Gastroenteropancreatic neuroendocrine tumors: diagnosis and treatment

Surgery

Surgery is the only potentially curative therapeutic strategy in localized disease. Radical oncological surgery is indicated except for small carcinoids (<2 cm) of the stomach, appendix or rectum, in which more conservative surgical or endoscopic resections may be appropriate due to their low malignant potential. Small pancreatic insulinomas also have a very good prognosis (90% are benign tumors) and tumor enucleation is generally sufficient [3]. No adjuvant therapy is recommended in completely resected, well-differentiated localized GEP-NETs. Adjuvant chemotherapy with platinum and etoposide may be considered in poorly-differentiated tumors.

Surgery also plays a major role in advance disease. Surgery of metastasic disease is recommended if complete resection is feasible. Major cytoreductive therapy with palliative purposes may be considered even if R0 is not achievable in patients with extensive liver metastasis and hormonal syndrome refractory to medical therapy. Prophylactic cholecystectomy to prevent cholelithiasis is recommended in patients undergoing surgery if treatment with somatostatin analogs is anticipated. Surgery of the primary tumor may be performed in selected patients to avoid obstruction due to the neoplasm or to the fibrotic reaction commonly associated with small-bowel carcinoids.

When a functioning tumor is diagnosed before surgery, there is a risk of carcinoid crisis when the tumor is operated. This should be prevented by the administration of continuous i.v. octreotide at a dose of 50 mg/h for 12 h prior to and at least 48 h after surgery [11]. Boluses of 100-200 mg octreotide can be given as required. It is also important to avoid drugs that release histamine or activate the sympathetic nervous system [12]. Similarly, prophylaxis with glucose infusion for insulinoma surgery, proton pump inhibitor and octreotide for gastrinomas may be required.

Interventional radiology

In patients not suitable candidates for surgery, regional control of liver metastases may be achieved by different ablative techniques such as radiofrequency ablation, laser ablation and cryotherapy, among others [3].

Reduction in tumor burden often leads to a reduction in hormone secretion and, consequently, an improvement in symptom control.

Other locoregional approaches include embolization of the hepatic artery by particles or cytotoxic agents (chemoembolization). These therapeutic strategies are based on the fact that, unlike normal hepatocytes, NET liver metastases are preferentially supplied by arterial rather than portal blood. They are generally employed with palliative purposes in patients with slow growing functional tumors refractory to medical therapy, but may also be useful to reduce tumor burden and control tumor progression in non-functioning tumors. Doxorubicin (DOX), streptozocin (STZ), mitomycin and fluorouracil (5-FU) are commonly used agents in this context, although randomized studies that properly evaluate the benefit-risk ratio of chemoembolization with that of mechanical embolization are lacking. Clinical responses have been reported in up to 80% of the patients and radiological responses in about 50%. Median duration of response extends up to 18 months [13]. Common adverse events include pain, fever or elevation of liver enzymes. Severe complications occur in 10% of cases and include acute liver or renal failure, liver abscess, cholecystitis or carcinoid crisis.

Although these results have documented the beneficial effects of hepatic arterial embolization (HAE) and chemoembolization (HACE), doubt remains whether chemoembolization offers any therapeutic advantage over particulate embolization alone. In a retrospective study of Gupta et al [14], the addition of intraarterial chemotherapy to embolization did not improve the overall survival (OS) or progression-free survival (PFS) in patients with carcinoid tumors. In contrast, a tendency toward prolonged survival (31.5 vs. 18.2 months) and improved response rate (50% vs. 25%) was noted in patients with islet cell carcinomas who received HACE compared with patients who received HAE, although the differences did not reach statistical significance. They hypothesized that it is not unreasonable to expect that intraarterial chemotherapy will be more effective in patients with islet cell carcinomas, because carcinoid tumors are generally resistant to systemic chemotherapy, whereas islet cell carcinomas generally demonstrate a better response. In another retrospective review at three institutions by Pitt et al [15] OS was similar in patients managed by HACE or HAE.

