| Term 
 
        | What are the two phases of treating CINV? |  | Definition 
 
        | Prevention: - Select antiemetic based on regimen and patient factors - Subsequent cycles may be altered based on response   Breakthrough: - Treatment of CINV after it occurs, in spite of appropriate prevention regimen |  | 
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        | Term 
 
        | What are the main principles of CINV prevention? |  | Definition 
 
        | - Prevention is goal - Risk of emesis is 4 days in high risk regimens and 3 days in moderate risk, protect throughout - Correctly convert doses, and pay attention to antiemetic SE's - Choice of agent depends on: emetic risk, prior antiemetic experience, patient factors - Rule out other causes of emesis - Consider PPI or H2 blocker for dyspepsia - For multiple-drug regimens, treat against chemo agent with greatest emesis risk |  | 
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        | Term 
 
        | What factors put a PATIENT at risk for emesis? |  | Definition 
 
        | - Being a woman (LOL) - Anxiety/expection of n/v - roommate experiencing n/v (see them puking?) - H/o emesis to prior chemo - Prego - Motion sickness - Lack of sleep - Poor food intake - Basically, being an alcoholic PROTECTS YOU from emesis, weird. |  | 
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        | Term 
 
        | What factors make a REGIMEN more likely to cause emesis? |  | Definition 
 
        | - Combination regimens - Rapid infusion - >once daily administration - Chemo > 1 day - Pay attention to Grunberg levels |  | 
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        | Term 
 
        | If a regimen's Grunberg Scale is <90%, what will we give them pre-chemo and post-chemo? |  | Definition 
 
        | Pre-Chemo:  Aprepitant + 5HT3 + Dex   Post-Chemo:  Aprepitant x 2 days + Dex 12mg PO or IV |  | 
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        | Term 
 
        | If a regimen's Grunberg Scale is 30-90%, what will we give them pre-chemo and post-chemo? |  | Definition 
 
        | Pre-chemo:  Same as high for some OR  5HT3 for most   Post-chemo:  Same as high OR Dex alone OR 5HT3 alone |  | 
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        | Term 
 
        | If a regimen's Grunberg Scale is 10-30%, what will we give them pre-chemo and post-chemo? |  | Definition 
 
        | Pre-chemo:  Dex only OR Prochlorperazine only OR metoclopramide   Post-Chemo:  Nothing needed |  | 
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        | Term 
 
        | If a regimen's Grunberg Scale is <10%, what will we give them pre-chemo and post-chemo? |  | Definition 
 
        | Pre-chemo:  Nothing needed   Post-chemo:  Nothing needed |  | 
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        | Term 
 
        | What is significant in regards to Emend (Aprepitant/Fosaprepitant)? |  | Definition 
 
        | - NK1 and substance P inhibitor - Approved for high and moderate risk - Expensive and messes with P450 3A4 in EVERY way - Give 125mg po pre-chemo, then 80mg/day x 2 days after - Fosaprepitant 115mg IV pre-chemo, then aprepitant 80mg/day x 2 days |  | 
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        | Term 
 
        | Give four examples of 5HT3 antagonists and their doses.  What is a retarded pneumonic to remember the order of the doses? |  | Definition 
 
        | - DOGP (Dogs pee?)   Dolasetron (Anzemet): 100mg IV pre-chemo x 1, 100mg po daily x 2-4 days   Ondansetron (Zofran):  8mg IV or 16mg PO x 1 dose pre-chemo, 8mg BID or 16mg IV x 2-4 days after   Granisetron (Kytril):  1mg IV x 1 dose pre-chemo, 1mg po BID or 2mg PO x 2-4 days after   Palonosetron (Aloxi):  0.25mg IV x 1 dose pre-chemo (lasts 3 days) or 0.5mg PO pre-chemo |  | 
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        | Term 
 
        | What is significant regarding Dexamethasone for prevention of emesis? |  | Definition 
 
        | - Unknown MOA - 12mg IV/PO pre-chemo and for 2-4 days post chemo depending on risk - Might mess with blood sugar, best if taken in morning to prevent insomnia |  | 
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        | Term 
 
