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Neoadjuvant Therapy for
Esophageal Cancer
Daniel Morgensztern, M.D.
Overview
• Background
• Neoadjuvant radiotherapy
• Neoadjuvant chemotherapy
• Neoadjuvant chemoradiotherapy
• Neoadjuvant or definitive chemoradiotherapy
• The significance of pathologic CR
• Strategies to improve outcome
• Conclusions
Epidemiology
Worldwide
Worldwide estimates for 2000
• Eight most common cancer
with 412,000 new cases
• Sixth most common cause of
cancer death with 338,000
deaths
• 2002 update
462,000 new cases
386,000 deaths
Parkin DM, Lancet Oncol 2001; 2: 533-543
Parkin DM, CA Cancer J Clin. 2005;55:74-108
Epidemiology
US
US estimates for 2005
• 14,520 new cases
- 11,220 male
- 3,300 female
• 13,570 deaths
Jemal A CA Cancer J Clin. 2005;55:10-30
AJCC Staging
T Stage
AJCC Staging
N stage
AJCC Staging and Prognosis After Complete
Surgical Removal of the Tumor
Ezinger PC, N Engl J Med 2003; 349:2241-2252
Neoadjuvant Radiotherapy
Rationale
• Decrease tumor size with potential increase in resectability
• Improve local control
• Decrease the number of viable cells with possible minimization of
intraoperative spilling
Disadvantages
• No effect in micrometastatic disease
• Delay in definitive therapy
Neoadjuvant Radiotherapy
Randomized Trials
Study Patients Dose of RT Median survival (months) 5-year survival (%) p Value
Launois (1981) RT + S 62
S 47
40 Gy 10
12
10
12
NS
Gignoux (1988) RT + S 115
S 114
33 Gy 48
45
10
9
NS
Wang (1989) RT + S 104
S 102
40 Gy NA
NA
35
30
NS
Arnott (1992) RT + S 90
S 86
20 Gy 8
8
9
17
NS
Fok (1994) RT + S 58
S 50
35-53 Gy 11
22
10
16
NS
Neoadjuvant Radiotherapy
Meta-analysis
Oesophageal Cancer Collaborative Group
- 5 trials including 1147 patients
- Increased 2-year survival from 30% to 34% (95% CI 0-9%)
- Increased 5-year survival from 15% to 18% (95% CI 0-8%)
Arnott SJ, Int J Radiat Oncol Biol Phys 1998; 41: 579-583
Arnott SJ, Cochrane Database Syst Rev 2000; 4: CD001799
Neoadjuvant chemotherapy
Rationale
• Downstage of the disease with potential increase in resectability
• Improvement in local control
• Eradication of micrometastatic disease
• Pathologic evaluation of treatment response with possible selection of adjuvant
therapy
Disadvantages
• Delay in definitive therapy with risk of disease spreading
• Limited efficacy of the available chemotherapeutic agents
Neoadjuvant chemotherapy
Randomized Trials
Study (year) Patients Chemotherapy pCR (%) Median
Survival (mo)
5-year
Survival (%)
P value
Roth (1988) C + S 19
S 20
Neo: C,Vin, Bleo
Adjuvant: C,
Vin
NA 9
9
NA
NA
NS
Nygaard (1992) C + S 50
S 41
C, Bleo NA 8
8
3-y 3
9
NS
Ancona (2001) C + S 47
S 47
CF X 2 or 3 13% 25
24
34
22
NS
Schlag (1992) C + S 22
S 24
CF X 3 NA 10
10
NA NS
INT 0113 (1998) C + S 213
S 227
Neo CF X 3
Adj CF X 2
2.5% 14.9
16.1
2 y 35
37
NS
MRC (2002) C + S 400
S 402
CF X 2 4% 16.8
13.3
2 y 43
34
P = 0.004
Neoadjuvant chemotherapy
INT 0113 and MRC Trials
INT (S) INT (CS) MRC (S) MRC (CS)
Patients
S (%)/A (%)
227
47/53
213
46/54
401
31/67
400
31/66
Chemotherapy ----------- C 100 D1, F 1000 D1-5
q4wX3
Adjuvant C 75 F 1000 X 2
------------ C 80 D1, F 1000 D1-4 q3wX2
Percentage receiving all
neoadjuvant therapy
----------- 71 ------------ 90
Surgery (%)
R0 (%)
92
59
80
62
97
54
92
60
pCR ----------- 2.5% ------------ 4%
Median time to surgery
(days)
9 93 16 63
