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The International Federation
          of Head and Neck Oncologic Societies
Current Concepts in Head and Neck Surgery and Oncology 2012




Side Effects of Radiotherapy
   To the Head and Neck


                    Dan Fliss
Acute vs. Late Effects
       •  Acute (early) RT toxicity:
         –  during or within a few weeks after
           completion of treatment
         –  tissues with high cell turnover rate
           (mucosal membranes, skin)
         –  usually transient
         –  tissues with high α/β ratio
         –  dose per fraction not very
2012

           important
Acute vs. Late Effects

       •  Late RT toxicity:
         –  months to years after therapy

         –  tissues with slow cell turnover rate
           (low α/β ratio)

         –  usually persistent and progressive

         –  fraction size matters
2012
             (BED)
Late Oropahryngeal Side Effects:

       •  Persistent Xerostomia
       •  Burning and Pain
       •  Mucositis
       •  Dysphagia
       •  Osteoradionecrosis
       •  Rampant caries/ dental disease
2012

                               Head and Neck Cancer: Multimodality Management
                                                            By Jacques Bernier
Consequential Late Effects

        •  Severe early toxicity may be causally
          related to subsequent late effects

        •  Both phases are manifestations of an
          ongoing sequence of events initiated
          immediately after injury

        •  Autocrine, paracrine and endocrine
          messages resulting in dysregulation of
2012


          the tissue environment
Consequential Late Effects




2012
Defining Late Toxicity - Difficulties

       •  Late effects are underscored and
        underreported
       •  Selection of clinically relevant
        outcomes
       •  Uniform grading of late effects
       •  Multi-modality therapy
2012   •  Tumor and host factors may interact
        with therapy
Grading Systems

•  The US NCI Common Terminology
 Criteria for Adverse Events

•  SOMA scale (Subjective, Objective,
 Management, Analytic procedures)


 2012
Mucositis




2012
Mucositis
       •  Dose-limiting toxicity of H&N RT

       •  Severe pain, dysphagia, weight loss

       •  Psychological distress, isolation,
        depression

       •  The most common cause of treatment
        interruptions à possible negative
2012


        impact on treatment efficacy
Mucositis
       •  Concurrent CRT is associated with
        increased rates and more severe
        grades of mucositis compared with
        radiotherapy alone

       •  The mucositis also occurs earlier

2012
        during treatment and lasts longer
Mucositis

       •  ~2/3 of patients have severe
        mucositis during concurrent
        CRT

       •  ~1/3 of patients in earlier trials
        were unable to complete their

2012
        planned treatment d/t toxicity
Mucositis

       •  Usually begins ~2 weeks
        after starting RT

       •  Symptoms continue for
        4-5 weeks after
        completion of therapy

2012
WHO s Oral Toxicity Scale
             World Health Organization s Oral Toxicity
                              Scale
                                            Severe Mucositis


        Grade 1        Grade 2        Grade 3          Grade 4
                                     Ulcers with
                      Erythema,                      Mucositis
                                     extensive
                                                     to the extent
                      ulcers;        erythema;
       Soreness                                      that
                      patient can    patient
       ± erythema                    cannot
                                                     alimentation
                      swallow                        is not
                      solid food     swallow
                                                     possible
                                     food




2012
Mucositis
       •  Wide variation in the methods of
         capturing, grading and reporting (NCI-
         CTC, WHO criteria, RTOG scale)
       •  The reported rates of mucositis vary
         considerably among studies (25% to
         higher than 80%)
       •  Physician-reported vs. patient-reported
         symptoms
2012
Mucositis – Risk factors
       •  Patient-related:
         –  Poor nutritional status
         –  Poor dental condition, poorly fitting dentures or
           oral appliances
         •  Pre-treatment dental evaluation and treatment is
         beneficial in reducing severity of mucositis and
         ORN
         –  Habits (Alcohol, smoking, tobacco chewing)

2012
         –  Reduced/impaired salivary function
         –  Previous cancer treatment
Mucositis – Risk factors

       •  Treatment related:
         –  Concurrent chemotherapy, agent (5-FU,
          MTX) and dose

         –  Radiation dose, fractionation, treatment
          site

         –  More sensitive: lips, pharyngeal wall, soft
2012      palate, tonsillar pillars, buccal mucosa,
          lateral tongue, floor of mouth
The 5-stage Model of Mucositis




                            Blijlevens N , Sonis S Ann Oncol
                                   2006;18:817-826

                           © 2006 European Society for Medical
                            Oncology




2012
Mucositis – Prevention and Treatment


       •  No evidence-based guidelines!!!
       •  Self-care regimens for oral hygiene

       •  Avoidance of :
          –  Chemical irritants (tobacco, alcohol, spicy food, citrus fruits
            and juices)

          –  Physical irritants (extremes of hot and cold foods, hard or

            coarse foods)

       •  Dietary changes as needed (pureed or liquid diet)
2012
Mucositis – Treatment

•  Pain medications

•  Antibacterial or antifungal treatment
       as needed
       –  Candida Albicans is the most common
        infection in pts receiving H&N RT à

2012
Salivary Hypofunction
                 Xerostomia
•  Proportional to the surface of salivary
  glands receiving > 3000- 3500 Gy
•  Effect is not reversible
•  Low salivary output, viscous, sticky
  saliva



  2012
Dose-Volume Data

                          Complication
                           probability
                          curves as a
                      function of the
                          mean parotid
                              dose



