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Family Practice Oncology Network Upper Gastrointestinal Cancer (Suspected) Part 2 External Review Effective Date: TBD SCOPE: Part 2 of this guideline outlines recommendations for the prevention, screening, diagnosis, treatment and follow-up of upper gastrointestinal (GI) malignancies, ncluding pancreatic cancer, neuroendocrine tumours (NETs) of the pancreas and duodenum, and cancer of the extrahepatic biliary tract. The primary targett audience for this guideline is community general practitioners providing first contact or primary health care. KEY RECOMMEND DATIONS Screening for upper GI cancers, including extrahepatic biliary and pancreatic cancers, is not recommended. Painless jaundice should be considered to be pancreatic cancerr until proven otherwise. If pancreatic cancer is suspected, investigations should be expedited. There is no evidence that routine imaging or laboratory investigations, including Ca 19-9, are useful in detecting recurrent metastatic disease. 1,2 Patients facing potentially life-limiting conditionss may benefitt from advance care planning (see Resources). PREVENTION The risk of many of these cancers increases with smoking. 3,4 Excessivee alcohol consumption, as well as the presence of diabetes and chronic pancreatitis increase the risk of pancreatic cancer. 3 As with many other cancers, preventative measures include reducing alcohol intake, maintaining a healthy weight, and smoking cessation. SCREENING Theree are no recommended screening guidelines for pancreatic or bile duct cancer. 2,5 The incidence of these cancers is low (e.g. the incidence of pancreatic cancer in B.C. is 12.55 cases per 100 000 population, and bile duct cancer 1-2 cases perr 100 000 population). 6,7 Screening with EUS or MRI may be indicated in patients at high risk (seee Risk Factors) for pancreatic cancer. 5,8 Risk Factors The incidence of pancreatic cancer increases significantlyy from the age of 60. 6 Non-hereditary and Helicobacter pylori infection. 3 Hereditary pancreatic cancer account forr 5-10% of cases. 8 People at higher risk risk factors include smoking, chronic pancreatitis, diabetes mellitus, obesity, include: 5 individuals with two or more first degree relativess with pancreatic carcinoma carriers of BRCA2 mutations carriers of p16 mutations patients with Lynch syndrome with affected first degree relatives patients with Peutz-Jeghers syndrome Pancreatic NETs (pnets) are rare and can occur at any age, and in both sexes equally. 9 Page 1 of 5

Pancreatic neoplasms can occur as part of four hereditary conditions: 9 multiple endocrine neoplasia type 1 (MEN1), von Hippel-Lindau disease (VHL), neurofibromatosis 1 (NF-1; von Recklinghausen disease), and tuberous sclerosis complex (TSC) The most common association of pnets is with MEN-1 (80%). 9 Bile duct cancer occurs equally in men and women, and incidence peaks in the sixth and seventh decade. 7 Prevalence is higher in South East Asia, and may be related to chronic infection with Clonorchis sinensis and Opisthorchis viverrini. 10 Risk factors for bile duct cancer in Western populations include: 10 inflammatory bowel disease primary sclerosing cholangitis congenital choledochal cysts possible exposure to environmental toxins (i.e. dioxins, asbestos, nitrosamines, Thorotrast) The incidence of cholangiocarcinoma in patients with underlying primary sclerosing cholangitis is 9-40%. 10 DIAGNOSIS Pancreatic Cancer Pancreatic cancers are of exocrine or endocrine origin. Exocrine tumors are the most common type of pancreatic cancer, of which 85% are adenocarcinoma. 11 Approximately 10% are adenosquamous carcinoma; the remainder are endocrine tumours (pnets) amouting to <4% of all pancreatic neoplasms. 9 Pancreatic exocrine carcinomas are associated with poor prognosis, 12 and patients are often asymptomatic until late in the course of the disease. Ampullary cancers have a better prognosis than pancreatic adenocarcinoma. 11 Neuroendocrine Tumours Neuroendocrine tumours arise from the diffuse neuroendocrine system of the gut. 13 They are rare and include NETs of the stomach, duodenum and pancreas. Bile Duct Cancer Intrahepatic cholangiocarcinoma is often mistaken for hepatocellular carcinoma, or metastatic disease from an unknown primary site. 14 Over 90% of bile duct carcinomas are adenocarcinomas. 14 Signs and Symptoms This is a difficult diagnosis to make as many of the symptoms of these cancers are non-specific and can mimic benign and other malignant conditions (e.g. ovarian cancer, gastric cancer, primary peritoneal cancer). In pancreatic cancer, the two most common presenting symptoms are abdominal pain and jaundice. 15 Other non-specific symptoms are included below: Painless jaundice is considered to be pancreatic cancer until proven otherwise. Fatigue, anorexia, weight loss, dull epigastric pain, early satiety. 12 Abdominal pain, back pain or weight loss are usually signs of late-stage disease. 8 Persistent abdominal pain and ongoing weight loss should prompt appropriate investigations. Page 2 of 5