Median survival (months) 16.2 14.9 13.3 16.8
2-year survival (%) 37 35 34 43
Neoadjuvant chemotherapy
Meta-analysis
Cochrane Database 2003
• 11 Randomized trials involving 2051 patients
• Clinical relevance based on median survival and 1 to 5
year survival
• When specific survival was not available, it was
calculated from the published survival curves
- Pooled response rate to chemotherapy was about 36%
with 3% pCR
- No difference in survival at 1 and 2 years
- Survival advantage starts at 3 years and reaches
statistical significance at 5 years
Cochrane Database Syst Rev 2003; 4: CD001556
Neoadjuvant chemotherapy
MAGIC Trial
Cunningham ASCO 2005
Neoadjuvant chemotherapy
MAGIC Trial
• Overall, both median survival (24 m vs 20 m) and
5-year OS (36 vs 23%) favored neoadjuvant
therapy
• On multivariate analysis, treatment effect was
unchanged after adjustment for primary site
• Perioperative chemotherapy significantly
increased both PFS and OS in patients with gastric
or lower esophageal cancer
Neoadjuvant Chemoradiotherapy
Rationale
• Combine the benefits from both therapeutic modalities: Downstage of the
tumor facilitating surgical resection and eradication of micrometastatic disease
• Increase the number of pathologic complete remissions which may translate
into improved survival
Disadvantages
• Patients may not undergo surgery due to toxicity or tumor progression
• Increased post-operative mortality
Neoadjuvant Chemoradiotherapy
Non-Randomized Trials
• 46 trials from 1981 to 1999
• 2704 patients – 69% SCC, 31% Adenocarcinoma
• RT dose from 30 to 60 Gy
• Majority of studies used 5-FU and cisplatin
• Resection rate 74%
• Pathologic CR: 24% (32% surgical patients)
• Patterns of recurrence after surgical resection
- Locoregional 9%
- Distant 31%
- Both 6%
Geh JI, Br J Surg 2001; 88:338-356.
Neoadjuvant Chemoradiotherapy
Randomized Trials
Study Patients Histology Chemotherapy
RT
Surgical
mortality
(%)
pCR (%) Median
Survival (mo)
3-year survival
(%)
P value
Nygaard
(1992)
S 41
CS 47
S Cis + Bleo
35 Gy
13
24
NA 7.5
7.5
9
17
NS
Le Prise (1994) S 45
CS 41
S Cis + 5-FU
20 Gy
7
8.5
10 10
10
14
19
NS
Apinop (1994) S 34
CS 35
S Cis + 5-FU
40 Gy
15
14
7
10
20
26
NS
Walsh (1996) S 55
CS 58
A Cis + FU
40 Gy
4
8
22 11
16
6
32
P = 0.01
Law (1998) S 30
CS 30
S Cis + 5-FU
40 Gy
0
0
25 27
26
NA
NA
NS
Bosset (1997) S 139
CS 143
S Cis
37 Gy
4
12.3
26 19
19
37
39
NS
Urba (2001) S 50
CS 50
S (25%)
A (75%)
Cis + 5-Fu + Vin
45 Gy
2
7
28 18
17
16
30
NS
Burmeister
(2002)
S 128
CS 128
S (36%)
A (61%)
Cis + 5-FU
35 Gy
NA 15% 22
19
NA
NA
NS
Neoadjuvant Chemoradiotherapy
Meta-analyses
Urschel J, Am J Surg 2003; 185: 538-543
- Neoadjuvant chemoradiation improves 3-year survival, with more
significant benefit in the concurrent studies (OR 0.45, 95% CI 0.26
to 0.79, p = 0.005)
- Decrease LR but not distant recurrences
Fiorica F, Gut 2004;53: 925-930
- Neoadjuvant chemoradiotherapy significantly reduces the 3-year
mortality rate (OR 0.53, 95% CI 0.26 to 0.72, p = 0.03)
- Risk of postoperative mortality is higher in the neoadjuvant
group ( OR 2.10, 95% CI 1.18-3.73, p = 0.01)
Greer SE, Surgery 2005; 137: 172-177
- Neoadjuvant chemoradiotherapy is associated with a small, non-
statistically significant improvement in overall survival (RR of
death in neoadjuvant group 0.86, 95% CI 0.74 to 1.01, p = 0.07)
Malthaner RA, BMC Med 2004; 2: 35
