Lung Cancer Flashcards

1
Q

Describe the general treatment approach of solid tumors and the relative importance of treatments for cure.

A
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2
Q

LIST common toxicities and MOA for cisplatin.

A
  • Platinum agent; forms DNA crosslinks that impairs DNA replication, leading to cell death.
  • N/V, nephrotoxicity (hypokalemia, hypomagnesemia), ototoxicity, neuropathy, and gonadal toxicity (risk of infertility)
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3
Q

LIST common toxicities and MOA for carboplatin.

A
  • Platinum agent; forms DNA crosslinks that impairs DNA replication, leading to cell death.
  • More bone marrow suppression (thrombocytopenia)
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4
Q

LIST common toxicities and MOA for paclitaxel.

A
  • Taxane/plant alkaloid; binds to tubulin, promotes microtubule assembly, prevents disassembly (paclitaxel paralyzes)
  • Hypersensitivity reactions (cremophor; pre-medication required = dexa, diphen, H2RA), peripheral neuropathy
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5
Q

LIST common toxicities and MOA for bevacizumab.

A
  • VEGF targeting agent; prevents from binding to receptor - works outside the cell
  • Hypertension, proteinuria, impaired wound healing, bleeding, thromboembolic events
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6
Q

LIST common toxicities and MOA for docetaxel.

A
  • Taxane/plant alkaloid; binds to tubulin, promotes microtubule assembly, prevents disassembly
  • Hypersensitivity reactions (less common than paclitaxel), edema (requires premedication of dexa), peripheral neuropathy, greater myelosuppression than paclitaxel
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7
Q

LIST common toxicities and MOA for pemetrexed.

A
  • Anti-folate; inhibits multiple enzymes in the folate pathway (DHFR, TS, GARFT, AICARFT)
  • Requires premedication: folic acid 400 mcg to 1000 mcg daily, vitamin B12 1000 mcg IM q9w (both are given to reduce myelotoxicity; begin 1 week before initiation), dexamethasone 4 mg PO BID x 3 days beginning the day before treatment (reduces cutaneous reactions)
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8
Q

LIST common toxicities and MOA for EGFR TKIs.

A
  • EGFR inhibitors; response best in tumors with activating EGFR mutations
  • Acne-like rash, diarrhea, interstitial lung disease (besides lapatinib - targets HER2 as well, only diarrhea no rash, decreases LVEF no ILD)
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9
Q

LIST common toxicities and MOA for etoposide.

A
  • Topoisomerase II inhibitor; epipodophyllotoxin
  • Hypotension (rate limiting), secondary leukemia (11q23/MLL gene mutations)
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10
Q

LIST common toxicities and MOA for ALK TKIs.

A
  • ALK inhibitor
  • Bradycardia, pancreatitis, QT prolongation, ILD
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11
Q

LIST common toxicities and MOA for immune checkpoint inhibitors.

A
  • PD-1 monoclonal antibodies
  • Immune mediated (liver, endocrine, GI, skin, cardiac), adrenal insufficiency, hypothyroidism
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12
Q

Identify brand/generic name of osimertinib.

A

Tagrisso

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13
Q

Identify brand/generic name of nivolumab.

A

Opdivo

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14
Q

Identify brand/generic name of pembrolizumab.

A

Keytruda

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15
Q

Identify brand/generic name of pemetrexed.

A

Alimta

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16
Q

Compare the pathophysiology, natural disease course, and treatment of non-small cell lung cancer (NSCLC) with small cell lung cancer (SCLC).

A
17
Q

Differentiate the role of chemotherapy for NSCLC vs. SCLC.

A
18
Q

LIST the risk factors for lung cancer.

A
19
Q

Plan a supportive care regimen to prevent/limit toxicity for cisplatin.

A
19
Q

Plan a supportive care regimen to prevent/limit toxicity for carboplatin.

A
20
Q

Plan a supportive care regimen to prevent/limit toxicity for paclitaxel.

A
21
Q

Plan a supportive care regimen to prevent/limit toxicity for docetaxel.

A
22
Q

Plan a supportive care regimen to prevent/limit toxicity for gemcitabine.

A
23
Q

Plan a supportive care regimen to prevent/limit toxicity for pemetrexed.

A
24
Q

Plan a supportive care regimen to prevent/limit toxicity for etoposide.

A
25
Q

Plan a supportive care regimen to prevent/limit toxicity for osimertinib.

A
26
Q

Plan a supportive care regimen to prevent/limit toxicity for bevacizumab.

A
27
Q

Plan a supportive care regimen to prevent/limit toxicity for nivolumab.

A
28
Q

Plan a supportive care regimen to prevent/limit toxicity for pembrolizumab.

A
29
Q

Identify immune-related adverse events (irAEs) from PD-1 or PD-L1 inhibitors.

A
30
Q

Design a plan to treat irAEs.

A
31
Q

Describe the concept of “personalized medicine” as it relates to lung cancer treatment in essay form.

A
32
Q

Select systemic cancer treatment (i.e. chemo, TKIs, etc.) that are appropriate for 1st line treatment of lung cancer using the tenets of personalized medicine and medication safety.

A