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ARCON for T2-4 laryngeal cancer:
  a phase III randomized trial



              Hans Kaanders
      Department of Radiation Oncology
  Radboud University Nijmegen Medical Centre
              The Netherlands
ARCON
      Accelerated Radiotherapy + CarbOgen + Nicotinamide
          Tumor cell proliferation                     Chronic hypoxia      Acute hypoxia
                                        S
 D                   D S S        D S S S
                                          D
S S D                 S S S        S S D S S
                          D S    D S S S S
 D S                 D S                    S
                         S        S D S S
                                           S
                                      S S

           D S DS
     D D        S   S
           S
   S SS S D S D S
 S D S      S       S DS
 S S     S S S D      S SS S
D S D D         D S
             S S  S S      D S         S S
D    D S                D S           S D    S S
D  D       D S D S D        S      S S    S S D
      D      D S D D S D S               S S      S
 S SS D                  S        D
                                     S D D
                                              S S S
SS      S D S D D S S S           S          S S S
 D
    D
       S  S SS D D S         D       D
                                       S
                                         S S D
   S     SS      S       S D     S               S D
      S       D    D SS                S D S
                                              D
   S     D                S      S SS D          S
     SS S D D S                            D S
          D D D SSD S               S S
                                         S D D S
                  D                                        Carbogen         Nicotinamide
                                                          98% O2 + 2% CO2


        Accelerated fractionation



                                         S
 D                   DS S         D S S S
S S D                 S S S        S S  D SD
                                             S
                          D S    D S S S S
 D S                 D S                     S
                         S        S D S S
                                            S
                                       S S


S    stem cell
D    differentiated cell
ARCON in a mouse mammary carcinoma



 Enhancement     2.1
                                                                                 ARCON
  ratio at the    2
  TCD50 level                                                     conventional
                 1.9                                accelerated     carbogen
        -                                            carbogen     nicotinamide
                 1.8
   relative to
 conventional    1.7
                                     conventional
 radiotherapy    1.6                  carbogen
      in air
                 1.5
                 1.4
                 1.3   accelerated

                 1.2
                 1.1
                  1



Rojas 1996
ARCON, phase II trial in H&N cancer



          UMC Nijmegen
          Oct. 1993 – Oct. 2000



215 patients                      larynx:        100
Stage III-IV                      hypopharynx: 50

                                  oropharynx:    52
Median follow-up:
68 months (37-127)                oral cavity:   13
ARCON phase II trial:
             high local control rates in T3-4 tumors
Local control (%)


                                                       44 patients
                                       oropharynx
                                         larynx


                                                       79 patients
                                       hypopharynx




                         oral cavity
                                                       21 patients




                                                       12 patients
                      Time (months)
Dutch multicenter randomized trial
              ARCON vs Accelerated RT
               in laryngeal carcinoma

                                        Secondary endpoints:
                                        • larynx preservation
Primary objective:                      • regional control
• To improve local tumor control        • toxicity
                                        • quality of life
                                        • disease-free survival
                                        • overall survival




Translational side study:
   Is the hypoxic status of the tumor predictive for outcome?
ARCON for T2-4 squamous cell carcinoma of the larynx
                               Randomization



  Accelerated Radiotherapy                       Accelerated Radiotherapy
                                                             +
                                                carbogen and nicotinamide




 Fractionation schedule:



                                      primary          metastatic nodes
         Acc. RT                      68 Gy                  68 Gy
         ARCON                        64 Gy*                 68 Gy

          *Aim: improve tumor control with equal toxicity between arms!
Patient characteristics (N = 345)


                             Standard   Experimental
                               arm          arm

Total                          174           171
Female                         39            30
Male                           135           141


Mean age (SD)                61 (9.1)     62 (9.9)


WHO performance status
                         0     140           137
                         1      34            33
Tumor site and T/N-stage (UICC 1997)

                    Standard      Experimental
                      arm             arm
Glottic               74              74
Supraglottic          100             97


T2 (advanced)         67              55
T3                    80              95
T4                    27              21


N0                    117             115
N1                    20              23
N2                    37              33
N3                     -               -
Acute toxicity: mucositis


Patchy/confluent mucositis(%)