A significant difference in the risk of mortality at 3-years favors
neoadjuvant chemoradiation (RR 0.87, 95% CI 0.80-0.96, p =0.004)
*None of the meta-analysis included Burmeister’s
study, which has been recently published (Lancet
Oncol 2005) and at that time was available only in
abstract form
The Role of Surgery after
Chemoradiotherapy
• The 5-year survival for chemoradiotherapy in
patients with unresectable locally advanced
esophageal cancer was 26% in the RTOG 85-01
trial
• The subsequent INT 0123 showed a 2-year survival
of 40% in the control standard-dose RT arm
• These results are similar to those achieved with
surgery alone or neoadjuvant chemoratiotherapy
followed by surgery
Cooper JS, JAMA 1999; 281: 1623-1627
Minsky BD, J Clin Oncol 2002; 20: 1167-1174
INT 0123
The Role of Surgery after
Chemoradiotherapy
FFCD 9102 Bedenne ASCO 2002 (abstract # 519)
FC X 2 + RT
Responders randomized to S or additional CRT
S CRT
2-year OS 34% 40% OR 0.91, p = 0.56
Median survival 17.7 m 19.3m
• No significant difference in survival
• Surgery was associated with improved local control
- Decreased use of stent (13% versus 27% ; p = 0.005)
- Decrease use of dilations (22% versus 32% ; p = 0.07)
The Role of Surgery after
Chemoradiotherapy
GOCSG Stahl M, J Clin Oncol 2005; 23: 2310-2317
FLEP X 3 → EP + 40 Gy → surgery (89 patients)
FLEP X 3 → EP + > 66Gy (88 patients)
S CRT
3-year OS 31.3% 24.4%
Median survival 16.4 m 14.9 m
- CRT resulted in equivalent survival with preserved
esophagus
- Surgery significantly increased local control
- Survival curves appear to spread after 3 years but without
reaching statistical significance
- Patients responding to induction therapy appear to have
good prognosis regardless of surgical intervention
OS
S
CRT
FLRP
S
CRT
Pathologic CR
• Pathologic CR in randomized clinical trials
- Neoadjuvant chemotherapy – 2.5% to 15%
- Neoadjuvant chemoradiotherapy – 10% to 28%
• Several trials have demonstrated improved survival in patients
achieving pCR
Pathologic CR
Study Patients who
underwent surgery
Median survival (mo) Survival (%) P value
Urba (2001) pCR 14
No pCR 36
49.7
12
3y 64
19
P = 0.01
Chirieac (2005) pCR 77
No pCR 158
133
10.5 to 38.1
5y 65
29
P = 0.003
Swisher (2005) pCR 86
PR 98
> 50% Residual 53
3y 74
54
24
P < 0.001
Berger (2005) pCR 42
PR 13
No response 76
50
49
25
5y 48
34
15
P = 0.015
New Strategies
• Incorporation of new chemotherapy agents
Taxanes, irinotecan, oxaliplatin
• Addition of a targeted agent
- COX-2 inhibitors, EGFR inhibitors, bevacizumab
• Intensification of neoadjuvant therapy
- Triplets with concomitant RT (CF + taxane)
- Triplets without RT (ECF, CF + taxane)
• Induction chemotherapy followed by concomitant chemoratiotherapy
Conclusions
• Surgery remains the mainstay for a curative approach in esophageal cancer
• Neoadjuvant RT does not appear to decrease local relapse or improve survival
in patients with resectable esophageal cancer
• The role of neoadjuvant chemotherapy remains undefined with a small 5-year
benefit obtained in a meta-analysis but conflicting results from two large
randomized trials
• The impact of the MAGIC trial is unclear due to the small number of patients
with esophageal cancer
• NCCN v1.2005: Preoperative chemotherapy is not recommended as the
standard of care
Conclusions
• Neoadjuvant chemoradiotherapy has been widely accepted in US despite the