2012
Salivary Hypofunction
               Xerostomia
       •  Dryness typically not relieved
        by sipping water
       •  Impaired speech
       •  Burning
       •  Pain

2012
       •  Difficulty in chewing and swallowing
Salivary Hypofunction
               Xerostomia

       •  Taste disturbances
        aggravated by lack of
        normal salivary function

       •  Chapped lips

       •  Major effect on nutrition,
        social function, QOL
2012
Salivary Hypofunction
               Xerostomia

•  In the long term major effects on
 dental health

•  Normal protective effects of saliva
 are not available

•  Caries, periodontal inflammation

•  Lifelong increased risk for ORN!!
 2012
IMRT

       •  Reduced dose to the noninvolved
        oral cavity

       •  Reduced and limited extent of acute
        mucositis

       •  Sparing of minor salivary glands
2012    may further improve xerostomia
Xerostomia
       •  Common late toxicity with a huge impact on QoL
       •  Leads to multiple problems:
         –  Difficulty speaking

         –  Difficulty chewing and swallowing
         –  Halitosis

         –  Altered taste
         –  Complaint of burning mouth, lips, or tongue

         –  Dental problems, a propensity to oral infections
2012
         –  Sleep disturbances
Sparing of the parotid glands only
             may not be sufficient!

2012
Limited Success in Relieving
               Xerostomia




2012
RT Skin Effects
       •  RT-induced damage to the basal layer of
         the epidermis; cells shed more rapidly

       •  Inflammatory response à edema and
         erythema

       •  Melanin rises to the surface à
         characteristic hyperpigmentation of

2012
         irradiated skin
RT Skin Effects
       •  Begins 2-3 weeks after starting
         RT, continues for 3-4 weeks after
         completion of therapy

       •  The effect is cumulative

       •  Mild erythema
         àhyperpigmentation à

         dry desquamation (dryness,
2012
         pruritus) à moist desquamation
2012
RT Skin Effects – Risk Factors

       •  Patient-related:
         –  Poor nutritional status

         –  Fair complexion?

         –  Diabetes

         –  Connective tissue disease

         –  Burned skin, skin donor site etc.
2012
RT Skin Effects – Risk Factors
       •  Treatment-related:
         –  Large field, electron-beam therapy,
           tangential fields
         –  Post-op RT
         –  Concurrent chemotherapy
         –  Thin epidermis (face, neck)
         –  Bony prominences
         –  Susceptible sites: skin folds, lips, ear
2012
           lobes, incision lines or wounds,
           peristomal skin
RT Skin Effects - Treatment
       •  No evidence-based guidelines
         –  General skin care (cleaning,
          moisturizing)
         –  Avoidance of sun exposure
         –  Steroid cream +/- antibacterial
          ointments
         –  Silvadene ointment
2012

         –  Pain killers
Late Skin Effects

       •  Thinning

       •  Telangiectasia

       •  Hair loss in the treated area

       •  Loss of sweat and sebaceous
        glandular function
2012
       •  Hyper/hypopigmentation
H&N RT: Late Effects
       •  Xerostomia
       •  Swallowing dysfunction
       •  Vocal dysfunction
       •  Laryngeal edema à necrosis
       •  Osteoradionecrosis (ORN)
       •  Hearing impairment
2012


       •  Visual complications
Other Oral-Oropharyngeal Side-Effects
        •  Trismus: Limitations in mouth opening and
         jaw movements caused by fibrosis of
         irradiated muscles
          –  Pain
          –  Impaired chewing
          –  Impaired oral hygiene procedures
          –  Problems in dental treatment

        •  More severe in patients who also have
 2012    surgery involving mandible
Other Oral-Oropharyngeal Side-Effects

        •  Taste alterations

        •  Loss of taste, loss of appetite
          –  Transient but may become persistent

          –  Major effect on choice of food,
           malnutrition, weight loss

 2012
Dysphagia

       •  Field length greater than 82 mm at
         second phase of Rx

       •  Concurrent chemotherapy

       •  Site

       •  Increasing age

2012
       •  All increase risk for long term
         dysphagia
Survival Vs QOL

       •  EORTC QLQC-30, EORTC H&N 30
        peak complaints at 2-3 months from
        start of treatment
       •  Major problems:
         –  Nutrition
         –  Pain
2012
                                       Head and Neck Cancer:
         –  Psychiatric disorders   Multimodality Management
                                           By Jacques Bernier
Esophageal Pathology in Patients After Treatment
             for Head and Neck Cancer

        •  100 patients, Mean age 64 (± 10) years;
          75% were male.

        •  Mean time between the end of treatment and
          endoscopy 40 (± 51) months.

        •  81% of HNCA was advanced stage (3 or 4).