                                                                 ARCON
                                                                 Acc. RT




                                Weeks after start of treatment
Late toxicity

                                     Standard   Experimental
                                       arm          arm


Severe subcutaneous fibrosis           12           16


Mucosal ulceration                     14           11


Nasogastric tube feeding               11           11
(> 6 m after randomisation)


Chondritis                             17           22


Cartilage necrosis                     15           12
   tracheostomy                        4            5
   laryngectomy                        0            0
ARCON for larynx carcinoma, local control


Local control (%)

        100


         90


         80


         70


         60          ARCON
                     Acc. RT
         50
              0     12         24   36     48   60
                           Time (months)
ARCON for larynx carcinoma, regional control


Regional control (%)

        100


         90                                             p = 0.04


         80


         70


         60             ARCON
                        Acc. RT
         50
              0        12         24   36     48   60
                              Time (months)
ARCON for larynx carcinoma, survival


Survival (%)

        100


         90


         80


         70


         60         ARCON
                    Acc. RT
         50
               0   12         24   36     48    60
                          Time (months)
Pimonidazole: an exogenous marker of hypoxia
Hypoxic marker injection prior to biopsy
                                           well oxygenated tumor




    Immunohistochemical staining
                        Pimonidazole          hypoxic tumor




        Blood vessels
ARCON improves regional control in hypoxic tumors
              but not local control (N = 79)


                   well oxygenated           hypoxic

                                     92%                  93%
                                                          91%
                                     80%

local
control




                   well oxygenated           hypoxic
                                     96%                 100%
                                     92%



regional                                                 55%

control
ARCON vs Acc RT - Conclusions

• High local-regional control rates with ARCON and Acc RT.

• Equal levels of acute and late toxicity.

• No improvement of local tumor control rate
  (4 Gy lower dose in ARCON arm).

• Significant improvement of regional control rate
  (therapeutic gain).

• Oxygenation status of the primary tumor is predictive
  for outcome. ARCON is only effective in hypoxic
  tumors.
What about hemoglobin?
Pre-treatment Hb is associated with poor prognosis
                                      (larynx carcinomas)




                                                            high Hb



                                                            low Hb

                                         p = 0.007




Haugen et al., Clin Cancer Res 2004
Randomized trial with EPO
                           in H&N cancer patients with anemia

               Locoregional
             tumor control (%)
                       100

                           80
                                                   p = 0.04
                           60
                                                              placebo
                           40

                           20                              Epoetin β

                            0
                                0   12        24      36        48      60   72
                                         Time after treatment (months)
Henke et al, Lancet 2003
Randomized trial with blood transfusions
           in H&N cancer patients with anemia (DAHANCA 5)

                           100
  Locoregional
tumor control (%)
                             75

                                                      p = 0.04
                             50


                             25


                               0
                                     0    12      24       36     48     60
                                         Time after treatment (months)
Hoff et al, Radiother. Oncol. 2011
ARCON for T2-4 squamous cell carcinoma of the larynx
                           Randomization



  Accelerated Radiotherapy                Accelerated Radiotherapy
                                                      +
                                         carbogen and nicotinamide




 Fractionation schedule:



                               primary        metastatic nodes
         Acc. RT                68 Gy              68 Gy
         ARCON                 64 Gy*              68 Gy
Anemic patients have a worse outcome




                Accelerated RT
100

80

                                              20%
60

40

20                               normal Hb
          p < 0.01               low Hb
 0
      0        12      24   36    48     60
                       months
ARCON improves loco-regional control in anemic patients




                 Accelerated RT                                   ARCON
 100                                               100

  80                                               80

                                             20%
  60                                               60

  40                                               40

  20                            normal Hb          20                        normal Hb
           p < 0.01             low Hb                                       low Hb
   0                                                0
       0        12    24   36    48     60               0   12   24    36    48     60
                      months                                       months
and disease-free survival….




                Accelerated RT                                   ARCON
100                                               100

80                                                 80

60                                          24%    60

40                                                 40

20                             normal Hb           20                       normal Hb
          p < 0.01             low Hb                                       low Hb
 0                                                  0
      0        12    24   36    48     60               0   12   24    36    48     60
                     months                                       months
…but not overall survival.




