Epidemiology, aetiology and the patient pathway in oesophageal and pancreatic cancers

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Epidemiology, aetiology and the patient pathway in oesophageal and pancreatic cancers Dr Ian Chau Consultant Medical Oncologist Women's cancers Breast cancer introduction 3 What profession are you in? 1) Academic general practice 2) Non-academic general practice 3) Nursing 4) Managerial 5) Others Put in order the commonest cause of cancer death worldwide A) colorectal cancer B) breast cancer C) gastric cancer D) lung cancer E) hepatocellular carcinoma Answers: Vote 1 D, B, A, C, E Vote 2 B, D, A, E, C Vote 3 D, C, E, A, B Vote 4 D, E, A, C, B 1

Match the five-year survival rate with the following cancer in the UK A) colorectal cancer B) breast cancer C) oesophageal cancer D) lung cancer E) hepatocellular carcinoma F) pancreatic cancer Answers: Vote 1: 82% (CRC), 15% (Breast), 50% (Oesophageal), 7% (Lung), 5% (HCC), 3% (Pancreatic) Vote 2: 50% (CRC), 82% (Breast), 13% (Oesophageal), 7% (Lung), 5% (HCC), 4% (Pancreatic) Vote 3: 45% (CRC), 60% (Breast), 13% (Oesophageal), 10% (Lung), 10% (HCC), 15% (Pancreatic) Vote 4: 45%(CRC), 60% (Breast), 5% (Oesophageal), 8% (Lung), 25% (HCC), 8% (Pancreatic) Epidemiology of upper GI cancers Cancer Oesophagus Stomach Pancreas Liver World incidence 481,000 988,000 278,000 749,000 World mortality 406,000 736,000 266,000 694,000 World ranking of cancer-related deaths 6 th 2 nd 7 th 3 rd UK incidence 8,477 7,266 8,463 4,241 UK mortality 7,610 4,960 7,901 3,789 UK 5-year survival 13% 17.9% 3.7% 5.5% GLOBOCAN 2008 (IARC); Cancer Research UK CancerStats accessed July 2013 Oesophageal Cancer Epidemiology UK Incidence of oesophageal cancer rises with age More common in males than females Incidence in males continues to rise whereas incidence in female started to fall at the turn of the century Cancer Research UK CancerStats accessed July 2013 2

Percentage distribution of cases in oesophageal cancer, UK 2008-2010 Cancer Research UK CancerStats accessed July 2013 Risk factors for oesophageal cancer 2 types of cancer of the oesophagus: squamous cell carcinoma and adenocarcinoma. Adenocarcinoma of the oesophagus is increasing rapidly in Western populations but the underlying reasons for this are unclear. Tobacco use increases the risk of both types of oesophageal cancer. Alcohol consumption increases the risk of squamous cell carcinoma of the oesophagus. Some of the highest risks of squamous cell carcinoma of the oesophagus occur in people who combine a smoking habit with regularly drinking alcohol. Around two-thirds of oesophageal cancers in the UK are caused by smoking and around one-fifth are linked to alcohol. Being overweight or obese ( acid reflux) - risk of adenocarcinoma of the oesophagus. One of the strongest risk factors for adenocarcinoma of the oesophagus is the pre-cancerous condition known as Barrett s oesophagus. Pancreatic Cancer Epidemiology UK Incidence of pancreatic cancer rises with age Similar incidence in males and females Incidence generally stable although there is a small decline in males Cancer Research UK CancerStats accessed July 2013 3

Which risk factor is the most important for pancreatic cancer in the UK? 1) Type 2 diabetes 2) Type 1 diabetes 3) Chronic pancreatitis 4) Smoking 5) Obesity Risk factors for pancreatic cancer About 30% pancreatic cancers in the UK are caused by smoking. People with type I or II diabetes have roughly twice the risk of developing pancreatic cancer. Chronic pancreatitis is associated with increased risk of pancreatic cancer. Being overweight or obese increases the risk of pancreatic cancer, with around 1,000 cases in the UK each year linked to excess bodyweight. Eating processed meat may increase risk of pancreatic cancer. People with a family history of pancreatic cancer have a higher risk of developing the disease Case history 1 62 years old male Jan 09 presented with dyspepsia OGD showed malignant lesion from 39-46cm Biopsy poorly differentiated signet ring adenocaricnoma 4

