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Cancer
- Oncology Nursing
- No Oncology Nursing in the Philippines
- Other countries have oncology nursing
o For Chemotherapy Administration
o Certifications and Trainings
- From the form: Cancri or Crab-like
o It goes in any direction
o No specific direction of growth
Ex. Lung cancer affecting the brain or liver
o Begins with an abnormal cell that is transformed by the genetic mutation of
cellular DNA
All cancers are the result of mutations in oncogenes and tumor
suppressor genes
Oncogenes – precursor for cancer cells
o A group of heterogeneous diseases that share common biologic properties
The same but different areas of events
o Not a singles disease; disorder of altered cell differentiation and growth
Breast cancer is not only in the breast
Cell are transformed from one type of cell into another
Ex. Stomach cells change shape from example square to circle or
triangle
Anaplasia – change of one type of cell to another
A precursor of malignant cells
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FACTS of CANCER
1. Increasing mortality rate
2. A lot of Filipinos diagnosed with cancers than the westerners
a. Filipino tech is obsolete
b. Filipinos are used to having check-ups during the worst conditions already
3. In the Philippines, leading cancers are as follows:
a. Breast cancer
b. Lung cancer
c. Liver cancer
d. Colon cancer
e. Cervical cancer - Phi
f. Leukemia cancer
g. Stomach cancer
h. Prostate cancer
i. Brain / Nervous System cancer
j. Ovary cancer
4. Phils has highest Breast Cancer Incidence in the World
5. Feb 4: World Cancer Day
GROWTH PATTERNS
Cell Proliferation – cell division to form new cell types
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CANCER NOMENCLATURE
OMA – suffix
o Presumption of having a cancer or preceding a cancer
i. Carcinoma – parenchymal cells or functional cells
ii. Sarcoma
1. Except: hepatoma (hepatocellular carcinoma), lymphoma,
melanoma, glioma – no BENIGN, always MALIGNANT
PERMANENT CELLS
1. Cardiac cells
2. Neurons cells
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CARCINOGENESIS
_______ and derangement theory
a. The cells usually undergoing cellular transformation is removed through removal
of stimulus
b. Continuous stimulus deranges the cells
c. Transformation of the cells makes the cells abnormal
d. Slow transformation and change which are copied by the cells thus
“abnormalizes” the cells
2. Failure of the Immune Response Theory
a. The check points in the cell cycle are inactive
b. Copying of the abnormal cells due to failing of the immune system of the body
CARCINOGENESIS
1. 2 stage theory
2. 3 Stage theory
- Initiation > Start; irreversible mutation of a gene that leads to malignant transformation
- Promotion > Stage of duplication; Promoting agent stimulates the growth and division of a
cell; stimulation of the ONCOGENES
*- Progression > Start of cells building their own group
- Transformation > series of changes that lead to the characteristics of undifferentiated cell
- Metastasis > Tumor has properties needed to spread to other organs in the body
CARCINOGENESIS FACTORS
Host
Female – more common to breast cancer due to change in estrogen
Male – more common to lung cancer due to smoke
Status of the Host – Socio-economic Status
Life Style of the Host
Environmental Agents
Chemical Agents
o Direct Acting –
Ionizing radiation, light, cell phone, microwave, tanning beds, Cosmic
Waves, X-rays.
