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149 Cards in this Set

  • Front
  • Back
Cancer warning signs
Changes in bowel or bladder habits
Sores that do not heal
Unusual bleeding or discharge
Thickening or lump in breast or elsewhere
Indigestion or Trouble Swallowing
Obvious change in wart or mole
Nagging cough or hoarseness
Neurotoxicity Management
Venlafaxine, Gabapentin
Vincristine
HD
Reduce dose by 50% with TBili > 1.5 mg/dl
Don't use if TBili > 3.0 mg/dl
Do NOT use intrathecally
Constipation, Neuropathy, Alopecia
Myelosuppression is not severe
DOES NOT CAUSE MYELOSUPPRESSION AND NVD
Bleomycin
HD
Idiosyncratic Reactions, Dose-related pulmonary toxicity
Pulmonary toxicity risk increases with age > 70 and cumulative lifetime dose of >400 units.
Premedicate with acetaminophen to prevent fever
High risk Breast Cancer for 5 year risk
35-59 with 5 year risk of at least 1.66%
Tamoxifen
Decreases osteoporotic risk
Increases thromboembolic risks
Increases endometrial cancer
Only one indicated for premenopausal
Avoid black cohash to treat menopausal symptoms
Poor 2D6 metabolizers...
Decreases breast cancer incidence
More effective than raloxifene for reducing risk of noninvasive breast cancer
Raloxifene
Better AE profile than Tamoxifen
Indicated for osteoporosis
60 mg po qd x 5 years
Reduction of risk of invasive breast cancer in post-meno women at high risk
INTX: Cholestyramine, Warfarin
Exemestane
Maybe more efficacious than raloxifene and tamoxifen in reducing incidence of cancer
Increases osteoporosis risk
No survival benefit
Better for DVT risk?
Take after a meal, administration with high fat meals increases absorption by 40%
3A4 metabolized so increase dose if given with 3A4 inhibitor
TC
Docetaxel and Cyclophosphamide
Dose Dense AC
Doxorubicin and cyclophosphamide followed by paclitaxel
ALWAYS use growth factor support
TCH
Docetaxel, Carboplatin, Trastuzumab
AC
Doxorubicin and cyclophosphamide followed by paclitaxel and trastuzumab
Doxorubicin
Breast Cancer and HD
Total cumulative lifetime dose not to exceed 550 mg/m2 due to heart failure
Vessicant if it gets into tissue
Turns urine bright red (not dangerous)
Comes as liposomal product, different dosing
Cyclophosphamide
Breast Cancer and HD
Prodrug via 2B6
Cardiotoxic due to endothelial capillary damage (manage this with diuretics/BB)
Cystitis at high dose (manage with fluids and/or Mesna)
Do not crush
Carboplatin
NSCLC
Thrombocytopenia
Avoid nephrotoxins (ibuprofen, aminoglycosides) on day of administration
Electrolyte abnomralities due to lots of urine being pushed.
Monitor urine for blood and contact doctor immediately if so
Blindness, Anaphylaxis, Secondary Malignancies
Paclitaxel
NSCLC
Hypersensitivities much more common (to taxane of creamaphor)
Peripheral neuropathy is a class effect of M phase inhibitors
Give taxane derivatives before platinum derivatives to limit myelosuppression and enhance efficacy
Premedicate with dexamethasone, diphenhydramine, and ranitidine for hypersensitivity
Infuse through in line filter and nonabsorbing administration set
Avoid with clozapine
Docetaxel
For Metastatic Prostate, MM
Fluid retention, often around lungs
Infuse with nonsorbing tubing, do not need in line filter.
Premedicate with dexamethasone for 3 days to avoid fluid retention
Avoid with clozapine
Trastuzumab
Cardiotoxic (d/c if MUGA drops)
Avoid with doxyrubicin/cyclophosphamide due to cardiotoxicity
Premedicate with diphenhydramine and APAP
Monitor/Dose reduce for ejection fraction
Pertuzumab
Binds to different part of HER-2 than trastuzumab
Same as Trastuzumab, only use in combo with it
Risk Factors for CINV
<50 years
Female
Lower risk if alcoholic
Motion sickness
Previous history of N/V
Dolasetron
5-HT3 Receptor Antagonist for Antiemesis
100 mg daily
Only one that is only oral
Very expensive
QT interval prolongation!
Granisetron
5-HT3 Receptor Antagonist for Antiemesis
2 mg po or 1 mg IV or patch (1-2 days before chemo)
Ondansetron
5-HT3 Receptor Antagonist for Antiemesis
16-24 mg po, 8 mg iv
Headache common, switch to granisotron if so
Max IV dose is 16 mg due to QTC prolongation above that
Lots of formulations
Avoid 3A4 interactions
Palonosetron
5-HT3 Receptor Antagonist for Antiemesis
Only IV only
Very long half life
0.25 mg IV
Most expensive
Aprepitent
Neurokinin Antagonist for antiemesis
125 mg oral or one time
Fatigue, Constipation, Hiccups
Fosaprepitant is IV form
3A4 substrate
Reduce dexamethasone to 12 mg if used concurrently
Dexamethasone
Corticosteroid for antiemesis
12 mg po
Hyperglycemia, GI upset
3A4 intx
No need to taper
Take with food for GI upset
Oral Chemo that is pH dependent
Vismodegib
Erlotinib
Dasatinib
Ponatinib
Guidelines for chemo that is ph dependent
Antacids separate by 2 hours
H2 antagonists separate by 12 hours
DONT use PPI's
5-HT3 receptor antagonists INTX
Apomorphine due to hypotension
Metoclopramide
Serotoninc receptor antagonist only at high dose
Words by increasing gastric emptying as PRN anti-emetic
Sedation, diarrhea, EPS, neuroleptic syndrome
Not used for prevention
Benzo's
Used for anti-emesis, mainly lorazepam due to having the shortest half life
Used for anticipatory CINV and breakthrough CINV
Phenothiazines
Prochlorperazine, Promethazine
For mild emetogenic chemo
Sedation, Hypotension
Breakthrough N+V rescue options
Proclorperazine
Metoclopramide
Lorazepam
Ondansetron
Granisetron
Treating breakthrough N+V secondary prevention options
Dolasetron
Haloperidol
Dronabinol
Dexamethasone
Promethazine
Olanzapine
G-CSF dosing
Do not administer on day of chemo, give 24-72 hours after
Stop ANC > 2000 x 2 days
SubQ
Do not dose escalate
G-CSF interactions
Bleomycin (increased pulmonary toxicity)
Topotecan increased topo AE
Clinical presentation of febrile neutropenia
Fever > 101.5 with ANC < 500
Respiratory, skin lesions, neurologic, septic shock
How to treat early satiety?
Metoclopramide
Cachexia appetite stimulants
Megesterol
Prednisone
Cachexia depression treatment
Mirtazapine
Megesterol
Synthetic Progestin
Appetite stimulant
Break throguh bleeding, diarrhea, edema
Thromboembolic events
Hypercalcemia cutoffs for chemo
Mild = 12-13.5 mg/dl
Severe > 13.5 mg/dl
Hypercalcemia symptoms
Confusion, N/V, HA, Irritability, Muscle Weakness
Pamidronate
Max single dose 90 mg
D/C if creatinine deteriorates
Takes several days for effect, do not re-dose more than once a week
Single dose over 2-24 hours
Avoid concurrent nephrotoxins
Zoledronic Acid
Max single dose is 4 mg
Zometa for oncology
Reclast for osteoporosis
Single dose
Avoid concurrent nephrotoxins
Spinal Cord Compression Treatment
Radiation
Chemo
Dexamethasone
Terminal Sedation
Dying within hours to days in opinion of 2 physicians