NETs present as functional or nonfunctional tumours: Functional tumours are characterized by excess hormone production resulting in clinical syndromes (e.g. carcinoid syndrome) and are named according to the hypersecreted hormone (e.g. insulinomas, gastrinomas). 13 Non-functional tumours are not due to excess hormone production, and alternatively present due to tumour bulk; tumours are slow growing and metastatic disease is usually present at diagnosis. The patient may present with intermittent abdominal discomfort for months or years, often interpreted to be a functional disorder. 13 Investigations While the incidence of these cancers is low, it is important to maintain a high index of suspicion in patients with persistent symptoms. If cancer is suspected, investigations should be expedited (urgent request for abdominal imaging). Initial investigations should include abdominal imaging (US and CT scan), and bloodwork (CBC, creatinine, liver function tests, tumour markers). CA 19-9 serum antigen is the tumour marker for pancreatico-biliary malignancy, however, this marker is not specific to these cancers. 14 Indications for Referral to a Specialist A person should be referred urgently to a specialist if they have obstructive jaundice. A person with an upper abdominal mass should be referred urgently to a specialist. STAGING The TNM classification system is the international standard. Refer to the BC Cancer Agency gastrointestinal guidelines (Refer to Resources), for a link to staging diagrams and definitions for T, N, and M descriptors. TREATMENT Treatment is as recommended by the surgeon and the oncologist/bc Cancer Agency team. Pancreatic Cancer Surgical treatment offers the only potential cure for resectable carcinoma of the pancreas. Adjuvant therapy may be offered following surgery. Surgery, chemotherapy, or radiation therapy may be indicated for palliation. Neuroendocrine Tumours A multidisciplinary approach to the treatment of NETs is recommended. 9,13 Patients with resectable NETs can expect a good intermediate term prognosis. Resectable NETs are managed by endoscopic or surgical resection. Unresectable metastatic disease may benefit from debulking for palliation. For gastrin-producing NETs, proton pump inhibitors should be used to control acid-related symptoms. 13 Biliary Tract Cancer Surgery of resectable tumours is the only potentially curative treatment available. 16 The role of adjuvant chemotherapy remains undefined. 16 Patients with advanced disease may achieve a prolonged period of palliation through surgical, endoscopic and radiological drainage procedures. 16 In a palliative setting, chemotherapy may provide a benefit. 16 FOLLOW-UP At the discretion and direction of the oncologist, the patient may be discharged to the primary care provider. Page 3 of 5

Follow-up care may include the following: Surveillance for recurrent disease or late effects of treatment when indicated. Monitoring and treating complications and/or side effects. Providing patient support. Symptom management, best supportive care and the involvement of palliative services. There is no evidence that routine imaging or laboratory investigations, including Ca 19-9, are useful in detecting recurrent metastatic disease. Early detection of asymptomatic metastases does not enhance survival. Investigations should be performed based the clinical presentation of a patient who is suspected of having recurrent or metastatic disease. 1,2 Patients with a life-limiting disease or illness may benefit from the development of an advance care plan (ACP) (see Resources) that incorporates the patient s values and personal goals, indicates potential outcomes, and outlines linkages with other healthcare professionals that would be involved in the care and their expected roles. The ACP is an opportunity to also identify the patient s alternate substitute decision maker or legal health representative. Specific recommendations will be provided in the patient s discharge letter. At any time the patient and/or primary care provider may consult with the BC Cancer Agency for any follow-up questions or concerns. RESOURCES REFERENCES 1 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 8. Pancreas 8.7 Follow Up [updated June 2013; cited 2015 February 6]. 