o Indirect Acting (Procarcinogens)
Radiation
o UV Radiation (A,B,C)
Chromosomal Damage in cells
Skin Cancer
UV-A Rays – strongest type of UV Radiation; Avobenzene – protects body
from UV-A, and automatically UV-B
o Inonizing Radiation
X-Rays
Gamma Rays
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Industrial Sources
o Polyvinyl Chloride
o Cd, Cr
o Ni and Zn ores
From the Work Place
o Coal tars and soot
o Dyes
o Asbestos
o Ar
o Wood dust
Dietary Substances
o Alcohol
o Fats
o Nitrites and Nitrates
o Red Meat
Normal Tissue
- Mitotic Division: New Cells = Old / Dying Cells
- Growth Pattern
Malignant Cells
1. Self Sufficiency in growth signals
a. Tumors possess the capability to proliferate without external stimuli
b. Proliferation of Oncogenes
2. Insensitivity to growth-inhibitory signals
a. Tumor suppressor genes
Categories of TSG
Gate Keepers – controls the rate of proliferation
Care Takers – ones responsible for controlling the mutation
o Tumor Suppressor Genes – EGF
3. Evasion of Apoptosis
a. Reproduction of abnormal cells due to the invasion of apoptosis
b. Abnormal Cells overcomes the p53
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4. Defects in the DNA Repair
a. Change in the DNA structure
b. No proper signals that limit and control reproduction
c. Check-points are not functional
5. Limitless Replication Potential
a. Uncontrolled reproduction
6. Sustained Angiogenesis (VEGF)
a. Continuation of angiogenesis
b. Number of cells go out of the containing area
7. Ability to invade and metastasize
a. Moving on to other areas
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CANCER TREATMENT MODALITIES
GOAL
1. Cure 2. Control 3. Palliate
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Karnofsky’s Performance Scale – KPS (100%-0%)
> The lower the scale, the higher the percentage of dying
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Model for Palliative Care
3 SPECIFIC GOALS
Cure, Control, Palliation
Oncology Team:
Oncologist – Cancer Doctor
Secondary Oncologist – Assisting Practitioner
General Practitioner (MD) – to detect any co-morbidity present
Oncology Nurse – cancer nursing practitioner
Pathologist – checks the removed part
Radiologist – supportive diagnosis and radiation therapy
Surgeon – for removal of cancer in invasive program
Anaesthetist -
Dietician / Nutrition Specialist -
Oncologic Pharmacist
STAGE 4 PATIENTS
1. Palliative Care
- Given at the start of the stage of cancer
- Patient is already dead
2. Cure and Control
- Becomes small as time progresses
- Hospice: a place for treating chronically ill person
- Limitation on the bereavement care – up until the patient dies
- Bereavement: <6 Months
- >6 Months: Patient will have depression
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TREATMENTS
1. Surgery – simplest and the fastest way to remove cancer
Purpose:
a. Cure – removal of tumor / mass
b. Control – remove marginal tissues or tissues adjacent or beside the mass
c. Palliative – remove tumor / mass blocking vital function
D. Diagnosing, Staging, and Grading
Stage – extent of the disease
Grading – type of the cells
Principle:
A - as
L - low
A - as
R - reasonably
A – achievable
> In cancer cells, the active ones are the ones outside because they have more nutrients or
receive more nutrients.
Ex. 6000 gy (grays) – removes the cancer but kills the patient
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> Fractionated Dose – portion of the total amount of dosage a patient can tolerate for the
radiation therapy
Patient:
> Mild, not scented
> Do not rub dried area
> Etc.
Tele therapy
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Chemotherapy
Directly kills the cancer cells and the normal cells
Purposes
Not used in palliative purposes
o Makes the patient weaker, using up energy of the patient
1. Primary – main therapy
2. Induction Chemotherapy – high doses (Loading Dose) and then lesser doses
3. Neoadjuvant – removes the part of the tumor prior to treatment; shrinks the cancer
tumor
4. Combination Chemotherapy
5. Adjuvant Therapy – after the primary treatment (surgery) to remove remaining cancer
cells, or as prophylaxis
6. Myeloblative Therapy (Myeloablation) – high dose chemo therapy (already given high
doses for successive therapy)