        | What are the principles of breakthrough CINV? |  | Definition 
 
        | - *Add agent from different class* - Schedule ATC doses instead of PRN - Hydration/fluids, etc. - Rule out other causes of N/V - For next cycle, treat regimen as if ONE Grunberg level higher - Consider changing regimen/doses if treatment is palliative - Add H2-blocker or PPI if dyspepsic - Add lorazepam +/- behavioral therapies if anxious |  | 
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        | Term 
 
        | What are the agents and doses of drugs you could add to a regimen for breakthrough CINV? Pneumonic for remembering these?! |  | Definition 
 
        | - Lorazepam 1mg IV/PO and then q8h prn - Prochlorperazine 10mg q4-6hprn or 25mg PR q12h - Promethazine 12.5mg-25mg PO/IV q4hprn - Metoclopramide 10-40mg IV or PO q4-6h prn +/- Benadryl 25-50mg PO/IV q4-6h for dystonic reactions - Haloperidol 1-2mg PO or IV q4-6h - Olanzapine 2.5-5mg PO daily (Black box for diabetics and demented elderly) **Medical Marijuana better for anorexia than N/V, elderly experience adverse events)** - Dronabinol 5-10mg PO q3-6h - Nabilone 1-2mg PO BID   *Other Hard Drugs Make Prevention Look Pretty Null* LPPMHODN |  | 
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        | Term 
 
        | What are the required components of pain management in oncology patients? |  | Definition 
 
        | - Pain intensity must be quantified - Formal pain assessment must be performed - Reassess pain at specified intervals - Psychosocial support must be available - Specific educational material must be provided to patient |  | 
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        | Term 
 
        | When assessing cancer pain using imaging studies and a physical exam, what are considered oncologic emergencies? |  | Definition 
 
        | - Bone fracture or impending fracture - Brain, epidural, leptomeningeal mets - Infection - Perforated viscera (acute abdomen)   **Needs to be distinguished if acute pain! **Pain mgmt plus surgery, steroids, XRT, abx, etc. |  | 
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        | Term 
 
        | What the the different cancer pain syndromes? |  | Definition 
 
        | - pain from inflammation - Bone pain w/o oncologic emergency - Nerve compression or inflammation - Neuropathic pain - Severe refractory pain/imminent death |  | 
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        | Term 
 
        | What are the general principles of opioid dosing, and how does this apply to the dosing seen in cancer pain? |  | Definition 
 
        | - Appropriate dose which relieves pain with no SE's - Depends on if pt is taking opioids or is opioid naive - Calculate increase or decrease by TOTAL amount taken previous day - Equillibrium reached in 5 T1/2 - If increasing, increase both ATC and PRN doses - Never exceed 4g/APAP/Day - If unmanageable SE's and pain <4, decrease total dose by 25% - Always start bowel regimen at same time |  | 
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        | Term 
 
        | What are the approximate doses of opioid-equivalents? |  | Definition 
 
        |   
|        Opioid  | PO  | IV | Half-life |  
| Codeine | 200 mg | 130 mg | 2.9 h |  
| Hydrocodone | 30-200 mg | n/a | 3.5-4 h |  
| Oxycodone | 15 – 20 mg | n/a | 3.2 h |  
| Morphine | 30 mg | 10 mg | 1.5 – 2 h |  
| Hydromorphone | 7.5 mg | 1.5 mg | 2.5 h |  
| Fentanyl IV | n/a | 100 mcg | 1-3h |  
| Fentanyl patch | n/a | 50 mcg | 1-3 h |  |  | 
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        | Term 
 
        | How should we dose methadone in cancer patients? |  | Definition 
 
        | - Tricky, has long half-life, accumulates after 2-5 days(side effects) - High potency - Dose q4h initially, then may need to increase to q6-8h after steady state (1-2 weeks)   |  | 
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        | Term 
 
