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CANCER OF LARYNX
the larynx is consists of a cartilaginous skeleton with
  ligaments,which carries the muscles and mostly is covered
  by mucous membrane .
 skeleton of the larynx ;-
1)Thyroid cartilage ;- consist of tow lateral laminae which are
  fused in front (bow ship). At the tip of bow is a notch (Adam
  apple) . The superior and inferior horn arise from the
  posterior edge of each laminae
2) Caricoid cartilage ;-it is ship is like signet ring .it is lamina is
  2-2.5 cms lies posterior .the upper edage of the lamina has
  tow articular surface for the arytenoid cartilage .the lateral
  surface on each side has articular surface for the inferior
  horn of the thyriod cartilage .
Arytenoid cartilage ;-pair of cartilage sited on the
  upper edge of the lamina of the cricoid cartilage .it
  has the shap of triangular pyramid .
The vocal cord are two thickened uppper end of the
  conus attached posterior to the vocal process of
  both arytenoids cartilage and interiorly to the inner
  surface of the angle of the thyroid
  cartilagecricoarytenoid muscles .
Epiglottis ;-lies against the middle of the thyroid
  cartilage
Laryngeal ligaments ;-is a membrane composed of a
  dense elastic fiber net which lies below the mucous
  memberane of the larynx and has different
  sickness in different region (conus elasticus-vocal
  cord –median cricothyroid ligament l-quadrangular
  membrane –vestibular ligament …)
New case in 2009 is 12,290 with ca larynx .with men
   affected four time more than female .deaths from
   ca larynx is 3,660 . With modern care the deaths
   dropped from 2,97 per 100,000 to 2,24 per 100,000 .
Risk factors ;-
1) Age > 55 yrs .
2)Gender male to female ratio 4:1
3)Cigarette smoking (2-25X increase)
4) Alcohol consumption (2-6 increase ) the .
The combination of cigarette and alcohol ↑(40-100) .
5) Race African –American are more affected .
6) Past medical history of head and neck cancer
   ↑risk of ca larynx .
7) Genetic factors ;- e.g fanconia anemia and
   dyskeratosis congenita (condation→aplastic
   anemia ↑ risk of ca larynx .
8) Condition → ↓ immunity (AIDS –organ
   transplant ) .↑risk of ca larynx .
The majority of ca larynx which arise from the
  mucosal surface is squamous cell carcinoma .
The most are well to mode differentiated .


     Ca larynx sub site           percent

     supraglottic                  35%
     glottic                       65%
     subglottic                     1%
spread occur by one of the three ;-
A) Local extension ;- the most common ,spread to
  cartilages→ sclerosis then by additional growth
  causes cartilage erosion → destruction and
  penetration of cartilages .
B) Lymph nodes met- Occur less common .the
  lymphatic drainage depend on the origin of the 1ry
  sites .
C) Distant mets- ;-the most common site of
  hematogenous spread is the bones then less
  common to the lungs .
ipsilateral nodes         contralateral nodes
    11      111    1v v        1    11     111 1v       v
1su
pr
1% 39%      26% 8% 5%          O% 12%      5% 3% 3%


 lymph nodes involved in the ca larynx (supraglottic)
 Clinical presentation ;-
Early presentation is hoarseness of the voice
Change in the quality of the voice .
While advance presentation is difficulty in the swallowing .
  Cervical adenopathy . Weight loss . Throat pain . Referred
  pain . Air way obstruction .
Head and neck examination :- inspection of the scalp,ears,
Nose, and mouth . Palpation of the neck, mouth, tongue
Mobility, base of the tongue, and floor of mouth.
Endoscope to nasal cavity,nasopharynx,oropharynx,
Hypopharynx and larynx . Carefully cranial nerve
  examination
Diagnosis and clinical staging depends on finding from
  history ,physical examination ,imaging and lab tests
  . Pathological staging depends on finding from
  surgical resection and histological examination .
There are American joint committee on cancer (AJCC)
And Tumor, Node, and Metastasis .(TNM)
AJCC ,TNM classification of carcinoma
   Primary tumor ;-

Tx        primary tumor can not be assessed
T0        No evidence of primary tumor
T is      Carcinoma insitu
supraglottis ;-