                Accelerated RT                                   ARCON
100                                         100

 80                                          80

 60                                          60

 40                                          40

 20                            normal Hb     20                             normal Hb
          p < 0.01             low Hb                 p = 0.03              low Hb
 0                                           0
      0        12    24   36    48     60         0       12     24    36    48     60
                     months                                       months
Other prognostic clinical parameters

lysis:         N-stage
               WHO performance status



                                Locoregional     Disease-free      Overall
                                  control          survival        survival
 Multivariate analysis
 (p-value)                      AR      ARCON   AR      ARCON   AR      ARCON




 N-stage:      N0 vs. N+        < .01    .11    < .01     .02   < .01     .14



 Hemoglobin:   low vs. normal   < .01    .91    < .01     .21   .06       .02



 WHO perf.:    0 vs. 1          .54      .72    .99       .67   < .01     .15
Other prognostic clinical parameters

lysis:         N-stage
               WHO performance status



                                Locoregional     Disease-free      Overall
                                  control          survival        survival
 Multivariate analysis
 (p-value)                      AR      ARCON   AR      ARCON   AR      ARCON




 N-stage:      N0 vs. N+        < .01    .11    < .01     .02   < .01     .14



 Hemoglobin:   low vs. normal   < .01    .91    < .01     .21   .06       .02



 WHO perf.:    0 vs. 1          .54      .72    .99       .67   < .01     .15
Pimonidazole: an exogenous marker of hypoxia
Hypoxic marker injection prior to biopsy
                                           well oxygenated tumor




    Immunohistochemical staining
                        Pimonidazole          hypoxic tumor




        Blood vessels
No correlation between Hb and pimonidazole…


      1                             Normal values
                                      M: 8.5 – 11.0
                                      F: 7.5 – 10.0




   0.1




  0.01
   0.0001

            6   7   8    9    10   11     12
                    HB (mmol/ml)
Effect of carbogen breathing

                       air breathing                   carbogen breathing




                                        HF=16,3%                    HF=5,3%
                 hypoxia             vessels           hypoxia    vessels

Ljungkvist et al., Int J Radiat Oncol Biol Phys 2000
“Reduced cord radius theory” (D. Hirst 1986)


   Normal Hb


                             air breathing         carbogen breathing




   Anemic


                                             blood transfusion or erythropoietin




   Anemic


                             air breathing         carbogen breathing

Hirst, Int J Radiat Oncol Biol Phys 1986
ARCON in anemic patients - Conclusions

•   ARCON is the first treatment modality to demonstrate improved outcome
    in anemic patients.
ARCON in anemic patients - Conclusions

•   ARCON is the first treatment modality to demonstrate improved outcome
    in anemic patients.

•   But…, patients with low Hb do not have more hypoxic tumors.
ARCON in anemic patients - Conclusions

•   ARCON is the first treatment modality to demonstrate improved outcome
    in anemic patients.

•   But…, patients with low Hb do not have more hypoxic tumors.

•   Suggested mechanism:
    -   shorter O2 diffusion distances in tumors of anemic patients.
    -   no compensatory increase of tumor cord thickness with ARCON.
ARCON in anemic patients - Conclusions

•   ARCON is the first treatment modality to demonstrate improved outcome
    in anemic patients.

•   But…, patients with low Hb do not have more hypoxic tumors.

•   Suggested mechanism:
    -   shorter O2 diffusion distances in tumors of anemic patients.
    -   no compensatory increase of tumor cord thickness with ARCON.

•   Other potential mechanisms:
    -   increased plasma flow with low hematocrit (increased effect of
    carbogen, glycolytic switch).
    -   different effect of ARCON on red blood cell 2,3-DPG and
    subsequent O2 unloading in anemic patients.
    -   carboxyhemoglobin deblocking by carbogen in smokers.
Translational studies….
High EGFR-expression correlates with
           poor treatment outcome




Ang KK et al. Cancer Res 2002;62:7350-7356
EGFR-expression in larynx carcinoma




no expression   intermediate     high
EGFR-expression: intensity vs fraction


             Median EGFR fraction: 0.43
                   (0.003 – 0.93)
    180

    160

    140

    120

    100

     80

     60

     40
       0.0   0.2      0.4     0.6         0.8   1.0
                     EGFR fraction
Accelerated radiotherapy can improve outcome
              of high EGFR expressing tumors




