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RADIOTHERAPY IN ENT
DR.DIVYA.K.V
DEFINITION
The application of radiation for the purpose of
therapeutic gain.
 Radiation is the process of emitting radiant energy in
the form of waves or particle.
Aim of Radiotherapy
 Delivering tumoricidal dose to a defined target
volume
 Respecting the normal tissue tolerance
 Trying to achieve an optimum therapeutic ratio
 Improvement of quality of life
MECHANISM OF RADIOTHERAPY
 Radiations act on biological cells by ionization
which can be direct or indirect.
Direct ionization(Electron, Heavy Ion
radiations)
photons hit matter
produce secondary electrons
damage DNA directly
Indirect ionization( X-ray, Neutrons )
photons hit matter
produce secondary electrons
with water and oxygen free radicals damage DNA
 Indirect ionization is more common ( > 2/3rd )
 Radiations also causes cell reproduction failure by
inhibiting mitosis.
BIOLOGICAL EFFECTS OF RADIATIONS
Affects cell by breaking strands of DNA
 Single strand breaks - repairable than double strand
breaks which are lethal.
 Sub-lethal damage refers to DNA damage that can be
repaired if given the right cellular conditions and
sufficient time.
 Sub-lethal damage is less efficient in tumor cells,
hypoxia or low pH.
 DNA damage is repairable with low radiation dose
and the relation is proportional. (Absorbable dose )
TUMOR CELL KINETICS AND RESPONSE TO RT
CELL PROLIFERATION AND LOSS
 radiosensitive in the G(2)-M phase,
 less sensitive in the G(1) phase
 least sensitive during the latter part of the S phase
INTRINSIC RADIOSENSITIVITY
 Lesser the SF2 better the radiosensitivity/prognosis.
 X-rays are more effective on cells which have a
greater reproductive activity
HYPOXIA - radioresistant
The response of a tumour to radiotherapy is dependent
upon
 Inherent Radiosensitivity
 Tumour cell Repopulation
 Redistribution through the cell cycle (G2/M is the
most sensitive phase of the cell cycle, late-S phase is
the most radioresistant)
 Repair of radiation induced damage- atleast 6hrs to
complete.
 Reoxygenation of tumour tissues between fractions
i.e. Hypoxic cells re-oxygenate and become
radiosensitive.
FACTORS INFLUENCING THE EFFECTIVENESS OF RT
FACTOR CHANGE IN LOCAL CONTROL
CONCURRENT CHEMOTHERAPY
OR BIOLOGICAL
AGENTS
10% INCREASE
70Gy rather than 66Gy 5% INCREASE
DELAYS IN STARTING
RADIOTHERAPY
15% DECREASE PER MONTH
TREATMENT INTERRUPTIONS 1.4% DECREASE PER EXTRA
DAY
ANEMIA 10-15% DECREASE
SMOKING 10-15% DECREASE
TYPES OF RADIOTHERAPY
 External Beam Radiotherapy or Teletherapy
 Brachytherapy or Sealed Source Radiotherapy
 Systemic Radioisotope therapy or Unsealed Source
Radiotherapy
EXTERNAL BEAM RADIOTHERAPY
 Radiation beam is directed from a machine placed
outside the patient to a treatment volume located
within.
SOURCE OF RADIATIONS
X-Ray Machines Particle accelerators
Gamma rays i) LINAC
(Cobalt 60) ii) Betatron
iii)Cyclotron
iv) Nuclear Reactors
v) Radionuclides
COBALT 60 MACHINE
 Gamma rays
 Beam is weak
 Cheap
Disadvantage : Decaying source causing reduced
output & requires change of source every 5-7 years
 Does not give ideal depth dose and require
complicated plans to deliver the effective tumor dose
Radiotherapy  indications and complications
LINAC MACHINE[ Linear accelerator]
 High, Medium , Low energy X-rays, Electrons
 Beam is much superior.
 Expensive
 No decaying source
 Good penetration
BRACHYTHERAPY
 Radioactive material is introduced directly to within
the tumor or tumor bearing area.
 Radium needles were first to be used.
 Iridium (Ir-192) wire is the source of choice for
modern head and neck brachytherapy.
 Brachytherapy can be temporary or permanent.
INDICATIONS OF BRACHYTHERAPY
 Site oral cavity , base of tongue
 Localized disease
 Small (T1) lesion
 Accessible site
 Substantial local recurrence rate
 Lesions away from bone
 The temporary sources
are usually placed by a
technique called
Afterloading.
 In afterloading a hollow
tube or applicator is
placed surgically in the
organ to be treated, and
the sources are loaded
into the applicator after
the applicator is
implanted.
 This minimizes radiation exposure to health care
personnel.
 Advantage - high dose in small area
 Limitation - need for adequate radiation protection
and cant be done in cases where wider field
irradiation is required.
Doses in Brachytherapy
 Low dose rate = <2 Gy/hr ( used in oral, lip, tongue
CA )
 High dose rate = >12 Gy/hr
 Pulsed dose rate (uncommon) = 2-12 Gy/hr
SYSTEMIC RADIOISOTOPE THERAPY
 Systemic radioisotope therapy (RIT) is a
form of targeted therapy.
 The radioisotopes are delivered through
infusion (into the bloodstream) or ingestion.
 Examples : Infusion of meta-
iodobenzylguanidine (MIBG) to treat
neuroblastoma,
Oral iodine-131 to treat thyroid cancer or
thyrotoxicosis.