Thiopental
Midazolam
Agents for Neuropathic Pain
Amitriptyline
Duloxetine
Venlafaxine
Buproprion
Gabapentin
Pregabalin
Antidepressant titration schedule
Every 3-5 days
Opioids for Mild to Moderate Pain
Codeine
Tramadol
Hydrocodone
Codeine
1/100th potency of morphine
Prodrug converted via 2D6
Produces the most constipation and nausea!
Bad with impaired renal function
Busulfan, isoniazide, warfarin etc INTX
Tramadol
Weak Mu agonist, SNRI action
Not controlled
Max dose: 400 mg/day
IR only 50 mg
Lots of N/V
Titrate over several weeks
Seizures
Serotonin Syndrome
Hydrocodone
More potent and longer lasting than codeine
Prodrug metabolized by 2D6
Only available in combo products with non-opioids
Meperidine
Not recommended due to fast on/off due to high lipophilicity
Morphine
2 biologically active metabolites
Induces histamine release
-Hypotension, Pruritis
Hydrophilic (slower onset, longer duration)
High FPM. 3:1
Starting dose = 30mg SR q 12 h
Hydromorphone
5-7x more potent than morphine
Same AE profile to morphine
Less histamine than morphine
No active metabolites (good for renal impairment)
Short acting formulations only
Quite high FPM 5:1
Oxycodone
3:2 more potent than morphine
Less histamine
Prodrug metabolized by 2D6 (parent compound also active)
Requires less dose reductions with renal impairment than morphine
Starting dose in opioid naive is 10 mg
More abuse potential
Oxymorphone
Twice as potent as oxycodone
More lipophilic than morphine
Fast onset, LONGER half life
Fentanyl
100's more potent than morphine
Selective for mu receptor
Near immediate onset of action when given IV, VERY lipophilic
May be stored in fat leading to prolonged effects
No active metabolites. Safest in renal failure
Initial patch dose is 25 mcg/hr
Titrate q 3 days with initial patch, then no more often than q6days
Absorption of patch increased when febrile by up to 30%
Effects last 12 hours after patch removed
NOT FOR OPIOID NAIVE PATIENT
Methadone
Inexpensive
Good for people who need high doses of others but have significant AE
Longest half life (lots of variance)
Duration of analgesia shorter than half-life
What opioid patients should call about?
New pain
N/V that prevents eating for a day
No BM for 3 days
Confusion
Actinic Keratosis
Pre-cancerous sun-induced skin lesions.