T1  Tumor limited to 1 sub site of supraglottis ,with normal
    vocal cord mobility
T2 Tumor in more than 1 adjacent sub site of the
    supraglottis or glottis .with out fixation of the larynx
T3 tumor limited to larynx with vocal cord fixation, or
    invades following postcricoid area preepiglottic space
    Or inner cortex of thyroid cartilage
T4a Moderate advanced local disease, tumor invade thyroid
    cartilage or pre -larynx tissues
T4b Very advanced local disease ,tumor invade prevertedral
    space,carotid artery,or invades mediastinal structure
Glottis
T1    Tumor limited to 1 vocal cord with normal mobility
T1b   Tumor involve both vocal cord with normal
      mobility

T2    Tumor extends to supraglottis or subglottis with
      impaired vocal cord mobility.
T3    Tumor limited to the larynx with vocal cord fixation
      Or involve paraglottic space ,or inner cortex of
      thyroid cartilage .
T4a   Moderately advanced local disease ,outer cortex of
      thyroid cartilage or tissues surrounding the larynx
T4b   Very advanced local disease prevertebral space or
      mediastinal structures .
Sub glottis ;-
T1    tumor limited to the subglottis

T2    Tumor extend to vocal cord with normal or
      impaired mobility
T3    Tumor limited to the larynx with vocal cord fixation

T4    Moderately advanced local disease .invading of the
      cricoid or thyroid cartilage or tissue around the
      larynx .
T4b Very advanced local disease ,invading the
    prevertebral space ,cartoid artery ,meditational
    structure .
Regional lymph nodes ;-
Nx    Can not be assessed
N0    no lymph nodes metastasis
N1     metastasis in the ipsilateral lymph nodes≤3 cm
      (greater dimension)
N2a   Metastasis in single ipsilateral lymph nodes>3cm
      but≤6cm in greater dimension
N2b   Metastasis in multiple ipsilateral lymph nodes
      none >6 cm
N2c   Metastasis in bilateral or contra lateral lymph
      nodes none > 6cm
N3    Metastasis in lymph nodes >6cm in greater
      dimension
Ca larynx suspected

          Complete history & physical exam

                   Endoscopy and biopsy

         imaging            Lab
                                             interventi
          study            study
                                                 on


