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Nursing Considerations With the Use of Targeted Therapy

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Adapted from Jain RK. Nat Med 2001;7:987 9. Willett CG et al. Nat Med 2004;10:145 7 ... Common side effect with this class of drug. Baseline BP reading is essential ... – PowerPoint PPT presentation

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Title: Nursing Considerations With the Use of Targeted Therapy


1
Nursing Considerations With the Use of Targeted
Therapy
  • Fadi Sami Farhat
  • Head of Division Hematology Oncology,
  • Hammoud Hospital University Medical Centre,
  • Lecturer St-Joseph University

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Amphi-regulin(1)
NRG3(4)
NRG2(4)
NRG1(3,4)
NRG4(4)
Cytokines
HB-EGF(1,4)
b-cellulin(1)
Epiregulin(1,4)
EGF(1)
TGFa(1)
LPA,thrombinET, etc.
Ligands
a
a
b
b
Inputlayer
2
2
2
2
4
1
4
3
4
1
1
4
2
4
3
1
3
3
3
1
Receptordimers
Src
Jak
Cbl
Shc
Crk
Ras-GDP
Adaptorsand enzymes
PLCg
Grb7
PI3K
Vav
Grb2
Shp2
Nck
GAP
Sos
Rac
Ras-GTP
Signal-processinglayer
RAF
Akt
PAK
Cascades
Abl
MEK
JNKK
S6K
Bad
PKC
MAPK
JNK
Jun
Transcriptionfactors
Myc
Sp1
Elk
Fos
Egr1
Stat
Outputlayer
Differentiation
Apoptosis
Migration
Growth
Adhesion
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Normal HER2 expression
6
HER2 amplification leads toHER2 overexpression
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HER2 overexpression leads totumour proliferation
8
Binding of Herceptin to HER2
9
New Challenges For Oncology Nurses
  • Understanding new mechanisms of actions
  • Toxicities are highly variable among patients
  • Unique side-effect profiles
  • Proactive side effect management
  • Controls disease vs. curing disease
  • Some medications Oral administration and
    decreased patient/nurse interaction

Moldawer N, Wood LS. Kidney Cancer J. 2006425.
10
  • Some Examples

11
Avastin
  • Bevacizumab

12
Normal Angiogenesis in Adults
13
Tumour Angiogenesis
5. Intravasation
1. Secretion of angiogenic factors
Tumour
4. Appearance of new tumour vasculature
2. Proteolytic destruction of extracellular
matrix
3. Endothelial cell proliferation and migration
Sprouting capillary
14
Avastin effects on human tumor vasculature
Avastin
Normalized
Normal
Abnormal
Reduces interstitial fluid pressure vessel
density Increases drug delivery
Adapted from Jain RK. Nat Med 200179879 Willett
CG et al. Nat Med 2004101457 Tong R et al.
Cancer Res 20046437316
15
Dosing and Administration
  • Usual dosage of bevacizumab in the treatment of
  • Colorectal, breast, lung cancer -5 mg/kg IV every
    2 weeks
  • renal cancer is 10 mg/kg IV every 2 weeks 1,2
  • Can be associated with hypersensitivity reactions
    during administration

1. Avastin (bevacizumab) Full Prescribing
Information. Genentech, Inc. March 2008. 2.
National Cancer Institute website.
http//www.cancer.gov/clinicaltrials/search.
16
Serious Adverse Events
Percent of patients with grade 3 toxic
effects ? 1 or 150 mg/24 hrs Grade 3
hypertension was defined as hypertension not
completely controlled by one standard
medication Grade 3 proteinuria was defined as
urinary excretion of gt3.5 g of protein per 24 hrs
Yang CH et al. N Engl J Med. 2003349427.
ALT Alanine Aminotransferase
17
  • Adverse Events Nursing Considerations

18
Bleeding
  • Obtain patient history of unusual bleeding or
    clotting, GI perforation, and use of
    anticoagulants
  • Avoid anticoagulant therapy if possible,
  • Educate patient about signs of bleeding (ie,
    epistaxis bleeding gums during tooth brushing
    red or black, tarry stools vomiting blood)