Treated with ingenol mebutate gel
Ingenol Mebutate Gel
For actinic keratosis
Eye edema, Eye Pain, Conjunctivitis, Skin flaking, scaling erythema
Allow treated area to dry for 15 minutes after application, don't touch area or get it wet for 6 hours after application.
Basal Cell Carcinoma
Most common cancer
More common whites
More common in men
Chronic Immunosuppression is risk
Only use drugs if stage 1 or 4.
Those treated are more likely to have another non-melanoma skin cancer within 5 years.
Mohs Surgery
Treatment for Basal Cell Carcinoma
Highest cure rate, preserves lots of normal tissue.
Can be done outpatient.

Costly, longer procedure, scarring risk.
Topical Basal Cell Carcinoma Treatments
5FU - Inflammatory rxn, stinging, edema, secondary infections

Imiquimod - Inflammatory Reaction, Fatigue, Flu-Like Symptoms
Vismodegib
Basal Cell Carcinoma Stage IV treatment (or in patients with recurrence post surgery)
Hedgehog signaling pathway inhibitor
Alopecia, Taste Loss, Weight Loss, N/D (rare, report immediately)
PPI's/H2RA/Antacids reduce absorption
Must conduct pregnancy test within 1 week of initiating therapy
Concerning Features of Melanoma
Asymmetry
Border Irregularity
Color change
Diameter change
Evolution of the lesion
Interferon Alpha-2b
Adjunct for melanoma Stage III
Contraindicated in liver disease
May worsen psychiatric symptoms, increased risk of suicide.
May worsen ID, autoimmune disease
Hepatotoxicity
Myelosuppression
Visual Loss
Chest Pain
N/V/D
Avoid with interleukin-2, zidovudine, ribavirin, telbuvudine due to increased AE
Dose in evening for tolerability
Melanoma Metastatic Regimens
No drugs if Stage I or II