   Lesion
                               Advanced       Advanced
incapable of     LESION
                                 lesion         lesion
  regional      CAPABLE
                              suitable for     beyond
    met-           OF
                                 organ          organ
GLOTTIC T1-    REGIONAL
                             conservation    conservation
   2N0M0         *Mets-
                                   **            ***
   The out come of treatment of ca larynx is
    varies substantially, from excellent to poor.
    The most important prognostic factors
    include extent/stage at diagnosis, the exact
    site of origin of disease and patient’s
    performance status /ability to tolerate the
    desired therapy
Localized lesion incapable of regional
 metastasis ; this include the SCC of glottis (T1 or
  T2, N0 ) .this treated by radiation therapy to the
  primary site only . Surgery is second option but
  radiation is preferable due to subsequent voice
  quality .
Radiation therapy ;- is indicated for all early stage .
  The techniques ;- small opposed portals (e.g. 5x5 or
  6x6 cm ) treating the primary tumor only .the dose
  is 63 Gy in 28 fr/ 2.25 CGY/day in 5.6 weeks .
Usually the portals extend from hyoid bone to the
   bottom of the cricoids cartilage (upper/lower) and
   from the flash of the skin to the anterior aspect of
   the vertebral body (anterior/posterior) .
Usually we use tow parallel opposed 4-6 MV photon
Beam field .
In recent years arandomized study done concurring
   the fraction schaclat for T1N0M0 glottic cancer were
   treated either with 2,0 or 2.25 Gy ,the 5yrs local
   control rate favored the group that received 2.25 Gy
(92 versus 77%) . But the cause specific survival rate
   were similar (100 and 97%) .
Localized lesion capable of regional metastasis
Limited extent SCC of the supraglottic larynx
(T1N0-smallN1 and most T2N0 . In treatment of the
   these type of the lesion the tow type of the
   treatment can be done radiation and surgery but
   the radiation is preferable due to less morbid .
Radiation ;- suitable for all case . Specially if the
   extend of the disease required total laryngectomy
   to repair the surgery .
The techniques ;-
For small supraglottic include the primary lesion pulse the
   upper and mid cervical (level1&11) .
For more extensive supraglottic lesion also include low,
   anterior cervical (level1v) nodes .
If N1 anterior cervical disease the posterior cervical (level
   5) should be treated .
Radiation technique ;-usually lateral and parallels op-
Posed fields are used . For T1 supraglottic lesion a dose of
66 GY in 33fr 2fr/day .for T2 supraglottic 70 GY in35 fr .
Advanced lesion suitable for organ preservation
T3 –T4 ;- this lesion traditionally treated by
  laryngectomy(with or without pharyngectomy)
  .now these is larynx sparing therapy these is no
  deferent in the cervival between surgery and the
  larynx sparing therapy .but not all lesion are suitable
  for organ preservation therapy (unreliable
  patients,pts contuse smoking during treatment
  ,hypertensive,pts who cannot tolerate discomfort
  of the surgery)
The treatment modal which used for organ
  preservation;-
Indicated for advanced lesion that have not
  penetrated cartilage .(cord fixation is not contra-
Indication).
Techniques ;-the primary tumor and clinical involved
Nodes should receive 70 GY in 35 frs .
All anterior and posterior cervical andsupraclavicular
  clinically uninvolved are at risk for sub clinical
  involvement and need to receive minimum of 50 GY
The chemotherapy ;- include cisplatin I.V on day 1,22
       &43 of radiotherapy .
     Clinical evidence ;-
     Randomized trials ;-
Departmen       pts number= 332 ( stage 111 or 1v ca larynx ). Median fallow up 33
t of veteran   months
affairs        Compared 3 cycles of indication cisplatin + flurouracil chemotherapy
larynx         Versus laryngectomy postoperative radiation.
               The survival rate is equal in both arm for 2 yrs =68% ( p=0.098)
               .there were
               More local recurrence (p=0.005)and fewer distant metastases
               (p=0.016)
               In the chemotherapy group than in the other group
EORTC2489 Randomized of patent number202 with ca
1b        larynx of the pyriform sinus stage 11-1v follow
          up to 51 months .
          Compared cycles of inducation cisplatin
          chemotherapy and thenradiotherapy verus
          larngectomy and postoperative radiotherapy
          median cervival was 44months in inducation
          chemotherapy arm and 25 months in surgery
          arm .
          Local and regional recurrence was similar in
          both arm
RTOG    Randomized care of 520 patients who wise
       Required laryngectomy .
       Comparing inducation cisplatin plus fluoro-
       Uracil and then radiotherapy versus radiotherapy
       with concurrent administration of cisplatin versus
       radiotherapy alone .
       The primary end point of preservation of the
       larynx significantly favored concurrent
       Therapy 2yrs-88% while inducation chemo-
       75% and the radiotherapy 70%.
       2nd end point of loco regional control significantly
       Favored concurrent therapy 78% while with
       inducation chemo-61% and 56% with radiotherapy
       Alone .overall survival was similar in all groups
Resectable advanced lesions not suitable for organ
Preservation ;-the important part in preservation is
the preservation of the function .once function is
Irreparably lost , these is little benefit to preserving
The anatomy .in other cases concurrent chemo-may be
   toxic due to other diseases or refuse stop smoking /co-
   morbidities /unreliable who cutting medication /patients
   who emotionally would prefer
Surgery / cartilage destroyed or extracapssular extension.
   2studies show that stage111 loco regional
Control improved by adding cisplatin concurrent with
Radiation therapy tech- ;-the fields include the
  primary site (tumor +ve LNs) +subclinical LNS
The upper border includes the nodes in the upper
  jugular region. both the ipsilateral and contra lateral
Posterior are include in the treatment portals if
  anterior chain +ve.
The primary site &area with↑risk(dissected and has
Altered vascular supply)60-66GY 33fr .
While area of low risk(not dissected) will receive
50-54 fr .
unresectable advanced lesion not suitable for organ
Preservation ;- in unresectable patients with good
  general condition with no heamatogenus spread
  can be approached with curative- intent
  chemotherapy-enhanced radiation therapy . In very
Fit patients inducation chemotherapy succeeded by
Chemo—enhanced radiation therapy .for patient with
Already distant metastasis role will be palliation
Post-operative radiation therapy .
Radiation is indicated for all lesion extent
Tech – 60-66 GY to operative bed and drainage
Nodes .
Chemo- ;-indicated for microscopically involved
  mucosal margin /extra capsular extension of nodal
Disease .
Tech- I-V ;-cisplatin 1 on day 1 ,22 and 43 of
  radiotherapy treatment .
The volume delineation ;-
The primary tumor site,all nodal beds at risk of
  subclinical disease and operative bed . The upper
  border include the nodes in jugular region .the high
Risk region→ 60-66 GY .low risk→50-54 GY .
Supporting clinical evidence

