Child with Cancer (NUR 320) – Comprehensive Exam Study Notes
Epidemiology & Etiology of Childhood Cancer
- Second leading cause of death in the pediatric population (after unintentional injuries)
- Etiology is largely unknown
- Current theory: multifactorial interaction among
- Genetic alterations
- Environmental exposures (radiation, toxins, viral triggers, etc.)
- Immune‐system dysfunction or inadequate tumor surveillance
- Psychosocial / developmental overlay
- Diagnosis collides with critical growth stages ⇒ regression, altered body image, school disruption
- Family-centered care is ethically imperative; parents/guardians are primary partners in decision-making
- Family stressors: financial strain, anticipatory grief, caregiver role strain, cultural/spiritual questions
Fundamental Tumor Biology
- Neoplasm = any new growth or tumor
- Tumors classified as benign or malignant
- Benign: localized, usually encapsulated, non-invasive
- Malignant:
- Life-threatening potential
- Invasion of contiguous tissue
- Metastasis via blood, lymph, or CSF
- Cells poorly differentiated / anaplastic
Clinical Presentation – Pediatric Specifics
- Pediatric cancers often present with covert, nonspecific complaints ("the cold that lingers")
- Typical red-flag signs & symptoms
- Mass or swelling
- Purpura / unexplained bruising
- Pallor or anemia-related fatigue
- ↓ weight (unintentional)
- Persistent or projectile vomiting
- Recurrent or low-grade fevers
- Bone or joint pain, limp
- Headache (especially a.m.)
- Lymphadenopathy (firm, non-tender nodes)
- Gait, personality, or balance changes
- General fatigue / malaise
- NCLEX-style recall: fatigue, headache, weight loss, lymphadenopathy are classic; polydipsia is NOT
Diagnostic Work-Up
- Laboratory studies
- CBC: pancytopenia, leukocytosis, or isolated cytopenias
- Chemistry: electrolyte shifts, ↑ uric acid, ↓ albumin
- Procedures
- Bone-marrow aspiration/biopsy (posterior iliac crest; prone with pillow)
- Lumbar puncture (evaluate CNS involvement; intrathecal chemo route)
- Imaging modalities
- X-ray, ultrasound, CT, MRI, PET
- Pathology / flow cytometry for definitive cell typing
Nursing Considerations for Invasive Procedures
- Obtain informed consent; developmentally appropriate explanations (use play/visual aids)
- Sedation for young or anxious children; allow parental presence
- Positioning: prone with small pillow under hips for marrow aspiration
- Coping techniques: singing, counting, deep breathing during needle entry (<10 sec discomfort)
- Post-procedure
- Pressure dressing if platelet count <50{,}000/\text{mm}^3
- Monitor VS, puncture site for hemorrhage or infection
Treatment Modalities Overview
- Surgery (curative, debulking, biopsy)
- Radiation therapy (external beam, fractionated doses)
- Chemotherapy (multi-agent protocols)
- Biologic / immunotherapy (e.g., monoclonal antibodies, CAR-T)
- Complementary & alternative modalities (massage, art therapy) – evaluate evidence & safety
- Hematopoietic stem-cell transplant (HSCT) – autologous or allogeneic
Central Venous Access Devices (CVADs)
- Long-term routes: Port-a-Cath, PICC, tunneled catheters
- Access with non-coring (Huber) needle; sterile technique imperative
- Teaching: flushing schedule, infection-prevention, swimming restrictions, when to seek help
Chemotherapy Essentials
- Mechanism: cytotoxic to rapidly dividing cells ⇒ high collateral on GI mucosa, hair follicles, marrow
- Routes: PO, IV, IM, SQ, intrathecal
- Setting: inpatient, outpatient clinic, or home infusion
- Common adverse effects
- Bone-marrow suppression: thrombocytopenia, neutropenia, anemia
- Nausea / vomiting (anticipatory, acute, delayed)
- Mucositis / stomatitis
- Alopecia
- Photosensitivity, fatigue, diarrhea
- Nursing priorities
- Reverse isolation & neutropenic precautions (ANC <500/\text{mm}^3)
- Strict infection control; no fresh flowers, raw produce
- Transfusion support (PRBCs, platelets)
- Bleeding & injury prevention; soft toothbrushes, no rectal temps
- Nutrition: high-calorie, high-protein; TPN if necessary
- Pain & nausea management (opioids, antiemetics BEFORE chemo)
- Sun protection, activity clustering, developmentally appropriate play
Preparing & Administering Chemotherapy (OSHA High-Alert)