If no BRAF mutation: Ipilumumab +/- dacarbazine (THESE ARE MORE EFFECTIVE IN COMBO)
If Mutation: Dabrafenib or vemurafenib (chosen by toxicity)
Decarbazine
Metastatic Melanoma Mutation Negative
Hepatotoxicity, Bone marrow Suppression, Secondary malignancies
1A2 and 2E1 substrate
Hair loss, N/V, Flu-like symptoms
Immediately report easy brusing or bleeding, yellowing of eyes or skin, change in color of urine or blackened stool.
No overall survival benefit
Ipilimumab
Metastatic melanoma Mutation Negative
Hold for hepatic toxicity
Potentially fatal immune-mediated AE due to T-Cells (TEN, Hepatitis, etc)
Rash, N/V, Fatigue, lots of others
Can require several months for effect
In REMS (assess for serious symptoms before each dose, d/c permanently if seen and start high dose corticosteroid)
Vemurafenib
Metastatic Melanoma BRAF mutation positive
BRAF kinase inhibitor
QTC prolongation
Hand-Foot syndrome
Fast response, but maybe short duration
Skin exams and sun protection
Dabrafenib
Metastatic Melanoma BRAF mutation positive
BRAF kinase inhibitor
Adjust for hepatic dysfunction
QTC prolongation
Hyperglycemia
Premedicate with APAP for febrile reactions
Fast response, but maybe short duration
Skin Exams and Sun Protection
Mammography
Every 2 years once 50-74
Improves overall survival
False positives very common (more so in younger)
High risk screening for Breast Cancer
Known BRCA mutation
First degree relative with BRCA
Lifetime risk of 20-25%+
Radiation therapy to chest between ages of 10-30
Li-Fraumeni, Cowden Syndrome, Hereditary diffuse gastric cancer

For all of these, annual MRI and mammography
Stage I + II Breast Cancer Treatment
Her-2 Positive: Trastuzumab
ER/PR positive: Tamoxifen or Aromatase
Node Positive: Chemo
Node Negative: Oncotype DX >31 chemo
Metastatic Breast Cancer Treatment
Palliative
Premenopausal: Antiestrogen or LHRH
Post: Antiestrogen or Aromatase Inhibitor
(Continue until disease progression)
If no response, then chemo
Slow Opioid Titration
Pain score 4-6
Naive: Morphine SR 15-30 mg po bid
Not naive: Increase dose 25-5-% daily morphine
Prostate Cancer Screening
No significant effect of PSA based screening on mortality after 10 years
Risk of ED/incontinence, CV events
PSA limits by age
40-49 = 1.0 ng/ml
50-59 = 3.5
60-69 = 4.5
70-79 = 6.5
Finasteride
30% risk reduction in developing prostate cancer over 7 years.
If PSA < 3 (less than), and are regularly screened, may be beneficial to use this or dutasteride
Decreases observed PSA by 50%, double for cancer monitoring
May take 6 months for effect
Bad news in women even touching it
Prostate Cancer Localized Treatment
Active Surveillance (curative) observation (palliative)
Radiation +/- androgen deprivation therapy
Prostatectomy (curative/better survival but leads to incontience, impotence, diarrhea)
Prostate Cancer Metastatic Treatment
Hormone Therapy (eliminate androgens)
-LH-RH +/- antiandrogen
-Orchiectomy (removal of testes)
Chemo
LH-RH
For metastatic prostate cancer
Leuprolide, Goserelin, Triptorelin
Gynecomastia, Osteoporosis, Weight gain, Edema, CV events, Diabetes
Monitor serum testosterone @ 4 weeks for efficacy
Monitor PSA for efficacy
Cause tumor flare early on
Gonadotropin Receptor Antagonists
For metastatic prostate cancer
Degralix
No tumor flare
Gynecomastia, Osteoporosis, Weight gain, Edema, CV events, Diabetes
Monitor serum testosterone @ 4 weeks for efficacy
Monitor PSA for efficacy
Antiandrogens
For metastatic prostate cancer
Reduce tumor flare from LH-RH agonists
Flutamide, Biclutamide, Nilutamide, Enzalutamide
Inferior to LH-RH in monotherapy
Edema, GI, Fatigue
Flutamide
Antiandrogen for metastatic prostate cancer
Diarrhea, Methemoglobinemia
Bicalutamide
Antiandrogen for metastatic prostate cancer
D/C if ALT double ULN
Nilutamide
Antiandrogen for metastatic prostate cancer
Visual disturbances
Alcohol intolerance
Interstitial pneuomonitis
Enzalutamide
Antiandrogen for metastatic prostate cancer
Musculoskeletal disorders
Asthenia
Peripheral Edema
HA/Dizziness
Seizures
Denosumab vs Zoledronic Acid for Prostate
Denosumab has lower skeletal event rate
Asymptomatic metastatic prostate cancer treatment
Sipleucel-T
Abiraterone
Both show survival benefit
Abiraterone
For Asymptomatic metastatic prostate cancer
Always given with prednisone 10 mg
C/I in women. 2 forms of birth control
Give on empty stomach
Metastatic (castration resistant) symptomatic prostate cancer Treatment
Docetaxel (survival benefit)
Mitoxantrone