RTOG 9501 459 patients . Who ,after definitive surgery , had
          histologic invasion
          Of tow or more regional LNs/extra capsular extension
          of nodal disease
          Or mucosal resection margin.
          Randomized to radiotherapy alone o(60-66GY) versus
          identical treatment
          +concurrent cisplatin on day 1 ,22 &43 .
          The primary end point of loco regional control favored
          concurrent chemotherapy at 2 yrs 82% ( with
          chemotherapy ) versus 72% (no chemotherapy ).
          The secondary end point of disease free survival also
          favored concurrent
          Therapy ( p=0.04) but over all survival not different
EORTC   Patients number 334 ,who after definitive surgery had
22931   histological
        Evidence of extra nodal spread , + ve margin , per neural
        involvement
        Or vascular tumor embolism (median fallow up 60
        months )
        Randomized to radiotherapy alone (66 GY in 33 fr)
        versus identical treatment +concurrent cisplatin in day
        1, 22 &43 .
        The primary end point of disease free survival favored
        concurrent therapy
        At 5 yr s4% with chemotherapy verus36% (no
        chemotherapy) p=o.o4
        Second end point of overall survival(p=0.02) and loco
        regional control
        (p=0.007) both significantly favored concurrent therapy
schedule          frequency

First follow up   2weeks after radiation →for acute reaction

Yrear0-1          Every month

Year 1-2          Every 2 months

Year2-3           Every 3 months

Year 3+           Every 6 months
From the previous data of RTOG 9501and EORTC
  22931
Which concurring the benefit of chemotherapy.
Were the ECE (extra capsular extenation) or +ve SM.
Involvement of2 more LNs by tumor is not predict
Benefit from chemotherapy .
The emis is to controlling thedistressing loco-
Regional signs or symptoms of disease for during the
  patient remaining alive .
For who have one or tow non life threatening lesion
  .with good response to chemotherapy ,the radiation
Therapy that approaches the intensity of definitive
Treatment. With more advanced metastatic disease
The author tends to favor asplit-course( eg;-30GY in
  2weeks the tow weeks rest ,followed by another
30 GY in 2weeksto smaller field never over lap the
  spinal cord.for patient live more we can do quad
Shot technique
Supporting clinical evidence ;-
For M0tumor   Multi-institutional phase 111 trial includeing 295 patient with
              unresectable
              Nondisseminated ,head and neck cancer.
              Randomized to stander radiation therapy alone (70YG in 30 fr ) versus
              Identical radiation +concurrent bolus cisplatin on day 1 ,22 ,34 versus
              Split-course radiation therapy + bolus cisplatin and continuous –infusion
              Fluorourcil . The with concurrent cisplatin is associated with improve of
              The survival,at the cost increase the toxicity .the 3yrs overall survival
              37% .
For M0   166 patients with locally advanced ( 74% operable and 26%
tumor    unoperable)laryngeal and hypophyaryngealcancer .
         Randomized to to treatment with docetaxel (taxotere) ,cisplatin
         And 5-fluorourcil inducation then chemoradiotherapy versus
         Cisplatin and fluorourcil (pf) then chemoradiotherapy .
         For inoperable 2 yrs overall survival was 55% with TPF AND 41%
         In the PF .
          for inoperable tumor ,the 2 yrs progression free survival was 42%
         In TPF and 30% in the PF .
For MI   30 patients who had advanced head and neck nearly stage 1v
TUMOR    With performance score of 2-3 .
         Quad shot =14 GY in 4fr given twice a day at least 6hours apart
         Over 2 consecutive days ahd repeated up to twice more every
         4 weeks .
         53% objective reponse rate ( complete reponse,2, partial response
         ,4.) .
         Median progression free survival3,1 months . Median overall
         survival 57 months .
         44% patients had measurable improvement in the quality of life
Dose limitation gude line in the ca larynx

