Systemic Effects of Chemo Flashcards

1
Q

What is the most common dose-limiting side effect of chemo? Why?

A
  • Myelosuppression

- All types of blood cells divide rapidly regardless of development stage and are therefore very vulnerable

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2
Q

What chemo agents are likely to cause myelosuppresion?

A
  • Because AA’s and nitrosurea’s affect both cycling or non-cycling, they are most likely to destroy bone marrow stem cells
  • Antimetabolites, vinca alkaloids and antitumor antibiotics are cell cycle specific and so cause less severe myelosuppresion
  • Combination therapies tend to cause more severe suppression
  • Anti-angiogenic agents and targeted therapies can also cause a more mild suppression
  • High risk in tumor cells of the bone marrow and previous chemo/rad
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3
Q

What are colony stimulating factors?

A
  • Exogenous type stimulates stem cells in the bone marrow to grow and differentiate into different colonies of blood cells
  • In Ca care most often refers to stimulating production of WBC’s, especially neutrophils
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4
Q

Why is chemo induced anemia less frequent than neutropenia?

A
  • RBC lifespan of 120 days, therefore the marrow has time to recover before the number of circulating RBC’s decreases
  • If a stimulating factor (EPO) is given, it is typically after ~4 weeks post treatment, and primary purpose is to avoid transfusion
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5
Q

Why does thrombocytopenia occur?

A
  • Platelet life span is 7-10 days, and penia usually appears 8-14 days after chemo along with neutropenia
  • Chemo may be temporarily stopped if platelets drop below 50,000 to 75,000 cells/mm
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6
Q

What stimulating factors are given for chemo induced thrombocytopenia?

A

Interleukin-II (increases stem cell proliferation) and is given until cells >50,000 before next cycle

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7
Q

What levels of WBC would chemo be withheld?

A
  • WBC between 1000-3000 cells/mm or if absolute neutrophil count (ANC) is less than 1000 to 1500 cells/mm (under 1500 is the official definition for neutropenia)
  • Life threatening ANC is <500 cells/mm
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8
Q

Why might we not see the standard signs of infection in a patient with neutropenia?

A
  • Major function of neutrophils is phagocytosis > invasion of pathogens can increase in frequency in severity while in a neutropenic state, particularly around days 7-10
  • Typical signs of infection may be inhibited, making the only sign a fever
  • Neutrophils usually cause the overt signs of infection like inflammation and redness
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9
Q

What are the advantages of using colony stimulating factors to improve neutrophil counts?

A
  • Doesn’t change the rate of decline but it does improve the recovery rate and shortens the duration of neuropenia, reducing risk of mortality and morbidity from infections
  • Full doses of chemo can be used
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10
Q

How do we manage myelosuppression?

A
  • Monitor labs and alter chemo dose/schedule as needed
  • Assessment and education for infection prevention and identification of febrile neutropenia
  • Avoid dental care and other procedures if able to during periods of neutropenia
  • Appropriate hygiene (hand washing, avoid touching face, oral care)
  • Safe food handling (maintain appropriate temperatures, wash all foods, avoid food sources with high risk exposure to bacteria like street vendors)
  • Colony stimulating factors, particularly for neutropenia (granulate-CSF)
  • Monitor VS when indicated (eg. daily temperature)
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11
Q

What causes diarrhea in chemo?

A
  • causes necrosis of the cells lining the intestinal crypt, causing ++ wall inflammation
  • Without crypt cells replacement of GI cells are hampered and the surface for absorption is reduced - therefore imbalance with absorption causes diarrhea
  • Diarrhea can cause other problems like lethargy, weakness and electrolyte imbalance; without management can cause malnutrition, dehydration and CV collapse
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12
Q

What is the difference between early onset and late onset diarrhea?

A
  • Early onset is within 24 hours and late is >24 hours
  • Early onset can be managed with atropine; usually cramping, watery eyes, rhinitis and salivation is also present
  • Late can be prolonged and lead to potentially fatal dehydration and electrolyte imbalance if not managed
  • Must be treated immediately with immodium
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13
Q

What are the recommendations for immodium dosages?

A

Two tablets (4 mg) after 1st loose stool, then one tablet (2 mg) q2h until diarrhea free for 12 hours

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14
Q

What special considerations must be made for immune-mediated adverse reactions and diarrhea?

A
  • imAE’s can cause severe and fatal immune-mediated adverse reactions of the multiple systems, but especially GI (enterocolitis, perforations)
  • Permanent d/c of treatment is recommended for severe reactions
  • Onset usually occurs during beginning of treatment but may occur months after last dose
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15
Q

What are prevention and management techniques for diarrhea?