RADIOTHERAPY IN HEAD AND
NECK CANCER
More than 70% of oncological cases receive RT
Modalities of RT used in head and neck cases are 
 Definitive/Curative/Radical RT- Stage I-IV A
 Palliative RT  Stage IV B- IV C, unresectable /
metastatic disease with good general condition
 Neo-Adjuvant RT- adjuvant treatment given prior to
definitive treatment
 Concurrent treatment : Chemoradiation
PRE-RT ASSESSMENT
 Examination under anesthesia
 Tumor biopsy
 Imaging  CT/MRI of head and neck
 CXR/ CT thorax
 Full Blood count
 Urea and electrolytes
 LFT
 Dietician assessment
 Dental assessment
 Speech Therapist
CONTRA-INDICATIONS OF RT
 Cachexia
 Anemia
 Leukopenia
 Acute septic states
 Decompensated states of heart, liver, kidneys
 Active tuberculosis
 Extension of tumors to adjacent hollow organs
 Growth into great blood vessels.
 An inflammatory process
DOSIMETRY
 It is the measurement, calculation and assessment of
the ionizing radiation dose absorbed by the human
body.
 It can be internal or external dosimetry.
 Medical dosimetry is the calculation of absorbed
dose and optimization of dose delivery in radiation
therapy.
 Grays (Gy) is the S.I unit of absorbed dose
 Sieverts is the S.I unit of dose equivalence.
 1 Gy = 100 rads = 1J/kg
Dose required for disease control
 Subclinical disease : 45-50Gy
 Microscopic disease : 60-65Gy
 Gross disease : 65-80Gy
Selection total radiation dose in head and neck cancer
depends on
 Primary tumor
 Neck node size
 Fractionation
 Clinical circumstances
 Concurrent systemic therapy used or not
To ensure accurate radiation
therapy, the following
measures are taken
 Positioning and immobilization
of patient ( moulded
thermoplastic shield, custom
made cabulite)
Target definition and delineation by imaging
(Gross tumor volume(GTV) , Clinical target
volume(CTV), Planning target volume(PTV)
 Coverage of Organ at risk
 Field arrangement ( Lateral parallel opposed
fields and a wedged pair field are the most
common used)
 Beam Modification ( wedges and shielding )
RADIOTHERAPY FRACTIONATION
CONVENTIONAL FRACTIONATION
 1.8-2Gy/day for 5 days/week.
 Curative doses  66-70Gy in 33-35
 Fractions over 6.5-7weeks
HYPERFRACTIONATION
 <1.8Gy/day
 Increases time
 Reduces risk for late damage
 Reduce effectiveness
HYPOFRACTIONATION
 > 2Gy/day
 Shorter duration
 Limits tumor repopulation
 Increases risk for late damage
ACCELERATED FRACTIONATION
 Treatment time reduced
 Hyperfractionation treating two-three times each day
 Time between fractions should be minimum 6 hours
 Reduced risk of normal tissue damage
CHART( Continuous hyperfractionated accelerated
radiotherapy)
 1.5Gy three times/daily for 12 days = 54 Gy ( total
dose)
 No weekend break
DEFINITIVE /CURATIVE
RADIOTHERAPY
Dose of curative radiotherapy by EBRT is dependent on
the sites
 The maximum dose limits are 70 Gy (2Gy/day) for the
following sites 
 Lip, oral cavity, oropharynx, hypopharynx, glottic
larynx, supraglottic larynx, occult primary, salivary
gland tumors
 Cancer pharynx with high subclinical risk should be
given 2.12Gy/day radiations for total dose of 69.96
Gy for 6-7 weeks ( Mon-Fri ).
 3D-Conformal RT and sequential planned IMRT 44-
50 Gy.
 For IMRT, some suggest 54-63 Gy.
PALLIATIVE RADIOTHERAPY
 Palliative RT considered in advanced cancer when
curative intent is not appropriate.
 Basic principle of palliative RT is to avoid any
regimen that causes severe toxicities.
 Hypofractionated regimen should be preferred in end
stage diseases.
Recommended RT regimens
 50 Gy in 20 fractions
 37.5 Gy in 5 fractions
 30 Gy in 10 fractions
 44.4 Gy in 12 fractions, in 3 cycles
POST-OPERATIVE RT
Post-operative RT is recommended based on 
 T-stage  T3/T4 disease
 Close or positive margins of excision
 Depth of invasion
 Multiple positive nodes ( without extracapsular nodal
spread)
 Perineural/lymphatic/vascular invasion.
Higher doses of post-operative RT alone (60-66 Gy) or
with systemic therapy are recommended for the high-
risk features of extracapsular disease and/ or positive
margins.
 The preferred interval is 6 weeks or less, between
resection and commencement of postoperative RT
FOLLOW-UPAFTER RT
 Assessment of thyroid function (i.e. TSH test ever 6-
12 months)
 Clinical assessment at 4-8 weeks or CT-evaluation
with or without contrast at 8 weeks after completion
of RT alone or chemoradiation.
 Follow up 3-6 monthly
REIRRADIATION
 Repeating course of RT carries greater risk of damage
to normal tissue.
 Reirradiation has to be weighed against other
treatment options and against the risk and
consequences of normal tissue damage.
General rule-
 Minimize dose to critical normal tissues esp. spinal
cord and optic tracts. ( IMRT, IGRT etc )
 6 months gap between previous RT and reirradiation.
