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10 - Treatment of locally advanced and metastatic pancreatic cancer

Published online by Cambridge University Press:  23 December 2009

Jay Heiken
Affiliation:
Mallinckrodt Institute of Radiology
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Summary

Introduction

Despite recent advances in multi-modality and targeted antineoplastic therapy, efforts to improve clinical outcomes for patients with pancreatic adenocarcinoma remain challenging. The potential for cure is applicable only to patients whose tumors are initially resectable or those with borderline, potentially resectable locally advanced tumors. However, these patients constitute < 10% of all newly diagnosed patients with pancreatic cancer [1]. For most patients with pancreatic cancer, the goal of therapy is palliation, and the prognosis is very poor. Patients with locally advanced pancreatic cancer have a median life expectancy of 6–10 months, and patients with metastatic disease have an even shorter median survival of approximately 3–6 months [2]. Current standard and experimental therapeutic options for patients with locally advanced and metastatic pancreatic cancer are evolving and are discussed below.

Locally advanced pancreatic adenocarcinoma

A multi-disciplinary approach is required for the proper assessment and treatment of patients with locally advanced pancreatic cancer. Optimal imaging of the pancreas and its surrounding tissues may delineate tumors that truly are unresectable and those with “borderline” resectability. Whereas the median survival of patients with unresected locally advanced pancreatic cancer is 6–10 months [2], survival times of 21 months can potentially be achieved in patients who have had resection of their tumor after preoperative therapy [3]. This survival time is comparable to the median survival time achieved with upfront pancreatic cancer resection followed by adjuvant therapy.

Type
Chapter
Information
Pancreatic Cancer , pp. 166 - 174
Publisher: Cambridge University Press
Print publication year: 2008