Abiraterone
Enzalutamide
Lung Cancer Prevention
Reduces mortality but not widely implemented due to cost
Stop smoking
No effective chemoprevention agents
NSCLC Doublet Selection
Cisplatin + Paclitaxel - Better activity, more toxicity (preferred in academic centers)
Carboplatin + Paclitaxel - Preferred in community/elderly
Cisplatin + Docetaxel - Second line
Cisplatin + Gemcitabine - Less effective than cisplatin + permetrexed
NSCLC Addition of Bevacizumab
Increased overall survival
Increased hemorrhage
Increased hypertension
Increased proteinuria
Bevacizumab
Prevents angiogenesis in NSCLC
GI perforation
Impaired wound healing
Hemorrhage
Lots of DI
Avoid surgery within 28 days
Do not use if CNS metastisis
Cisplatin
NSCLC
Hypersensitivity, ototoxicity, renal issues.
Prevent renal toxicity with normal saline and electrolyte repletion
Avoid concurrent nephrotoxins on same day
Permetrexed
NSCLC
Begin folic acid daily 7 days prior to treatment. Continue for 21 days post last dose.
Being B12 7 days prior to treatment and then every 3 cycles
Begin Dexamethasone bid for 3 days starting day before treatment to reduce hypersensitivity
Erlotinib
First line for EGFR+ NSCLC
Expensive!
Dose until disease progression
Edema (diuretics), Rash, Diarrhea (dose reduce), LFT's (dose reduce)
Bleeding, interstitial lung disease
Food affects absorption, take on empty stomach
Afatanib
First line for EGFR+ NSCLC (effective in patients with erlotinib resistance)
Expensive!
Longer progression free survival and better objective response than cisplatin/permetrexed
Edema (diuretics), Rash, Diarrhea (dose reduce) LFT's (dose reduce)
Bleeding, Interstitial Lung disease
PGP substrate
Take on empty stomach
Crizotinib
ALK+ NSCLC
Edema (diuretics), NVD, LFT (dose reduce), Vision issues
QTC prolongation, Pneumonitis
No food effect
Hodgkins Lymphoma Treatment
Curable, cure while minimizing long term AE
If, after chemo patient does not have complete response, additional cycles or stem cell transplant.
ABVD
Chemo treatment for HD
Doxorubicin
Bleomycin
Vinblastine
Dacarbazine
Stanford V
Chemo Treatment for HD
Doxorubicin
Vinblastine
Mechorethamine
Vincristine
Bleomycin
Etoposide
prednisone
BEACOPP
Chemo for HD
Bleomycin
Etoposide
Adriamycin
Cyclophosphamide
Vincristine
Procarbazine
prednisone
HD Treatment Complications
Joint replacement (steroids)
Cardiac (doxorubicin)
Cognitive Dysfunction
Pulmonary (Bleomycin)
Gonadal dysfunction
Secondary Malignancies
Autologous vs Allogenic
Autologous is patient's own stem cells. Must be under 70
Allogenic is donors (also allows immune response against cancer cells) must be under 60
-Matched for HLA type