Addition of chemotherapy increases the effectiveness
of reirradiation without increasing late morbidity.
Field cancerization  biological process in which
large areas of cells at a tissue surface or within
an organ affected by carcinogenic alterations.
Commonly seen in head and neck carcinoma ,
oral carcinoma , lung carcinoma
ORAL CAVITY
Buccal mucosa , floor of mouth , retromolar trigone
皰 T1 and small T2 tumours- Radical implantation
皰 Larger lesions- EBRT and implantation
皰 In case of bone invasion  surgery followed by EBRT
皰 In case of retromolar trigone  surgery followed by
postoperative EBRT or EBRT alone
LIP
T1, T2  surgery (wide excision)
RT (radical radiotherapy/ brachytherapy)
T3, T4  surgery + postoperative radiotherapy
N0  observe or Supraomohyoid neck dissection
N+ - Modified neck dissection
Tongue
皰 SmallLarger T2 and T3 lesion  EBRT followed by
interstitial implantation
皰 Early tumors with mobile lymph nodes  Surgery/
interstitial implant for primary and neck dissection
for lymph nodes
皰 superficial tumors - Surgery
皰 T1 and small T2 tumors- Interstitial implants
Brachytherapy
 Tumour < 1 cm: Hairpin technique
 Tumour upto 2 cm: Plastic loop technique
DOSE IN ORAL CAVITY
Brachytherapy
 Radical treatment-65-70 Gy to the 85% reference iso
doseusing Paris system
 Boost treatment:25-30 Gy to the 85% reference iso
doseusing Paris system
EBRT
 Radical treatment:66-70 Gy in 33-35 fractions over
6.5-7 weeks
 Preimplantation:40-50 Gy in 20-25 fractions given 4-
5 weeks
OROPHARYNX
 Early T1-T2 tumours: Radiotherapy alone
 T3-T4 tumours:Concomitant chemotherapy +
Radiotherapy
 T1-T2,N2-N3:Concomitant chemotherapy +
Radiotherapy followed by neck salvage if residual
nodes are present
 In node negative patients- Elective neck irradiation is
done
 Mobile unilateral nodes: block dissection followed by
radiotherapy
 Fixed bilateral nodes:Radical radiotherapy if residual
nodes- Surgery
Dose for Oropharynx:
 66 Gy in 33 fractions over 6.5 weeks for T1-T2
nonbulky
 70 Gy in 35 fraction over 7 weeks for T2(bulky)-T4
LARYNX
 Choice of treatment depends upon
 Voice preservation
 Local control rate
 Fitness for surgery
 Reliability of follow up
Supraglottic tumours
 T1-T2- radiotherapy or partial laryngectomy
 T3-T4-laryngectomy and post op radiotherapy
 N0 disease  target volume includes primary tumor,
upper deep cervical and midjugular lymphnodes.
Glottic tumour
 T1 and T2  radical radiotherapy; 5yr survival rate
being 80-95%
 T3  radiotherapy and surgery; 5 yr survival rate
being 50%
Target volume
 T1 T2  5x5 field size , center lies below the
promontory of thyroid cartilage
 If T2 disease with supraglottic or subglottic
extension; volume larger to include the extension and
margins
 T3 and T4  radiotherapy n postoperative setting and
target volume is to cover the potential sites of
recurrence.
Subglottic tumour
 T1 and T2- radiotherapy or partial laryngectomy
 T3 and T4  laryngectomy and postoperative
radiotherapy
 Target volume  primay tumour , pre and paratracheal
lymph nodes, lower jugular lymph nodes and superior
mediastinum
 Dose  66Gy in 33 fractions over 6.5 weeks
 In postoperative , 58-60Gy is required
Hypopharynx
 Pyriform fossa  radiotherapy in postoperative to
reduce the local recurrence
 Postcricoid tumors without lymphadenopathy or with
mobile lymph node  laryngopharyngectomy .
Radical RT is given in palliative settings for advanced
cases
Posterior pharyngeal wall tumors  radical radiotherapy
is treatment o choice
Ear
 Given in postoperative settings
 Palliative settings
 Inoperable cases
Assessment of disease
Clinical examination- parotid region, ear, facial nerve ,
mastoid region, regional lymphatics
Otoscopy
Ct scan
Indications for radiotherapy in Glomus
tumor
 Larger tumors
 Inoperable sites: glomus jugulare , glomus
tympanicum
 Extensive bone destruction
 Intracranial involvement
 Jugular foramen syndrome
Dose : 45-55 Gy in 5 weeks
Nasal cavity and Ethmoid sinuses
 Limited disease : target volume  includes medial
maxillary sinus , ethmoid sinus , medial portion of
orbit , nasopharynx , sphenoid sinus and base of skull
Nasopharynx
 For all stages  radiotherapy is treatment of choice
and intent is radical
 Bilateral neck irradiation  mandatory even it is
unilateral involvement
 T3 , T4 with any N status- concurrent chemotherapy
and radiotherapy
Dose
Patients without lymphadenopathy
Nasopharyngeal and neck fields  56Gy in 28 fractions
given in 5.5 weeks
Nasopharynx alone  10-14 Gy in 5-8 fractions in 1-1.5
weeks
Patients with lymphadenopathy
Large lateral fields 40Gy in 20 fractions over 4
weeks
Nasopharyngeal field 26 Gy in 13 fractions over
2.5 weeks
Neck field boost 26Gy in 13 fractions over 2.5
weeks
TREATMENT MORBIDITY OF RT IN
HEAD AND NECK CA
 ACUTE TOXICITY
 Dose-response relationship
 Starts from 3rd week onwards
TOXICITIES MANAGEMENT
Xerostomia ( damage to the plasma
membrane of
secretory granules both in Parotid &
Submandible gland)
Non alcoholic Anti-septic mouth wash,
narcotic analgesic, anti-fungals for oral
candidiasis, saliva
replacement gel
Ageusia ( Increased by Xerostomia )
Mucositis ( erythemapatchy
mucositisconfluent
mucositis)
Analgesics, Zinc supplementation,
Amifostine
Odynophagia/dysphagia AnalgesicNG tubePEG
Skin erythemaMoist desquamation Aqueous creamHydrocolloid
dressing
Lethargy Resolves itself in 6months
 CHRONIC TOXICITY
 Toxicity is based on dose and latency of
tissues at risk.