lack of conclusive evidence from phase III trials
 The confirmatory trial CALGB 9781 was terminated early due to poor accrual
• Benefit from trimodality therapy may be restricted to patients achieving
significant response or pCR and non-responders may have worse outcome
compared with patients treated with surgery only
• Small benefit observed in the 4 published meta-analysis may change with the
inclusion of Burmeister’s study
 Ongoing Cochrane review
• NCCN v1.2005: Although neoadjuvant chemoradiotherapy represents a
reasonable approach, it remains investigational due to conflicting results from
RCTs
Conclusions
• Surgery following neoadjuvant chemoratiotherapy improves
local and regional control but not overall survival
• Post-therapy pathologic status may be a better predictor for
outcome than the baseline clinical AJCC staging system
• The pathologic status achieved with neoadjuvant therapy may
provide an early surrogate benchmark to speed up comparative
trials
Conclusions
• Distant relapse continues to be a major challenge in patients
presenting with locally advanced disease
• More intense chemotherapy regimens using third-generation
agents may increase the eradication of micrometastatic disease
• Patients treated with induction chemotherapy may benefit from
early evaluation of response to avoid unnecessary delays in
surgery
• Larger randomized trials of neoadjuvant chemotherapy or
chemoradiotherapy are needed to identify optimal regimens
capable of producing higher pCR rates with acceptable toxicity

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Neoadjuvant therapy for esophageal cancer

  • 1. Neoadjuvant Therapy for Esophageal Cancer Daniel Morgensztern, M.D.
  • 2. Overview • Background • Neoadjuvant radiotherapy • Neoadjuvant chemotherapy • Neoadjuvant chemoradiotherapy • Neoadjuvant or definitive chemoradiotherapy • The significance of pathologic CR • Strategies to improve outcome • Conclusions
  • 3. Epidemiology Worldwide Worldwide estimates for 2000 • Eight most common cancer with 412,000 new cases • Sixth most common cause of cancer death with 338,000 deaths • 2002 update 462,000 new cases 386,000 deaths Parkin DM, Lancet Oncol 2001; 2: 533-543 Parkin DM, CA Cancer J Clin. 2005;55:74-108
  • 4. Epidemiology US US estimates for 2005 • 14,520 new cases - 11,220 male - 3,300 female • 13,570 deaths Jemal A CA Cancer J Clin. 2005;55:10-30
  • 7. AJCC Staging and Prognosis After Complete Surgical Removal of the Tumor Ezinger PC, N Engl J Med 2003; 349:2241-2252
  • 8. Neoadjuvant Radiotherapy Rationale • Decrease tumor size with potential increase in resectability • Improve local control • Decrease the number of viable cells with possible minimization of intraoperative spilling Disadvantages • No effect in micrometastatic disease • Delay in definitive therapy
  • 9. Neoadjuvant Radiotherapy Randomized Trials Study Patients Dose of RT Median survival (months) 5-year survival (%) p Value Launois (1981) RT + S 62 S 47 40 Gy 10 12 10 12 NS Gignoux (1988) RT + S 115 S 114 33 Gy 48 45 10 9 NS Wang (1989) RT + S 104 S 102 40 Gy NA NA 35 30 NS Arnott (1992) RT + S 90 S 86 20 Gy 8 8 9 17 NS Fok (1994) RT + S 58 S 50 35-53 Gy 11 22 10 16 NS
  • 10. Neoadjuvant Radiotherapy Meta-analysis Oesophageal Cancer Collaborative Group - 5 trials including 1147 patients - Increased 2-year survival from 30% to 34% (95% CI 0-9%) - Increased 5-year survival from 15% to 18% (95% CI 0-8%) Arnott SJ, Int J Radiat Oncol Biol Phys 1998; 41: 579-583 Arnott SJ, Cochrane Database Syst Rev 2000; 4: CD001799
