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15 - Management of cancer of the exocrine pancreas

Published online by Cambridge University Press:  05 November 2015

Rhian Sian Davies
Affiliation:
Velindre Cancer Centre, Velindre Hospital, Cardiff, UK
Sarah Gwynne
Affiliation:
South West Wales Cancer Centre, Singleton Hospital, Swansea, UK
Somnath Mukherjee
Affiliation:
Oxford Cancer Centre, Oxford, UK
Louise Hanna
Affiliation:
Velindre Cancer Centre, Velindre Hospital, Cardiff
Tom Crosby
Affiliation:
Velindre Cancer Centre, Velindre Hospital, Cardiff
Fergus Macbeth
Affiliation:
Velindre Cancer Centre, Velindre Hospital, Cardiff
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Summary

Introduction

Pancreatic cancer is the fifth commonest cause of cancer mortality in the UK. The major risk factors include smoking, diet and a history of previous total gastrectomy. There is also an association between long-standing diabetes and pancreatic cancer. Surgery is the only curative option, but fewer than 20% of patients are suitable for this. Chemotherapy is the mainstay of treatment for fit patients with advanced or metastatic cancers. Chemoradiation is an option for locally advanced inoperable (LAPC) or borderline resectable disease. Palliative care and psychosocial support are important in the management of this challenging disease.

Types of pancreatic tumour

Benign cysts can be congenital and arise from anomalous development of the pancreatic ducts. Pseudocysts are loculated collections of fluid arising from necrosis, inflammation or haemorrhage, which usually occur as a complication of acute pancreatitis. They are often solitary, can measure 5–10 cm and are often found adjacent to the pancreas in the region of the tail. Benign cystadenomas occur in elderly women and are found incidentally at autopsy or during other investigations. Microcystic and papillary–cystic are other variants found in younger women. The types of pancreatic tumour are shown in Table 15.1.

Incidence and epidemiology

There are about 8800 new cases of pancreatic cancer in the UK each year and 8700 die from the disease. The annual incidence is 9.7/100,000; peak incidence occurs for men in their eighth decade and women in their ninth decade.

Pancreatic cancer is the fifth leading cause of cancer death overall (5% of cancer mortality). The incidence is roughly equal in males and females. Most cases of the disease (80%) occur in the head of the pancreas.

Carcinoma of the exocrine pancreas

Risk factors and aetiology

Three per cent of pancreatic cancers may be inherited. Cancer family syndromes include inherited chronic pancreatitis, inherited diabetes mellitus and ataxia telangectasia syndrome.

Cigarette smoking doubles the risk. More than 1 in 4 pancreatic cancers in the UK are caused through smoking. The use of smokeless tobacco also increases the risk.

A diet rich in protein and carbohydrates and poor in fruit and fibre increases the risk of pancreatic cancer; processed meat may increase the risk.

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Publisher: Cambridge University Press
Print publication year: 2015