Staging CT/PET T3N1M0 Case history 1 (cont d) EUS T3N1 type 1 OGJ adenocarcinoma with extension below the OGJ Laparoscopy no peritoneal disease, no evidence of disease even at OGJ Mar to May 09 Randomised in OEO 5 study to have pre-operative ECX Oesophago-gastric cancer: patient pathway Typical symptoms: Dysphagia, dyspepsia, weight loss Upper GI endoscopy Cancer suspected Localised disease Endoscopic ultasound PET Laparoscopy Histology CT HER 2 testing Metastatic disease Palliative chemotherapy Peri-operative treatment + 5

Multimodality treatment for resectable oesophageal cancer Squamous cell carcinoma Adenocarcinoma Oesophagus Oesophagogastric junction Definitive chemoradiation Pre-operative chemoradiation Pre-operative chemotherapy Pre-operative Pre-operative chemoradiation chemotherapy Post-operative chemotherapy Post-operative chemoradiation Multimodality treatment in operable gastric cancer Post-operative chemotherapy Post-operative chemoradiation Pre-operative chemotherapy Post-operative chemotherapy UK Second National Oesophago-Gastric Cancer Audit 2013 National audit for all patients diagnosed between 1 Apr 2011 and 31 mar 2012 with OG cancer in England and Wales Data on 11,516 pts submitted Overall 35% of patients had curative treatment plan The Royal College of Surgeons, National Oesophago-Gastric Cancer Audit 2013 6

Proportion of tumours diagnosed by location Oesophagus 47.3% OGJ 22.7% Stomach 30.0% The Royal College of Surgeons, National Oesophago-Gastric Cancer Audit 2013 What proportion of patients with newly diagnosed oesophago-gastric cancer was referred initially by GP? 1) Two-thirds 2) Three-quarters 3) One-tenth 4) 100% Of the patients with newly diagnosed oesophago-gastric cancer who was referred initially by GP, what proportion was referred in as an urgent suspected cancer? 1) 10% 2) 30% 3) 50% 4) 70% 5) 90% 7

Patterns of referral Total Oesophageal Stomach + OGJ GP referral 67% 71% 56% Emergency admission 15% 11% 25% Referral from another hospital consultant 18% 18% 19% - Of the GP referrals, 71% were referred as USC: 74% oesophageal vs. 64% stomach; p<0.0001 - Patients presented as emergency admission were less likely to have a radical treatment plan The Royal College of Surgeons, National Oesophago-Gastric Cancer Audit 2013 Oesophago-gastric cancer: patient pathway Typical symptoms: Dysphagia, dyspepsia, weight loss Upper GI endoscopy Cancer suspected Localised disease Endoscopic ultasound PET Laparoscopy Histology CT HER 2 testing Metastatic disease Palliative chemotherapy Peri-operative treatment + National audit OG cancer: patient pathway (n=17,279) Typical symptoms: Dysphagia, dyspepsia, weight loss Upper GI endoscopy Cancer suspected Histology HER 2 testing Localised disease CT (91%) Metastatic disease Endoscopic ultasound (62%) PET Laparoscopy (57%) Peri-operative treatment + Palliative chemotherapy 84% had either EUS or PET The Royal College of Surgeons, National Oesophago-Gastric Cancer Audit 2013 8

