• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/35

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

35 Cards in this Set

  • Front
  • Back
Adjuvant vs Neoadjuvant Therapy (general)
Adjuvant: eliminate undetectable mets after removing primary tumor

Neoadjuvant: eliminate undetectable mets before removal of primary tumor
Chemotherapy (Cytotoxic) Agents vs Targeted (Biologic) Therapies (general)
Chemo: targets DNA or other cell processes used in cell replication (such as mitotic spindle)

Targeted/biologic Tx: targets markers expressed on cancer cells, genes, or intracellular pathways inappropriately activated or inactivated (tumor suppressors) in cancer cells, or elements of stroma that support tumor growth/mets
Common toxicities of chemotherapy.
Effects on cell proliferation: Myelosuppression (cytopenia)

Hair loss, mouth/anal sores, diarrhea (due to thinning of bowel wall)

Nausea (natural response to poisons), vomiting, anorexia

Tumor lysis syndrome (breakdown of cancer cells more rapidly than body can handle; metabolite imbalances)
How long after chemo administration is cytopenia seen? Why isn't it develop right away?
Takes about a week to see drop in WBC count. Causes system to 'restart' and WBC production resumes after 10-14 days.

Chemo only affects cells that are replicating/dividing. WBCs stop dividing (replicating DNA) at the metamyelocyte stage.

So cells that were already metamyelocytes at time of administration will continue to differentiate.
Antimetabolites:
MOA
Target S phase of cell cycle; inhibit synthesis of DNA
Topoisomerase Inhibitors:
MOA
Target S phase of cell cycle
Antimicrotubule Inhibitors:
MOA
Target M phase of cell cycle
Intercalating Agents:
MOA
Target S phase of cell cycle
Alkylating Agents:
MOA
Toxicities
Attach alkyl group to DNA, usually 7-nitrogen of guanine:

(unbolded):
-DNA fragmented by repair enzymes trying to excise altered nucleotides

-forms cross-links for cDNA strand, preventing DNA transcription/replication.

Toxicities are the same as chemo: myelosuppression, nausea, vomiting, anorexias, mucositis (mouth sores)
Cyclophosphamide:
Drug Class
Alkylating agents - Nitrogen Mustards

require hepatic metabolism to active form

toxic byproducts may cause bladder irritation and hemorrhagic cystitis
This drug requires hepatic metabolism to its active form.
Cyclophosphamide
Ifosfamide
This drug can cause bladder irritation and hemorrhagic cystitis.
Irrirates bladder and causes hemorrhagic cystitis via creation of toxic byproducts!

Cyclophosphamide
Ifosfamide

also have typical chemotx toxicities (myelosuppression, nausea, vomiting, alopecia)
Chlorambucil:
Drug Class
Toxicities
Alkylating agent - Nitrogen Mustard

Toxicities same as alkylating agents: myelosuppression, nausea/vomiting, anorexia
Melphalan:
Drug Class
Toxicities
Alkylating agents - nitrogen mustards

Typical toxicities: myelosuppression (can be prolonged if sem cells damaged), nausea/vomiting, anorexia

ALOPECIA is RARE
This drug rarely causes alopecia.
Melphalan
Busulfan
(Bendamustine NEVER causes alopecia)
Bendamustine:
Drug Class
Toxicities
Alkylating agent- Nitrogen mustard

Typical toxicities for alkylating agent: myelosuppression, n/v/anorexia

NO ALOPECIA
This drug never causes alopecia.
Bendamustine
Busulfan:
Drug Class
Toxicities
Alkylating agent - Alkylsulfonate

Typical Toxicities: myelosuppression, n/v/anorexia, alopecia rare

PULMONARY FIBROSIS
This drug can result in pulmonary fibrosis.
Busulfan
Camustine:
Drug Class
Toxicities
Alkylating agent - Nitrosureas

Myelosuppression (often prolonged)
Lomustine:
Drug Class
Toxicities
Alkylating agent - Nitrosureas

Myelosuppression (often prolonged)
Procarbazine:
Drug Class
Toxicities
Non-classic alkylating agent

Tox: myelosuppression, hypertensive crises when eating tyramine-rich foods (aged cheeses/meats, overripe fruits, wine)
Ingestion of aged cheese, meat, fruit, or wine is contraindicated in this drug.
Procarbazine--bc can cause hypertensive crisis
Methotrexate:
Drug Class
MOA
Toxicities
Antimetabolite: Anti-folates

Blocks enzyme whose product is needed for thymidine (and thus DNA) synthesis

Tox: Myelosuppression, n/v/a
6-mercaptopurine:
Drug Class
Toxicities
Antimetabolite: Purine Analogue

Tox: myelosuppression, tumor lysis syndrome, veno-occlusive disease of liver
6-thioguanine:
Drug Class
Toxicities
Antimetabolite: Purine Analogue

Tox: myelosuppression, tumor lysis syndrome, veno-occlusive disease of liver
This drug's toxicity can be increased by administration of allopuriniol.
6-MP: 6-mercaptopurine
5-fluoruracil:
Drug Class
MOA
Antimetabolite: Pyrimidine Analogue

When bioactivated, binds thymidylate synthetase, depleting cell of thymidine and preventing DNA synthesis
Capecitabine:
Drug Class
Indications
Anti-pyrimidine

Oral pro-drug (converted to 5-FU by liver) used to tx BrCa, ColorectalCa, and other GI cancers
Cytarabine:
Drug Class
Toxicities
Pyrimidine

CNX tox, cerebellar damage
This drug can result in cerebellar damage.
Cytarabine (Ara-C)
Gemcitabine:
Drug Class
Antimetab: Pyrimidine analogue
Hydroxyurea:
MOA
Indication
Toxicities
Antimetabolite: anti deoxyribonucleotide

INhibits ribonucleotide reductase, depleting cells of deoxyribonucleotides (so it's an antimetabolite)

used to bring down blood counts acutely in acute leukemias, CML

also to reduce frequency of crises in sickle cell

Tox: myelosuppression
Thalidomide:
MOA
Indications
Toxicities
Unclear, may suppress angiogenesis

Multiple myeloma

Tox: birth defects
Lenalidomide:
MOA
Indications
Toxicities
MOA: unclear, may suppress angiogenesis

Tox: myelosuppression, birth defects