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Management of Gastroenteropancreati Neuroendocrine Tumour an update Joint Hospital Surgical Grand Round Dr Chan Kwan Kit Caritas Medical Centre

Management of Gastroenteropancreatic Neuroendocrine T umour: a n update

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Management of Gastroenteropancreatic Neuroendocrine T umour: a n update. Joint Hospital Surgical Grand Round Dr Chan Kwan Kit Caritas Medical Centre. Neuroendocrine Tumours (NETs). Epithelial neoplasms with predominant neuroendocrine differentiation - PowerPoint PPT Presentation

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Page 1: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Management of Gastroenteropancreatic Neuroendocrine Tumour:an update

Joint Hospital Surgical Grand RoundDr Chan Kwan Kit

Caritas Medical Centre

Page 2: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Neuroendocrine Tumours (NETs)

Epithelial neoplasms with predominant neuroendocrine differentiation

Considered rare traditionally, comprising ~0.5% of all malignancies

Increasing incidence and prevalence, 2.5 -5/100,000 people per year Increasing awareness Improvement in diagnostic modalities

Page 3: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Distribution

Gastrointestinal tract: ~65% Bronchopulmonary system: ~25% Other locations ~10%:

thymus gonadsheart kidneysprostate

Page 4: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Gastroenteropancreatic NETs (GEPNETs)

Page 5: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Classifications

WHO classification: tumour sitedegree of differentiation and grading functionality

TNM classification

Page 6: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Presentation Asymptomatic Non-functional: non-specific symptoms

abdominal pain, small bowel obstruction, gastrointestinal bleeding, anorexia, weight loss

Functional: hormone/ peptides-related Serotonin: carcinoid syndrome Insulin: Whipple’s triad Gastrin Vasoactive intestinal peptide etc.

Page 7: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 8: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Investigation

Biochemical markers Radiological imaging

Page 9: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Investigation: biochemical markers

Specific markers depending on origin Urinary 5-hydroxyindoleacetic acid (5-HIAA):

main metabolite of serotoninGastrin InsulinGlucagon etc.

Page 10: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Investigation: biochemical markers

Chromogranin A Co-secreted by different neuroendocrine cell

types Correlates with tumour burden and stage Established roles in literatures:

Diagnosis Treatment response monitoring Relapse detection

Page 11: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Chromogranin A

Relatively high sensitivity 53-85%Ben L. Endocrinol Metab Clin N Am 40 (2011) 111–134

Non-specific Elevated in non-NETs condition:

Non-neoplastic: chronic atrophic gastritis; renal failure; liver cirrhosis

Neoplastic: HCC; colon cancers Drugs: proton pump inhibitors

Page 12: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Investigation: radiology

Computed tomography: arterial enhancing lesions with washout in

venous phase Magnetic resonance imaging:

more sensitive for liver and bone marrow metastases

Page 13: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 14: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Endoscopic ultrasound

High sensitivity for tumours at esophagus, stomach, duodenum, and pancreas

Allows image-guided biopsy

Page 15: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 16: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Octreoscan

Somatostatin (SST) receptor scintigraphy Principle: 80-90% of NETs express SST

receptors

Inflammatory lesions and some non-NET malignancies may give false positive results

Page 17: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 18: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Positron Emission Tomography

Ga-68 DOTATOC: high binding affinity for SST receptors

18-FDG: identifies clinically aggressive lesions with high metabolism

Page 19: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

PET: pros and cons

Better spatial and contrast resolution giving higher sensitivity

Specific radioisotopes not widely available Hasn’t been fully validated with strong

evidence yet

Page 20: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Principle of imaging for GEPNETs

CT or MRI combining with functional imaging to obtain maximal information

Currently Octreoscan is still the gold standard for radionuclide imaging

Will likely be replaced by PET scan with specific radioisotopes

Page 21: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Cehic G et al. COSA. Nov 2010

Page 22: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Management

Surgical Non-surgical

Page 23: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Management

Surgery remains the only curative treatment

Curative surgery should always be considered if feasible

Page 24: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Palliative surgery in metastatic disease:Debulking Resection of primary tumour

Proven benefit for local and hormonal symptom control

Page 25: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Surgery

Surgical plan dictated by:Tumour’s site of originDegree of tumour burdenGeneral health or debility of the patient

Page 26: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Operative consideration

Perioperative somatostatin analogsPrevents excessive hormone release during

manipulationParticularly important for intestinal carcinoids

Page 27: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Somatostatin (SST) analogs First line medication Acts through SST receptors on NETs

Inhibition of cellular proliferation and hormonal release

Available for clinical use: octreotide and lanreotide

Page 28: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

SST analogs

Reduction in tumour size: <10% Stabilization of tumour: 40-60% Biochemical response: 50-70% Symptomatic response: 70-90%