Organ at risk   Dose limitation (GY)
spinal cord              45
brachial                60
plexus
mandible                70
posterior       <35 (astrip of normal tissue should
neck            be left to facilitate
                Drainge )

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Canaer of larynx

  • 2.
  • 3.
  • 4.
  • 5.
  • 6. the larynx is consists of a cartilaginous skeleton with ligaments,which carries the muscles and mostly is covered by mucous membrane . skeleton of the larynx ;- 1)Thyroid cartilage ;- consist of tow lateral laminae which are fused in front (bow ship). At the tip of bow is a notch (Adam apple) . The superior and inferior horn arise from the posterior edge of each laminae 2) Caricoid cartilage ;-it is ship is like signet ring .it is lamina is 2-2.5 cms lies posterior .the upper edage of the lamina has tow articular surface for the arytenoid cartilage .the lateral surface on each side has articular surface for the inferior horn of the thyriod cartilage .
  • 7. Arytenoid cartilage ;-pair of cartilage sited on the upper edge of the lamina of the cricoid cartilage .it has the shap of triangular pyramid . The vocal cord are two thickened uppper end of the conus attached posterior to the vocal process of both arytenoids cartilage and interiorly to the inner surface of the angle of the thyroid cartilagecricoarytenoid muscles . Epiglottis ;-lies against the middle of the thyroid cartilage
  • 8. Laryngeal ligaments ;-is a membrane composed of a dense elastic fiber net which lies below the mucous memberane of the larynx and has different sickness in different region (conus elasticus-vocal cord –median cricothyroid ligament l-quadrangular membrane –vestibular ligament …)
  • 9.
  • 10. New case in 2009 is 12,290 with ca larynx .with men affected four time more than female .deaths from ca larynx is 3,660 . With modern care the deaths dropped from 2,97 per 100,000 to 2,24 per 100,000 . Risk factors ;- 1) Age > 55 yrs . 2)Gender male to female ratio 4:1 3)Cigarette smoking (2-25X increase)
  • 11. 4) Alcohol consumption (2-6 increase ) the . The combination of cigarette and alcohol ↑(40-100) . 5) Race African –American are more affected . 6) Past medical history of head and neck cancer ↑risk of ca larynx . 7) Genetic factors ;- e.g fanconia anemia and dyskeratosis congenita (condation→aplastic anemia ↑ risk of ca larynx . 8) Condition → ↓ immunity (AIDS –organ transplant ) .↑risk of ca larynx .
  • 12. The majority of ca larynx which arise from the mucosal surface is squamous cell carcinoma . The most are well to mode differentiated . Ca larynx sub site percent supraglottic 35% glottic 65% subglottic 1%
  • 13.
  • 14.
  • 15. spread occur by one of the three ;- A) Local extension ;- the most common ,spread to cartilages→ sclerosis then by additional growth causes cartilage erosion → destruction and penetration of cartilages . B) Lymph nodes met- Occur less common .the lymphatic drainage depend on the origin of the 1ry sites . C) Distant mets- ;-the most common site of hematogenous spread is the bones then less common to the lungs .
  • 16.
  • 17. ipsilateral nodes contralateral nodes 11 111 1v v 1 11 111 1v v 1su pr 1% 39% 26% 8% 5% O% 12% 5% 3% 3% lymph nodes involved in the ca larynx (supraglottic)
  • 18.  Clinical presentation ;- Early presentation is hoarseness of the voice Change in the quality of the voice . While advance presentation is difficulty in the swallowing . Cervical adenopathy . Weight loss . Throat pain . Referred pain . Air way obstruction . Head and neck examination :- inspection of the scalp,ears, Nose, and mouth . Palpation of the neck, mouth, tongue Mobility, base of the tongue, and floor of mouth. Endoscope to nasal cavity,nasopharynx,oropharynx, Hypopharynx and larynx . Carefully cranial nerve examination
  • 19. Diagnosis and clinical staging depends on finding from history ,physical examination ,imaging and lab tests . Pathological staging depends on finding from surgical resection and histological examination . There are American joint committee on cancer (AJCC) And Tumor, Node, and Metastasis .(TNM)
  • 20. AJCC ,TNM classification of carcinoma Primary tumor ;- Tx primary tumor can not be assessed T0 No evidence of primary tumor T is Carcinoma insitu