Bentzen SM et al. Journal of Clinical Oncology 2005
Accelerated radiotherapy can improve outcome
              of high EGFR expressing tumors



                                                                Accelerated arm of larynx study
                                                      100


                                                       75


                                                       50


                                                       25
                                                                                       EGFR low
                                                                                       EGFR high
                                                        0
                                                            0       12     24     36    48        60
                                                                            months




Bentzen SM et al. Journal of Clinical Oncology 2005
ARCON can improve outcome
  of low EGFR expressing tumors
            100


            75



AR arm      50


            25
                                       EGFR low
                                       EGFR high
             0
                  0    12    24   36    48    60
                             months
            100


            75


ARCON arm   50


            25
                                       EGFR low
                  p = 0.02             EGFR high
             0
                  0    12    24   36    48    60
                             months
ARCON can improve LRC and DFS
             of low EGFR expressing tumors
100                                    100


 75                                    75


 50                                    50


 25                                    25
                           EGFR low                                EGFR low
      p = 0.02             EGFR high         p = 0.05              EGFR high
  0                                     0
      0    12    24   36    48    60         0    12    24    36    48    60
                 months                                  months
ARCON can improve LRC and DFS
                of low EGFR expressing tumors
   100                                           100


    75                                            75


    50                                            50


    25                                            25
                               EGFR low                                      EGFR low
         p = 0.02              EGFR high               p = 0.05              EGFR high
     0                                             0
         0    12    24    36    48     60              0    12    24    36    48     60
                    months                                         months

Independent prognostic factor in MV analysis (age, sex, T, N, subsite, grade, Hb, EGFR)
HR 2.43 (1.01 – 5.87), p = 0.05.
ARCON can improve LRC and DSS
                of low EGFR expressing tumors
   100                                           100


    75                                            75


    50                                            50


    25                                            25
                               EGFR low                                      EGFR low
         p = 0.02              EGFR high               p = 0.05              EGFR high
     0                                             0
         0    12    24    36    48     60              0    12    24    36    48     60
                    months                                         months

Independent prognostic factor in MV analysis (age, sex, T, N, subsite, grade, Hb, EGFR)
HR 2.43 (1.01 – 5.87), p = 0.05.


Why are high expressing EGFR tumors resistant to ARCON?
•better defense mechanisms after “O2-shock” and simultaneous radiotherapy?
•induction of HIF-1 pathway by EGFR through hypoxia-independent mechanisms?
•more rapid activation of DNA-repair processes?
Acknowledgements


• Nijmegen UMC St. Radboud                         • Groningen UMC
  G. Janssens                                        H. Bijl
  S. Rademakers
                                                   • Maastro Clinic
  I. Hoogsteen
                                                     P. van den Ende
  P. Span
  J. Bussink                                       • Leiden UMC
• Utrecht UMC                                        A. Chin
  Ch. Terhaard                                     • London Mt Vernon
• Amsterdam VUMC                                     M. Saunders
  P. Doornaert
  R. De Bree
                                                              Financial support:




                 Dutch Cooperative Head and Neck
                          Oncology Group

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Hypoxia as a target for personalized medicine

