Melanoma Flashcards

1
Q

What is a melanoma

A

Cancer that arises in melanocytes

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2
Q

What are the most common of mutations seen in melanoma

A

MAP kinase (enhance proliferation) PI3K/AKT (diminishes apoptosis)

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3
Q

What are genetic risk factors for melanoma

A

Family or personal history of melanoma, history of atypical skin lesions, age, complexion/hair and eye color

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4
Q

What are the enviornmental risk factors for melanoma

A

Sun/UV light exposure, multiple sunburns, residence in sun/nearer to equator

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5
Q

What are the ABCDEs of screening for melanoma

A
A: Asymmetry
B: Boarder
C: Color
D: Diameter
E: Evolving
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6
Q

T/F: The deeper melanoma grows the less overall survival

A

True

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7
Q

What is the first line treatment for a patient with stage 0, 1a, 1b, 2 melanoma

A

Excision with or without a nodal biopsy

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8
Q

What is the first line treatments for a patient with stage 3 (nodal involvement)

A

Excision, Radiation with or without Adjuvant therapy

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9
Q

What are the possible adjuvant therapy treatments for

A

Nivolumab, Pembrolizumab, Dabrafenib/Trametinib

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10
Q

What are the first line treatment for metastatic melanoma

A

Nivolumab, Pembriolizumab, Nivolumab/Ipilimumab

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11
Q

What chemotherapy can be given if a patient has a positive BRAF V600 mutation in Stage 3 melanoma, Stage 4 melanoma

A

Dabrafenib/trametinib/ Dabrafenib/trametinib, vemurafenib/cobimetinib, Encorafenib/binimetinib

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12
Q

What is the most important oncology clinical trial

A

Overall survival

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13
Q

T/F: Immunotherapy causes immediate reduction in tumor therapy

A

False: A patient may have pseudoprogression in the first weeks and when therapy is continued the tumor shrinks

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14
Q

What are the immunotherapy categories

A

PD-1 inhibitors and CTLA-4 inhibitors

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15
Q

What is the mechanism of action for CTLA-4 inhibitors, what is the one CTLA-4 inhibitor

A

Blocks CTLA-4 in order to increase the likelihood that a T-cell is activated by APC, Ipilimumab

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16
Q

T/F: Ipilimumab has the capability of causing high adverse effects and death but also curing melanoma

A

True

17
Q

What is the MOA of PD-1 inhibitors, what are the PD-1 inhibitors

A

Blocking the interaction of PD-1 and programmed cell death ligand 1 (PDL-1) resulting in decreased cell anergy/ Nivolumab and Pembrolizumab

18
Q

What is the risk of mixing a PD-1 inhibitor and a CTLA-4 inhibitor. risk

A

Increase response with much more toxicity that is more intense and frequent

19
Q

What mutation is seen in half of the patients with melanoma

A

BRAF mutation

20
Q

What is the MOA of BRAF inhibitors, what are the BRAF inhibitors

A

Inhibition of mutant BRAF V600E and V600K/ Vemurafenib, Dabrafenib, Encorafenib

21
Q

What patients cant recieve BRAF inhibitors, why

A

BRAF wild type patients, the melanoma becomes worse

22
Q

What are the adverse effects of BRAF

A

New primary malignancies (Keratoacanthomas), skin toxicities, Fevers, QTc prolongation (Hold if greater than 500 ms), Increased creatinine

23
Q

What are the MEK inhibitors

A

Cobimetinib, Trametinib, Binimetinib

24
Q

What are the adverse effects of MEK inhibtors

A

Cardiomyopathy (if LEVF is less than 50% no use), DVT and pulmonary embolism, ocular toxicity

25
Q

When the patients have combination of BRAF and MEK inhibitors what are the most common adverse effects

A

Pyrexia, serum creatinine increase

27
Q

Which cancer drug acts as a vector for a protein that stimulates an immune response on the cancer, what is the major side effect

A

Talimogene Laherparepvec, herpes

28
Q

T/F: Since immunotherapy takes longer than expected if someone has symptoms from there melanoma they should be given a BRAF and MET inhibitor if they have the right mutations

A

True