Late effect latency
Osteoradionecrosis
(mandible/ maxilla)
Mostly 1-3 yrs
Loss of teeth 1-5yrs
trismus 6-12 months
Larynx necrosis 6-18months
Cartilage necrosis 6-18 months
Spinal cord damage 6 months  5 yrs
Optic nerve damage 6months  5 yrs
OSTEORADIONECROSIS
 Inflammatory condition of bone(osteomyelitis) due to
high doses of radiation given for malignancy of head
and neck region.
 Mandible is particularly susceptible( microanatomy
and less vasculature)
 Dose above 50Gy cause irreversible damage
 Hallmark : Loss of mucosal covering and exposed
bone
 Pain +/-
 Swelling present and drainage extraorally
 Necrosis of bone- result of loss of vasularity from
periosteum and sequestra
Radiologically
Early changes : well defined area of bone resorption
Later changes : lytic or sclerotic or mixture
Management
 Administration of antibiotics , rinsing
 Use of narcotic analgesics, hydration , nutrition
 Ultrasound therapy
RADICAL METHOD
 Hyerbaric O2 therapy  reduces hypoxia and
increases healing
 Sequestrectomy , local debridement
NEWER TECHNIQUES OF RT
 3D conformal Radiotherapy
 Intensity Modulated Radiotherapy ( IMRT )
 Volumetric Modulated Arc Radiotherapy ( VMAT )
 TomoTherapy
 Image Guided Radiotherapy (IGRT)
 Proton Beam Therapy (PBT)
 Stereotactic Body Radiation Therapy (SBRT)
Advanced radiation technologies mostly offer the
advantage of sparing of important organs at risk and
tight conformal doses to cancer targets
INTENSITY MODULATED RADIOTHERAPY
 The intensity of radiation beam can
be modulated to decrease doses
to normal tissue without
compromising the doses to the
cancer targets
 Advanced form of 3D-conformal RT
 IMRT dose painting refers to the
medthod of assigning different
dose levels to different structures
within the same treatment
fraction resulting in different total
doses to different targets.
 Useful in oropharyngeal, paranasal
sinus and nasopharyngeal cancers
 Xerostomia decreased greatly
Volumetric modulated arc radiotherapy (VMAT)
 VMAT is a new type of IMRT
technique.
 The radiotherapy machine
rotates around the patient
during treatment. The
machine continuously
reshapes and changes the
intensity of the radiation
beam as it moves around the
body
IMAGE GUIDED RADIOTHERAPY
 Images of each beam are
obtained, stored and reviewed
electronically
 Used to confirm that set up is
within tolerance i.e. 3mm for
head and neck cancer and no
unacceptable deviation from the
original treatment plan.
IGRT involves both fitting the linear accelerator with
CT capability so that patient position may be
confirmed prior to treatment and programming the
linear accelerator to carry out any necessary shifts in
treatment position.
 Helical Tomotherapy is advanced technique of IGRT
PET- BASED RT PLANNING
 Potential to improve
accuracy of target
definition.
 PET images obtained
using hypoxia marker
offers possibility of
delivering a greater
does to hypoxic areas in
order to overcome their
relative radioresistance.
PROTON BEAM THERAPY
 Uses Proton particle as
radiation
 Highly Conformal RT
 Lower mean doses.
 Typically used in patients
with most challenging
disease for which other
RT options were not safe
or of any benefit.
PBT for treatment of sinonasal cancer is associated with
good locoregional control, freedom from distant
metastasis and acceptable toxicity.
 Serious toxicities encountered in trials but in less rate.
STEREOTACTIC BODY RADIATION THERAPY (SBRT)
 Advanced technique of
EBRT.
 Delivers large ablative doses
of radiation.
 Shorter treatment time,
promising local control rates
and acceptable toxicities.
 Less evidence for treatment
of Head and neck cancers.
 Beneficial for palliation or
older adults.
PRINCIPLE
 Uses 3D imaging to target high dose of radiation
 Minimal impact to the surrounding tissue
 Works by damaging the DNA of the targeted cells
 Delivery of radiation is accurate to within 1-2mm
Radiation is delivered only when the outer and inner
collimators are aligned.
USES
 Brain tumours  pituitary adenomas ,
craniopharyngiomas, meningiomas etc
 Vestibular schwannoma
 Glomus jugulare
 Arteriovenous malformations
 Trigeminal neuralgia
RADIOSURGERY/CYBERKNIFE THERAPY
 Radiosurgery is a form of
radiation therapy that uses
precisely targeted radiation
to destroy tumors.