        •  Oropharynx (38%), larynx (33%), oral cavity
          (17%), unknown primary (10%),
          hypopharynx (1%), and nasopharynx (1%).
 2012



                            Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
Esophageal Pathology in Patients After Treatment
             for Head and Neck Cancer

        •  Treatment modalities included
          – Surgery alone (15%)

          – Surgery with radiation (34%)

          – Radiation alone (6%)

          – Chemoradiation alone (24%)

          – Chemoradiation with surgery
 2012


           (20%)      Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
Esophageal Pathology in Patients After Treatment
             for Head and Neck Cancer
        •  The findings on esophagoscopy included
          –  Peptic esophagitis (63%)
          –  Stricture (23%)
          –  Candidiasis (9%)
          –  Barrett metaplasia (8%)
          –  Gastritis (4%)
          –  Carcinoma (4%)
 2012     –  Only 13% had a normal esophagoscopy
                       Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
Esophageal Pathology in Patients After Treatment
             for Head and Neck Cancer


        •  Esophageal changes after treatment for HNCA are likely
          multifactorial and related to:
           –    Changes in bacterial flora

           –  Mucosal injury from chemoradiation therapy

           –  Fibrosis Xerostomia and its resultant change in pH

           –  Use of a PPI was not associated with the endoscopic
                diagnosis of esophagitis in this cohort (P > 0.05)It is
                unclear if the severity of the esophagitis would have

 2012
                been worse had they not been on the PPI

                                 Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
2012
2012
Dose-Volume Data

       •  Limited

       •  Minimizing dose to the
        pharyngeal constrictors and
        larynx to < 60 Gy when possible

       •  Other causes – fibrosis, vascular
2012    and nerve injury
2012
Severe acute mucositis is a surrogate risk index for long-
                   term dysphagia
 2012
Osteoradionecrosis

  •  Bone within the radiation
       field becomes devitalized
       and exposed through the
       overlying skin or mucosa,
       persisting as a non-
       healing wound for three
2012

       months or more
Evolution of the concept of ORN
       •  1983, Marx suggested etiopathology

       •  Endarteritis

       •  Tissue hypoxia

       •  Hypocellularity

       •  Hypo-vascularity

2012
       •  Tissue breakdown and chronic non-
        healing wounds
Evolution of the Concept of ORN

       •  Suppression of osteoclast
        related bone turnover is
        the initial event in
        development of ORN
2012


                     Ruggiero SL et al J Oral Maxillofac Surg 2004;62:527–34.
Evolution of the Concept of ORN

       •      Fibro-Atrophic Theory :
            –  fibroblast populations undergo total cellular
             depletion but also show a reduced ability to
             produce and secrete collagen; free radical
             formation, endothelial dysfunction,
             inflammation, microvascular thrombosis,
             fibrosis and remodeling, and finally bone and
2012
             tissue necrosis
                                  Delanian S, Lefaix JL. Radiother Oncol 2004;73:119–31
Epidemiology of ORN

       •  Most frequently noted in the first few years
            after completion of treatment (70–94%)
       •      Early onset ORN (<2 ) related to
            radiation doses > 70 Gy or surgical trauma
       •     Late onset ORN, is thought to arise from
            trauma in a chronically hypoxic tissue
            environment
2012
Mandibular Osteoradionecrosis in Squamous Cell
 Carcinoma of the Oral Cavity and Oropharynx:
          Incidence and Risk Factors


        •  73 patients treated for stage I - IV SCC of
         the oral cavity and oropharynx 2000 -
         2007

        •  Treatment modalities included both RT
         with curative intent and adjuvant RT
 2012
         following tumor surgery.
                                Monnier Y et al. Otolaryngol Head Neck Surg. 2011
Mandibular Osteoradionecrosis in Squamous Cell
 Carcinoma of the Oral Cavity and Oropharynx:
          Incidence and Risk Factors
        •  Results
          The incidence of mandibular ORN was 40%
          at 5 years.
        •  Conclusions:
          –  Mandibular ORN is a frequent long-term
            complication of RT for oral cavity and
            oropharynx cancers.
 2012     –  Mandibular surgery before irradiation is
            the only independent risk factor.
Factors Predictive of Severity of
        Osteoradionecrosis of the Mandible

       •  METHODS: Retrospective analysis,

       •  46 patients 2002 – 2009

       •  93% had mandibular ORN, staged 0-III (Store
         and Boysen).

       •  RESULTS: Advanced age, stage IV, RT dose,
         post-RT extractions, and lack of pre-RT dental
         extractions appeared predictive of severe
2012     mandibular ORN

                               Chopra S, et al. Head Neck. 2011 Epub ahead of print
Additional Risk Factors
       Drugs:

       •  Abuse of alcohol and tobacco is
         clearly identified as risk factor for
         ORN.

       •  89% of patients with ORN generally
         continue smoking.
2012


       B.R. Goldwaser, S.K. Chuang, L.B. Kaban and M. August, Risk factor assessment for the development
                                   of osteoradionecrosis, J Oral Maxillofac Surg 65 (11) (2007):2311–2316
Additional modalities
       •  COMPLETE RESTORATION OF REFRACTORY MANDIBULAR
         OSTEORADIONECROSIS BY PROLONGED TREATMENT
         WITH A PENTOXIFYLLINE-TOCOPHEROL-CLODRONATE
         COMBINATION (PENTOCLO): A PHASE II TRIAL

       •  Conclusion:

          •  Long-term PENTOCLO treatment is effective, safe, and
             curative for refractory ORN and induces mucosal and
             bone healing with significant symptom improvement.
2012




              DELANIAN S et al.Int. J. Radiation Oncology Biol. Phys., Vol. 80, No. 3, pp. 832–839, 2011
ORN After IMRT
       •  RTOG-0022 study reported an incidence
        of 6% ORN in oropharynx cancer patients
        treated at fraction size of 2.2–66 Gy
        without chemotherapy.




2012
ORN After IMRT
       •  The University of Michigan reported on 176
         patients treated with IMRT.

       •  At a median follow-up of 34 months, no cases of
         ORN developed (attribute to conformality of
         IMRT, meticulous dental hygiene as well as
         salivary gland sparing )

       •  Similarly Studer reported a 1.3% incidence of
2012
         ORN after parotid sparing IMRT
HBO in Treatment of ORN of
                 Jaws???

