

  • mild nausea, diarrhea, upset stomach
  • muscle or joint pain
  • skin rash
  • headache, dizziness
  • stuffy nose, cough, sore throat
  • depression, sleep problems (insomnia) tired feeling.
25
Mechanism of angiogenesis inhibitors?
Inhibition of angiogenesis usually involves the **neutralization** of angiogenic factors such as **VEGF** (vascular endothelial growth factor) or **bFGF** (basic fibroblast growth factor)
26
What is Bevacizumab (Avastin)? Uses?
Angiogenesis inhibitor - An **IgG1** monoclonal Ab _Uses:_ - **Colorectal** cancer that has **spread** to other parts of the body (with other drugs) - Some **non-small cell lung** cancers - Some **breast** cancers that have **spread** to other parts of the body. _Other similar drugs have been approved for:_ - Multiple myeloma - Mantle cell lymphoma - GI stromal tumors - Kidney cancer
27
Name a proteosome inhibitor agent
Bortezomib (Velcade)
28
What is Bortezomib (Velcade)? - Mechanism - Uses
Proteosome inhibitor - **Reversible inhibitor** of the **26S proteasome**, (a multienzyme protease that degrades misfolded or redundant proteins) involved in signal transduction and regulation of the cell cycle - Blockade of this pathway results in **accumulation** of unwanted proteins and cell death -\> **apoptosis** - Cancer cells, because they are more highly proliferative than normal cells, have higher rates of protein translation and degradation _Uses:_ - Newly diagnosed and refractory **multiple myeloma** - Relapsed **mantle cell lymphoma (MCL)**
29
ASEs of Bortezomib?
- General weakness - Nausea - Vomiting - Diarrhea - Stomach pain - Anxiety - Back pain - Bone, joint, or muscle pain - Muscle cramps - Difficulty falling asleep or staying asleep
30
SUMMARY: **_Traditional Chemotherapy_** is a form of cancer treatment that involves taking one or more drugs that interfere with the DNA (genes) of fast-growing cells. These drugs are further subdivided into specific classes such as alkylating agents, antimetabolites, anthracyclines, and topoisomerase inhibitors. **_Targeted Cancer Therapies_** are drugs that block the growth and spread of cancer by interfering with specific molecules involved in tumor growth and progression while sparing normal healthy cells.
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31
Summary Table