 Radiosurgery is non-invasive
 there is no cutting
involved.
 The CyberKnife System is a
unique, robotic system
designed to deliver high-
precision radiosurgical and
SBRT procedures.
 Patient lies comfortably on a treatment table while the
machine's robotic arm moves around him/her, aiming
and firing targeted radiation beams from numerous
angles.
The cumulative dose of radiation kills tumor cells while
minimizing exposure to the surrounding healthy
tissue.
 Single high dose radiation fraction.
 Used in acoustic neuroma, skull base tumors.
THANK YOU

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Radiotherapy indications and complications

  • 2. DEFINITION The application of radiation for the purpose of therapeutic gain. Radiation is the process of emitting radiant energy in the form of waves or particle. Aim of Radiotherapy Delivering tumoricidal dose to a defined target volume Respecting the normal tissue tolerance Trying to achieve an optimum therapeutic ratio Improvement of quality of life
  • 3. MECHANISM OF RADIOTHERAPY Radiations act on biological cells by ionization which can be direct or indirect. Direct ionization(Electron, Heavy Ion radiations) photons hit matter produce secondary electrons damage DNA directly
  • 4. Indirect ionization( X-ray, Neutrons ) photons hit matter produce secondary electrons with water and oxygen free radicals damage DNA Indirect ionization is more common ( > 2/3rd ) Radiations also causes cell reproduction failure by inhibiting mitosis.
  • 5. BIOLOGICAL EFFECTS OF RADIATIONS Affects cell by breaking strands of DNA Single strand breaks - repairable than double strand breaks which are lethal. Sub-lethal damage refers to DNA damage that can be repaired if given the right cellular conditions and sufficient time. Sub-lethal damage is less efficient in tumor cells, hypoxia or low pH. DNA damage is repairable with low radiation dose and the relation is proportional. (Absorbable dose )
  • 6. TUMOR CELL KINETICS AND RESPONSE TO RT CELL PROLIFERATION AND LOSS radiosensitive in the G(2)-M phase, less sensitive in the G(1) phase least sensitive during the latter part of the S phase INTRINSIC RADIOSENSITIVITY Lesser the SF2 better the radiosensitivity/prognosis. X-rays are more effective on cells which have a greater reproductive activity HYPOXIA - radioresistant
  • 7. The response of a tumour to radiotherapy is dependent upon Inherent Radiosensitivity Tumour cell Repopulation Redistribution through the cell cycle (G2/M is the most sensitive phase of the cell cycle, late-S phase is the most radioresistant) Repair of radiation induced damage- atleast 6hrs to complete. Reoxygenation of tumour tissues between fractions i.e. Hypoxic cells re-oxygenate and become radiosensitive.
  • 8. FACTORS INFLUENCING THE EFFECTIVENESS OF RT FACTOR CHANGE IN LOCAL CONTROL CONCURRENT CHEMOTHERAPY OR BIOLOGICAL AGENTS 10% INCREASE 70Gy rather than 66Gy 5% INCREASE DELAYS IN STARTING RADIOTHERAPY 15% DECREASE PER MONTH TREATMENT INTERRUPTIONS 1.4% DECREASE PER EXTRA DAY ANEMIA 10-15% DECREASE SMOKING 10-15% DECREASE
  • 9. TYPES OF RADIOTHERAPY External Beam Radiotherapy or Teletherapy Brachytherapy or Sealed Source Radiotherapy Systemic Radioisotope therapy or Unsealed Source Radiotherapy
  • 10. EXTERNAL BEAM RADIOTHERAPY Radiation beam is directed from a machine placed outside the patient to a treatment volume located within. SOURCE OF RADIATIONS X-Ray Machines Particle accelerators Gamma rays i) LINAC (Cobalt 60) ii) Betatron iii)Cyclotron iv) Nuclear Reactors v) Radionuclides
  • 11. COBALT 60 MACHINE Gamma rays Beam is weak Cheap Disadvantage : Decaying source causing reduced output & requires change of source every 5-7 years Does not give ideal depth dose and require complicated plans to deliver the effective tumor dose
  • 13. LINAC MACHINE[ Linear accelerator] High, Medium , Low energy X-rays, Electrons Beam is much superior. Expensive No decaying source Good penetration
  • 14. BRACHYTHERAPY Radioactive material is introduced directly to within the tumor or tumor bearing area. Radium needles were first to be used. Iridium (Ir-192) wire is the source of choice for modern head and neck brachytherapy. Brachytherapy can be temporary or permanent.
  • 15. INDICATIONS OF BRACHYTHERAPY Site oral cavity , base of tongue Localized disease Small (T1) lesion Accessible site Substantial local recurrence rate Lesions away from bone
  • 16. The temporary sources are usually placed by a technique called Afterloading. In afterloading a hollow tube or applicator is placed surgically in the organ to be treated, and the sources are loaded into the applicator after the applicator is implanted.
  • 17. This minimizes radiation exposure to health care personnel. Advantage - high dose in small area Limitation - need for adequate radiation protection and cant be done in cases where wider field irradiation is required.
  • 18. Doses in Brachytherapy Low dose rate = <2 Gy/hr ( used in oral, lip, tongue CA ) High dose rate = >12 Gy/hr Pulsed dose rate (uncommon) = 2-12 Gy/hr
  • 19. SYSTEMIC RADIOISOTOPE THERAPY Systemic radioisotope therapy (RIT) is a form of targeted therapy. The radioisotopes are delivered through infusion (into the bloodstream) or ingestion. Examples : Infusion of meta- iodobenzylguanidine (MIBG) to treat neuroblastoma, Oral iodine-131 to treat thyroid cancer or thyrotoxicosis.