Exclusions: CHF, Uncontrolled DM, Active infections, Renal Insufficiency
Stem Cell Transplant Complications
Mucositis
Sinusoidal Obstructive Syndrome
Transplant related infetions (mouth, gut, skin)
Pancytopenia
Graft Rejection
Secondary Tumors
Need repeat vaccinations
Types of Non-Hodgkins Lymphomas
Low grade = Chronic Lymphocytic Leukemia
Intermediate = Follicular, Diffuse large Cell
High Grade = Burkitts, mantle cell
Low Grade lymphomas Treatment
Incurable, watchful waiting is acceptable
Treat if recurrent infections, organ function decay, massive bulk, patient preference
Chlorambucil
For Low Grade NHL
Hypersensitivity, Interstitial Pneumonia, Secondary Malignancies
Must store in refrigerator, protect from light
Take on empty stomach
Fludarabine
For Low Grade NHL
Blindness, coma, hemolytic anemia, Immunosuppression, Neurotoxicity
Must receive acyclovir and TMP/Sulfa for antiinfective prophylaxis
CLL suportive care
Infections (evaluate IgG, if less than 500 mg/dl start IVIG)
Avoid all live vaccines, get pneumococcal every 5 years
Intermediate NHL treatment
rCHOP
Rituximab
Part of rCHOP for intermediate NHL treatment
Infusion reactions, mucocutaneous reactions, progressive multifocal leukoencephalopathy, tumor lysis syndrome (high tumor burden increases risk of tumor lysis)
Edema, Rash, Fever, etc
Philadelphia chromosome
Generates abnormal Bcr-Abl fusion gene
Leads to CML
CML labs
Leukocytes over 25,000
CML Phases
Chronic Phase - Indolent, WBC increase

Accelerated Phase - Progressive myeloid maturation, WBC continue to increase

Blast Crisis - Acute Leukemia, death can occur quickly
CML goals
CHR - Complete hematologic response (no blasts in peripheral blood)

CCyR - Complete cytogenetic response (No phili chromosome cells in bone marrow or peripheral blood)

CMR - Complete Molecular Response (No BCR-ABL protein)

If no CHR and CCyR at 3 months, go to alternative therapy
CML Treatment
Only allogeneic stem cell transplant is curative
Almost all patients first started on Tyrosine Kinase Inhibitor, transplant it failed.

Imatinib (typically first choice due to cost and lots of data), Nilotinib, or Dasatinib first
-Bosutinib, Ponatinib if failed
Tyrosine Kinase Inhibitors
Imatinib, Dasatinib, Nilotinib, Bosutinib, Ponatinib
3A4 intx
Imatinib
For CML first line
Increased progression free survival vs Interferon alfa + cytarabine. Very high response rates
3A4
Take with food
GI, Edema, Fatigue, Rash
TKI resistances
Bcr-Abl kinase domain mutations may lead to only dasatanib working