UK National Oesophago-Gastric Cancer Audit 2013: Curative treatment decisions Planned Rx Oes SCC Oeso Adeno Oeso Adeno OGJ Stomach Upper/Mid Lower/S1 SII/III alone 12% 22% 18% 21% 47% (Total: 25%) RT alone 10% 5% 4% 2% 1% (Total: 4%) Chemo + surgery 35% 55% 62% 70% 46% (Total: 54%) Definitive chemorad 38% 8% 8% 3% 2% (Total: 11%) ChemoRT + surgery 3% 1% 2% 1% 1% (Total: 2%) EMR 2% 9% 6% 3% 4% (Total: 4%) Overall 35% of patients had radical treatment plan The Royal College of Surgeons, National Oesophago-Gastric Cancer Audit 2013 Of the patients with newly diagnosed oesophago-gastric cancer who could not be treated with curative intent, what proportion were treated with palliative care alone? 1) 20% 2) 40% 3) 60% 4) 80% 5) 100% UK The Royal National Marsden Oesophago-Gastric Cancer Audit 2013: Palliative treatment decisions Planned Rx Oes SCC Oeso Adeno Oeso Adeno OGJ Stomach Upper/Mid Lower/S1 SII/III Best supportive care 36% 40% 36% 36% 55% (Total: 42%) Palliative Oncology (chemotherapy or radiotherapy) (Total: 47%) 49% 45% 52% 57% 38% Palliative chemotherapy (Total: 64%) 44% 56% 64% 73% 80% Palliative radiotherapy (Total: 29%) 46% 35% 28% 23% 16% Palliative chemoradiation (Total: 7%) 10% 9% 8% 5% 4% Stenting 14% 15% 11% 7% 4% (Total: 9%) The Royal College of Surgeons, National Oesophago-Gastric Cancer Audit 2013 9

Case history 2 77 years old male Sep 11 presented with obstructive jaundice ERCP and plastic stent inserted Biliary brushing negative for malignancy Staging CT and PET/CT scan Case history 2 (cont d) CT and PET/CT showed locally advanced pancreatic cancer and suspicious liver metastases (Diffusion weighted) MRI scan confirmed low volume liver metastases Metal biliary stent inserted and further biliary brushing negative 10

Case history 2 (cont d) CT guided percutaneous biopsy of the pancreas confirmed adenocarcinoma Patients commenced on palliative chemotherapy with gemcitabine plus capecitabine Pancreatic cancer: patient pathway Typical symptoms: Obstructive jaundice, pain, weight loss Ultrasound Cancer suspected CT/ERCP Serum CA19-9 Biliary brushing/ cytology Localised operable PET Laparoscopy + adjuvant treatment Locally advanced Histology Chemotherapy (Chemoradiation) Metastatic Histology Palliative chemotherapy Pancreatic cancer treatment paradigm Pancreatic cancer Localised Locally advanced * Metastatic Chemoradiation Chemotherapy alone alone Chemotherapy alone Adjuvant chemo Adjuvant chemoradiation Chemoradiation * Considered to be unresectable based on at least one of the following: i) extensive peripancreatic lymph node involvement ii) encasement or occlusion of SMV or SMV/portal vein confluence iii) direct involvement of SMA, coeliac axis, IVC or aorta Chemotherapy alone 11

Case history 3 81 years old male Aug 11 presented with obstructive jaundice ERCP and plastic stent inserted Biliary brushing negative for malignancy Staging CT Case history 3 (cont d) Serum CA19-9 = 6,073 U/ml US guided biopsy showed cholangiocarcinoma Commenced on reduced dose gemcitabine plus cisplatin 12

Bile duct cancer: patient pathway Typical symptoms: Obstructive jaundice, pain, weight loss Localised disease MRI/MRCP PET Laparoscopy Ultrasound Cancer suspected ERCP CT Multiple liver mets of unknown origin Biliary brushing/ cytology Locally advanced disease Metastatic disease Histology Palliative chemotherapy ± Consolidation radiotherapy Conclusions Upper GI cancers are highly lethal cancers Two-thirds of newly diagnosed OG cancer patients are referred by GP Curative treatment plans are only possible in 35% of patients Multi-disciplinary approach is required for these cancers Enrolment into clinical trials would be paramount to improve survival of these patients 13