A
  • Encourage monitoring stool quality and frequency (will determine if severe and needs escalation of care to hospital)
  • Encourage 10-12 cups fluids/day
  • Increase soluble fiber (peeled fruits, bananas, white rice/pasta) and decrease insoluble fiber (skins of fruits and vegs, leafy greens, nuts/seeds)
  • Small, frequent meals
  • Avoid spicy foods, deep fried/greasy foods, alcohol
  • Avoid meds that can cause or worsen diarrhea (eg. laxatives, maxeran) in collab c MRP
  • Take immodium
  • Protect skin integrity to perianal skin
  • Hand hygiene
  • If diarrhea not resolving in 24 hours, and/or S&S of fever/infection present, seek urgent care to r/o other causes (eg. cdiff) and to receive appropriate supports (eg. IV fluids, labs, etc.)
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16
Q

What chemo drugs cause diarrhea?

A
  • Capecitabine
  • 5-FU
  • Irinotecan
  • Leucovorin
  • TKI’s
  • Checkpoint inhibitors (-mabs) and biotherapy (high dose interferon or interleukin-2)
17
Q

What is acute n/v?

A
  • Occurs from a few minutes to 1-2 hours post treatment, resolving within 24 hours
  • Primarily mediated by serotonin release
18
Q

What is delayed n/v?

A
  • Develops 24 hours post chemo, typically days 2-3 at it’s worst
  • If nausea is well controlled within first 24 hours delayed n/v is less likely to occur
19
Q

What is anticipatory n/v?

A
  • Usually 12 hours prior
  • Conditioned from stimuli associated with chemo, usually after a few sessions and when efforts to control emesis have failed
  • Ativan is helpful
20
Q

What causes n/v with chemo?

A
  • Emesis is coordinated by the vomiting center in medulla
  • VC is rich in neurotransmitter receptors that are sensitive to chemical toxins in the blood and CSF
  • Chemo can cause damage to tissues that then release messengers (eg. serotonin) that trigger the VC
21
Q

Which chemo drugs are considered highly emetic?

A
  • Carmustine *
  • Cisplatin **
  • Cyclophosphamide
  • Dacarbazine
  • Catinomycin and streptozotocin
  • Mechlorethamine
22
Q

What ending does anthracycline drugs end in?

A
  • Type of antibiotic that tx many types of cancer by damaging Ca DNA cells
  • -rubicin
23
Q

How can nausea and vomiting be managed, non-pharm?

A
  • Eat small, bland meals served cool (eg. rice, crackers, toast)
  • Sip water and other fluids, aim for 8-10 glasses/day
  • Oral hygiene
  • Restrict fluids with meals
  • Try tea/smoothies made with ginger, lemon zest or mint leaves
  • Ginger candies or flat ginger ale
  • Avoid solid food for 30-60 min after emesis, then slowing start to eat again (CF > dry starchy food > protein rich foods > dairy foods)
  • Avoid smoking and alcohol
  • Sit upright 30-60 min after meals
  • Breath in fresh air (open window or walk)
  • If anticipatory, use distraction techniques
  • Acupressure
24
Q

What are some pharm management strategies for n/v?

A
  • Avoid or d/c meds that cause of worsen n/v (talk c MRP about this)
  • Anti-emetics and appropriate scheduling/administration
  • allow 30-60 min after anti-emetic before eating
  • zofran, dex, maxeran and prochlorperazine common drugs
  • If taking highly emetogenic chemo, may be given haldol, nozinan, and gravol suppository
  • If nausea/vomiting is decreasing oral intake, weight, and emesis is not resolving or increasing (24 hours), the pt needs urgent care
25
Q

What are cancer related factors that contribute to n/v?

A
  • Treatments such as chemo, immunotherapy, radiation and surgery/anesthesia
  • Cancer of the GI tract
  • Brain mets/increased ICP
  • Constipation (bowel obstruction)
  • Vestibular dysfunction
  • Anxiety
  • metabolic changes (hyperglycemia, hypercalcemia, hyponatremia)
  • Infections
  • Pain/HA
  • Gastritis (if n/v present and on immunotherapy, consider an autoimmune reaction that may need immediate attention)
26
Q

What are the risk factors for mucositis? (Referring to inflammation throughout the entire GI tract):

A
  • Chemo-induced is believed to be d/t inflammatory events medicated by cytokines, and direct toxic effects on the basal epithelium, connective tissue and condition of oral cavity
  • Aggressive regime with more prolonged or repetitive exposures
  • More likely in hematologic malignancies compared to solid tumors
  • Younger and elderly patients at risk
  • Pre-existing oral disease (eg. cavities), poor oral hygiene, and local irritants (eg. poor fitting dentures, smoking/alcohol)
  • Infection/inflammation of the gums can increase in bacterial and fungal organisms drastically
  • Malnutrition (esp low protein) increase risk of infection
27
Q

What is the potential serious complication from mucositis?