  • 21. supraglottis ;- T1 Tumor limited to 1 sub site of supraglottis ,with normal vocal cord mobility T2 Tumor in more than 1 adjacent sub site of the supraglottis or glottis .with out fixation of the larynx T3 tumor limited to larynx with vocal cord fixation, or invades following postcricoid area preepiglottic space Or inner cortex of thyroid cartilage T4a Moderate advanced local disease, tumor invade thyroid cartilage or pre -larynx tissues T4b Very advanced local disease ,tumor invade prevertedral space,carotid artery,or invades mediastinal structure
  • 22. Glottis T1 Tumor limited to 1 vocal cord with normal mobility T1b Tumor involve both vocal cord with normal mobility T2 Tumor extends to supraglottis or subglottis with impaired vocal cord mobility. T3 Tumor limited to the larynx with vocal cord fixation Or involve paraglottic space ,or inner cortex of thyroid cartilage . T4a Moderately advanced local disease ,outer cortex of thyroid cartilage or tissues surrounding the larynx T4b Very advanced local disease prevertebral space or mediastinal structures .
  • 23. Sub glottis ;- T1 tumor limited to the subglottis T2 Tumor extend to vocal cord with normal or impaired mobility T3 Tumor limited to the larynx with vocal cord fixation T4 Moderately advanced local disease .invading of the cricoid or thyroid cartilage or tissue around the larynx . T4b Very advanced local disease ,invading the prevertebral space ,cartoid artery ,meditational structure .
  • 24. Regional lymph nodes ;- Nx Can not be assessed N0 no lymph nodes metastasis N1 metastasis in the ipsilateral lymph nodes≤3 cm (greater dimension) N2a Metastasis in single ipsilateral lymph nodes>3cm but≤6cm in greater dimension N2b Metastasis in multiple ipsilateral lymph nodes none >6 cm N2c Metastasis in bilateral or contra lateral lymph nodes none > 6cm N3 Metastasis in lymph nodes >6cm in greater dimension
  • 25. Ca larynx suspected Complete history & physical exam Endoscopy and biopsy imaging Lab interventi study study on Lesion Advanced Advanced incapable of LESION lesion lesion regional CAPABLE suitable for beyond met- OF organ organ GLOTTIC T1- REGIONAL conservation conservation 2N0M0 *Mets- ** ***
  • 26. The out come of treatment of ca larynx is varies substantially, from excellent to poor. The most important prognostic factors include extent/stage at diagnosis, the exact site of origin of disease and patient’s performance status /ability to tolerate the desired therapy
  • 27. Localized lesion incapable of regional metastasis ; this include the SCC of glottis (T1 or T2, N0 ) .this treated by radiation therapy to the primary site only . Surgery is second option but radiation is preferable due to subsequent voice quality . Radiation therapy ;- is indicated for all early stage . The techniques ;- small opposed portals (e.g. 5x5 or 6x6 cm ) treating the primary tumor only .the dose is 63 Gy in 28 fr/ 2.25 CGY/day in 5.6 weeks .
  • 28. Usually the portals extend from hyoid bone to the bottom of the cricoids cartilage (upper/lower) and from the flash of the skin to the anterior aspect of the vertebral body (anterior/posterior) . Usually we use tow parallel opposed 4-6 MV photon Beam field . In recent years arandomized study done concurring the fraction schaclat for T1N0M0 glottic cancer were treated either with 2,0 or 2.25 Gy ,the 5yrs local control rate favored the group that received 2.25 Gy
  • 29. (92 versus 77%) . But the cause specific survival rate were similar (100 and 97%) . Localized lesion capable of regional metastasis Limited extent SCC of the supraglottic larynx (T1N0-smallN1 and most T2N0 . In treatment of the these type of the lesion the tow type of the treatment can be done radiation and surgery but the radiation is preferable due to less morbid . Radiation ;- suitable for all case . Specially if the extend of the disease required total laryngectomy to repair the surgery .
  • 30. The techniques ;- For small supraglottic include the primary lesion pulse the upper and mid cervical (level1&11) . For more extensive supraglottic lesion also include low, anterior cervical (level1v) nodes . If N1 anterior cervical disease the posterior cervical (level 5) should be treated . Radiation technique ;-usually lateral and parallels op- Posed fields are used . For T1 supraglottic lesion a dose of 66 GY in 33fr 2fr/day .for T2 supraglottic 70 GY in35 fr .