Liver transplantation

Unlike other types of tumors, due to the slow growth of NET, the possibility of liver transplantation exists. A small group of patients with bilobar liver metastases without extrahepatic disease can be considered for total tumor hepatectomy with liver transplantation in two situations: 1) with the intent to cure; or 2) to palliate from life-threatening hormonal disturbances [16]. In most series, a high rate of recurrence was reported, with a 5-year survival not exceeding series without liver transplantation and high morbidity and mortality. Survival is better with metastatic small intestinal NETs compared with metastatic pancreatic NETs (pNETs). Patients <50 years of age, with low expression of Ki-67 and E-cadherin, are most likely to benefit [17].

Somatostatin analogs

The foundation of current NET therapy is based on the long-acting somatostatin analogs. They act to alleviate symptoms in carcinoid syndrome, stabilize tumor growth and improve quality of life.

There are at least five subtypes of the somatostatin receptor (sst1–5), a G-protein-coupled membrane receptor to which native somatostatin peptides bind to with high affinity. SSTRs, predominantly sst5, are present in the majority of NETs (70-95%) but in only half of insulinomas and less in poorly-differentiated NETs and somatostatinomas. As a result of ligand activation, there is inhibition of the release of many hormones and impairment of hormonally-mediated exocrine function. By this mechanism, somatostatin analogs prevent spontaneous and provoked flushing and secretory diarrhea in patients with carcinoid syndrome.

The elimination half-life of natural somatostatin peptides is only a few minutes, which necessitated the need for a synthetic agent, octreotide, with a half-life of several hours, and a high affinity for sst2 and sst5. It is administered by s.c. injection or i.v. infusion with s.c. dosing starting at 50-100 µg b.i.d. or t.i.d. to a maximum daily dose of 3000 µg. Other short-acting somatostatin analogs include lanreotide. In a prospective crossover study, no differences in symptom control or biochemical response were seen between octreotide and lanreotide [18]. Short-acting somatostatin analogs are used in testing patient tolerability, immediate relief of carcinoid syndromic symptoms and stabilization of symptoms for 10-14 days before converting to long-acting therapy [19]. It is also used in rescue therapy when carcinoid syndrome symptoms occur despite long-acting analogs and also perioperatively to prevent and treat carcinoid crises by either s.c. or i.v. routes. Nevertheless, the mainstay of NET therapy is in the form of long-acting somatostatin analogs. The development of long-acting depot formulations, octreotide LAR and lanreotide Autogel, has allowed clinically practical administration of these drugs by i.m. and deep s.c. routes every 28 days. Biochemical response rates with an inhibition of hormone production are seen in 30-70% with symptom control in the majority of patients [20,21]. Escalation of dose is often required over time for symptom control due to poorly understood ‘tachyphylaxis’. Minor differences may exist between long-acting octreotide and long-acting lanreotide but it has been demonstrated that tumors refractory to one analog may respond to the treatment of another [22].

Recently, it has been confirmed that somatostatin analogs have a role in non-functioning small intestinal tumors. Data derived from the PROMID phase III study has shown that long-term administration of octreotide LAR inhibits tumor growth in midgut NETs with low-volume metastatic disease, with time to progression twice as long as the placebo arm [23].

Few side effects have been reported with somatostatin analogs and these include fat malabsorption, gallstones, gall bladder dysfunction, vitamins A and D malabsorption, headaches, diarrhea, dizziness and hypo- and hyperglycemia.