A
  • For the oral cavity, it is susceptible to infection esp while in neutropenic states; gram-negative organisms can flourish in the oral cavity and overgrow (eg. oral thrush [candida], herpes simplex virus)
  • Mucous in the oral cavity is a first line of defense, so when it is poor it can further contaminate the lungs and GI tract, possibly leading to systemic complications
  • Reduced intake ** causing malnutrition and weight loss
  • Decreased quality of life
  • Pain
  • Difficulty talking
  • Depression
  • Sleep disturbances
  • Trouble swallowing (xerostomia)
  • d/t risks for nutrition deficits and infection, it can also be a costly complication if hospitalized for tube feeds/TPN
28
Q

What is involved in the assessment of mucositis, specifically oral?

A
  • Presence of dentures and if fit is appropriate
  • Visual inspection of fall aspects of the oral cavity
  • Assess oral habits both before treatment and during
  • Assess for risk factors (eg. are they an active smoker)
  • Have pt referred to a dental professional for exam before starting tx
  • Assess for changes like:
  • Bleeding or changes in color (white patches?)
  • changes in cleanliness (odor, debris)
  • Changes in integrity (ulcers, cracks, lesions, erosions)
  • Changes in perception (hoarseness, difficulty swallowing, pain)
  • Taste ability
29
Q

What are interventions for mucositis, specifically oral?

A
  • Good oral care, including proper tooth brushing (soft brush), flossing, and rinsing oral cavity
  • If unable to tolerate a brush, can use sponges or gauze
  • Oral rinse 4x a day with water-baking sosa
  • Moisturize lips with water-based products
  • Smoking cessation
  • Avoid alcohol and foods/liquids that are spicy, acidic, rough or hot)
  • Try to maintain adequate fluid intake to keep mucous membranes moist
  • Sugarless candies for xerostomia
  • Education re: how to assess the oral cavity and what changes to report
30
Q

What are some integumentary changes that can occur with Ca treatment?

A
  • All chemo agents have a tendency to cause some type of skin reaction and often affect QOL and can cause non-adherence to treatment
  • Hyperpigmentation
  • Dryness
  • Nail changes
  • Erythema, rash, hand-foot syndrome (can cause loss of fingerprints) **
  • Pruritus
  • Photosensivity
  • Alopecia
31
Q

What are some interventions for integumentary changes?

A
  • To prevent PPE, avoid pressure like tight-fighting clothing and to avoid excessive heat around time of tx
  • Antihistamine therapy for pruritus
  • Skin care and comfort for pruritus - medicated baths, anesethetic creams, steroid creams, and emollient creams
  • Soaps for sensitive skin
  • Avoid use of perfumes, cosmetics and deodorants for + sensitive and itchy skin
  • Keep room humid and the temperature cool
  • Gentle methods of itching - using a soft cloth
  • Educate re: sun exposure and sun safety (have a SPF of at least 30, but higher amounts might be irritating)
  • For irritated nail-beds, wear loose-fitting shoes and do good nail care hygiene
  • Educate re: skin self-assessments
  • Promote adequate hydration/nutrition
  • Avoid exposure to hot water
  • Gently pat skin dry
32
Q

How do we assess integ changes?

A
  • Assess all aspects of face, torso, extremities, scalp, areas of pressure/friction
  • Color - erythema (patchy or uniform), change in pigmentation
  • Thickening (esp of soles and hands)
  • Moisture
  • Integrity (any peeling, rashes, ulcers or blisters)
  • Desquamation/bleeding
  • Swelling
  • Sensory changes
  • Assess timing of onset
  • Assess for pain, infection, bleeding and if altered integrity may need wound care/dressings
  • Take into consideration conditions that can affect skin care (eg. DM)
33
Q

What classifications of chemo drugs are responsible for alopecia?

A
  • Antimetabolites
  • AA’s (cyclophosphamide)
  • Anthracycline antibiotics
  • Vinka alkaloids, taxanes (paclitaxel)