  • 1. ARCON for T2-4 laryngeal cancer: a phase III randomized trial Hans Kaanders Department of Radiation Oncology Radboud University Nijmegen Medical Centre The Netherlands
  • 2. ARCON Accelerated Radiotherapy + CarbOgen + Nicotinamide Tumor cell proliferation Chronic hypoxia Acute hypoxia S D D S S D S S S D S S D S S S S S D S S D S D S S S S D S D S S S S D S S S S S D S DS D D S S S S SS S D S D S S D S S S DS S S S S S D S SS S D S D D D S S S S S D S S S D D S D S S D S S D D D S D S D S S S S S D D D S D D S D S S S S S SS D S D S D D S S S SS S D S D D S S S S S S S D D S S SS D D S D D S S S D S SS S S D S S D S D D SS S D S D S D S S SS D S SS S D D S D S D D D SSD S S S S D D S D Carbogen Nicotinamide 98% O2 + 2% CO2 Accelerated fractionation S D DS S D S S S S S D S S S S S D SD S D S D S S S S D S D S S S S D S S S S S S stem cell D differentiated cell
  • 3. ARCON in a mouse mammary carcinoma Enhancement 2.1 ARCON ratio at the 2 TCD50 level conventional 1.9 accelerated carbogen - carbogen nicotinamide 1.8 relative to conventional 1.7 conventional radiotherapy 1.6 carbogen in air 1.5 1.4 1.3 accelerated 1.2 1.1 1 Rojas 1996
  • 4. ARCON, phase II trial in H&N cancer UMC Nijmegen Oct. 1993 – Oct. 2000 215 patients larynx: 100 Stage III-IV hypopharynx: 50 oropharynx: 52 Median follow-up: 68 months (37-127) oral cavity: 13
  • 5. ARCON phase II trial: high local control rates in T3-4 tumors Local control (%) 44 patients oropharynx larynx 79 patients hypopharynx oral cavity 21 patients 12 patients Time (months)
  • 6. Dutch multicenter randomized trial ARCON vs Accelerated RT in laryngeal carcinoma Secondary endpoints: • larynx preservation Primary objective: • regional control • To improve local tumor control • toxicity • quality of life • disease-free survival • overall survival Translational side study: Is the hypoxic status of the tumor predictive for outcome?
  • 7. ARCON for T2-4 squamous cell carcinoma of the larynx Randomization Accelerated Radiotherapy Accelerated Radiotherapy + carbogen and nicotinamide Fractionation schedule: primary metastatic nodes Acc. RT 68 Gy 68 Gy ARCON 64 Gy* 68 Gy *Aim: improve tumor control with equal toxicity between arms!
  • 8. Patient characteristics (N = 345) Standard Experimental arm arm Total 174 171 Female 39 30 Male 135 141 Mean age (SD) 61 (9.1) 62 (9.9) WHO performance status 0 140 137 1 34 33
  • 9. Tumor site and T/N-stage (UICC 1997) Standard Experimental arm arm Glottic 74 74 Supraglottic 100 97 T2 (advanced) 67 55 T3 80 95 T4 27 21 N0 117 115 N1 20 23 N2 37 33 N3 - -
  • 10. Acute toxicity: mucositis Patchy/confluent mucositis(%) ARCON Acc. RT Weeks after start of treatment
  • 11. Late toxicity Standard Experimental arm arm Severe subcutaneous fibrosis 12 16 Mucosal ulceration 14 11 Nasogastric tube feeding 11 11 (> 6 m after randomisation) Chondritis 17 22 Cartilage necrosis 15 12 tracheostomy 4 5 laryngectomy 0 0
  • 12. ARCON for larynx carcinoma, local control Local control (%) 100 90 80 70 60 ARCON Acc. RT 50 0 12 24 36 48 60 Time (months)
  • 13. ARCON for larynx carcinoma, regional control Regional control (%) 100 90 p = 0.04 80 70 60 ARCON Acc. RT 50 0 12 24 36 48 60 Time (months)
  • 14. ARCON for larynx carcinoma, survival Survival (%) 100 90 80 70 60 ARCON Acc. RT 50 0 12 24 36 48 60 Time (months)
  • 15. Pimonidazole: an exogenous marker of hypoxia Hypoxic marker injection prior to biopsy well oxygenated tumor Immunohistochemical staining Pimonidazole hypoxic tumor Blood vessels
  • 16. ARCON improves regional control in hypoxic tumors but not local control (N = 79) well oxygenated hypoxic 92% 93% 91% 80% local control well oxygenated hypoxic 96% 100% 92% regional 55% control
  • 17. ARCON vs Acc RT - Conclusions • High local-regional control rates with ARCON and Acc RT. • Equal levels of acute and late toxicity. • No improvement of local tumor control rate (4 Gy lower dose in ARCON arm). • Significant improvement of regional control rate (therapeutic gain). • Oxygenation status of the primary tumor is predictive for outcome. ARCON is only effective in hypoxic tumors.