         A systematic review in 2008 did not show value of
             hyperbaric oxygen therapy for
             osteoradionecrosis




Pitak-Arnnop P et al: Management of osteoradionecrosis of the jaws: An analysis of evidence. Eur J Surg Oncol
                                                                                               34:1123, 2008
2012
                                                                  Pitak-Arnnop P et al. J Oral Maxillofac Surg.

                                                                                         2010;68(10):2644-5.
Radiotherapy Effects on Larynx

       •  Dysphonia and laryngeal edema are potential
         long-term complications of radiotherapy for HNCa
       •  The impact of dysphonia can result in severe
         distress and potential financial loss from sick
         leave
       •  Irradiation of the neck results in dryness of the
         submucosal laryngeal glands, abnormal vocal cord
         vibration, and in severe case laryngeal edema
2012
         with resulting chronic dysphonia
                      G. Sanguineti, et al. Int J Radiat Oncol Biol Phys, 68 (3) (2007), pp. 741–749
                                Nguyen et al. Oral Oncol. 2011 Sep;47(9):900-4. Epub 2011 Jul 2.
Radiotherapy Effects on Larynx
       •  Laryngeal edema severity correlates
        with the radiation dose delivered to the
        larynx
       •  Significant when mean dose > 43.5 Gy
       •  For laryngeal and hypopharyngeal
        cancers, high doses to the larynx are
        unavoidable frequently resulting in
        long-term vocal cord edema.
2012




                 G. Sanguineti, et al. Int J Radiat Oncol Biol Phys, 68 (3) (2007), pp. 741–749
Laryngeal sparing
effect of
TomoTherapy in a
patient with locally
advanced
nasopharyngeal
cancer: despite the
presence of a left
cervical node (yellow
circle) adjacent to
the larynx (red)
treated to 70 Gy,
and the area at risk
for extracapsular
extension (light
green) treated to
63 Gy, mean
laryngeal dose was
only 17.8 Gy.

   2012
Radiotherapy Effects on Larynx
       •  96 patients, median age was 55 years,
          82% men.
       •  Primary site of cancer was
         –  Oropharynx 43
         –  Hypopharynx/larynx 17
         –  Oral cavity 13
         –  Nasopharynx 11
         –  Maxillary sinus 2
         –  Unknown primary 10

2012

          Caglar HB et al. Dose to larynx predicts for swallowing complications after intensity-modulated
                                                                                             radiotherapy.
                                                 Int J Radiat Oncol Biol Phys. 2008 Nov 15;72(4):1110-8
Radiotherapy Effects on Larynx
       •  85% underwent definitive RT and
          15% postoperative RT.
       •  28 patients underwent induction
          chemotherapy followed by
          concurrent chemotherapy,
       •  59 received concurrent
          chemotherapy
       •  9 patients underwent RT alone.
       •  The median follow-up was 10
2012      months.
         Caglar HB et al. Dose to larynx predicts for swallowing complications after intensity-modulated
                                                                                            radiotherapy.
                                               Int J Radiat Oncol Biol Phys. 2008 Nov 15;72(4):1110-8.
Radiotherapy Effects on Larynx
       •  31 (32%) had clinically significant
         aspiration and 36 (37%) developed a
         stricture.
       •  the volume of the larynx receiving
         >or=50 Gy and volume of the inferior
         constrictor receiving >or=50 Gy were
         significantly associated with both
2012     aspiration and stricture.
         Caglar HB et al. Dose to larynx predicts for swallowing complications after intensity-modulated
                                                                                            radiotherapy.
                                               Int J Radiat Oncol Biol Phys. 2008 Nov 15;72(4):1110-8.
Quality of Life in Patients Treated for Advanced
     Hypopharyngeal or Laryngeal Cancer
       •  A retrospective 2-center study included 100 patients in
         remission from squamous cell carcinoma, treated
         between 1998 and 2009.
       •  70 (24 hypopharynx, 46 larynx) treated by total
         (pharyngo-) laryngectomy followed by external radiation
         therapy,
       •  30 (13 hypopharynx, 17 larynx) underwent an organ-
         conservation protocol with concurrent radiochemotherapy
         or with induction chemotherapy using platin-5FU or
         taxan-platin-5FU followed by radiation therapy.
       •  All patients responded to the quality of life questionnaires
2012     (EORTC QLQ-C30 and QLQ-H&N35).

                M. Guiberta et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Nov;128(5):218-23.
Quality of Life in Patients Treated for Advanced
     Hypopharyngeal or Laryngeal Cancer

       •  Advanced tumor stages IVa and IVb were
         significantly more frequent in the surgery groups
       •  In pharyngeal cancer, the only significant difference
         between surgical treatment and laryngeal
         conservation was for sensory disorder (taste and
         odor), with better results in case of laryngeal
         conservation (p < 0.0001).
       •  For the other items, there was a trend for quality of
         life to appear better in patients with laryngeal
2012     conservation (p = NS).

                M. Guiberta et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Nov;128(5):218-23.
Quality of Life in Patients Treated for Advanced
     Hypopharyngeal or Laryngeal Cancer

       •  In laryngeal cancer, the only significant
        difference was for dry mouth , which
        was significantly less invalidating with
        surgical treatment (p < 0.001).