  • 31. Advanced lesion suitable for organ preservation T3 –T4 ;- this lesion traditionally treated by laryngectomy(with or without pharyngectomy) .now these is larynx sparing therapy these is no deferent in the cervival between surgery and the larynx sparing therapy .but not all lesion are suitable for organ preservation therapy (unreliable patients,pts contuse smoking during treatment ,hypertensive,pts who cannot tolerate discomfort of the surgery)
  • 32. The treatment modal which used for organ preservation;- Indicated for advanced lesion that have not penetrated cartilage .(cord fixation is not contra- Indication). Techniques ;-the primary tumor and clinical involved Nodes should receive 70 GY in 35 frs . All anterior and posterior cervical andsupraclavicular clinically uninvolved are at risk for sub clinical involvement and need to receive minimum of 50 GY
  • 33. The chemotherapy ;- include cisplatin I.V on day 1,22 &43 of radiotherapy . Clinical evidence ;- Randomized trials ;- Departmen pts number= 332 ( stage 111 or 1v ca larynx ). Median fallow up 33 t of veteran months affairs Compared 3 cycles of indication cisplatin + flurouracil chemotherapy larynx Versus laryngectomy postoperative radiation. The survival rate is equal in both arm for 2 yrs =68% ( p=0.098) .there were More local recurrence (p=0.005)and fewer distant metastases (p=0.016) In the chemotherapy group than in the other group
  • 34. EORTC2489 Randomized of patent number202 with ca 1b larynx of the pyriform sinus stage 11-1v follow up to 51 months . Compared cycles of inducation cisplatin chemotherapy and thenradiotherapy verus larngectomy and postoperative radiotherapy median cervival was 44months in inducation chemotherapy arm and 25 months in surgery arm . Local and regional recurrence was similar in both arm
  • 35. RTOG Randomized care of 520 patients who wise Required laryngectomy . Comparing inducation cisplatin plus fluoro- Uracil and then radiotherapy versus radiotherapy with concurrent administration of cisplatin versus radiotherapy alone . The primary end point of preservation of the larynx significantly favored concurrent Therapy 2yrs-88% while inducation chemo- 75% and the radiotherapy 70%. 2nd end point of loco regional control significantly Favored concurrent therapy 78% while with inducation chemo-61% and 56% with radiotherapy Alone .overall survival was similar in all groups
  • 36. Resectable advanced lesions not suitable for organ Preservation ;-the important part in preservation is the preservation of the function .once function is Irreparably lost , these is little benefit to preserving The anatomy .in other cases concurrent chemo-may be toxic due to other diseases or refuse stop smoking /co- morbidities /unreliable who cutting medication /patients who emotionally would prefer Surgery / cartilage destroyed or extracapssular extension. 2studies show that stage111 loco regional Control improved by adding cisplatin concurrent with
  • 37. Radiation therapy tech- ;-the fields include the primary site (tumor +ve LNs) +subclinical LNS The upper border includes the nodes in the upper jugular region. both the ipsilateral and contra lateral Posterior are include in the treatment portals if anterior chain +ve. The primary site &area with↑risk(dissected and has Altered vascular supply)60-66GY 33fr . While area of low risk(not dissected) will receive 50-54 fr .
  • 38. unresectable advanced lesion not suitable for organ Preservation ;- in unresectable patients with good general condition with no heamatogenus spread can be approached with curative- intent chemotherapy-enhanced radiation therapy . In very Fit patients inducation chemotherapy succeeded by Chemo—enhanced radiation therapy .for patient with Already distant metastasis role will be palliation
  • 39. Post-operative radiation therapy . Radiation is indicated for all lesion extent Tech – 60-66 GY to operative bed and drainage Nodes . Chemo- ;-indicated for microscopically involved mucosal margin /extra capsular extension of nodal Disease . Tech- I-V ;-cisplatin 1 on day 1 ,22 and 43 of radiotherapy treatment .