  • 11. Neoadjuvant chemotherapy Rationale • Downstage of the disease with potential increase in resectability • Improvement in local control • Eradication of micrometastatic disease • Pathologic evaluation of treatment response with possible selection of adjuvant therapy Disadvantages • Delay in definitive therapy with risk of disease spreading • Limited efficacy of the available chemotherapeutic agents
  • 12. Neoadjuvant chemotherapy Randomized Trials Study (year) Patients Chemotherapy pCR (%) Median Survival (mo) 5-year Survival (%) P value Roth (1988) C + S 19 S 20 Neo: C,Vin, Bleo Adjuvant: C, Vin NA 9 9 NA NA NS Nygaard (1992) C + S 50 S 41 C, Bleo NA 8 8 3-y 3 9 NS Ancona (2001) C + S 47 S 47 CF X 2 or 3 13% 25 24 34 22 NS Schlag (1992) C + S 22 S 24 CF X 3 NA 10 10 NA NS INT 0113 (1998) C + S 213 S 227 Neo CF X 3 Adj CF X 2 2.5% 14.9 16.1 2 y 35 37 NS MRC (2002) C + S 400 S 402 CF X 2 4% 16.8 13.3 2 y 43 34 P = 0.004
  • 13. Neoadjuvant chemotherapy INT 0113 and MRC Trials INT (S) INT (CS) MRC (S) MRC (CS) Patients S (%)/A (%) 227 47/53 213 46/54 401 31/67 400 31/66 Chemotherapy ----------- C 100 D1, F 1000 D1-5 q4wX3 Adjuvant C 75 F 1000 X 2 ------------ C 80 D1, F 1000 D1-4 q3wX2 Percentage receiving all neoadjuvant therapy ----------- 71 ------------ 90 Surgery (%) R0 (%) 92 59 80 62 97 54 92 60 pCR ----------- 2.5% ------------ 4% Median time to surgery (days) 9 93 16 63 Median survival (months) 16.2 14.9 13.3 16.8 2-year survival (%) 37 35 34 43
  • 14. Neoadjuvant chemotherapy Meta-analysis Cochrane Database 2003 • 11 Randomized trials involving 2051 patients • Clinical relevance based on median survival and 1 to 5 year survival • When specific survival was not available, it was calculated from the published survival curves - Pooled response rate to chemotherapy was about 36% with 3% pCR - No difference in survival at 1 and 2 years - Survival advantage starts at 3 years and reaches statistical significance at 5 years Cochrane Database Syst Rev 2003; 4: CD001556
  • 16. Neoadjuvant chemotherapy MAGIC Trial • Overall, both median survival (24 m vs 20 m) and 5-year OS (36 vs 23%) favored neoadjuvant therapy • On multivariate analysis, treatment effect was unchanged after adjustment for primary site • Perioperative chemotherapy significantly increased both PFS and OS in patients with gastric or lower esophageal cancer
  • 17. Neoadjuvant Chemoradiotherapy Rationale • Combine the benefits from both therapeutic modalities: Downstage of the tumor facilitating surgical resection and eradication of micrometastatic disease • Increase the number of pathologic complete remissions which may translate into improved survival Disadvantages • Patients may not undergo surgery due to toxicity or tumor progression • Increased post-operative mortality
  • 18. Neoadjuvant Chemoradiotherapy Non-Randomized Trials • 46 trials from 1981 to 1999 • 2704 patients – 69% SCC, 31% Adenocarcinoma • RT dose from 30 to 60 Gy • Majority of studies used 5-FU and cisplatin • Resection rate 74% • Pathologic CR: 24% (32% surgical patients) • Patterns of recurrence after surgical resection - Locoregional 9% - Distant 31% - Both 6% Geh JI, Br J Surg 2001; 88:338-356.