       •  The impairment of the other quality of
        life items did not differ between
        surgical and conservative treatment.
2012




              M. Guiberta et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Nov;128(5):218-23.
Complications After Radiation
         Treatment Base of Skull
       •  Endocrinopathy
       •  Cranial neuropathy
       •  Visual deficits
       •  The exposure of the optic apparatus,
        pituitary stalk, and brainstem must
        be considered during planning to
2012
        minimize complications.
                            Hauptman et al. Int J Radiat Oncol Biol Phys. 2011 in press
Complications After Radiation
         Treatment Base of Skull
       •  If the optic apparatus is included in
          the 80% isodose line, it might be
          best to fractionate therapy
       •  Exposure of the pituitary stalk
          should be kept to <30 Gy to
          minimize endocrine dysfunction.
       •  Brainstem exposure should be
          limited to <60 Gy in fractions.
2012



                        Hauptman et al. Int J Radiat Oncol Biol Phys. 2011 in press
2012

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Complications from radiation therapy to the head and neck by D. Fliss

  • 1. The International Federation of Head and Neck Oncologic Societies Current Concepts in Head and Neck Surgery and Oncology 2012 Side Effects of Radiotherapy To the Head and Neck Dan Fliss
  • 2. Acute vs. Late Effects •  Acute (early) RT toxicity: –  during or within a few weeks after completion of treatment –  tissues with high cell turnover rate (mucosal membranes, skin) –  usually transient –  tissues with high α/β ratio –  dose per fraction not very 2012 important
  • 3. Acute vs. Late Effects •  Late RT toxicity: –  months to years after therapy –  tissues with slow cell turnover rate (low α/β ratio) –  usually persistent and progressive –  fraction size matters 2012 (BED)
  • 4. Late Oropahryngeal Side Effects: •  Persistent Xerostomia •  Burning and Pain •  Mucositis •  Dysphagia •  Osteoradionecrosis •  Rampant caries/ dental disease 2012 Head and Neck Cancer: Multimodality Management By Jacques Bernier
  • 5. Consequential Late Effects •  Severe early toxicity may be causally related to subsequent late effects •  Both phases are manifestations of an ongoing sequence of events initiated immediately after injury •  Autocrine, paracrine and endocrine messages resulting in dysregulation of 2012 the tissue environment
  • 7. Defining Late Toxicity - Difficulties •  Late effects are underscored and underreported •  Selection of clinically relevant outcomes •  Uniform grading of late effects •  Multi-modality therapy 2012 •  Tumor and host factors may interact with therapy
  • 8. Grading Systems •  The US NCI Common Terminology Criteria for Adverse Events •  SOMA scale (Subjective, Objective, Management, Analytic procedures) 2012
  • 10. Mucositis •  Dose-limiting toxicity of H&N RT •  Severe pain, dysphagia, weight loss •  Psychological distress, isolation, depression •  The most common cause of treatment interruptions à possible negative 2012 impact on treatment efficacy
  • 11. Mucositis •  Concurrent CRT is associated with increased rates and more severe grades of mucositis compared with radiotherapy alone •  The mucositis also occurs earlier 2012 during treatment and lasts longer
  • 12. Mucositis •  ~2/3 of patients have severe mucositis during concurrent CRT •  ~1/3 of patients in earlier trials were unable to complete their 2012 planned treatment d/t toxicity
  • 13. Mucositis •  Usually begins ~2 weeks after starting RT •  Symptoms continue for 4-5 weeks after completion of therapy 2012
  • 14. WHO s Oral Toxicity Scale World Health Organization s Oral Toxicity Scale Severe Mucositis Grade 1 Grade 2 Grade 3 Grade 4 Ulcers with Erythema, Mucositis extensive to the extent ulcers; erythema; Soreness that patient can patient ± erythema cannot alimentation swallow is not solid food swallow possible food 2012
  • 15. Mucositis •  Wide variation in the methods of capturing, grading and reporting (NCI- CTC, WHO criteria, RTOG scale) •  The reported rates of mucositis vary considerably among studies (25% to higher than 80%) •  Physician-reported vs. patient-reported symptoms 2012
  • 16. Mucositis – Risk factors •  Patient-related: –  Poor nutritional status –  Poor dental condition, poorly fitting dentures or oral appliances •  Pre-treatment dental evaluation and treatment is beneficial in reducing severity of mucositis and ORN –  Habits (Alcohol, smoking, tobacco chewing) 2012 –  Reduced/impaired salivary function –  Previous cancer treatment
  • 17. Mucositis – Risk factors •  Treatment related: –  Concurrent chemotherapy, agent (5-FU, MTX) and dose –  Radiation dose, fractionation, treatment site –  More sensitive: lips, pharyngeal wall, soft 2012 palate, tonsillar pillars, buccal mucosa, lateral tongue, floor of mouth
  • 18. The 5-stage Model of Mucositis Blijlevens N , Sonis S Ann Oncol 2006;18:817-826 © 2006 European Society for Medical Oncology 2012