- Verify height & weight ⇒ calculate body-surface area (BSA) m2
- Double-check dose with 2nd RN, cross-reference protocol (COG, institutional)
- Review CBC within 48 h; hold if counts below threshold
- Confirm CVAD patency; new peripheral IV for vesicants
- Have emergency meds & extravasation kits at bedside
- Don appropriate PPE per OSHA/NIOSH
Radiation Therapy – Key Points
- Delivered in fractionated doses to limit toxicity
- Acute side-effects
- Fatigue
- Dermatitis / skin breakdown in radiation field
- Alopecia in field
- Nausea / vomiting, anorexia
- Myelosuppression
- May also see late effects months–years later (endocrine dysfunction, secondary malignancies)
Stem-Cell / Bone-Marrow Transplant (HSCT/BMT)
- Stem-cell sources: bone marrow, peripheral blood, cord blood
- Autologous (self) vs allogeneic (matched donor)
- Infused cells migrate to marrow ⇒ restore hematopoiesis
- Common acute toxicities: mucositis, profuse diarrhea, fevers, epistaxis
- Core nursing care
- Strict neutropenic isolation; positive-pressure room if available
- GVHD surveillance (rash, liver dysfunction, diarrhea)
- Antirejection / immunosuppressant management
- Nutritional, emotional, and developmental support
Pediatric Oncologic Emergencies
- Tumor Lysis Syndrome (TLS)
- Rapid lysis ⇒ release of K+, phosphate, uric acid; ↓ calcium
- Risk of renal failure; maintain aggressive hydration, allopurinol/rasburicase, monitor labs & urine output
- Hyperleukocytosis (> 100×109/L) ⇒ viscosity, stroke risk
- Superior Vena Cava (SVC) Syndrome ⇒ facial/upper-body edema, respiratory compromise
- Spinal-Cord Compression ⇒ back pain, motor loss, bladder dysfunction
- Disseminated Intravascular Coagulation (DIC) ⇒ bleeding & microthrombi; support with blood products, treat trigger
General Acute Side Effects Across Therapies
- Infection / sepsis
- Hemorrhage
- Anemia & fatigue
- Nausea / vomiting (anticipatory, acute, delayed)
- Altered nutrition & weight loss
- Mucositis / ulcerations of GI tract
- Neurotoxicity / peripheral neuropathies
- Hemorrhagic cystitis (e.g., cyclophosphamide metabolite acrolein) ⇒ MESNA prophylaxis, hydration
- Steroid-related: mood swings, hyperglycemia, cushingoid appearance
Acute Leukemias
- Malignancy of marrow & lymph tissues ⇒ “liquid tumors”
- Most common childhood cancer (<15 yrs)
- Pathophysiology: uncontrolled proliferation of immature blasts crowding healthy cells ⇒ pancytopenia
Acute Lymphoblastic Leukemia (ALL)
- Accounts for majority; 5-yr disease-free survival >85%
- Diagnostics
- CBC: pancytopenia, ↑ lymphocytes
- Bone-marrow aspirate: ≥25% lymphoblasts (confirmatory)
- LP: evaluate CNS spread
- Flow cytometry: B- vs T-cell lineage
- Clinical staging (I–IV) by node & organ involvement (diagram review)
- Therapy: multi-phase chemotherapy per Children’s Oncology Group (induction, consolidation, maintenance); potential HSCT
- Focused Nursing Issues
- Infection control (ANC monitoring)
- Hemorrhage & bruising surveillance, nose-bleed management
- Nutrition: high-calorie, antiemetics, weight tracking
- Psychosocial: alopecia preparation, school re-entry facilitation
Lymphomas
- Malignancies of lymphoid tissue
- Two main entities
- Hodgkin Lymphoma (HL)
- Typically localized, single node chain
- Reed-Sternberg cells pathognomonic
- Non-Hodgkin Lymphoma (NHL)
- Rapid, diffuse, often mediastinal mass
- “B-symptoms”: night sweats, fever, >10\% weight loss
- Painless, firm lymphadenopathy; hepatosplenomegaly; abdominal pain (NHL)
- Treatment: risk-adapted chemo ± radiation; monitor TLS risk
Overview of Solid Tumors
- Brain & CNS tumors
- Neuroblastoma
- Bone & muscle tumors (Osteosarcoma, Ewing sarcoma, Rhabdomyosarcoma)
- Wilms tumor (nephroblastoma)
- Retinoblastoma
- Germ-cell & hepatic tumors
Brain Tumors
- Most common solid pediatric tumor
- Presentation
- Early-morning headache, vomiting
- Abnormal neuro exam; cranial nerve deficits
- ↑ intracranial pressure (ICP): papilledema, behavior change, decreased pulse pressure
- Diagnostics: MRI preferred; CT, PET, LP (cautious), tissue biopsy
- Management: surgical resection, chemo, targeted radiation
- Post-op Nursing
- Neuro checks, ICP control, positioning, fluid balance, comfort
- Family emotional support & rehabilitation planning
Neuroblastoma