  • 20. RADIOTHERAPY IN HEAD AND NECK CANCER More than 70% of oncological cases receive RT Modalities of RT used in head and neck cases are Definitive/Curative/Radical RT- Stage I-IV A Palliative RT Stage IV B- IV C, unresectable / metastatic disease with good general condition Neo-Adjuvant RT- adjuvant treatment given prior to definitive treatment Concurrent treatment : Chemoradiation
  • 21. PRE-RT ASSESSMENT Examination under anesthesia Tumor biopsy Imaging CT/MRI of head and neck CXR/ CT thorax Full Blood count Urea and electrolytes LFT Dietician assessment Dental assessment Speech Therapist
  • 22. CONTRA-INDICATIONS OF RT Cachexia Anemia Leukopenia Acute septic states Decompensated states of heart, liver, kidneys Active tuberculosis Extension of tumors to adjacent hollow organs Growth into great blood vessels. An inflammatory process
  • 23. DOSIMETRY It is the measurement, calculation and assessment of the ionizing radiation dose absorbed by the human body. It can be internal or external dosimetry. Medical dosimetry is the calculation of absorbed dose and optimization of dose delivery in radiation therapy. Grays (Gy) is the S.I unit of absorbed dose Sieverts is the S.I unit of dose equivalence. 1 Gy = 100 rads = 1J/kg
  • 24. Dose required for disease control Subclinical disease : 45-50Gy Microscopic disease : 60-65Gy Gross disease : 65-80Gy
  • 25. Selection total radiation dose in head and neck cancer depends on Primary tumor Neck node size Fractionation Clinical circumstances Concurrent systemic therapy used or not
  • 26. To ensure accurate radiation therapy, the following measures are taken Positioning and immobilization of patient ( moulded thermoplastic shield, custom made cabulite)
  • 27. Target definition and delineation by imaging (Gross tumor volume(GTV) , Clinical target volume(CTV), Planning target volume(PTV) Coverage of Organ at risk Field arrangement ( Lateral parallel opposed fields and a wedged pair field are the most common used) Beam Modification ( wedges and shielding )
  • 28. RADIOTHERAPY FRACTIONATION CONVENTIONAL FRACTIONATION 1.8-2Gy/day for 5 days/week. Curative doses 66-70Gy in 33-35 Fractions over 6.5-7weeks HYPERFRACTIONATION <1.8Gy/day Increases time Reduces risk for late damage Reduce effectiveness
  • 29. HYPOFRACTIONATION > 2Gy/day Shorter duration Limits tumor repopulation Increases risk for late damage ACCELERATED FRACTIONATION Treatment time reduced Hyperfractionation treating two-three times each day Time between fractions should be minimum 6 hours Reduced risk of normal tissue damage
  • 30. CHART( Continuous hyperfractionated accelerated radiotherapy) 1.5Gy three times/daily for 12 days = 54 Gy ( total dose) No weekend break
  • 31. DEFINITIVE /CURATIVE RADIOTHERAPY Dose of curative radiotherapy by EBRT is dependent on the sites The maximum dose limits are 70 Gy (2Gy/day) for the following sites Lip, oral cavity, oropharynx, hypopharynx, glottic larynx, supraglottic larynx, occult primary, salivary gland tumors
  • 32. Cancer pharynx with high subclinical risk should be given 2.12Gy/day radiations for total dose of 69.96 Gy for 6-7 weeks ( Mon-Fri ). 3D-Conformal RT and sequential planned IMRT 44- 50 Gy. For IMRT, some suggest 54-63 Gy.
  • 33. PALLIATIVE RADIOTHERAPY Palliative RT considered in advanced cancer when curative intent is not appropriate. Basic principle of palliative RT is to avoid any regimen that causes severe toxicities. Hypofractionated regimen should be preferred in end stage diseases.
  • 34. Recommended RT regimens 50 Gy in 20 fractions 37.5 Gy in 5 fractions 30 Gy in 10 fractions 44.4 Gy in 12 fractions, in 3 cycles
  • 35. POST-OPERATIVE RT Post-operative RT is recommended based on T-stage T3/T4 disease Close or positive margins of excision Depth of invasion Multiple positive nodes ( without extracapsular nodal spread) Perineural/lymphatic/vascular invasion.
  • 36. Higher doses of post-operative RT alone (60-66 Gy) or with systemic therapy are recommended for the high- risk features of extracapsular disease and/ or positive margins. The preferred interval is 6 weeks or less, between resection and commencement of postoperative RT
  • 37. FOLLOW-UPAFTER RT Assessment of thyroid function (i.e. TSH test ever 6- 12 months) Clinical assessment at 4-8 weeks or CT-evaluation with or without contrast at 8 weeks after completion of RT alone or chemoradiation. Follow up 3-6 monthly
  • 38. REIRRADIATION Repeating course of RT carries greater risk of damage to normal tissue. Reirradiation has to be weighed against other treatment options and against the risk and consequences of normal tissue damage. General rule- Minimize dose to critical normal tissues esp. spinal cord and optic tracts. ( IMRT, IGRT etc ) 6 months gap between previous RT and reirradiation. Addition of chemotherapy increases the effectiveness of reirradiation without increasing late morbidity.
