14.3 (12.3) Radiotherapy in symptom management Flashcards
What are two types of damage caused to DNA by ionizing radiation?
Which is more important to controlled tumor growth?
Radiation-> direct and indirect damage to DNA
Direct damage = base deletions, breaks in the DNA chain
Indirect damage = results from toxic FREE RADICALS produced from the interaction between radiation and water molecules in cells
- Indirect damage is the more important cause of cell death
- with very high doses (>10Gy) damage to endothelial cells may occur which may cause cell death from damage to blood supply
List 4 types of particle radiation therapies
- Electrons - used to treat superficial sites
- Beta particles - i.e. systemic Strontium
- Alpha particles - i.e. systemic Radium
- Proton therapy - i.e. base of skull tumours, but not indicated in palliative Rx
List 2 contributors to radiosensitivity of cancer cells compared to normal cells
- Differences in repair capacity (Cancer cells are less able than normal cells to repair ‘sublethal’ radiation damage)*
- Oxygenation (hypoxic cells are relatively radioresistant)
-The number of cells actively dividing (cells in certain phases of the cell cycle are more sensitive than others) -> non-cycling
cells are relatively radioresistant*
-rate of repopulation within the tumour
FS: cancer cells have less ability to repair and more dividing cells
- What are the 2 aims of radical radiotherapy?
- What are the 2 aims of palliative radiotherapy?
- Radical:
-Complete eradication of tumour cells
-Minimize long-term normal tissue damage - Palliative:
-Control of symptoms
-Minimal acute radiation reaction
- When delivering XRT, how is normal tissue damage minimized?
- For curative-intent treatment, how is the schedule adjusted to reduce tumour repopulation? List 2 ways.
- For palliative treatment, how is acute reaction minimized?
- What is the relationship between tumour shrinkage and symptom control?
- Radiation dose is built up with daily treatment over several weeks
- Acceleration - giving treatment over a shorter period of time (but limited by acute reaction)
- Hyperfractionation - higher dose is delivered by increasing number of fractions (multiple per day) but over same time period
- Low dose radiation given over short course
- Symptom control does not require complete eradication of tumour
(i.e. for metastatic bone pain, symptom response seems independent of tumour shrinkage. Mechanism unclear - related to osteoclast activity?)
List the 3 main types of radiation delivery
- External beam treatment (most common)
- Brachytherapy (internal radiation)
- Systemic radioisotopic therapy
List 5 modes of external beam radiotherapy and the anatomical site of their use
***Do we need to know this??
See Table 14.3.1 (energy/source/depth of penetration excluded here - ?relevant):
- Superficial x-rays: surface skin tumours
- Orthovoltage x-rays: surface tumours, superficial bones (ribs, sacrum)
- Electrons: surface tumours, superficial bones, lymph nodes
- Megavoltage x-rays: main radiation for sites other than above
- Gamma rays: all sites except superficial skin
What is the device used to deliver radiotherapy? How does it work?
Linear accelerator
produces high energy X-ray beams (or for superficial lesions, an electron beam)
- How does brachytherapy work?
- When are systemic radioisotopes used? Give 2 cancer examples and their isotopes
- Bracytherapy - use of a radioactive source placed directly onto/within treatment area so radiation is given directly into the tumour
- Systemic radioisotopes - given when specific tissues can be targeted (oral or IV)
- radioiodine - thyroid cancer
- strontium and radium - bone metastases
Brachytherapy:
List 3 ways it can be placed
List 2 isotopes used
Table 14.3.2 (12.3.2)
Intracavitary -> Iridium, cobalt
- Intrauterine
- Intravaginal
- Endo-oesophageal
- Endobronchial
- Endorectal
Interstitial -> Iridium, cobalt, iodine, caesium
- Tongue, floor of mouth
- Buccal mucosa
- Breast
- Anal canal
- Vulva/vagina
Surface (Mould) -> Iridium, Cobalt
- Skin
- Penis
List the 4 steps of radiation treatment planning
- IMMOBILIZATION
- to avoid normal tissue/critical structures - TREATMENT VOLUME LOCALIZATION
- i.e. CT for clear definition of non-superficial lesions - DOSIMETRIC PLANNING
- i.e. single beam vs 2 opposing vs stereotactic - VERIFICATION
List 3 scenarios in which more complex radiation planning may be needed
- Tumour sites close to the spinal cord
- Retreatments close to critical organs
- Treatment of oligometastases (<3 mets) when higher doses may be considered
- What is the underlying mechanism of ACUTE radiation toxicity?
- How does recovery happen?
- How long does recovery take?
- What happens if there is poor healing?
- Loss of surface EPITHELIAL CELLS resulting in skin erythema or desquamation mucositis (i.e. esophagitis, cystitis, GI irritation)
- Repair of the denuded surface (if stem cell population not damaged irreparably)
- Usually within a few days or weeks. May take longer in sites of less efficient skin healing (lower leg, back)
- Rarely, poor healing may lead to radiation necrosis (i.e. secondary to infection or trauma)
List 6 acute side effects of XRT
Table 14.3.3:
- Skin: erythema, desquamation
- CNS: transient demyelination (Lhermitte’s sign)
- Eye: Keratitis
4: Oral cavity: Mucositis
- Pharynx: Dry mouth, taste loss
- Lung: pneumonitis
- Gastrointestinal tract: N/V, anorexia, Diarrhea
- Bladder: Sterile cystitis
FS:
Dermatitis
Mucositis
Pneumonitis
Gastritis
Proctitis
Cystitis
- LATE radiation damage - what is the underlying mechanism?