Factors to Consider
1. Patient Eligibility
2. Cancer cell type
a. The smaller the cancer the more dangerous
3. Rate of drug absorption
a. Dependent on the body mass
4. Tumor Location
a. Chemotherapy is not able to penetrate the blood brain barrier
5. Tumor Load
a. Amount of the tumor
6. Tumor Resistance
a. Resisting factor of the tumor
Intravenous Routes
- Central Lines (connected to the Inferior or Superior Vena Cava
- Highly Vesicant Drugs (easily destroys the linings of the blood vessels)
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Preparation: BSC
BSC – Biohazard Safety Cabinet
- Has safety vents
Handling
- Must be in complete PPE
CLASSIFICATION
Cell-cycle non specific
o Alkylatting Agent (MMEANT)
Mustargens or Mustard Derivatives
Metal Salts (~platine) – highly emetic drugs
Ethyl Alkyllating Agents (Ethyl Amines)
Alkyl Sulfonates
Nitrosureas – can cross the Blood-Brain Barrier
Thiazines
o
o Anti-tumor antibiotics
o Hormonal Agents
Cell-Cycle Specific
o S-Phase = antimetabolics and Topoisomerase Inhibitors
o M-Phase = Mitotic Inhibitors (Vinca Alkaloids and Taxanes (~cristines)
o
Miscellaneous
Highly Toxic
Tinca Alkaloids
CHEMOTHERAPY
SFANCH
S – stomatitis or mucositis (use water to clean)
F – Fatigue (due to systemic Chemotherapy effects)
A2 – Anorexia; Anxiety
N – Nausea (bland food, crackers)
C3 – Cardiovascular Changes, Cardio Toxicity, Constipation
H2 – Hairloss (women), Hyper Calcemia
Concern: Nausea and Vomiting
CINV – Chemotherapy Induces Nausea and Vomiting
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Anticipatory Acute Delayed
> 24 hours before therapy > Day 1- > Day 2-5
> Psychological Mechanism > Serotonin dependent > Substance P dependent
> Antiemetics ineffective mechanism (peripheral) mechanism (central)
> Behavioural therapy helpful
Refractory
- N/V in subsequence cycles of chemotherapy due to failure of the initial treatment
GIT
-all GI contents will be expelled
- 5-HT3
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Chemotherapy Administration
Calculation of drug dosage
Mosteller Formula
Ex.
Doxorubicin hcl
Adriamycin PFS, Adriamycin RDF, Rubex
Dosages (adult)
60-75 mg/m2 IV as single dose q21D
Note: Dosages come in ranges. Get the higher dose of the medication
Note: Use only 1 decimal place BEFORE continuing with the formula.
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PREVENTION and DIAGNOSIS
2 Types of Prevention
1. Primary – steps taken to prevent disease occurrence
2. Secondary – the early detection (at risk)
a. Must follow screening guidelines
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PRIMARY PREVENTION
> Fiber – 25 – 35g / day
> Top 10 Cancer Foods
- Cruciferous
> BMI (18.5-25 = N>)
Normal = 19.5 – 25
Overweight => 25 – 29.99
Obese = >30 – 35.99
Severely Obese = >36 – 39.99
Morbidly Obese = >40
Tumor Markers – protein excreted by the cancer cells / Supportive DX test / Monitoring Cancer
Progress Tx
CA – Cancer Antigen
CEA – CARCINO EMBRYONIC ANTIGEN – any organ
CA19-9 = GIT
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CA 27 -29 = more specific (breast cancer)
CA 15-3 =
PSA = Prostate Cancer
AFP = Alphafeto Protein (Amniotic fluid, blood)
HCG = Human Chorionic Gonadotropin – (testicular & ovatrian) – secretes
CA 125 – ovarian cancer – only at late stages
Looks like PMS (Pre Menstrual Syndrome)
If it happens in the right side, might look like Appendicitis
Thyroglobulin – thyroid or head and neck cancer
Beta2-Macroglubulin (B2M) – Multiple Myeloma
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Biopsy
– getting of a particular part of an organ
- Confirmative
Types:
1. Excisional Biopsy – tissue sample
a. Fine Needle Aspiration Biopsy
b. Core Needle biopsy – bigger needle
c. Ultra-sound guided biopsy
d. Sentinel Lymph Node Biopsy
i. First lymph node that will receive BIOPSY
Lymph Nodes Only
2. Incisional Biopsy – adjacent to the tumor
CANCER GRADING
- Classification of cells
- The Broders Classification of a simple grading system
GRADE STAGE
1 Well I Localized
Differentiated
2 Moderately II Lymph Node
3 Highly III Involvement
4 Poorly IV Metastasis
Differentiated
Autologous – self
Allogeneic – family members or relatives
Synergetic – twins
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