  • 40. The volume delineation ;- The primary tumor site,all nodal beds at risk of subclinical disease and operative bed . The upper border include the nodes in jugular region .the high Risk region→ 60-66 GY .low risk→50-54 GY .
  • 41. Supporting clinical evidence RTOG 9501 459 patients . Who ,after definitive surgery , had histologic invasion Of tow or more regional LNs/extra capsular extension of nodal disease Or mucosal resection margin. Randomized to radiotherapy alone o(60-66GY) versus identical treatment +concurrent cisplatin on day 1 ,22 &43 . The primary end point of loco regional control favored concurrent chemotherapy at 2 yrs 82% ( with chemotherapy ) versus 72% (no chemotherapy ). The secondary end point of disease free survival also favored concurrent Therapy ( p=0.04) but over all survival not different
  • 42. EORTC Patients number 334 ,who after definitive surgery had 22931 histological Evidence of extra nodal spread , + ve margin , per neural involvement Or vascular tumor embolism (median fallow up 60 months ) Randomized to radiotherapy alone (66 GY in 33 fr) versus identical treatment +concurrent cisplatin in day 1, 22 &43 . The primary end point of disease free survival favored concurrent therapy At 5 yr s4% with chemotherapy verus36% (no chemotherapy) p=o.o4 Second end point of overall survival(p=0.02) and loco regional control (p=0.007) both significantly favored concurrent therapy
  • 43. schedule frequency First follow up 2weeks after radiation →for acute reaction Yrear0-1 Every month Year 1-2 Every 2 months Year2-3 Every 3 months Year 3+ Every 6 months
  • 44. From the previous data of RTOG 9501and EORTC 22931 Which concurring the benefit of chemotherapy. Were the ECE (extra capsular extenation) or +ve SM. Involvement of2 more LNs by tumor is not predict Benefit from chemotherapy .
  • 45. The emis is to controlling thedistressing loco- Regional signs or symptoms of disease for during the patient remaining alive . For who have one or tow non life threatening lesion .with good response to chemotherapy ,the radiation Therapy that approaches the intensity of definitive Treatment. With more advanced metastatic disease The author tends to favor asplit-course( eg;-30GY in 2weeks the tow weeks rest ,followed by another 30 GY in 2weeksto smaller field never over lap the spinal cord.for patient live more we can do quad Shot technique
  • 46. Supporting clinical evidence ;- For M0tumor Multi-institutional phase 111 trial includeing 295 patient with unresectable Nondisseminated ,head and neck cancer. Randomized to stander radiation therapy alone (70YG in 30 fr ) versus Identical radiation +concurrent bolus cisplatin on day 1 ,22 ,34 versus Split-course radiation therapy + bolus cisplatin and continuous –infusion Fluorourcil . The with concurrent cisplatin is associated with improve of The survival,at the cost increase the toxicity .the 3yrs overall survival 37% .
  • 47. For M0 166 patients with locally advanced ( 74% operable and 26% tumor unoperable)laryngeal and hypophyaryngealcancer . Randomized to to treatment with docetaxel (taxotere) ,cisplatin And 5-fluorourcil inducation then chemoradiotherapy versus Cisplatin and fluorourcil (pf) then chemoradiotherapy . For inoperable 2 yrs overall survival was 55% with TPF AND 41% In the PF . for inoperable tumor ,the 2 yrs progression free survival was 42% In TPF and 30% in the PF .
  • 48. For MI 30 patients who had advanced head and neck nearly stage 1v TUMOR With performance score of 2-3 . Quad shot =14 GY in 4fr given twice a day at least 6hours apart Over 2 consecutive days ahd repeated up to twice more every 4 weeks . 53% objective reponse rate ( complete reponse,2, partial response ,4.) . Median progression free survival3,1 months . Median overall survival 57 months . 44% patients had measurable improvement in the quality of life
  • 49. Dose limitation gude line in the ca larynx Organ at risk Dose limitation (GY) spinal cord 45 brachial 60 plexus mandible 70 posterior <35 (astrip of normal tissue should neck be left to facilitate Drainge )

Notes de l'éditeur

  1. *supraglottic T1N0-small N1. most ofT2N0 M0 ////**T2N1-3M0/T3N0-3M0 ///***T4N0-3M0-1 this then divided to operable &amp; inoperable