- How long after treatment can late radiation damage manifest?
- What are the clinical manifestations of this? List 1 minor and 1 major finding.
- How can late radiation damage be avoided during planning? What is 1 unavoidable risk factor?
- Due to VASCULAR damage with pathological changes (endarteritis obliterans –> closure of small blood vessels)
- Rarely seen before 9 months —> ongoing risk for many decades
Minor - skin atrophy, telangiectasia seen on treated skin/mucosal surfaces
Major - fibrosis, necrosis, stricture, fistula
- Every tissue has “tolerance dose” - up to which normal tissue damage NOT expected in “normal population”
Planning = avoid exceeding this dose but deliver effective dose to adjacent target
Some people are genetically predisposed to radiation damage even with conventional dose
List 4 late side effects of XRT
List 4 organs that may be involved
Table 14.3.3
- Skin - atrophy, fibrosis, telangiectasia, necrosis
- CNS - myelitis, necrosis, local edema
- Eye - cataract, entropion or ectropion, dry eye
- Oral cavity/pharynx - mucosal atrophy, telangiectasia/bleeding, dental caries, mandibular necrosis
- Lung - fibrosis
- GI - stricture, telangiectasia, bleeding, perf, malabsorption, chronic enteritis, colitis, proctitis
- Bladder - reduced volume, telangiectasia/bleeding, urethral stricture, ureteric stricture, fistula
FS: fibrosis, fistula, stricture, necrosis
List the 4 management tips of the following radiation side effect:
Skin reaction
- Relieve symptoms, allow to heal.
Mild skin reactions - no active Rx needed, avoid local applications
Desquamation - rare after pall dose XRT. Avoid topical preps, esp with metallic salts (can enhance reaction)
Starch powder to keep skin dry
FS: good source
http://www.bccancer.bc.ca/nursing-site/Documents/Symptom%20Management%20Guidelines/14RadiationDermatitis.pdf
Gentle cleaning - non perfumed soap, don’t rub
Water based lotion
Avoid sun
Avoid irritation products, shaving, etc
List the management of the following radiation side effect:
Nausea from irradiation to abdomen/pelvis
- simple
- complex
- prophylactic
- Simple anti-emetic therapy:
mild: metoclopramide
severe: ondansetron - Non-responsive to anti-emetics:
small dose steroid (i.e. prednisolone 10-30 mg daily) - Prophylactic anti-emetic (ondansetron 8mg) + steroid (dex 8 mg) 30 min prior to XRT to avoid severe symptoms
List 3 management of the following radiation side effect:
Radiation-induced acute diarrhea
- Low-fibre diet
- Loperamide after each loose BM
- Codeine phosphate on 3-4 times daily
List 4 management of the following radiation side effect:
Radiation cystitis
- Alpha blocker such as tamsulosin for severe bladder spasm
- Significant dysuria or strangury - systemic analgesics
- Potassium citrate or cranberry juice (supportive value, no objective evidence)
- Rule out secondary infectio
FS; usual tx of bladder spasm + rule out UTI
List 4 management of the following radiation side effect:
oropharygeal mucositis
- what should be considered if there is severe mucositis?
- what should be considered before radiation of head and neck?
- Maintain high level of oral hygiene (Regular chlorhexidine mouthwashes)
- Prophylactic anti-candidal prep with nystatin suspension or clotrimazole gel
- Local pain relief: soluble ASA or benzydamine mouthwashes
- Avoid smoking, ETOH during treatments (worse symptoms)
- If severe Sx + nutritional impairment, consider enteral feeding
- Formal pretreatment dental assessment (XRT to salivary glands –> mouth dryness –> dental caries; osteoradionecrosis of the jaw)
- List 2 presenting symptoms of radiation induced pneumonitis
- How long after treatment can pneumonitis occur?
- How is it diagnosed on imaging?
- What is the treatment?
- Dry cough and dyspnea
- Can present up to 4 months after treatment (considered acute SE)
- Interstitial pneumonitis - Appears on chest xray as patchy shadowing conforming to geometry of radiation field
- A 2-3 week course of systemic steroids with antibiotics for secondary infection (but continuing symptoms and late radiation fibrosis may ensue)
List 5 indications for radiotherapy in symptom palliation
Table 14.3.4 (12.3.4)
Pain - bone, visceral, neuropathic
local pressure - spinal canal compression, cranial nerve palsies
Obstruction - bronchus, esophagus, SVC, hydrocephalus
Bleeding - hemoptysis, hematuria, vaginal bleeding, rectal bleeding
Malignant fungating wounds
FS: WP = BOS
Wound
Pain
Bleeding
Obstruction
SCC