  • 19. Mucositis – Prevention and Treatment •  No evidence-based guidelines!!! •  Self-care regimens for oral hygiene •  Avoidance of : –  Chemical irritants (tobacco, alcohol, spicy food, citrus fruits and juices) –  Physical irritants (extremes of hot and cold foods, hard or coarse foods) •  Dietary changes as needed (pureed or liquid diet) 2012
  • 20. Mucositis – Treatment •  Pain medications •  Antibacterial or antifungal treatment as needed –  Candida Albicans is the most common infection in pts receiving H&N RT à 2012
  • 21. Salivary Hypofunction Xerostomia •  Proportional to the surface of salivary glands receiving > 3000- 3500 Gy •  Effect is not reversible •  Low salivary output, viscous, sticky saliva 2012
  • 22. Dose-Volume Data Complication probability curves as a function of the mean parotid dose 2012
  • 23. Salivary Hypofunction Xerostomia •  Dryness typically not relieved by sipping water •  Impaired speech •  Burning •  Pain 2012 •  Difficulty in chewing and swallowing
  • 24. Salivary Hypofunction Xerostomia •  Taste disturbances aggravated by lack of normal salivary function •  Chapped lips •  Major effect on nutrition, social function, QOL 2012
  • 25. Salivary Hypofunction Xerostomia •  In the long term major effects on dental health •  Normal protective effects of saliva are not available •  Caries, periodontal inflammation •  Lifelong increased risk for ORN!! 2012
  • 26. IMRT •  Reduced dose to the noninvolved oral cavity •  Reduced and limited extent of acute mucositis •  Sparing of minor salivary glands 2012 may further improve xerostomia
  • 27. Xerostomia •  Common late toxicity with a huge impact on QoL •  Leads to multiple problems: –  Difficulty speaking –  Difficulty chewing and swallowing –  Halitosis –  Altered taste –  Complaint of burning mouth, lips, or tongue –  Dental problems, a propensity to oral infections 2012 –  Sleep disturbances
  • 28. Sparing of the parotid glands only may not be sufficient! 2012
  • 29. Limited Success in Relieving Xerostomia 2012
  • 30. RT Skin Effects •  RT-induced damage to the basal layer of the epidermis; cells shed more rapidly •  Inflammatory response à edema and erythema •  Melanin rises to the surface à characteristic hyperpigmentation of 2012 irradiated skin
  • 31. RT Skin Effects •  Begins 2-3 weeks after starting RT, continues for 3-4 weeks after completion of therapy •  The effect is cumulative •  Mild erythema àhyperpigmentation à dry desquamation (dryness, 2012 pruritus) à moist desquamation
  • 32. 2012
  • 33. RT Skin Effects – Risk Factors •  Patient-related: –  Poor nutritional status –  Fair complexion? –  Diabetes –  Connective tissue disease –  Burned skin, skin donor site etc. 2012
  • 34. RT Skin Effects – Risk Factors •  Treatment-related: –  Large field, electron-beam therapy, tangential fields –  Post-op RT –  Concurrent chemotherapy –  Thin epidermis (face, neck) –  Bony prominences –  Susceptible sites: skin folds, lips, ear 2012 lobes, incision lines or wounds, peristomal skin
  • 35. RT Skin Effects - Treatment •  No evidence-based guidelines –  General skin care (cleaning, moisturizing) –  Avoidance of sun exposure –  Steroid cream +/- antibacterial ointments –  Silvadene ointment 2012 –  Pain killers
  • 36. Late Skin Effects •  Thinning •  Telangiectasia •  Hair loss in the treated area •  Loss of sweat and sebaceous glandular function 2012 •  Hyper/hypopigmentation
  • 37. H&N RT: Late Effects •  Xerostomia •  Swallowing dysfunction •  Vocal dysfunction •  Laryngeal edema à necrosis •  Osteoradionecrosis (ORN) •  Hearing impairment 2012 •  Visual complications
  • 38. Other Oral-Oropharyngeal Side-Effects •  Trismus: Limitations in mouth opening and jaw movements caused by fibrosis of irradiated muscles –  Pain –  Impaired chewing –  Impaired oral hygiene procedures –  Problems in dental treatment •  More severe in patients who also have 2012 surgery involving mandible
  • 39. Other Oral-Oropharyngeal Side-Effects •  Taste alterations •  Loss of taste, loss of appetite –  Transient but may become persistent –  Major effect on choice of food, malnutrition, weight loss 2012
  • 40. Dysphagia •  Field length greater than 82 mm at second phase of Rx •  Concurrent chemotherapy •  Site •  Increasing age 2012 •  All increase risk for long term dysphagia
  • 41. Survival Vs QOL •  EORTC QLQC-30, EORTC H&N 30 peak complaints at 2-3 months from start of treatment •  Major problems: –  Nutrition –  Pain 2012 Head and Neck Cancer: –  Psychiatric disorders Multimodality Management By Jacques Bernier
  • 42. Esophageal Pathology in Patients After Treatment for Head and Neck Cancer •  100 patients, Mean age 64 (± 10) years; 75% were male. •  Mean time between the end of treatment and endoscopy 40 (± 51) months. •  81% of HNCA was advanced stage (3 or 4). •  Oropharynx (38%), larynx (33%), oral cavity (17%), unknown primary (10%), hypopharynx (1%), and nasopharynx (1%). 2012 Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
  • 43. Esophageal Pathology in Patients After Treatment for Head and Neck Cancer •  Treatment modalities included – Surgery alone (15%) – Surgery with radiation (34%) – Radiation alone (6%) – Chemoradiation alone (24%) – Chemoradiation with surgery 2012 (20%) Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
