exam 2 lecture 5 (melanoma) Flashcards

1
Q

What are melanocytes? use? What is melanoma?

A

Melanocytes are dendritic pigmented cells located in skin and eye. They synthesize melanin to protect tissues from UV raditaion

melanoma results from malignant transformation of skin melanocytes

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2
Q

risk factors for melanoma

A

old white men.

tanning bed

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3
Q

WHAT ARE THE DIFFERENT GROWTH PATTERNS OF MELANOMA AND HOW PREVALENT THEY ARE, who are they common in

A
  1. Superficial spreading melanoma - 70% of cases, more in women
    nodular melanoma- 15% of cases, men
    Lentigo malina melanoma- elderly
    acral lentiginous melanoma- on palms and soles. In africans, asians, latinos
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4
Q

Clinical presentation of meanoma

A

ABCDE
- Asymmetric
- irregular Borders
- wide variety of Colors
- DIameter of >6mm
- Evolution of mole

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5
Q

how to diagnose melanoma

A

Biopsy of suspected lesion is gold standard
History and PE
CT scan if metastatic

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6
Q

treatment overview of melanoma based on stages

A

Stage IB or IIA (lymph node negative
-clinical trial or observation

stage IIB or IIC (lymph node negative)
- clinical trial, observation, pembrolizumab

Stage III
- Nivolumab, pembrolizumab (both immunotherapies)

or dabrafenib/trametinib (if bRAF mutant), with or without radiation FOR A YEAR

unresectable stage III
-T-VEC, topical imiquimod, radiation, limb perfusion

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7
Q

what is preferred adjuvant treatment in melanoma? What other drug is similar interms of efficacy and toxicity

A

nivolumab

pembrolizumab is similar interms of efficacy and toxicity

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8
Q

What adjuvant is used for completely resected stage III disease with BRAF V600E or V600K mutations

A

Dabrafenib + trametinib

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9
Q

Why are trametinib and dabrafenib given together

A

Trametinib is MEK inhibitor and BRAF like dabrafenib increases efficacy

BRAF inhibitor alone leads to resistance, that is why we add MEK inhibitor

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10
Q

first line treatment options for metastatic melanoma

A
  1. anti-PD-1 monotherapy
    -nivolumab
    -pembrolizumab
    -nivolumab and relatimab
  2. combination targeted therapy if BRAF V600 mutation
    -Dabrafenib/trametinib
    Vemurafenib/cobimetinib
    -encorafenib/binimetinib (preferred)
  3. certain circumstances
    - nivolumab/ipilimumab (lots of toxicities. Has to be a young and strong patient)

notice there are no chemo therapies.

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11
Q

toxicity of dabrafenib/trametinib

A

Pyrexia (fever), fatigue, nausea

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12
Q

2nd line tx options of metastatic tx of melanoma

A

same as 1st line except the addition of pembrolizumab/low dose ipilimumab if pt failed on anti PD-1 tx

and another difference is we MAY use chemo if we tried the anti PD-1 therapy (including pembro/ipili) and there are no BRAF mutations

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13
Q

If we have a BRAF mutation with melanoma do we always go with BRAF therapy

A

Yes, works quicker.

Immunotherapy takes weeks to work

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14
Q

What type of drug is vemurafenib? Unique toxicities?

A

BRAF inhibitor

toxicity- development of squamous cell carcinoma

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15
Q

What is used as MEK inhibitor with vemurafenib

A

cobimetinib

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16
Q

why is encorafenib/binimetinib used over vemurafenib/cobimetinib and dabrafenib and trametinib

A

Less fever, better tolerated

17
Q

what is something to know about immunotherapy compared to chemo

A

Make sure you do not stop immonotherapy treatment early, they make tumor worse before it gets better. Chemo is usually 2-3 cycles by immunotherapy needs about 4

18
Q

pembrolizumab toxicity

A

may cause colitis, diabetes, hypophysitis

give steroids if severe

19
Q

prognosis of melanoma

A

patients with melanoma>4mm thick have 50% risk of relapse

patients with lymph node involvement have a 50-85% risk

5 year overall survival 94%

20
Q

screening of melanoma? prevention?

A

full body exam

sunscreen
avoid tanning bed

21
Q
A