  • 19. Neoadjuvant Chemoradiotherapy Randomized Trials Study Patients Histology Chemotherapy RT Surgical mortality (%) pCR (%) Median Survival (mo) 3-year survival (%) P value Nygaard (1992) S 41 CS 47 S Cis + Bleo 35 Gy 13 24 NA 7.5 7.5 9 17 NS Le Prise (1994) S 45 CS 41 S Cis + 5-FU 20 Gy 7 8.5 10 10 10 14 19 NS Apinop (1994) S 34 CS 35 S Cis + 5-FU 40 Gy 15 14 7 10 20 26 NS Walsh (1996) S 55 CS 58 A Cis + FU 40 Gy 4 8 22 11 16 6 32 P = 0.01 Law (1998) S 30 CS 30 S Cis + 5-FU 40 Gy 0 0 25 27 26 NA NA NS Bosset (1997) S 139 CS 143 S Cis 37 Gy 4 12.3 26 19 19 37 39 NS Urba (2001) S 50 CS 50 S (25%) A (75%) Cis + 5-Fu + Vin 45 Gy 2 7 28 18 17 16 30 NS Burmeister (2002) S 128 CS 128 S (36%) A (61%) Cis + 5-FU 35 Gy NA 15% 22 19 NA NA NS
  • 20. Neoadjuvant Chemoradiotherapy Meta-analyses Urschel J, Am J Surg 2003; 185: 538-543 - Neoadjuvant chemoradiation improves 3-year survival, with more significant benefit in the concurrent studies (OR 0.45, 95% CI 0.26 to 0.79, p = 0.005) - Decrease LR but not distant recurrences Fiorica F, Gut 2004;53: 925-930 - Neoadjuvant chemoradiotherapy significantly reduces the 3-year mortality rate (OR 0.53, 95% CI 0.26 to 0.72, p = 0.03) - Risk of postoperative mortality is higher in the neoadjuvant group ( OR 2.10, 95% CI 1.18-3.73, p = 0.01) Greer SE, Surgery 2005; 137: 172-177 - Neoadjuvant chemoradiotherapy is associated with a small, non- statistically significant improvement in overall survival (RR of death in neoadjuvant group 0.86, 95% CI 0.74 to 1.01, p = 0.07) Malthaner RA, BMC Med 2004; 2: 35 A significant difference in the risk of mortality at 3-years favors neoadjuvant chemoradiation (RR 0.87, 95% CI 0.80-0.96, p =0.004) *None of the meta-analysis included Burmeister’s study, which has been recently published (Lancet Oncol 2005) and at that time was available only in abstract form
  • 21. The Role of Surgery after Chemoradiotherapy • The 5-year survival for chemoradiotherapy in patients with unresectable locally advanced esophageal cancer was 26% in the RTOG 85-01 trial • The subsequent INT 0123 showed a 2-year survival of 40% in the control standard-dose RT arm • These results are similar to those achieved with surgery alone or neoadjuvant chemoratiotherapy followed by surgery Cooper JS, JAMA 1999; 281: 1623-1627 Minsky BD, J Clin Oncol 2002; 20: 1167-1174 INT 0123
  • 22. The Role of Surgery after Chemoradiotherapy FFCD 9102 Bedenne ASCO 2002 (abstract # 519) FC X 2 + RT Responders randomized to S or additional CRT S CRT 2-year OS 34% 40% OR 0.91, p = 0.56 Median survival 17.7 m 19.3m • No significant difference in survival • Surgery was associated with improved local control - Decreased use of stent (13% versus 27% ; p = 0.005) - Decrease use of dilations (22% versus 32% ; p = 0.07)
  • 23. The Role of Surgery after Chemoradiotherapy GOCSG Stahl M, J Clin Oncol 2005; 23: 2310-2317 FLEP X 3 → EP + 40 Gy → surgery (89 patients) FLEP X 3 → EP + > 66Gy (88 patients) S CRT 3-year OS 31.3% 24.4% Median survival 16.4 m 14.9 m - CRT resulted in equivalent survival with preserved esophagus - Surgery significantly increased local control - Survival curves appear to spread after 3 years but without reaching statistical significance - Patients responding to induction therapy appear to have good prognosis regardless of surgical intervention OS S CRT FLRP S CRT