2 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 9 Gall Bladder, Extrahepatic and Intrahepatic (Peripheral), and Cholangiocarcinoma Cancer Management Guidelines. 9b.7 Follow-up [in press; cited 2015 February 6]. 3 Maisonneuve P, Lowenfels AB. Risk factors for pancreatic cancer: a summary review of meta-analytical studies. Int J Epidemiol. 2015;44(1):186-98. doi:10.1093/ije/dyu240. 4 Xiao-Hua Y, Jia-Ping H, Jin D, et al. Smoking, alcohol consumption, and the risk of extrahepatic cholangiocarcinoma: A meta-analysis. World J Gastroenterol. 2013;19(46):8780-788. doi:10.3748/wjg.v19.i46.8780. 5 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 8. Pancreas 8.1 Screening [updated June 2013; cited 2015 February 6]. 6 BC Cancer Agency. Statistics by Cancer Type - Pancreas [Internet]. 2012 [updated 2014 July 30, cited 2015 February 6]. Available from http://www.bccancer.bc.ca/hpi/cancerstatistics/ff/catype/default.htm 7 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 11. Bile Ducts [updated November 2005; cited 2015 February 6]. 8 Seufferlein T, Bachet JB, Van Cutsem E, et al. Pancreatic adenocarcinoma: EMSO-ESDO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2012;23(Supplement 7): vii33-vii40. doi:10.1093/annonc/mds224. 9 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 12. Neuroendocrine Tumors 12b. Pancreatic Neuroendocrine Tumors [updated 2013; cited 2015 February 6]. 10 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 11. Bile Ducts 11.1 Predisposing Factors/Prevention [updated November 2005; cited 2015 February 6]. 11 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 8. Pancreas [updated June 2013; cited 2015 February 6]. 12 Alberta Health Services. Clinical practice guideline GI-006 - Adenocarcinoma of the pancreas. [Internet]. 2014 [updated 2014 March, cited 2015 March 19]. Available from http://www.albertahealthservices.ca/hp/if-hp-cancerguide-gi006-pancreas.pdf. 13 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 12. Neuroendocrine Tumors 12a. Nonpancreatic Neuroendocrine Tumors [updated July 2013; cited 2015 February 6]. 14 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 11. Bile Ducts 11.2 Diagnosis [updated November 2005; cited 2015 February 6]. Page 4 of 5

15 New Zealand Guidelines Group. Suspected cancer in primary care Guidelines for investigation, referral, and reducing ethnic disparities. Evidence-based best practice guideline. Wellington: New Zealand Guidelines Group; 2009. 173 p. 16 BC Cancer Agency. Cancer Management Guidelines Gastrointestinal 9 Gall Bladder, Extrahepatic and Intrahepatic (Peripheral), and Cholangiocarcinoma Cancer Management Guidelines. 9b.6 Treatment Options [in press; cited 2015 February 6]. RESOURCES BC Cancer Agency, www.bccancer.bc.ca o Gastrointestinal Clinical Practice Guidelines http://www.bccancer.bc.ca/hpi/cancermanagementguidelines/gastrointestinal/default.htm o Hereditary Cancer Program, for referrals: 604-877-6000 (ext. 672198), http://www.screeningbc.ca/hereditary/forhealthprofessionals/default.htm BC Guidelines, BCGuidelines.ca o Dyspepsia with or without Helicobacter pylori Infection Clinical Approach in Adults December - 2009 o Palliative Care for the Patient with Incurable Cancer or Advanced Disease Part 1: Approach to Care 2010 Part 2: Pain and Symptom Management 2011 Part 3: Grief and Bereavement 2011 British Columbia Ministry of Health o My Voice Expressing my Wishes for Future Health Care Treatment Advance Care Planning Guide o Provincial advance care planning resources are available at www.gov.bc.ca/advancecare Healthlink BC, www.healthlinkbc.ca - (toll free in B.C.) 8-1-1, or TTY (Deaf and hearing-impaired) 7-1-1 ACRONYMS ACP advance care plan CBC complete blood count CT computed tomography GI gastrointestinal US ultrasound ASSOCIATED DOCUMENTS The following documents accompany this guideline: Family Practice Oncology Network Upper Gastrointestinal Cancer (Suspected) Part 1 (insert hyperlink) Hereditary Cancer Program Referral Form RENEWAL DATE: This guideline will be reviewed 3-5 years following the effective date, unless changes in clinical evidence warrant an earlier revision. The Family Practice Oncology Network (FPON) developed this clinical practice guideline following a documented guideline adaptation process. The recommendations in this guideline were adapted with permission from the BC Cancer Agency Gastrointestinal Cancer Management Guidelines, and unless otherwise stated, are based primarily on evidence sourced and evaluated by the BC Cancer Agency, as well as expert clinical opinion. Additional sources of evidence were cited as indicated. These recommendations were finalized following a clinical external review. Page 5 of 5