Interferon-α (IFN-α)

IFN-α was introduced as a treatment for GEP-NETs in the early 1980s and exerts an anti-proliferation and anti-secretory effect. Apart from inhibiting tumor cell cycle progression, it has anti-angiogenic properties. The usual dose is 3-5 million units s.c., three to five times a week. Symptomatic and biochemical responses have been noted in 50% of patients with disease stabilization in 60-80% at a follow up of 4 years. However, significant tumor reduction only occurs in 1015% [24]. Limitations in use of IFN include its side effects that include flu-like symptoms, bone marrow suppression, thyroid disorders, psychiatric phenomena and chronic fatigue syndrome. It has been suggested that patients not responding to either somatostatin analogs or IFN-α alone may show an improved response with inhibition of tumor growth and prolonged survival with the combination treatment of those two agents. However, prospective, randomized trials have not demonstrated any benefit [25].

Peptide-receptor radionuclide therapy (PRRT)

Patients with advanced disease and a positive octreoscan may be considered for PRRT. The optimal radionuclide is still to be determined, but treatment with 90Yttrium octreotide (90YDOTATOC), 90Y-lanreotide and Lu177-DOTA octreotate have been reported to achieve not only tumor stabilization but also tumor regression (objective partial responses) in up to 30% of GEP-NETs [26]. However, experience is limited to single-institution selected series and randomized controlled trials are lacking. In addition, the nonavailability of this therapeutic strategy in most countries further limits its widespread use. The appropriate timing of this therapeutic intervention or the relative long-term benefit-risk ratio compared to other treatment options are key questions that remain unanswered. Alternatively, 131Iodine-metaiodiobenzylguanidine (MIBG) therapy may be considered in advanced tumors with a positive MIBG scan (20-50% of NETs).

Chemotherapy

Systemic chemotherapy is widely used, but its precise role is not known due to studies including various grades, sites and inconsistent response criteria. Thus, there is no standard regimen. Systemic chemotherapy has been the standard treatment for pNETs based on the data from Moertel et al [27] with an objective response of 69%. This study used one of the first combinations with STZ and 5-FU. This group also demonstrated that the combination of STZ and DOX may be better than STZ/FU with a major response rate of 69 vs. 45%, respectively, but this was not confirmed in later studies, which demonstrates problems with comparing studies. The main indication for STZ, 5-FU or DOX includes well-differentiated malignant pancreatic NETs. STZ-based combinations in pancreatic NETs may help control symptoms and achieve tumor response in 40%. A recent study combined 5-FU, cisplatin and STZ (FCiSt) in chemo-naïve patients with metastatic or locally-advanced NETs [28]. Response rates were 38% for pancreatic and 25% for non-pancreatic sites with median time to progression 9.1 months and median OS 31.5 months with an acceptable toxicity profile and an advantageous 1-day outpatient administration.

It is difficult to assess whether subgroups of pancreatic NETs respond differentially due to small numbers, inconsistent assessment criteria and variable regimens amongst studies. Response rates treating pancreatic islet cell tumors with 5-FU, STZ and DOX vary between 40 and 70% [29]. However, in another study, none of the 11 patients with gastrinomas responded to STZ/5-FU/DOX whilst four of the nine (44%) patients with other functioning tumors responded according to RECIST criteria [30].

The use of chemotherapy in midgut and hindgut NETs has a much lower response rate, with <20% of patients benefitting, which may only last 6-8 months with STZ/5-FU/DOX, cyclophosphamide regimens [31]. A retrospective analysis found that temozolomide monotherapy achieved radiological response in 14% and stable disease in 53% [32]. It is generally well tolerated with minimal side effects including leukopenia, nausea and abdominal pain. Another more recent retrospective study of temozolomide combined with capecitabine in 30 chemo-naïve pNETs patients reported an objective radiographic response rate of 70% and median PFS of 18 months [33].

Side effects were relatively tolerable, with a grade 3/4 adverse event rate of only 12%.

Poorly-differentiated or anaplastic NETs are more aggressive, and etoposide and cisplatin combinations have been used to induce response rates of over 50% albeit with short median survival rates and significant toxicity [34].