  • 39. Field cancerization biological process in which large areas of cells at a tissue surface or within an organ affected by carcinogenic alterations. Commonly seen in head and neck carcinoma , oral carcinoma , lung carcinoma
  • 40. ORAL CAVITY Buccal mucosa , floor of mouth , retromolar trigone 皰 T1 and small T2 tumours- Radical implantation 皰 Larger lesions- EBRT and implantation 皰 In case of bone invasion surgery followed by EBRT 皰 In case of retromolar trigone surgery followed by postoperative EBRT or EBRT alone
  • 41. LIP T1, T2 surgery (wide excision) RT (radical radiotherapy/ brachytherapy) T3, T4 surgery + postoperative radiotherapy N0 observe or Supraomohyoid neck dissection N+ - Modified neck dissection
  • 42. Tongue 皰 SmallLarger T2 and T3 lesion EBRT followed by interstitial implantation 皰 Early tumors with mobile lymph nodes Surgery/ interstitial implant for primary and neck dissection for lymph nodes 皰 superficial tumors - Surgery 皰 T1 and small T2 tumors- Interstitial implants
  • 43. Brachytherapy Tumour < 1 cm: Hairpin technique Tumour upto 2 cm: Plastic loop technique
  • 44. DOSE IN ORAL CAVITY Brachytherapy Radical treatment-65-70 Gy to the 85% reference iso doseusing Paris system Boost treatment:25-30 Gy to the 85% reference iso doseusing Paris system EBRT Radical treatment:66-70 Gy in 33-35 fractions over 6.5-7 weeks Preimplantation:40-50 Gy in 20-25 fractions given 4- 5 weeks
  • 45. OROPHARYNX Early T1-T2 tumours: Radiotherapy alone T3-T4 tumours:Concomitant chemotherapy + Radiotherapy T1-T2,N2-N3:Concomitant chemotherapy + Radiotherapy followed by neck salvage if residual nodes are present
  • 46. In node negative patients- Elective neck irradiation is done Mobile unilateral nodes: block dissection followed by radiotherapy Fixed bilateral nodes:Radical radiotherapy if residual nodes- Surgery
  • 47. Dose for Oropharynx: 66 Gy in 33 fractions over 6.5 weeks for T1-T2 nonbulky 70 Gy in 35 fraction over 7 weeks for T2(bulky)-T4
  • 48. LARYNX Choice of treatment depends upon Voice preservation Local control rate Fitness for surgery Reliability of follow up
  • 49. Supraglottic tumours T1-T2- radiotherapy or partial laryngectomy T3-T4-laryngectomy and post op radiotherapy N0 disease target volume includes primary tumor, upper deep cervical and midjugular lymphnodes.
  • 50. Glottic tumour T1 and T2 radical radiotherapy; 5yr survival rate being 80-95% T3 radiotherapy and surgery; 5 yr survival rate being 50% Target volume T1 T2 5x5 field size , center lies below the promontory of thyroid cartilage
  • 51. If T2 disease with supraglottic or subglottic extension; volume larger to include the extension and margins T3 and T4 radiotherapy n postoperative setting and target volume is to cover the potential sites of recurrence.
  • 52. Subglottic tumour T1 and T2- radiotherapy or partial laryngectomy T3 and T4 laryngectomy and postoperative radiotherapy Target volume primay tumour , pre and paratracheal lymph nodes, lower jugular lymph nodes and superior mediastinum Dose 66Gy in 33 fractions over 6.5 weeks In postoperative , 58-60Gy is required
  • 53. Hypopharynx Pyriform fossa radiotherapy in postoperative to reduce the local recurrence Postcricoid tumors without lymphadenopathy or with mobile lymph node laryngopharyngectomy . Radical RT is given in palliative settings for advanced cases Posterior pharyngeal wall tumors radical radiotherapy is treatment o choice
  • 54. Ear Given in postoperative settings Palliative settings Inoperable cases Assessment of disease Clinical examination- parotid region, ear, facial nerve , mastoid region, regional lymphatics Otoscopy Ct scan
  • 55. Indications for radiotherapy in Glomus tumor Larger tumors Inoperable sites: glomus jugulare , glomus tympanicum Extensive bone destruction Intracranial involvement Jugular foramen syndrome Dose : 45-55 Gy in 5 weeks
  • 56. Nasal cavity and Ethmoid sinuses Limited disease : target volume includes medial maxillary sinus , ethmoid sinus , medial portion of orbit , nasopharynx , sphenoid sinus and base of skull
  • 57. Nasopharynx For all stages radiotherapy is treatment of choice and intent is radical Bilateral neck irradiation mandatory even it is unilateral involvement T3 , T4 with any N status- concurrent chemotherapy and radiotherapy
  • 58. Dose Patients without lymphadenopathy Nasopharyngeal and neck fields 56Gy in 28 fractions given in 5.5 weeks Nasopharynx alone 10-14 Gy in 5-8 fractions in 1-1.5 weeks
  • 59. Patients with lymphadenopathy Large lateral fields 40Gy in 20 fractions over 4 weeks Nasopharyngeal field 26 Gy in 13 fractions over 2.5 weeks Neck field boost 26Gy in 13 fractions over 2.5 weeks
  • 60. TREATMENT MORBIDITY OF RT IN HEAD AND NECK CA ACUTE TOXICITY Dose-response relationship Starts from 3rd week onwards
  • 61. TOXICITIES MANAGEMENT Xerostomia ( damage to the plasma membrane of secretory granules both in Parotid & Submandible gland) Non alcoholic Anti-septic mouth wash, narcotic analgesic, anti-fungals for oral candidiasis, saliva replacement gel Ageusia ( Increased by Xerostomia ) Mucositis ( erythemapatchy mucositisconfluent mucositis) Analgesics, Zinc supplementation, Amifostine Odynophagia/dysphagia AnalgesicNG tubePEG Skin erythemaMoist desquamation Aqueous creamHydrocolloid dressing Lethargy Resolves itself in 6months
  • 62. CHRONIC TOXICITY Toxicity is based on dose and latency of tissues at risk.