  • 19. Pre-treatment Hb is associated with poor prognosis (larynx carcinomas) high Hb low Hb p = 0.007 Haugen et al., Clin Cancer Res 2004
  • 20. Randomized trial with EPO in H&N cancer patients with anemia Locoregional tumor control (%) 100 80 p = 0.04 60 placebo 40 20 Epoetin β 0 0 12 24 36 48 60 72 Time after treatment (months) Henke et al, Lancet 2003
  • 21. Randomized trial with blood transfusions in H&N cancer patients with anemia (DAHANCA 5) 100 Locoregional tumor control (%) 75 p = 0.04 50 25 0 0 12 24 36 48 60 Time after treatment (months) Hoff et al, Radiother. Oncol. 2011
  • 22. ARCON for T2-4 squamous cell carcinoma of the larynx Randomization Accelerated Radiotherapy Accelerated Radiotherapy + carbogen and nicotinamide Fractionation schedule: primary metastatic nodes Acc. RT 68 Gy 68 Gy ARCON 64 Gy* 68 Gy
  • 23. Anemic patients have a worse outcome Accelerated RT 100 80 20% 60 40 20 normal Hb p < 0.01 low Hb 0 0 12 24 36 48 60 months
  • 24. ARCON improves loco-regional control in anemic patients Accelerated RT ARCON 100 100 80 80 20% 60 60 40 40 20 normal Hb 20 normal Hb p < 0.01 low Hb low Hb 0 0 0 12 24 36 48 60 0 12 24 36 48 60 months months
  • 25. and disease-free survival…. Accelerated RT ARCON 100 100 80 80 60 24% 60 40 40 20 normal Hb 20 normal Hb p < 0.01 low Hb low Hb 0 0 0 12 24 36 48 60 0 12 24 36 48 60 months months
  • 26. …but not overall survival. Accelerated RT ARCON 100 100 80 80 60 60 40 40 20 normal Hb 20 normal Hb p < 0.01 low Hb p = 0.03 low Hb 0 0 0 12 24 36 48 60 0 12 24 36 48 60 months months
  • 27. Other prognostic clinical parameters lysis: N-stage WHO performance status Locoregional Disease-free Overall control survival survival Multivariate analysis (p-value) AR ARCON AR ARCON AR ARCON N-stage: N0 vs. N+ < .01 .11 < .01 .02 < .01 .14 Hemoglobin: low vs. normal < .01 .91 < .01 .21 .06 .02 WHO perf.: 0 vs. 1 .54 .72 .99 .67 < .01 .15
  • 28. Other prognostic clinical parameters lysis: N-stage WHO performance status Locoregional Disease-free Overall control survival survival Multivariate analysis (p-value) AR ARCON AR ARCON AR ARCON N-stage: N0 vs. N+ < .01 .11 < .01 .02 < .01 .14 Hemoglobin: low vs. normal < .01 .91 < .01 .21 .06 .02 WHO perf.: 0 vs. 1 .54 .72 .99 .67 < .01 .15
  • 29. Pimonidazole: an exogenous marker of hypoxia Hypoxic marker injection prior to biopsy well oxygenated tumor Immunohistochemical staining Pimonidazole hypoxic tumor Blood vessels
  • 30. No correlation between Hb and pimonidazole… 1 Normal values M: 8.5 – 11.0 F: 7.5 – 10.0 0.1 0.01 0.0001 6 7 8 9 10 11 12 HB (mmol/ml)
  • 31. Effect of carbogen breathing air breathing carbogen breathing HF=16,3% HF=5,3% hypoxia vessels hypoxia vessels Ljungkvist et al., Int J Radiat Oncol Biol Phys 2000
  • 32. “Reduced cord radius theory” (D. Hirst 1986) Normal Hb air breathing carbogen breathing Anemic blood transfusion or erythropoietin Anemic air breathing carbogen breathing Hirst, Int J Radiat Oncol Biol Phys 1986
  • 33. ARCON in anemic patients - Conclusions • ARCON is the first treatment modality to demonstrate improved outcome in anemic patients.
  • 34. ARCON in anemic patients - Conclusions • ARCON is the first treatment modality to demonstrate improved outcome in anemic patients. • But…, patients with low Hb do not have more hypoxic tumors.
  • 35. ARCON in anemic patients - Conclusions • ARCON is the first treatment modality to demonstrate improved outcome in anemic patients. • But…, patients with low Hb do not have more hypoxic tumors. • Suggested mechanism: - shorter O2 diffusion distances in tumors of anemic patients. - no compensatory increase of tumor cord thickness with ARCON.
