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Squamous cell carcinoma of the head and neck (SCCHN) General Features and Treatment Guidelines Arafat Tfayli, MD Associate Professor of Clinical Medicine American University of Beirut Medical Center [email_address]
SCCHN ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Anatomic sites   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Oral cavity ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Pharynx ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Larynx ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Nasal cavity and paranasal sinuses ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Major salivary glands ,[object Object],[object Object],[object Object]
Lymph zones of the neck Level I: submental, submandibular Level II: upper jugular Level III: mid jugular Level IV: lower jugular Level V: posterior triangle (including spinal accessory or posterior cervical chain) Level VI: prelaryngeal (Delphian), pretracheal, paratracheal Other groups: sub-occipital retropharyngeal parapharyngeal buccinator (facial) preauricular periparotid intraparotid
Regional lymph node involvement ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Incidence and Mortality ,[object Object],[object Object],[object Object],[object Object]
Achievements ,[object Object],[object Object],[object Object],[object Object],[object Object]
Risk factors   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Viruses ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Figure 2. Human Papillomavirus (HPV) in Oropharyngeal Cancers. Recent studies confirm that oropharyngeal tumors are often HPV-positive and compose a distinct clinical and pathologic disease entity. In Panel A, a typical large tonsillar lesion (arrows) is shown. Panel B shows the typical basaloid appearance often seen in HPV-positive tumors. In Panel C, the same tissue section was subjected to in situ hybridization with an HPV-E7-specific probe. The dark brown spots indicate the presence of HPV DNA in virtually all the neoplastic cells. (Courtesy of Wayne M. Koch and William H. Westra.).
 
TNM Staging ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Salivary gland tumors with extraparenchymal extension are at least T3 regardless of size T staging is different for nasopharynx, hypopharynx, larynx subsites, and maxillary sinus, and is dependent on local extension as well as size for early lesions
TNM Staging ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TNM Staging ,[object Object],[object Object],[object Object],[object Object]
TNM Staging ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TNM Staging ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Management of SCCHN ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Multimodality Treatments in  LA-SCCHN ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Seiwert et al 2007
CRT: Answered questions ,[object Object],[object Object],[object Object],[object Object],Salama et al. JCO VOL 25  NUM 26  SEP 2007
CRT- Unanswered Questions ,[object Object],[object Object],[object Object],Salama et al. JCO VOL 25  NUM 26  SEP 2007
Concurrent CRT Is Superior to Radiotherapy Alone in Both the Definitive and Adjuvant Setting Salama et al. JCO VOL 25  NUM 26  SEP 2007
Meta-analysis of HNC (MACH-NC) Bourhis J: J Clin Oncol 24:489s, 2004 (suppl; abstr 5505)
Salama et al. JCO Vol 25  Num 26  Sep. 10 2007
Postoperative irradiation with or without concurrent chemotherapy for locally advanced head and neck cancer Bernier et al: 350:1945-1952, 2004
Postoperative irradiation with or without concurrent chemotherapy for locally advanced head and neck cancer NEJM 350:, 2004
Epidermal growth factor receptor
Study design Stage III and IV  nonmetastatic  SCCHN (n=424) RT (n=213) Erbitux + RT (n=211) Erbitux initial dose (400 mg/m 2 ) Erbitux (250 mg/m 2 ) + RT (wks 2–8) Bonner J et al. N Engl J Med 2006;354:567 –578 a Investigators’ choice R Primary endpoint:   Duration of locoregional control Secondary endpoints:   OS, PFS, RR, QoL, and safety ,[object Object],[object Object],[object Object],[object Object],[object Object]
Erbitux + RT: Locoregional control Hazard ratio=0.68 (95% CI: 0.52–0.89); p=0.005  Time (months) Erbitux + RT (n=211) Locoregional control (%) 100 80 60 40 20 0 0 10 20 30 40 50 60 70 RT (n=213) 14.9 months 24.4 months 47% (3-year control rate) 34% (3-year control rate) Bonner J et al. N Engl J Med 2006;354:567 –578
Erbitux + RT: Overall survival  5-year update Bonner J et al. Int J Radiat Oncol Biol Phys 2008; 72 (Suppl):Abs LB3 Hazard ratio=0.73 (95% CI: 0.56–0.95); p=0.018 1.0 0.9 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 0   10   20   30   40   50   60   70 Time (months) Probability of overall survival 29.3 months 49.0 months Erbitux + RT (n=211) RT (n=213) 36% (5-year survival rate) 46% (5-year survival rate)
Erbitux + RT:  Relevant grade 3–5 adverse events Bonner J et al. N Engl J Med 2006;354:567 –578 p<0.001 a p=0.01 a Patients (%) a Fisher’s exact test  b Listed for its relationship to Erbitux ,[object Object],b 0 10 20 30 40 50 60 Mucositis/stomatitis Dysphagia Radiation dermatitis Xerostomia Fatigue/malaise Acne-like rash Infusion reactions RT (n=212) Erbitux + RT (n=208)
Concurrent CRT Results in Superior Laryngeal Preservation Compared With Sequential CRT or RT Alone
 
 
 
The VA Trial : Conclusion Induction chemotherapy and definitive radiation therapy are effective in preserving the larynx in a high percentage of patients, without compromising overall survival .
 
