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Published byEthel Gregory Modified over 9 years ago
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CA Esophagus – Role of Chemoirradiation WH Chan Pamela Youde Nethersole Eastern Hospital
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Ca Esophagus Incidence: 4.5 cases per 100,000 in one year in Europe 1 8th commonest cause of cancer death in 2011 in HK (4.8 per 100,000) 2 Squamous cell carcinoma Adenocarcinoma 1.Esophageal Cancer: ESMO Clinical Practice Guidelines for Diagnosis, Treatment and Follow-up. M. Stahl; C. Mariette; K. Haustermans; A. Cervantes & D. Arnold, on behalf of the ESMO Guidelines Working Groups. Annals of Oncology 24 (Supplement 6), vi51-vi56, 2013 2.Hong Kong Cancer Registry
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Surgery High morbidity and mortality Worsened physical function, social function, long lasting deterioration in health-related quality of life 3 Recurrence Complete Resection may not be possible 3. Meta-analysis shows clinically relevant and long-lasting deterioration in health-related quality of life after esophageal cancer surgery. M. Jacobs; R.C. Macefield; R.G. Elbers; M.A.G. Sprangers. Qual Life Res (2014) 23: 1155-1176
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286 patients had surgery alone Median FU period: 49 months 30-day mortality: 3.7% Recurrence: - Stage I: 7.1%; Stage II/III/IV: 50.5% 5 year disease free survival: - Stage I: 76.3%; Stage II/III/IV: 30.8%
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Chemoirradiation Introduced in 1980s 5-FU, cisplatin Radiation of 40-50 Gy Improves survival, complete resection rate Surgically not fit patient ?Increase surgical morbidity
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20 RCTs were included 9 comparing neoadjuvant CRT vs surgery 8 comparing neoadjuvant chemotherapy vs surgery 3 comparing definitive CRT vs surgery
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Neoadjuvant CRT vs surgery alone 9 RCTs included 1099 patients: 554 received neoadjuvant CRT, 545 received surgery alone Mean age 60.8 Surgery performed 2-8 weeks after CRT (mean 3 weeks) Median FU time: 10-98 months
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R0 resection rate p-value = 0.043
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Morbidity p-value = 0.363
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30-day mortality p-value = 0.692
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Overall survival p-value = 0.008
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Conclusion Neoadjuvant chemoradiotherapy improved R0 resection and overall survival, but does not increase post-op morbidity or mortality
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Definitive chemoRT vs surgery 3 RCTs included All squamous cell carcinoma 512 patients: 252 received definitive chemoRT; 260 received surgery
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Morbidity p-value = 0.332
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30-day mortality p-value = 0.007
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Overall survival
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Conclusion Definitive chemoRT has lower 30-day mortality compared with surgery, but overall survival is similar
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Neoadjuvant chemotherapy vs surgery Neoadjuvant chemotherapy improved R0 resection rate, but no improvement in overall survival
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Definitive chemoirradiation Efficacy Tolerance and toxicity Any new regimen
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Traditionally is radiotherapy + 5-FU + cisplatin Cisplatin is difficult to administer as requiring prolonged hydration, nephrotoxic, emetogenic
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Study period 2004-2011 Exclusion: Metastasis Contraindication to chemoRT: tracheoesophageal fistula, recent AMI, etc 131 patients in FOLFOX; 128 patients in 5- FU + cisplatin
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Regimen Radiotherapy: 50Gy in 25 fractions Chemotherapy: FOLFOX: 6 cycles (each cycle 2 days), one cycle every 2 week, first 3 cycles concurrent with RT 5-FU + cisplatin: 4 cycles (each cycle 4 days), first 2 cycles with RT Completion rate: FOLFOX: 90/131 (68.7%) 5-FU + cisplatin: 96/128 (75%)
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No difference in progression free or overall survival Median survival: FOLFOX 20.2 months 5-FU + cisplatin 17.5 months P = 0.70
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Morbidity FOLFOX group: More paraesthesia, sensory neuropathy, elevation of liver enzyme 5-FU + cisplatin group: More mucositis, alopecia, renal impairment
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Mortality 1 in FOLFOX group (0.76%): pneumopathy plus denutrition 6 in 5-FU + cisplatin group (4.69%): 5 neutropenic sepsis, 1 cardiac ischemia p-value = 0.066
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Conclusion FOLFOX is a more convenient option, similar efficacy to 5-FU + cisplatin, with probably lower mortality
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New development
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Retrospective review 204 patients: 75 had neoadjuvant chemoRT, 129 had surgery alone Propensity score matching: 75 patients in each group with similar demographics and tumor staging 41.4 Gy, Paclitaxel and carboplatin
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Neoadjuvant chemoRT had better disease free and overall survival
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Distant recurrence Locoregional recurrence Complete Response
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Neoadjuvant chemoRT could improve disease free survival, overall survival and locoregional recurrence free survival Not improved distant recurrence free survival
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Future Development Any method to predict complete response to chemoRT EGFR inhibitors, HER-2 receptor inhibitors Adjuvant agents to reduce distant metastases
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Conclusion Neoadjuvant chemoirradiation improves survival of CA esophagus without increasing post-op morbidities Definitive chemoRT is an effective alternative to patients who are not fit for surgery New agents are needed to improve the complete response rate and survival of patients
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Reference 1. Esophageal Cancer: ESMO Clinical Practice Guidelines for Diagnosis, Treatment and Follow-up. M. Stahl; C. Mariette; K. Haustermans; A. Cervantes & D. Arnold, on behalf of the ESMO Guidelines Working Groups. Annals of Oncology 24 (Supplement 6), vi51- vi56, 2013 2. Meta-analysis shows clinically relevant and long-lasting deterioration in health-related quality of life after esophageal cancer surgery. M. Jacobs; R.C. Macefield; R.G. Elbers; M.A.G. Sprangers. Qual Life Res (2014) 23: 1155-1176 3. Meta-analysis of neoadjuvant treatment modalities and definitive non-surgical therapy for esophageal squamous cell cancer. M. Kranzfelder; T. Schuster; H. Geinitz; H. Friess; P. Buchler. British Journal of Surgery 2011; 98: 768-783 4. Definitive chemoradiotherapy with FOLFOX versus fluorouracil and cisplatin in patients with esophageal cancer (PRODIGE5/ACCORD17): final results of a randomized phase 2/3 trial. Thierry Conroy; Marie-Pierre Galais; Antonie Adenis. Lancet Onco 2014; 15: 305-14 5. Different Recurrence Pattern After Neoadjuvant Chemoradiotherapy Compared to Surgery Alone in Esophageal Cancer Patients. Justin K. Smit, MD; Sahin Guler, Bsc; John Th. M. Plukker, MD, PhD. Annals of Surgical Oncology (2013) 20; 4008-4015
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Thank You
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Staging method: CT scan, PET, EUS 752 clinical staging of T2N0 disease 482 underwent surgery directly 27.4% confirmed T2N0 disease 25.9% downstaged 46.7% upstaged
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