- Arises from sympathetic chain (neural crest)
- Often diagnosed as abdominal mass; can metastasize (bone, skin, orbit – “raccoon eyes”)
- Symptoms: protuberant abdomen, limping, jerks, eyelid droop, facial edema
- Diagnostics: biopsy, CT/MRI, catecholamine metabolite (HVA/VMA) elevations
- Treatment: multimodal – chemo, surgery, radiation, HSCT, immunotherapy
- Nursing: pain control, peri-op care, mobility support, parental coping
Bone & Muscle Tumors
- Osteosarcoma
- Peak adolescence; distal femur > prox tibia > prox humerus
- Pain, swelling, decreased ROM
- Ewing Sarcoma
- Flat bones (pelvis, ribs, vertebrae)
- Systemic symptoms (fever, weight loss)
- Rhabdomyosarcoma
- Soft-tissue tumor from mesenchyme (<10 yrs common)
- Multidisciplinary diagnosis (imaging, biopsy)
- Treatment: limb-sparing surgery, amputation (osteosarcoma), chemo, radiation
- Nursing: body-image counseling, prosthetic training, pain & function restoration
Wilms Tumor (Nephroblastoma)
- Most frequent renal malignancy
- Classic sign: painless abdominal mass; do NOT palpate vigorously (risk of rupture & seeding)
- Metastasis commonly to lungs
- Diagnostics: CT/MRI, UA, labs; staging I–V
- Treatment: nephrectomy, chemo ± radiation
- Pre-op: gentle handling, blood-pressure control; Post-op: output, infection, education on solitary kidney care
Retinoblastoma
- Malignancy of retinal cell layer; >90\% diagnosed <5 yrs
- Hallmark: leukocoria (“cat’s-eye” reflex) in photos, absent red reflex
- Other: strabismus, vision loss, orbital inflammation
- Diagnostics: fundoscopic exam under sedation, ocular US, CT/MRI
- Treatment: chemo, focal radiation, cryotherapy; enucleation if advanced
- Nursing: family preparation for prosthesis, genetic counseling (RB1 mutation)
Other Tumors
- Germ-cell tumors: gonadal/extragonadal (testes, ovaries, sacrococcyx, mediastinum); surgical resection is cornerstone
- Liver tumors
- Hepatoblastoma (infants/young) & Hepatocellular carcinoma (5–15 yrs)
- Surgery primary; transplant consideration
Survivorship & Late Effects
- Overall long-term survival now >80%
- Late effects
- Secondary malignancies (e.g., AML after etoposide)
- Endocrine: growth hormone deficiency, infertility
- Cardiac: anthracycline-induced cardiomyopathy
- Neurocognitive impairment, psychosocial challenges
- Lifelong, risk-based follow-up
- Screening, surveillance, health-promotion education (diet, exercise, smoking avoidance)
- Role of nurse: transition planning, advocacy, health-literacy reinforcement
Patient & Family Education Principles
- Continuous dialogue: diagnosis comprehension, treatment phases, expected side effects
- Skills teaching: CVAD care, medication administration, infection warning signs
- Encourage participation & shared decision-making
- Provide written & digital resources; connect with support groups, school liaison
- Address ethical considerations: assent, fertility preservation, advance directives in older adolescents
Ethical, Philosophical, & Practical Highlights
- Informed consent & child assent evolve with developmental stage
- Balance cure with quality of life; palliative care integration when appropriate
- Cultural sensitivity in discussing prognosis, complementary therapies
- Financial toxicity & healthcare disparity awareness
Quick Reference – Numerical Pearls
- ALL 5-yr DFS >85\%
- Neutropenia cutoff: ANC <500/\text{mm}^3
- Platelet precaution threshold: <50{,}000/\text{mm}^3
- Hyperleukocytosis: WBC >100\times10^9/\text{L}
- Majority of retinoblastoma cases present <5 yrs; >90% cured if localized
Mnemonic Aids
- “CHILD CANCER” for warning signs (Children’s Oncology Group mnemonic):
- Continued, unexplained weight loss
- Headaches with early-morning vomiting
- Increased swelling / persistent pain (bones, joints)
- Lump or mass (abdomen, neck, etc.)
- Development of whitish color behind pupil
- Constant infections
- Aches in bones, joints, back
- Neurologic changes (balance, gait)
- Constant fever
- Excessive bruising, bleeding
- Recurrent / persistent nausea
Summary
- Pediatric oncology nursing demands holistic care: biomedical precision + psychosocial scaffolding.
- Early recognition, protocol-driven treatment, meticulous supportive care, and family partnership yield high cure rates and improved lifelong outcomes.