  • 44. Esophageal Pathology in Patients After Treatment for Head and Neck Cancer •  The findings on esophagoscopy included –  Peptic esophagitis (63%) –  Stricture (23%) –  Candidiasis (9%) –  Barrett metaplasia (8%) –  Gastritis (4%) –  Carcinoma (4%) 2012 –  Only 13% had a normal esophagoscopy Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
  • 45. Esophageal Pathology in Patients After Treatment for Head and Neck Cancer •  Esophageal changes after treatment for HNCA are likely multifactorial and related to: –  Changes in bacterial flora –  Mucosal injury from chemoradiation therapy –  Fibrosis Xerostomia and its resultant change in pH –  Use of a PPI was not associated with the endoscopic diagnosis of esophagitis in this cohort (P > 0.05)It is unclear if the severity of the esophagitis would have 2012 been worse had they not been on the PPI Farwell et al. Otolaryng Head Neck Surg 2010 Sep;143(3):375-8.
  • 46. 2012
  • 47. 2012
  • 48. Dose-Volume Data •  Limited •  Minimizing dose to the pharyngeal constrictors and larynx to < 60 Gy when possible •  Other causes – fibrosis, vascular 2012 and nerve injury
  • 49. 2012
  • 50. Severe acute mucositis is a surrogate risk index for long- term dysphagia 2012
  • 51. Osteoradionecrosis •  Bone within the radiation field becomes devitalized and exposed through the overlying skin or mucosa, persisting as a non- healing wound for three 2012 months or more
  • 52. Evolution of the concept of ORN •  1983, Marx suggested etiopathology •  Endarteritis •  Tissue hypoxia •  Hypocellularity •  Hypo-vascularity 2012 •  Tissue breakdown and chronic non- healing wounds
  • 53. Evolution of the Concept of ORN •  Suppression of osteoclast related bone turnover is the initial event in development of ORN 2012 Ruggiero SL et al J Oral Maxillofac Surg 2004;62:527–34.
  • 54. Evolution of the Concept of ORN •  Fibro-Atrophic Theory : –  fibroblast populations undergo total cellular depletion but also show a reduced ability to produce and secrete collagen; free radical formation, endothelial dysfunction, inflammation, microvascular thrombosis, fibrosis and remodeling, and finally bone and 2012 tissue necrosis Delanian S, Lefaix JL. Radiother Oncol 2004;73:119–31
  • 55. Epidemiology of ORN •  Most frequently noted in the first few years after completion of treatment (70–94%) •  Early onset ORN (<2 ) related to radiation doses > 70 Gy or surgical trauma •  Late onset ORN, is thought to arise from trauma in a chronically hypoxic tissue environment 2012
  • 56. Mandibular Osteoradionecrosis in Squamous Cell Carcinoma of the Oral Cavity and Oropharynx: Incidence and Risk Factors •  73 patients treated for stage I - IV SCC of the oral cavity and oropharynx 2000 - 2007 •  Treatment modalities included both RT with curative intent and adjuvant RT 2012 following tumor surgery. Monnier Y et al. Otolaryngol Head Neck Surg. 2011
  • 57. Mandibular Osteoradionecrosis in Squamous Cell Carcinoma of the Oral Cavity and Oropharynx: Incidence and Risk Factors •  Results The incidence of mandibular ORN was 40% at 5 years. •  Conclusions: –  Mandibular ORN is a frequent long-term complication of RT for oral cavity and oropharynx cancers. 2012 –  Mandibular surgery before irradiation is the only independent risk factor.
  • 58. Factors Predictive of Severity of Osteoradionecrosis of the Mandible •  METHODS: Retrospective analysis, •  46 patients 2002 – 2009 •  93% had mandibular ORN, staged 0-III (Store and Boysen). •  RESULTS: Advanced age, stage IV, RT dose, post-RT extractions, and lack of pre-RT dental extractions appeared predictive of severe 2012 mandibular ORN Chopra S, et al. Head Neck. 2011 Epub ahead of print
  • 59. Additional Risk Factors Drugs: •  Abuse of alcohol and tobacco is clearly identified as risk factor for ORN. •  89% of patients with ORN generally continue smoking. 2012 B.R. Goldwaser, S.K. Chuang, L.B. Kaban and M. August, Risk factor assessment for the development of osteoradionecrosis, J Oral Maxillofac Surg 65 (11) (2007):2311–2316
  • 60. Additional modalities •  COMPLETE RESTORATION OF REFRACTORY MANDIBULAR OSTEORADIONECROSIS BY PROLONGED TREATMENT WITH A PENTOXIFYLLINE-TOCOPHEROL-CLODRONATE COMBINATION (PENTOCLO): A PHASE II TRIAL •  Conclusion: •  Long-term PENTOCLO treatment is effective, safe, and curative for refractory ORN and induces mucosal and bone healing with significant symptom improvement. 2012 DELANIAN S et al.Int. J. Radiation Oncology Biol. Phys., Vol. 80, No. 3, pp. 832–839, 2011
  • 61. ORN After IMRT •  RTOG-0022 study reported an incidence of 6% ORN in oropharynx cancer patients treated at fraction size of 2.2–66 Gy without chemotherapy. 2012
  • 62. ORN After IMRT •  The University of Michigan reported on 176 patients treated with IMRT. •  At a median follow-up of 34 months, no cases of ORN developed (attribute to conformality of IMRT, meticulous dental hygiene as well as salivary gland sparing ) •  Similarly Studer reported a 1.3% incidence of 2012 ORN after parotid sparing IMRT
  • 63. HBO in Treatment of ORN of Jaws??? A systematic review in 2008 did not show value of hyperbaric oxygen therapy for osteoradionecrosis Pitak-Arnnop P et al: Management of osteoradionecrosis of the jaws: An analysis of evidence. Eur J Surg Oncol 34:1123, 2008 2012 Pitak-Arnnop P et al. J Oral Maxillofac Surg. 2010;68(10):2644-5.