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References

Arslan, C. and Yalcin, S. (2014). Current and future systemic treatment options in metastatic pancreatic cancer. J. Gastrointest. Oncol., 5, 280–295.Google ScholarPubMed
Biankin, A. V., Waddell, N., and Kassahn, K. S. (2012). Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. Nature, 491, 399–405.CrossRefGoogle ScholarPubMed
Birkmeyer, J. D., Finlayson, S. R., Tosteson, A. N., et al. (1999). Effect of hospital volume on in-hospital mortality with pancreaticoduodenectomy. Surgery, 125, 250–256.CrossRefGoogle ScholarPubMed
Burris, H. A. III, Moore, M. J., Anderson, J., et al. (1997). Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a ramdomized trial. J. Clin. Oncol., 15, 2403–2413.CrossRefGoogle Scholar
Conroy, T., Desseigne, F., Ychou, M., et al. (2011). FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N. Engl. J. Med., 364, 1817–1825.CrossRefGoogle ScholarPubMed
Cunningham, D., Chau, I., Stocken, D. D., et al. (2009). Phase III randomized comparison of gemcitabine versus gemcitabine plus capecitabine in patients with advanced pancreatic cancer. J Clin Oncol., 27 (33), 5513–5518.CrossRefGoogle ScholarPubMed
Festa, V., Andriulli, A., Valvano, M.R., et al. (2013). Neoadjuvant chemo-radiotherapy for patients with borderline resectable pancreatic cancer: a meta-analytical evaluation of prospective studies. JOP, 14, 618–625.Google ScholarPubMed
Golcher, H., Brunner, T. B., Witzigmann, H., et al. (2015). Neoadjuvant chemoradiation therapy with gemcitabine/cisplatin and surgery versus immediate surgery in resectable pancreatic cancer: Results of the first prospective randomized phase II trial. Strahlenther. Onkol., 191, 7–16.CrossRefGoogle ScholarPubMed
Gurka, M. K., Collins, S. P., Slack, R., et al. (2013). Stereotactic body radiation therapy with concurrent full-dose gemcitabine for locally advanced pancreatic cancer: a pilot trial demonstrating safety. Radiat. Oncol., 8, 44.CrossRefGoogle ScholarPubMed
Hammel, P., Huguet, F. and Van Laethem, J-L. (2013). Comparison of chemoradiotherapy (CRT) and chemotherapy (CT) in patients with a locally advanced pancreatic cancer (LAPC) controlled after 4 months of gemcitabine with or without erlotinib: Final results of the international phase III LAP 07 study. J. Clin. Oncol., 31 (suppl; abstr LBA4003).CrossRefGoogle Scholar
Huguet, F., Hammel, P., Vernerey, D., et al. (2014). Impact of chemoradiotherapy (CRT) on local control and time without treatment in patients with locally advanced pancreatic cancer (LAPC) included in the international phase III LAP 07 study. J. Clin. Oncol., 32 (5 suppl.; abstr 4001).Google Scholar
Kalser, M. H. and Ellenberg, S. S. (1985). Pancreatic cancer. Adjuvant combined radiation and chemotherapy following curative resection. Arch. Surg., 120, 899–903.Google ScholarPubMed
Kelly, K. J., Greenblatt, D. Y., Wan, Y., et al. (2011). Risk stratification for distal pancreatectomy utilizing ACS-NSQIP: preoperative factors predict morbidity and mortality. J. Gastrointest. Surg., 15, 250–261.CrossRefGoogle ScholarPubMed
Klinkenbijl, J.H., Jeekel, J., Sahmoud, T., et al. (1999). Adjuvant radiotherapy and 5-fluorouracil after curative resection of cancer of the pancreas and periampullary region: phase III trial of the EORTC gastrointestinal tract cancer cooperative group. Ann. Surg., 230, 776–782.CrossRefGoogle ScholarPubMed
Mahadevan, A., Miksad, R., Goldstein, M., et al. (2011). Induction gemcitabine and stereotactic body radiotherapy for locally advanced nonmetastatic pancreas cancer. Int. J. Radiat. Oncol. Biol. Phys., 81, 615–622.CrossRefGoogle ScholarPubMed
Maraveyas, A.Waters, J., Roy, R., et al. (2012). Gemcitabine versus gemcitabine plus dalteparin thromboprophylaxis in pancreatic cancer. Eur. J. Cancer, 48, 1283–1292.CrossRefGoogle ScholarPubMed
Merchant, N. B., Conlon, K. C., Saigo, P., et al. (1999). Positive peritoneal cytology predicts unresectability of pancreatic adenocarcinoma. J. Am. Coll. Surg., 188, 421–426.CrossRefGoogle ScholarPubMed