  • 63. Late effect latency Osteoradionecrosis (mandible/ maxilla) Mostly 1-3 yrs Loss of teeth 1-5yrs trismus 6-12 months Larynx necrosis 6-18months Cartilage necrosis 6-18 months Spinal cord damage 6 months 5 yrs Optic nerve damage 6months 5 yrs
  • 64. OSTEORADIONECROSIS Inflammatory condition of bone(osteomyelitis) due to high doses of radiation given for malignancy of head and neck region. Mandible is particularly susceptible( microanatomy and less vasculature) Dose above 50Gy cause irreversible damage Hallmark : Loss of mucosal covering and exposed bone
  • 65. Pain +/- Swelling present and drainage extraorally Necrosis of bone- result of loss of vasularity from periosteum and sequestra Radiologically Early changes : well defined area of bone resorption Later changes : lytic or sclerotic or mixture
  • 66. Management Administration of antibiotics , rinsing Use of narcotic analgesics, hydration , nutrition Ultrasound therapy RADICAL METHOD Hyerbaric O2 therapy reduces hypoxia and increases healing Sequestrectomy , local debridement
  • 67. NEWER TECHNIQUES OF RT 3D conformal Radiotherapy Intensity Modulated Radiotherapy ( IMRT ) Volumetric Modulated Arc Radiotherapy ( VMAT ) TomoTherapy Image Guided Radiotherapy (IGRT) Proton Beam Therapy (PBT) Stereotactic Body Radiation Therapy (SBRT) Advanced radiation technologies mostly offer the advantage of sparing of important organs at risk and tight conformal doses to cancer targets
  • 68. INTENSITY MODULATED RADIOTHERAPY The intensity of radiation beam can be modulated to decrease doses to normal tissue without compromising the doses to the cancer targets Advanced form of 3D-conformal RT IMRT dose painting refers to the medthod of assigning different dose levels to different structures within the same treatment fraction resulting in different total doses to different targets. Useful in oropharyngeal, paranasal sinus and nasopharyngeal cancers Xerostomia decreased greatly
  • 69. Volumetric modulated arc radiotherapy (VMAT) VMAT is a new type of IMRT technique. The radiotherapy machine rotates around the patient during treatment. The machine continuously reshapes and changes the intensity of the radiation beam as it moves around the body
  • 70. IMAGE GUIDED RADIOTHERAPY Images of each beam are obtained, stored and reviewed electronically Used to confirm that set up is within tolerance i.e. 3mm for head and neck cancer and no unacceptable deviation from the original treatment plan.
  • 71. IGRT involves both fitting the linear accelerator with CT capability so that patient position may be confirmed prior to treatment and programming the linear accelerator to carry out any necessary shifts in treatment position. Helical Tomotherapy is advanced technique of IGRT
  • 72. PET- BASED RT PLANNING Potential to improve accuracy of target definition. PET images obtained using hypoxia marker offers possibility of delivering a greater does to hypoxic areas in order to overcome their relative radioresistance.
  • 73. PROTON BEAM THERAPY Uses Proton particle as radiation Highly Conformal RT Lower mean doses. Typically used in patients with most challenging disease for which other RT options were not safe or of any benefit.
  • 74. PBT for treatment of sinonasal cancer is associated with good locoregional control, freedom from distant metastasis and acceptable toxicity. Serious toxicities encountered in trials but in less rate.
  • 75. STEREOTACTIC BODY RADIATION THERAPY (SBRT) Advanced technique of EBRT. Delivers large ablative doses of radiation. Shorter treatment time, promising local control rates and acceptable toxicities. Less evidence for treatment of Head and neck cancers. Beneficial for palliation or older adults.
  • 76. PRINCIPLE Uses 3D imaging to target high dose of radiation Minimal impact to the surrounding tissue Works by damaging the DNA of the targeted cells Delivery of radiation is accurate to within 1-2mm Radiation is delivered only when the outer and inner collimators are aligned.
  • 77. USES Brain tumours pituitary adenomas , craniopharyngiomas, meningiomas etc Vestibular schwannoma Glomus jugulare Arteriovenous malformations Trigeminal neuralgia
  • 78. RADIOSURGERY/CYBERKNIFE THERAPY Radiosurgery is a form of radiation therapy that uses precisely targeted radiation to destroy tumors. Radiosurgery is non-invasive there is no cutting involved. The CyberKnife System is a unique, robotic system designed to deliver high- precision radiosurgical and SBRT procedures.
  • 79. Patient lies comfortably on a treatment table while the machine's robotic arm moves around him/her, aiming and firing targeted radiation beams from numerous angles. The cumulative dose of radiation kills tumor cells while minimizing exposure to the surrounding healthy tissue. Single high dose radiation fraction. Used in acoustic neuroma, skull base tumors.