  • 24. Pathologic CR • Pathologic CR in randomized clinical trials - Neoadjuvant chemotherapy – 2.5% to 15% - Neoadjuvant chemoradiotherapy – 10% to 28% • Several trials have demonstrated improved survival in patients achieving pCR
  • 25. Pathologic CR Study Patients who underwent surgery Median survival (mo) Survival (%) P value Urba (2001) pCR 14 No pCR 36 49.7 12 3y 64 19 P = 0.01 Chirieac (2005) pCR 77 No pCR 158 133 10.5 to 38.1 5y 65 29 P = 0.003 Swisher (2005) pCR 86 PR 98 > 50% Residual 53 3y 74 54 24 P < 0.001 Berger (2005) pCR 42 PR 13 No response 76 50 49 25 5y 48 34 15 P = 0.015
  • 26. New Strategies • Incorporation of new chemotherapy agents Taxanes, irinotecan, oxaliplatin • Addition of a targeted agent - COX-2 inhibitors, EGFR inhibitors, bevacizumab • Intensification of neoadjuvant therapy - Triplets with concomitant RT (CF + taxane) - Triplets without RT (ECF, CF + taxane) • Induction chemotherapy followed by concomitant chemoratiotherapy
  • 27. Conclusions • Surgery remains the mainstay for a curative approach in esophageal cancer • Neoadjuvant RT does not appear to decrease local relapse or improve survival in patients with resectable esophageal cancer • The role of neoadjuvant chemotherapy remains undefined with a small 5-year benefit obtained in a meta-analysis but conflicting results from two large randomized trials • The impact of the MAGIC trial is unclear due to the small number of patients with esophageal cancer • NCCN v1.2005: Preoperative chemotherapy is not recommended as the standard of care
  • 28. Conclusions • Neoadjuvant chemoradiotherapy has been widely accepted in US despite the lack of conclusive evidence from phase III trials  The confirmatory trial CALGB 9781 was terminated early due to poor accrual • Benefit from trimodality therapy may be restricted to patients achieving significant response or pCR and non-responders may have worse outcome compared with patients treated with surgery only • Small benefit observed in the 4 published meta-analysis may change with the inclusion of Burmeister’s study  Ongoing Cochrane review • NCCN v1.2005: Although neoadjuvant chemoradiotherapy represents a reasonable approach, it remains investigational due to conflicting results from RCTs
  • 29. Conclusions • Surgery following neoadjuvant chemoratiotherapy improves local and regional control but not overall survival • Post-therapy pathologic status may be a better predictor for outcome than the baseline clinical AJCC staging system • The pathologic status achieved with neoadjuvant therapy may provide an early surrogate benchmark to speed up comparative trials
  • 30. Conclusions • Distant relapse continues to be a major challenge in patients presenting with locally advanced disease • More intense chemotherapy regimens using third-generation agents may increase the eradication of micrometastatic disease • Patients treated with induction chemotherapy may benefit from early evaluation of response to avoid unnecessary delays in surgery • Larger randomized trials of neoadjuvant chemotherapy or chemoradiotherapy are needed to identify optimal regimens capable of producing higher pCR rates with acceptable toxicity