 
 
Concurrent CRT Is Associated With Increased Toxicity compared With RT Alone
 
 
Late toxicity associated with Concurrent CRT  Machtay et al, JCO VOL 26  NUM 21  JULY 20 2008
CRT: What Is the Optimal Chemotherapy Regimen? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Bourhis J: J Clin Oncol 24:489s, 2004 (suppl; abstr 5505)
What Is the Role of Neoadjuvant Chemotherapy for Patients Treated With Concurrent CRT? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Neoadjuvant Chemotherapy for Patients Treated With Concurrent CRT ,[object Object],[object Object],[object Object],[object Object]
 
 
 
 
 
 
Trials are ongoing to determine the role of induction chemotherapy in the setting of highly active CRT
Thank you
Case 1 ,[object Object],[object Object]
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Case 1 ,[object Object],[object Object],[object Object]
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Case 2 ,[object Object],[object Object]
Case 2 ,[object Object],[object Object],[object Object]
Case 2 ,[object Object],[object Object]
Case 2 ,[object Object],[object Object]
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A. Tfayli - Head and neck - Guidelines and clinical case presentation (2-3 cases)

  • 1. Squamous cell carcinoma of the head and neck (SCCHN) General Features and Treatment Guidelines Arafat Tfayli, MD Associate Professor of Clinical Medicine American University of Beirut Medical Center [email_address]
  • 2.
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  • 12. Lymph zones of the neck Level I: submental, submandibular Level II: upper jugular Level III: mid jugular Level IV: lower jugular Level V: posterior triangle (including spinal accessory or posterior cervical chain) Level VI: prelaryngeal (Delphian), pretracheal, paratracheal Other groups: sub-occipital retropharyngeal parapharyngeal buccinator (facial) preauricular periparotid intraparotid
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  • 18. Figure 2. Human Papillomavirus (HPV) in Oropharyngeal Cancers. Recent studies confirm that oropharyngeal tumors are often HPV-positive and compose a distinct clinical and pathologic disease entity. In Panel A, a typical large tonsillar lesion (arrows) is shown. Panel B shows the typical basaloid appearance often seen in HPV-positive tumors. In Panel C, the same tissue section was subjected to in situ hybridization with an HPV-E7-specific probe. The dark brown spots indicate the presence of HPV DNA in virtually all the neoplastic cells. (Courtesy of Wayne M. Koch and William H. Westra.).
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  • 29. Concurrent CRT Is Superior to Radiotherapy Alone in Both the Definitive and Adjuvant Setting Salama et al. JCO VOL 25 NUM 26 SEP 2007
  • 30. Meta-analysis of HNC (MACH-NC) Bourhis J: J Clin Oncol 24:489s, 2004 (suppl; abstr 5505)
  • 31. Salama et al. JCO Vol 25 Num 26 Sep. 10 2007
  • 32. Postoperative irradiation with or without concurrent chemotherapy for locally advanced head and neck cancer Bernier et al: 350:1945-1952, 2004
  • 33. Postoperative irradiation with or without concurrent chemotherapy for locally advanced head and neck cancer NEJM 350:, 2004
  • 35.
  • 36. Erbitux + RT: Locoregional control Hazard ratio=0.68 (95% CI: 0.52–0.89); p=0.005 Time (months) Erbitux + RT (n=211) Locoregional control (%) 100 80 60 40 20 0 0 10 20 30 40 50 60 70 RT (n=213) 14.9 months 24.4 months 47% (3-year control rate) 34% (3-year control rate) Bonner J et al. N Engl J Med 2006;354:567 –578
  • 37. Erbitux + RT: Overall survival 5-year update Bonner J et al. Int J Radiat Oncol Biol Phys 2008; 72 (Suppl):Abs LB3 Hazard ratio=0.73 (95% CI: 0.56–0.95); p=0.018 1.0 0.9 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 0 10 20 30 40 50 60 70 Time (months) Probability of overall survival 29.3 months 49.0 months Erbitux + RT (n=211) RT (n=213) 36% (5-year survival rate) 46% (5-year survival rate)
  • 38.
  • 39. Concurrent CRT Results in Superior Laryngeal Preservation Compared With Sequential CRT or RT Alone
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  • 41.  
  • 42.  
  • 43. The VA Trial : Conclusion Induction chemotherapy and definitive radiation therapy are effective in preserving the larynx in a high percentage of patients, without compromising overall survival .
  • 44.  
  • 45.  
  • 46.  
  • 47. Concurrent CRT Is Associated With Increased Toxicity compared With RT Alone
  • 48.  
  • 49.  
  • 50. Late toxicity associated with Concurrent CRT Machtay et al, JCO VOL 26 NUM 21 JULY 20 2008
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  • 60. Trials are ongoing to determine the role of induction chemotherapy in the setting of highly active CRT
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Hinweis der Redaktion

  1. As you know concomitant chemoradiation has become the standard of care
  2. Conclusion Severe late toxicity after CCRT is common. Older age, advanced T-stage, and larynx/hypopharynx primary site were strong independent risk factors. Neck dissection after CCRT was associated with an increased risk of these complications. These data suggest that the CCRT has reached the limits of acceptable long-term toxicity. Dose intensity can not be easily increased without some new and effective technique(s) of protection against late effects. In the future, these may include modern techniques in radiation therapy technology27,28 or biopharmacologic radioprotectors.29-31 Presently, however, these techniques have only succeeded in reducing xerostomia, not severe late dysphagia
  3. (LOOK UP) But there is one thing we should never forget: Don’t focus on the disease - Focus on the human being !