Evidence of tumour response AND improvement of quality of life are well established

Page 29: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

SST analogs

No conclusive evidence for survival benefit with use of SST analogs

Page 30: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Alpha-Interferon (IFN)

Induces apoptosis Antiproliferative and anti-angiogenic

effects Evidence suggested usage in low-

proliferating NETs only

Page 31: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Radionuclide therapy:Radiolabelled SST analogs SST analogs, IFN,

chemotherapies, and external irradiation all have poor response in advanced or rapidly progressing GEPNETs

Page 32: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Radiolabelled SST analogs GEPNETs: high level of SSTR expression and good

vascularization Studied radionuclide agents:

90Y-DOTA-octreotide 111In-pentetreotide 177Lu-DOTA-Tyr-octreotide

Page 33: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

90Y-DOTA-octreotide

Encouraging short and intermediate term results: 23-28% objective response rate 63-70% symptomatic response rate Longer progression free survival for pancreatic NETs

Waldherr et al. J Nucl Med. 2002; 32:133-140Paganelli G et al. Biopolymers 2008; 66: 393-398

No long term result available yet

Page 34: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Cytotoxic chemotherapy

Sensitivity of NETs correlates with primary tumour location and tumour grade low grade carcinoid tumours typically resistant

First line therapy only for metastatic/ unresectable pancreatic NETs combination of streptozotocin and 5-fluorouracil (5-

FU) Some evidence for use in high grade ileal NETs

Page 35: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Targeted therapy

Mammalian target of rapamycin (mTOR): serine kinase regulating cell growth and proliferation

mTOR inhibitor: everolimus Two recently completed phase III studies (RADIANT 2

and RADIANT 3) demonstrated statistically significant improvement in progression-free survival (PFS) in metastatic carcinoid tumours

Page 36: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Targeted therapy

NETs are highly vascular and frequently overexpress VEGF ligand and receptor

Bevacizumab and sunitinib: VEGF inhibitors

Phase II studies for both agents are promising

Multinational phase III study ongoing

Page 37: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Liver-directed therapies

Liver is the predominant site of metastases for GEPNETs

Metastatic liver disease gives more carcinoid syndrome

Treatment options:Liver resection/ ablationHepatic artery embolization

Page 38: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Liver resection/ ablation

Advocated if more than 90% of tumours can be successfully resected or ablated

Symptom palliation and survival prolongation well reported

Page 39: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Hepatic artery embolization Diffuse unresectable liver

metastases Rationale: tumours derived

majority of their blood supply from arterial circulation

Bilobar metastases: staged lobar embolization at 4-6 weeks interval

Page 40: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 41: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Conclusion

GEPNETs represent a complex and heterogenous tumour entity with rising incidence and prevalence

Diagnostic and therapeutic challenges due to its relative rarity

Page 42: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Conclusion

Diagnostic and treatment options for GEPNETs are expanding

Controversies exist for choice and sequencing of treatments requiring relevant expertise input

Multidisciplinary approach warranted for best outcome for patients

Page 43: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 44: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Pancreatic-NETs

Page 45: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 46: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Investigation: biochemical markers

Urinary 5-hydroxyindoleacetic acid (5-HIAA) Main metabolite of serotonin

helps diagnosing carcinoid syndrome

Not applicable for non-functional tumours

Page 47: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Operative consideration (2)

Role of prophylactic cholecystectomyRationale: somatostatin analogs treatment

leads to development of gallstonesHowever most of these stones are

asymptomaticNo conclusive evidence to recommend

prophylactic cholecystectomy

Page 48: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Side effects of SST analogs

Usually mild: flatulence; abdominal pain; diarrhea in less than 10% patients

Choledolithiasis: in 20-40% patients with long term SST analogs; acute symptoms rare

Page 49: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

SST analogs + IFN

Combination therapy as upfront treatment in therapy-naïve patients is not well established

Evidence for additive effect of tumour response: sequential use of the two drugs; and, combination after progression with single agent

No proven survival benefit

Page 50: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Side effect profile (Radiolabelled SST analogs) Toxic effects are mild in most patients Nausea and vomiting being the commonest

symptoms Severe lymphopenia and renal toxicity have been

reported

Waldherr et al. J Nucl Med. 2002; 32:133-140Paganelli G et al. Biopolymers 2002; 66: 393-398

De Jong M et al. Int J Cancer 2001 Jun 1; 92(5): 628-33Ebrahim S et al. Cancer biotherapy and radiopharmaceuticals Vol 23, No. 3, 2008

Page 51: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update
Page 52: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Hepatic artery embolization

Contraindication:Poor liver functionModerate to severe ascitesPortal venous thrombosis

Page 53: Management of Gastroenteropancreatic Neuroendocrine  T umour: a n update

Liver-directed therapies

Novel approaches:RadioembolizationLiver transplantation