        | Which opioid agents are NOT recommended in cancer patients? |  | Definition 
 
        | - Propoxyphene - renal, neuro - Meperidine - renal, neuro - Butorphanol - Buprenorphine - No morphine in renal failure   Pneumonic: BPBM (Bad Pharmacy Benefits Manager) |  | 
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        | Term 
 
        | What are the principles of maintenance dosing for cancer patients on opiods? |  | Definition 
 
        | - When patient is stable, convert to LA drugs - Give rescue doses of short-acting opioids for breakthrough, should be 10-20% of 24h dose q1h prn - Increase dose of LA form when prn dosing no longer effective   |  | 
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        | Term 
 
        | What are the equivalent morphine IV and PO doses when a cancer patient is on each different strength of a fentanyl patch? |  | Definition 
 
        |   
| Morphine PO  (dose in 24 hours)  | Morphine IV  (dose in 24 hours)  | Fentanyl patch  (mcg /hr)  |  
| 25 - 65 mg | 8 – 22 mg | 25 mcg |  
| 65 – 115 mg | 23 – 37 mg | 50 mcg |  
| 116 – 150 mg | 38 – 52 mg | 75 mcg |  
| 151 – 200 mg | 53 – 67 mg | 100 mcg |  
| 201 – 225 mg | 68 – 82 mg | 125 mcg |  
| 226 – 300 mg | 83 – 100 mg | 150 mcg |  |  | 
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        | Term 
 
        | How do we manage patients on each level of the pain scale if they HAVEN'T taken opioids before? |  | Definition 
 
        | 1-3:  consider NSAID or APAP; may start short-acting opioid   4-6:  Titrate short-acting opioid like morphine 5-15mg Reassess in 60 minutes, inc. by 50-100% if pain not resolved Reevaluate in 24-48h once stable   7-10:  Initiate opioid in same fashion, give same intial dose if still a 4-6 pain, continue same dose PRN if pain still 0-3 Reevaluate in 24h once stable, convert to long acting, calculate breakthrough pain dose (10-20% total dose q1h prn) |  | 
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        | Term 
 
        | What are the most important points when considering whether or not to use an ESA to treat Chemotherapy-Induced Anemia? |  | Definition 
 
        | - DO NOT use if NOT recieving chemo, Chemo and Procrit go hand-in-hand - DO NOT use if patient may be cured - DO NOT administer if Hgb > 12 --> VTE/Cardiac problems - Shorter overall survival and TTP (Time to tumor progression) in several cancers when Hgb >12 - Risk of shorter survival cannot be excluded even if Hgb <12 |  | 
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        | Term 
 
        | What is EPO and how does Procrit and Darbepoetin affect this? |  | Definition 
 
        | - Hematopoietic growth factor made in the kidneys, helps make RBC's; patients with levels >200mU/mL may be refractory to treatment or need higher levels - Procrit has same AA sequence as EPO, effective in 50-60% of patients - Dose is 50-100units/kg TIW or 40,000/week, response may take 4 weeks, SE's are HTN or flu-like sx. - Darbepoetin is glycosylated EPO, so half-life is longer - FDA approved for cancer patients 2.2mcg/kg qweek or 500mcg/kg q3w (SQ) - We almost always use 200mcg SQ QOW |  | 
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        | Term 
 
        | When do we treat anemia in cancer patients? |  | Definition 
 
        | Hgb <11 and ON chemo   Immediate correction: transfuse RBC's Chemo is curative: transfuse RBC's   Asymptomatic and......... no risks: Observe If risks and AID: IV or PO Iron If risks and FID: ESA after risk/benefit discussion   Symptomatic:  Transfuse or ESA after discussion |  | 
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        | Term 
 
        | What are the risks of developing symptomatic anemia that were discussed on the previous card? |  | Definition 
 
        |   nTransfusion in past 6 months nH/o prior myelosuppressive chemo nH/o XRT to >20% skeleton nMyelosuppressive potential of current chemo nCurrent Hgb level nComorbidities  qCardiac, chronic pulmonary, cerebral vascular dz  |  | 
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