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References

Jemal, A, Siegel, R, Ward, E, et al. Cancer statistics, 2007. CA Cancer J Clin 2007; 57(1): 43–66.CrossRefGoogle ScholarPubMed
Evans, D, Abbruzzesse, J, Willett, C.Cancer of the pancreas. In: DeVita, V, Helmman, S, Rosenberg, S, eds. Cancer: Principles and Practice of Oncology, 6th Edn, 2001, Philadelphia, Lippincott Williams & Wilkins. 2001.Google Scholar
Breslin, TM, et al. Neoadjuvant chemoradiotherapy for adenocarcinoma of the pancreas: treatment variables and survival duration. Ann Surg Oncol, 2001. 8(2): p. 123–132.CrossRefGoogle ScholarPubMed
Diehl, SJ, Lehmann, KJ, Sadick, M, Lachmann, R, Georgi, M. Pancreatic cancer: value of dual-phase helical CT in assessing resectability. Radiology 1998; 206(2): 373–378.CrossRefGoogle ScholarPubMed
Lowy, AM. Neoadjuvant therapy for pancreatic cancer. J Gastrointest Surg 2008; epublished Feb 8 2008.CrossRefGoogle ScholarPubMed
Crane, CH, et al. Is the therapeutic index better with gemcitabine-based chemoradiation than with 5-fluorouracil-based chemoradiation in locally advanced pancreatic cancer?Int J Radiat Oncol Biol Phys 2002; 52(5): 1293–1302.CrossRefGoogle ScholarPubMed
Gnant, M, Kuehrer, I, Teleky, B. Effect of neoadjuvant chemotherapy with gemcitabine and docetaxel on 3-year survival and resection rate in previously unresectable locally advanced pancreatic cancer. J Clin Oncol 2004; 22: 4234.CrossRefGoogle Scholar
Moertel, CG, et al. Therapy of locally unresectable pancreatic carcinoma: a randomized comparison of high dose (6000 rads) radiation alone, moderate dose radiation (4000 rads + 5-fluorouracil), and high dose radiation + 5-fluorouracil. The Gastrointestinal Tumor Study Group. Cancer 1981; 48(8): 1705–1710.3.0.CO;2-4>CrossRefGoogle Scholar
,Gastrointestinal Tumor Study Group. Treatment of locally unresectable carcinoma of the pancreas: comparison of combined-modality therapy (chemotherapy plus radiotherapy) to chemotherapy alone. Gastrointestinal Tumor Study Group. J Natl Cancer Inst 1988; 80(10): 751–755.CrossRefGoogle Scholar
Klaassen, DJ, MacIntyre, JM, Catton, GE, Engstrom, PF, Moertel, CG. Treatment of locally unresectable cancer of the stomach and pancreas: a randomized comparison of 5-fluorouracil alone with radiation plus concurrent and maintenance 5-fluorouracil -- an Eastern Cooperative Oncology Group study. J Clin Oncol 1985; 3(3): 373–378.CrossRefGoogle ScholarPubMed
Ikeda, M, Okada, S, Tokuuye, K, Ueno, H, Okusaka, T. A phase I trial of weekly gemcitabine and concurrent radiotherapy in patients with locally advanced pancreatic cancer. Br J Cancer 2002; 86(10): 1551–1554.CrossRefGoogle ScholarPubMed
Blackstock, AW, et al. Phase I trial of twice-weekly gemcitabine and concurrent radiation in patients with advanced pancreatic cancer. J Clin Oncol 1999; 17(7): 2208–2212.CrossRefGoogle ScholarPubMed
Li, CP, et al. Concurrent chemoradiotherapy treatment of locally advanced pancreatic cancer: gemcitabine versus 5-fluorouracil, a randomized controlled study. Int J Radiat Oncol Biol Phys 2003; 57(1): 98–104.CrossRefGoogle ScholarPubMed
Chauffert, B, Mornex, F, Bonnetain, F. Phase III trial comparing initial chemoradiotherapy (intermittent cisplatin and infusional 5FU) followed by gemcitabine versus gemcitabine alone in patients with locally advanced nonmetastatic pancreatic cancer. J Clin Oncol 2006; 24: 4008.Google Scholar
Huguet, F, et al. Impact of chemoradiotherapy after disease control with chemotherapy in locally advanced pancreatic adenocarcinoma in GERCOR phase II and III studies. J Clin Oncol 2007; 25(3): 326–331.CrossRefGoogle ScholarPubMed
Krishnan, S, et al. Induction chemotherapy selects patients with locally advanced, unresectable pancreatic cancer for optimal benefit from consolidative chemoradiation therapy. Cancer 2007; 110(1): 47–55.CrossRefGoogle ScholarPubMed
Burris, HA, 3rd, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol 1997; 15(6): 2403–2413.CrossRefGoogle ScholarPubMed
Cunningham, D, Chau, I, Stockton, . Phase III randomised comparison of gemcitabine versus gemcitabine plus capecitabine in patients with advanced pancreatic cancer. In: European Cancer Conference (ECCO 13). Paris, France. European Journal of Cancer Supplements 2005.Google Scholar
Sultana, A, Smith, CT, Cunningham, D, et al. Meta-analyses of chemotherapy for locally advanced and metastatic pancreatic cancer. J Clin Oncol 2007; 25(18): 2607–2615.CrossRefGoogle ScholarPubMed
Bramhall, SR, et al. Marimastat as first-line therapy for patients with unresectable pancreatic cancer: a randomized trial. J Clin Oncol 2001; 19(15): 3447–3455.CrossRefGoogle ScholarPubMed
Bramhall, SR, Schulz, J, Nemunaitis, J, et al. A double-blind placebo-controlled, randomised study comparing gemcitabine and marimastat with gemcitabine and placebo as first line therapy in patients with advanced pancreatic cancer. Br J Cancer 2002; 87(2): 161–167.CrossRefGoogle ScholarPubMed
Moore, MJ, et al. Comparison of gemcitabine versus the matrix metalloproteinase inhibitor BAY 12–9566 in patients with advanced or metastatic adenocarcinoma of the pancreas: a phase III trial of the National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol 2003; 21(17): 3296–3302.CrossRefGoogle ScholarPubMed
Kindler, HL, et al. Phase II trial of bevacizumab plus gemcitabine in patients with advanced pancreatic cancer. J Clin Oncol 2005; 23(31): 8033–8040.CrossRefGoogle ScholarPubMed
Kindler, H, et al. A double-blind, placebo-controlled, randomized phase III trial of gemcitabine (G) plus bevacizumab (B) versus gemcitabine plus placebo (P) in patients (pts) with advanced pancreatic cancer (PC): A preliminary analysis of Cancer and Leukemia Group B 80303. J Clin Oncol 2007; 25(18S): a4508.Google Scholar
Xiong, HQ, et al. Cetuximab, a monoclonal antibody targeting the epidermal growth factor receptor, in combination with gemcitabine for advanced pancreatic cancer: a multicenter phase II Trial. J Clin Oncol 2004; 22(13): 2610–2616.CrossRefGoogle ScholarPubMed
Philip, P, et al. Phase III study of gemcitabine [G] plus cetuximab [C] versus gemcitabine in patients [pts] with locally advanced or metastatic pancreatic adenocarcinoma [PC]: SWOG S0205 study. J Clin Oncol 2007; 25(18S): LBA4509.Google Scholar
Moore, MJ, et al. Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: a phase III trial of the National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol 2007; 25(15): 1960–1966.CrossRefGoogle ScholarPubMed
Wong, GY, et al. Effect of neurolytic celiac plexus block on pain relief, quality of life, and survival in patients with unresectable pancreatic cancer: a randomized controlled trial. J Am Med Assoc. 2004; 291(9): 1092–1099.CrossRefGoogle ScholarPubMed
Brentnall, TA. Management strategies for patients with hereditary pancreatic cancer. Curr Treat Options Oncol 2005; 6(5): 437–445.CrossRefGoogle ScholarPubMed

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