Tyrosine kinase and angiogenesis inhibitors

The tyrosine kinase receptor family comprises around 20 different classes including platelet-derived growth factor receptors (PDGFRs), c-kit and epidermal growth factor receptor (EGFR). Targeting PDGFR/c-kit, for example, using agents that are used in acute myelogenous leukemia such as imatinib mesylate, has been disappointing. Sunitinib, an oral tyrosine kinase inhibitor with action against all vascular endothelial growth factor (VEGF) receptor (VEGFR), PDGFR, stem cell factor receptor and FMS-like tyrosine kinase-3, has shown some promise in phaseII studies [35]. One hundred and seven patients received sunitinib with 16.7% of pancreatic NETs achieving objective response, 68% achieving stable disease; median time to progression 7.7 months in pNETs, 10.2 months in midgut NETs. The recent phase III study of sunitinib versus placebo in slowly progressing pNETs was halted due to an unplanned early analysis showing significant benefit with PFS of 11.4 months with Sunitinib versus 5.5 months with placebo [36].

Sorafenib, a small molecule inhibitor of Raf kinase, VEGFR-2 and PDGFR tyrosine kinase domains, has been explored in metastatic NETs with 10% partial response and 29% minor response in 41 patients. However, 43% in this study developed grade 3-4 toxicity [37].

NETs are highly vascular and express VEGF, a promoter of angiogenesis. A small phase II study looking at octreotide and bevacizumab versus octreotide and PEG-IFN found that 18% in the bevacizumab arm had partial response and 95% PFS at 18 weeks compared with one partial response and 68% PFS at 18 weeks in the IFN arm [38]. A phase II study looking at bevacizumab and temozolomide has also shown promising results [39].

Mammalian target of rapamycin (mTOR) inhibitors

mTOR is a threonine kinase and part of the phosphatidylinositol-3-kinase/AKT/mTOR pathway, which is crucial in regulation of cell survival and proliferation. It also mediates signalling downstream to growth factor receptors including insulin-like growth factor (IGF) receptor and EGFR. It has been shown that mTOR has a role to play in islet cell tumors in patients with tuberous sclerosis as well as in sporadic NETs [40]. Rapamycin and RAD001, inhibitors of mTOR, lead to a decrease in IGF1 and NET cell growth in studies on pancreatic neuroendocrine cell lines (BON-1) [41]. Thirty-six patients with advanced NETs and evidence of progressive disease were treated with the mTOR inhibitor, temsirolimus, as a single agent in a phase II study. Disease stabilization occurred in 58 cases and partial radiological response in two cases (6%) with median time to progression of 6 months [42]. This modest effect was balanced by adverse events such as fatigue, rash and hyperglycemia experienced in a number of patients.

Yao et al published the results of RAD001 in Advanced NETs-1 (RADIANT 1), a phase II study evaluating everolimus alone versus everolimus and depot octreotide in patients with advanced pancreatic NET who had progressed on first-line chemotherapy. In the combined treatment arm, 80% achieved stable disease and 4.4% partial response with a median PFS of 16.7 months [43]. In the arm with everolimus alone, partial responses were seen in 9.6% and stable disease in 67.8%; median PFS of 9.7 months. These promising results led to two everolimus trials, RADIANT-2 and RADIANT-3. RADIANT-2 was a randomized, double-blind, placebo-controlled, multicenter, phase III study of octreotide combined with everolimus or placebo in patients with advanced NETs. The RADIANT 2 trial demonstrated an improvement in PFS from 11 months on the placebo arm to 16 months on the active treatment arm.

On central radiologic review, the statistical significance of this trial was borderline (P = 0.026) [44]. RADIANT-3 was a randomized, double-blind, placebo-controlled, multicenter phase III study of everolimus plus best supportive care versus placebo and best supportive care in patients with progressive advanced pancreatic NETs. Results from the latter have recently been published and demonstrated a statistically and clinically significant PFS improvement with medians of 11.0 months with RAD001 (everolimus) compared with 4.6 months with placebo [45].