  • 36. ARCON in anemic patients - Conclusions • ARCON is the first treatment modality to demonstrate improved outcome in anemic patients. • But…, patients with low Hb do not have more hypoxic tumors. • Suggested mechanism: - shorter O2 diffusion distances in tumors of anemic patients. - no compensatory increase of tumor cord thickness with ARCON. • Other potential mechanisms: - increased plasma flow with low hematocrit (increased effect of carbogen, glycolytic switch). - different effect of ARCON on red blood cell 2,3-DPG and subsequent O2 unloading in anemic patients. - carboxyhemoglobin deblocking by carbogen in smokers.
  • 38. High EGFR-expression correlates with poor treatment outcome Ang KK et al. Cancer Res 2002;62:7350-7356
  • 39. EGFR-expression in larynx carcinoma no expression intermediate high
  • 40. EGFR-expression: intensity vs fraction Median EGFR fraction: 0.43 (0.003 – 0.93) 180 160 140 120 100 80 60 40 0.0 0.2 0.4 0.6 0.8 1.0 EGFR fraction
  • 41. Accelerated radiotherapy can improve outcome of high EGFR expressing tumors Bentzen SM et al. Journal of Clinical Oncology 2005
  • 42. Accelerated radiotherapy can improve outcome of high EGFR expressing tumors Accelerated arm of larynx study 100 75 50 25 EGFR low EGFR high 0 0 12 24 36 48 60 months Bentzen SM et al. Journal of Clinical Oncology 2005
  • 43. ARCON can improve outcome of low EGFR expressing tumors 100 75 AR arm 50 25 EGFR low EGFR high 0 0 12 24 36 48 60 months 100 75 ARCON arm 50 25 EGFR low p = 0.02 EGFR high 0 0 12 24 36 48 60 months
  • 44. ARCON can improve LRC and DFS of low EGFR expressing tumors 100 100 75 75 50 50 25 25 EGFR low EGFR low p = 0.02 EGFR high p = 0.05 EGFR high 0 0 0 12 24 36 48 60 0 12 24 36 48 60 months months
  • 45. ARCON can improve LRC and DFS of low EGFR expressing tumors 100 100 75 75 50 50 25 25 EGFR low EGFR low p = 0.02 EGFR high p = 0.05 EGFR high 0 0 0 12 24 36 48 60 0 12 24 36 48 60 months months Independent prognostic factor in MV analysis (age, sex, T, N, subsite, grade, Hb, EGFR) HR 2.43 (1.01 – 5.87), p = 0.05.
  • 46. ARCON can improve LRC and DSS of low EGFR expressing tumors 100 100 75 75 50 50 25 25 EGFR low EGFR low p = 0.02 EGFR high p = 0.05 EGFR high 0 0 0 12 24 36 48 60 0 12 24 36 48 60 months months Independent prognostic factor in MV analysis (age, sex, T, N, subsite, grade, Hb, EGFR) HR 2.43 (1.01 – 5.87), p = 0.05. Why are high expressing EGFR tumors resistant to ARCON? •better defense mechanisms after “O2-shock” and simultaneous radiotherapy? •induction of HIF-1 pathway by EGFR through hypoxia-independent mechanisms? •more rapid activation of DNA-repair processes?
  • 47. Acknowledgements • Nijmegen UMC St. Radboud • Groningen UMC G. Janssens H. Bijl S. Rademakers • Maastro Clinic I. Hoogsteen P. van den Ende P. Span J. Bussink • Leiden UMC • Utrecht UMC A. Chin Ch. Terhaard • London Mt Vernon • Amsterdam VUMC M. Saunders P. Doornaert R. De Bree Financial support: Dutch Cooperative Head and Neck Oncology Group

Notas del editor

  1. Mercury
  2. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  3. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  4. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  5. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  6. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  7. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  8. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  9. Mercury
  10. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.
  11. The EGFR expression was limited to the cell membrane. We found a large variation of the EGFR fractions between the biopsies. Here you can see examples of tumorcells with no expression of EGFR, intermediate expression and high expression. Besides a variation in overall fractions, we also observed a variation in the intensity of the staining.
  12. But overall, we found a good correlation between intensity and fraction EGFR. Biopsies with high overall expression also showed a mean high intensity. Therefore, patients were dichotomized in two groups based on low and high EGFR fractions and correlated with outcome. We did not found a correlation bewteen EGFR fraction and clinical parameters such as T&amp;N stage and differentiation.