Milano, M., Chmura, S. J., Garofalo, M. C., et al. (2004). Intensity-modulated radiotherapy in treatment of pancreatic and bile duct malignancies: toxicity and clinical outcome. Int. J. Radiat. Oncol. Biol. Phys., 59, 445–453.CrossRefGoogle ScholarPubMed
Mukherjee, S., Hurt, C. N., Bridgewater, J., et al. (2013). Gemcitabine-based or capecitabine-based chemoradiotherapy for locally advanced pancreatic cancer (SCALOP): a multicentre, randomised, phase 2 trial. Lancet Oncol., 14, 317–326.CrossRefGoogle ScholarPubMed
Neoptolemos, J. P., Russell, R. C., Bramhall, S., et al. (1997). Low mortality following resection for pancreatic and periampullary tumours in 1026 patients: UK survey of specialist pancreatic units. UK Pancreatic Cancer Group. Br. J. Surg., 84, 1370–1376.CrossRefGoogle ScholarPubMed
Neoptolemos, J. P., Stocken, D. D., Friess, H., et al. (2004). A randomized trial of chemoradiotherapy and chemotherapy after resection of pancreatic cancer. N. Engl. J. Med., 350, 1200–1210.CrossRefGoogle ScholarPubMed
Neoptolemos, J. P., Stocken, D. D., Bassi, C., et al. (2010). Adjuvant chemotherapy with fluorouracil plus folinic acid vs gemcitabine following pancreatic cancer resection: a randomized controlled trial. J. Am. Med. Ass., 304, 1073–1081.CrossRefGoogle ScholarPubMed
Neoptolemos, J. P., Moore, M. J., Cox, T. F., et al. (2012). Effect of adjuvant chemotherapy with fluorouracil plus folinic acid or gemcitabine vs observation on survival in patients with resected periampullary adenocarcinoma: the ESPAC-3 periampullary cancer randomized trial. J. Am. Med. Ass., 308, 147–156.CrossRefGoogle ScholarPubMed
NHS Executive. (2001). Guidance on Commissioning Cancer Services- Improving Outcomes in Upper Gastro-intestinal Cancers. NHS Executive Catalogue Number 23943. London: Department of Health.
Oettle, H., Neuhaus, P., Hochhaus, A., et al. (2013). Adjuvant chemotherapy with gemcitabine and long-term outcomes among patients with resected pancreatic cancer: the CONKO-001 randomized trial. J. Am. Med. Ass., 310, 1473–1481.CrossRefGoogle ScholarPubMed
Oettle, H., Riess, H., Stieler, J. M., et al. (2014). Second-line oxaliplatin, folinic acid, and fluorouracil versus folinic acid and fluorouracil alone for gemcitabine-refractory pancreatic cancer: outcomes from the CONKO-003 trial. J. Clin. Oncol., 32, 2423–2429.CrossRefGoogle ScholarPubMed
Pelzer, U., Schwaner, I., Stieler, J., et al. (2011). Best supportive care (BSC) versus oxaliplatin, folinic acid and 5-fluorouracil (OFF) plus BSC in patients for second-line advanced pancreatic cancer: A phase III-study from the German CONKO-study group. Eur. J. Cancer, 47, 1676–1681.CrossRefGoogle ScholarPubMed
Ravikumar, R., Sabin, C., Abu Hilal, M., et al. (2014). Portal vein resection in borderline resectable pancreatic cancer: a United Kingdom multicenter study. J. Am. Coll. Surg., 218, 401–411.CrossRefGoogle ScholarPubMed
Regine, W. F., Winter, K. A., Abrams, R., et al. (2011). Fluorouracil-based chemoradiation with either gemcitabine or fluorouracil chemotherapy after resection of pancreatic adenocarcinoma: 5-year analysis of the U.S. Intergroup/RTOG 9704 phase III trial. Ann. Surg. Oncol., 18, 1319–1326.CrossRefGoogle ScholarPubMed
Riess, U., Pelzer, G., Deutschinoff, B., et al. (2009). A prospective, randomized trial of chemotherapy with or without the low molecular weight heparin (LMWH) enoxaparin in patients (pts) with advanced pancreatic cancer (APC): Results of the CONKO 004 trial [abstract]J. Clin. Oncol., 27 (18 Suppl. 309, abstract 4033).CrossRefGoogle Scholar
UICC. (2009). TNM Classification of Malignant Tumours, ed. Sobin, L. H., Gospodarowicz, M. K. and Wittekind, Ch., 7th edn. Chichester: Wiley-Blackwell.
Van Laethem, J. L., Hammel, P., Mornex, F., et al. (2010). Adjuvant gemcitabine alone versus gemcitabine-based chemoradiotherapy after curative resection for pancreatic cancer: a randomized EORTC-40013-22012/FFCD-9203/GERCOR phase II study. J. Clin. Oncol., 28, 4450–4456.CrossRefGoogle ScholarPubMed
Von Hoff, D. D., Ervin, T., Arena, F. P., et al. (2013). Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N. Engl. J. Med., 369, 1691–1703.CrossRefGoogle ScholarPubMed

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