T315I causes resistance of imatinib, nilotinib, dasatinib (use ponatinib here)
Dasatinib
For CML when Bcr-Abl kinase domain mutation gives resistance to imatinib
Faster rates of complete response than imatinib, no change in OS or PFS
3A4
Edema, Bleeding, Pulmonary hypertension, QTC prolongation
Nilotinib
For CML resistant to imatinib
Better molecular response compared to imatinib
Empty stomach
QTc, Elevated serum lipase, Peripheral artery occlusive disease, pancreatitis
Bosutinib
For CML imatinib resistant mutations (except T315I and V299L)
3A4
With food
Diarrhea, Myelosuppression, Fluid retention
Ponatinib
For CML imatinib resistant (T315I mutation)
Improved major cytogenic response and hematologic response
Arterial thrombosis (temporarily suspended), Liver Toxicity
Omacetaxine
For CML resistant to 2 or more TKIs
Synthetic
SubQ
Myelosuppression, Hyperglycemia, Bleeding
MM Symptoms
Calcium (hypercalcemia)
Renal Dysfunction (due to accumulation of antibodies in kidney)
Anemia (Hbg <10)
Bone Disease (Bisphosphonate almost always)

Hyperviscosity
Thrombosis
Renal Dysfunction effect on MM treatment
Prefer dexamethasone over melphalan
When to give anticoag in MM
When receiving thalidomide, lenalidomide or pomalidomide

Aspirin if lower risk, LMWH or Warfarin if higher
Stem Cell Transplant Ineligibility in MM
Over 77
High bilirubin
Really high SCr
ECOG 3 or 4 unless due to bone pain
Functional Status III or IV
MM Treatment
Transplant Eligible:
-Lenalidomide/Dexamethasone
-Bortezomib/Thalidomide/Dexamethasone

Transplant Ineligible:
-Melphalan/Prednisone/Thalidomide
-Melphalan/Predisone/Bortezomib
MM Maintenance Therapy
Thalidomide or Lenalidomide preferred
Immune Modulators
For MM
Thalidomide, Lenalidomide
Take at bedtime at least 1 hour after evening meal
DI: Dexamethasone, Docetaxel (both increase thromboembolism)
AVOID IN PREGNANCY (2 forms of birth control)
Peripheral neuropathy, secondary malignancy
Very expensive!
REMS
Prophylactic anticoag needed!
Resistance to one does not mean resistance to other
PO
Bortezomib
Proteasome Inhibitor for MM
IV
3A4
Peripheral neuropathy, NVD, Fatigue, Fever, Hepatic failure, Acute respiratory distress syndrome
Very expensive!
Give subQ (non-inferior and fewer AE)
Must have prophylactic acyclovir
Capecitabine
For Colon Cancer
Oral agent, good for avoiding central line with 5FU
Very expensive!
FOLFOX versus FLOX
5FU bolus (MOSAIC) vs 5FU infusion (NSABP C07)
More neuropathy with FOLFOX
More GI with FLOX
FLOX easier
Metastatic Colon Cancer Treatment
Kras-: Cetuximab or panitumomab
Bevacizumab eligible: Bev
5-FU
For Colon Cancer
Myelosuppression dose limiting for bolus
Mucositis dose limiting for continuous infusion
DPD deficiency with severe toxicity (dihydropyridine dehydrogenase)
TS expression may predict efficacy
Leucovorin
For Colon Cancer
S enantiomer active
Stabilizes 5FU complex
Higher GI toxicity
Capecitabine
For colon cancer
Prodrug of 5FU
BBW: DI with warfarin
Take with water within 30 minutes after a meal
Hand-Foot
Ironotecan
For metastatic colon cancer
Dose alter for UGT1A1*28 homozygotes
Severe effects on bone marrow and severe diarrhea
Treat diarrhea with loperamide multiple times a day
Oxaliplatin
Stage III colon cancer after resection of primary tumor
Anaphylactic reactions (manage with epinephrine, steroids, antihistamines)
Neuropathy exacerbated by cold, avoid ice chips for mucositis. May be reversible with discontinuation
Cetuximab
EGFR inhibitor only for KRAS- colon cancer
Second line for metastatic colon cancer with ironotecan
Premedicate with diphenhydramine
Electrolyte abnormalities
Cardiopulmonary arrest
Panitumumab
EGFR inhibitor only for KRAS- colon cancer
Third line for metastatic colon cancer
Improved PFS compared to survival
Severe rash
Infusion reactions
Pulmonary fibrosis