Ignoffo RJ. Am J Health-Syst Pharm. 200461(Suppl
5)21.
19
Thrombosis Proteinuria
  • Educate patient about signs of thrombosis that
    include
  • Sudden chest pain
  • Difficulty breathing
  • Monthly monitoring of renal function and urine
    protein concentration

Ignoffo RJ. Am J Health-Syst Pharm. 200461(Suppl
5)21.
20
Hypertension
  • Establish baseline BP, monitor weekly during
    therapy
  • Ensure that patient has a BP monitor at home
  • Continue antihypertensive therapy in patients
    already taking it when bevacizumab is initiated
  • Initiate mild antihypertensive if patient
    develops hypertension during bevacizumab therapy

Ignoffo RJ. Am J Health-Syst Pharm. 200461(Suppl
5)21.
21
Erbitux
  • Cetuximab

22
EGFR inhibition by agents that target the EFGR
23
Erbitux Recommended Dosing Schedule
  • Once a week
  • an initial 400 mg/m2 2-h infusion, d1, week 1
  • subsequent 250 mg/m2 1-h infusions weekly from
    d1, week 2
  • Anti-allergic premedication (such as an
    antihistamine) must be used prior to the initial
    infusion and is recommended prior to all
    subsequent infusions

24
Erbitux Safety And Tolerability
  • Nail disorders, e.g. paronychia
  • Eye disorders
  • Respiratory disorders
  • Infusion-related reactions (IRRs)
  • mild to moderate reactions gt 10 of patients
  • severe reactions 1-10 of patients

25
Erbitux Skin reactions
  • Common feature of treatment with many EGFR
    inhibitors
  • In approx. 80 of patients treated with ERBITUX
  • 85 are mild-to-moderate
  • Acne-like rash (face, scalp, upper chest or back
    )
  • Pruritus, dry skin and nail disorders - less
    frequently
  • Generally manageable, rarely - discontinuing
    treatment
  • Majority - within the first 2-3 weeks and
    generally resolve, without sequelae, after
    cessation of treatment

26
Correlation between skin reactions and response
to treatment with Erbitux
  • The presence and/or intensity of skin reactions
    correlates strongly with response to ERBITUX and
    survival
  • This relationship has been observed in different
    tumor types, including CRC and SCCHN
  • However, patients not developing skin reactions
    may also respond to treatment with ERBITUX

27
Mabthera
  • Rituximab

28
MabThera anti-CD20 Monoclonal Antibody
1 ADCC2 Complement activity3 Sensitising
chemoresistant B-cells4 Induction of apoptosis
2
3
4
NK cell
1
B-cell (CD20-positive)
NK natural killer
29
MabThera administration
  • 375mg/m2 (Do not administer as i.v. push or
    bolus)
  • Premedication, about 1 hour before start of
    infusion
  • analgesic (i.e. paracetamol 1,000mg p.o.)
  • antihistamine (i.e. clemastine 2mg i.v. or p.o.)
  • First infusion must be applied in the hospital
    setting
  • Second infusion can be applied on an outpatient
    basis if no allergic reactions were present
    during the first infusion

30
MabThera pivotal trial in low-grade or follicular
NHL adverse events (n166)
180 160 140 120 100 80 60 40 20 0
NCI toxicity grade
Grade 1 Grade 2 Grade 3 or 4
Number of patients
First Second Third Fourth
Infusion
McLaughlin P, et al. Semin Oncol 1999267987
31
What special nursing considerations are
necessary?
  • Safety measures
  • Supervision available at all times by an
    experienced clinician
  • Stop antihypertensive medication 12 hours before
    infusion
  • Stop other protein-based drugs, e.g. interferons,
    mistletoe-based drugs
  • Should not be administered to pregnant women

32
What special nursing considerations are
necessary? (contd)
  • Adverse events
  • With the first infusion
  • With elevated infusion rates
  • infusion reaction
  • In high-risk patients
  • high tumour burden (bulky disease)
  • elevated lymphocyte count in peripheral blood
    (gt25,000/µL)