  • 64. Radiotherapy Effects on Larynx •  Dysphonia and laryngeal edema are potential long-term complications of radiotherapy for HNCa •  The impact of dysphonia can result in severe distress and potential financial loss from sick leave •  Irradiation of the neck results in dryness of the submucosal laryngeal glands, abnormal vocal cord vibration, and in severe case laryngeal edema 2012 with resulting chronic dysphonia G. Sanguineti, et al. Int J Radiat Oncol Biol Phys, 68 (3) (2007), pp. 741–749 Nguyen et al. Oral Oncol. 2011 Sep;47(9):900-4. Epub 2011 Jul 2.
  • 65. Radiotherapy Effects on Larynx •  Laryngeal edema severity correlates with the radiation dose delivered to the larynx •  Significant when mean dose > 43.5 Gy •  For laryngeal and hypopharyngeal cancers, high doses to the larynx are unavoidable frequently resulting in long-term vocal cord edema. 2012 G. Sanguineti, et al. Int J Radiat Oncol Biol Phys, 68 (3) (2007), pp. 741–749
  • 66. Laryngeal sparing effect of TomoTherapy in a patient with locally advanced nasopharyngeal cancer: despite the presence of a left cervical node (yellow circle) adjacent to the larynx (red) treated to 70 Gy, and the area at risk for extracapsular extension (light green) treated to 63 Gy, mean laryngeal dose was only 17.8 Gy. 2012
  • 67. Radiotherapy Effects on Larynx •  96 patients, median age was 55 years, 82% men. •  Primary site of cancer was –  Oropharynx 43 –  Hypopharynx/larynx 17 –  Oral cavity 13 –  Nasopharynx 11 –  Maxillary sinus 2 –  Unknown primary 10 2012 Caglar HB et al. Dose to larynx predicts for swallowing complications after intensity-modulated radiotherapy. Int J Radiat Oncol Biol Phys. 2008 Nov 15;72(4):1110-8
  • 68. Radiotherapy Effects on Larynx •  85% underwent definitive RT and 15% postoperative RT. •  28 patients underwent induction chemotherapy followed by concurrent chemotherapy, •  59 received concurrent chemotherapy •  9 patients underwent RT alone. •  The median follow-up was 10 2012 months. Caglar HB et al. Dose to larynx predicts for swallowing complications after intensity-modulated radiotherapy. Int J Radiat Oncol Biol Phys. 2008 Nov 15;72(4):1110-8.
  • 69. Radiotherapy Effects on Larynx •  31 (32%) had clinically significant aspiration and 36 (37%) developed a stricture. •  the volume of the larynx receiving >or=50 Gy and volume of the inferior constrictor receiving >or=50 Gy were significantly associated with both 2012 aspiration and stricture. Caglar HB et al. Dose to larynx predicts for swallowing complications after intensity-modulated radiotherapy. Int J Radiat Oncol Biol Phys. 2008 Nov 15;72(4):1110-8.
  • 70. Quality of Life in Patients Treated for Advanced Hypopharyngeal or Laryngeal Cancer •  A retrospective 2-center study included 100 patients in remission from squamous cell carcinoma, treated between 1998 and 2009. •  70 (24 hypopharynx, 46 larynx) treated by total (pharyngo-) laryngectomy followed by external radiation therapy, •  30 (13 hypopharynx, 17 larynx) underwent an organ- conservation protocol with concurrent radiochemotherapy or with induction chemotherapy using platin-5FU or taxan-platin-5FU followed by radiation therapy. •  All patients responded to the quality of life questionnaires 2012 (EORTC QLQ-C30 and QLQ-H&N35). M. Guiberta et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Nov;128(5):218-23.
  • 71. Quality of Life in Patients Treated for Advanced Hypopharyngeal or Laryngeal Cancer •  Advanced tumor stages IVa and IVb were significantly more frequent in the surgery groups •  In pharyngeal cancer, the only significant difference between surgical treatment and laryngeal conservation was for sensory disorder (taste and odor), with better results in case of laryngeal conservation (p < 0.0001). •  For the other items, there was a trend for quality of life to appear better in patients with laryngeal 2012 conservation (p = NS). M. Guiberta et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Nov;128(5):218-23.
  • 72. Quality of Life in Patients Treated for Advanced Hypopharyngeal or Laryngeal Cancer •  In laryngeal cancer, the only significant difference was for dry mouth , which was significantly less invalidating with surgical treatment (p < 0.001). •  The impairment of the other quality of life items did not differ between surgical and conservative treatment. 2012 M. Guiberta et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2011 Nov;128(5):218-23.
  • 73. Complications After Radiation Treatment Base of Skull •  Endocrinopathy •  Cranial neuropathy •  Visual deficits •  The exposure of the optic apparatus, pituitary stalk, and brainstem must be considered during planning to 2012 minimize complications. Hauptman et al. Int J Radiat Oncol Biol Phys. 2011 in press
  • 74. Complications After Radiation Treatment Base of Skull •  If the optic apparatus is included in the 80% isodose line, it might be best to fractionate therapy •  Exposure of the pituitary stalk should be kept to <30 Gy to minimize endocrine dysfunction. •  Brainstem exposure should be limited to <60 Gy in fractions. 2012 Hauptman et al. Int J Radiat Oncol Biol Phys. 2011 in press
  • 75. 2012