33
What adverse events might patients experience
with single-agent MabThera?
Figures based on events reported in ³5 of 356
patients
34
What actions should be taken should serious
adverse events occur?
  • If serious adverse events occur, e.g. fever,
    chills, hypotension
  • stop MabThera infusion
  • open saline infusion line
  • call for clinician
  • bed in top-down position and monitor closely
  • restart at 50 reduction in rate upon resolution
    of symptoms

35
  • Oral Targeted Therapy

36
Sutent
  • Sunitinib

37
Dosing and Administration
  • An orally administered tyrosine kinase inhibitor
    (TKI)
  • Approved for treatment of advanced RCC in January
    2006
  • Potent inhibitor of VEGFR, PDGFR, and FLT-31
  • May be taken with or without food
  • Drug formulation 50 mg, 25 mg and 12.5 mg
    capsules
  • Requires dose adjustment when administered with
    CYP3A4 inhibitors or inducers2
  • Important to assess concomitant medications
  • 50 mg daily x 28 days followed by 14 day rest
    period

1. Abrams TJ et al. Mol Cancer Ther.
20032471. 2. Motzer RJ. JAMA. 20062952516.
38
Most Common Adverse Events (20)
Sutent (sunitinib) Full Prescribing Information.
Pfizer Inc. October 2007.
39
Sunitinib and Sorafenib Adverse Events
  • Nursing Considerations1,2

1. Wood LS. Oncology Nurs News. 2007319. 2.
Wood LS. Oncology Nurs News. 2007437.
40
Diarrhea
  • Treat initially with diet modification (low
    residue) and loperamide consider fluid
    replacement as necessary
  • If loperamide insufficient, atropine ?
  • Additional options include tincture of opium,
    Culturelle? (oral probiotic), and Activia? yogurt
    containing bifidobacterium
  • May be a dose limiting toxicity

41
Fatigue Functional or clinical mucositis
  • Adjust activities to allow for rest periods and
    maximize fluid and caloric intake
  • Greater intensity during initial months of
    treatment
  • Avoidance of carbonated beverages and spicy foods
  • Eating foods at room temperature
  • Can be a dose limiting side effect

1. Wood LS. Oncology Nurs News. 2007319. 2.
Wood LS. Oncology Nurs News. 2007437.
42
Taste changes and anorexia Medications
  • Maximize caloric intake
  • Encourage 6 small meals per day
  • Use of flavorings and gravy to enhance food taste
  • Topical lidocaine or Xylocaine
  • BMX Solution (Benadryl/Mylanta/Xylocaine)
  • Rincinol (OTC topical solution containing aloe
    vera)
  • Nystatin suspension or clotrimazole troches for
    clinical mucositis

1. Wood LS. Oncology Nurs News. 2007319. 2.
Wood LS. Oncology Nurs News. 2007437.
43
Dermatologic Toxicities
  • Dry skin, Rash, Hand-foot skin reaction, Hair
  • Alopecia, Thinning, De-pigmentation, Scalp
    pruiritis/burning
  • Application of lotions/creams as part of initial
    education
  • Avoid hot showers/steam
  • Rash may present in many ways
  • Maculopapular, Exfoliative dermatitis, Acneform,
    Erythema multiform-appearing eruptions

44
Hypertension
  • Common side effect with this class of drug
  • Baseline BP reading is essential
  • Monitor BP weekly x 6
  • gt20 mg/m increase in diastolic or gt150/100
    warrants intervention
  • Antihypertensive agents may need to be added or
    increased during therapy

45
  • Targeted Therapies

46
Patient Education and Management
  • Assess patient at initiation of therapy and
    reinforce treatment goals, treatment schedule and
    duration of therapy
  • Ensure that patient sees an MD or RN at the
    beginning of each treatment cycle
  • Instructions about cancer treatment and side
    effect management

Moore SH. Online educational activity 2006.
47
Patient Education and Management
  • Patient should be instructed to contact
    healthcare provider immediately when experiencing
    any side effects
  • Targeted therapies have manageable side effects
    with appropriate nursing interventions
  • Patients have prolonged survival with control of
    their cancer

Moore SH. Online educational activity 2006.
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