Gastrointestinal Neuroendocrine Tumors Market Set to Surge by 2034 Amidst Advancements in Treatment Options | DelveInsight

The gastrointestinal neuroendocrine tumors market is experiencing steady growth driven by increasing disease prevalence, improved diagnostic capabilities, and rising awareness of targeted therapies. Additionally, growing investment in research and development, along with the launch of emerging therapies such as ITM-11 (n.c.a. 177Lu-edotreotide) (ITM Solucin GmbH), CAM2029 (Camurus), RYZ101 (Actinium-225 DOTATATE) (Bristol Myers Squibb/RayzeBio), and others, is expected to accelerate the expansion of the GI-NET market.

LAS VEGAS, Oct. 15, 2025 /PRNewswire/ -- DelveInsight's Gastrointestinal Neuroendocrine Tumors Market Insights report includes a comprehensive understanding of current treatment practices, gastrointestinal neuroendocrine tumors emerging drugs, market share of individual therapies, and current and forecasted market size from 2020 to 2034, segmented into leading markets (the US, EU4, UK, and Japan). 

Gastrointestinal Neuroendocrine Tumors Market Summary

• The market size for gastrointestinal neuroendocrine tumors in the leading markets is expected to grow significantly by 2034.
• The United States accounted for the highest gastrointestinal neuroendocrine tumors treatment market size in 7MM in 2024, in comparison to the other major markets, i.e., EU4 countries, the United Kingdom, and Japan.
• The total number of incident cases of GI-NETs in the US was nearly 15,500 cases in 2024 and is projected to increase by 2034.
• Leading gastrointestinal neuroendocrine tumors companies developing emerging therapies, such as ITM Solucin GmbH, Camurus, Bristol Myers Squibb, RayzeBio, and others, are developing new therapy for gastrointestinal neuroendocrine tumors that can be available in the gastrointestinal neuroendocrine tumors market in the coming years. 
• The promising gastrointestinal neuroendocrine tumors therapies in clinical trials include ITM-11 (n.c.a. 177Lu-edotreotide), CAM2029, RYZ101 (Actinium-225 DOTATATE), and others.

Discover the gastrointestinal neuroendocrine tumors new treatment @ New Treatments for Gastrointestinal Neuroendocrine Tumors

Key Factors Driving the Growth of the Gastrointestinal Neuroendocrine Tumors Market 

Rising GI-NET Incident Cases 

The total number of incident cases of GI-NETs in the US was nearly 15,500 cases in 2024 and is projected to increase by 2034 due to improved diagnostic capabilities and enhanced imaging and endoscopic techniques, which enable earlier and more accurate detection of these tumors.

Advancements in Diagnostic Technologies

Innovations in diagnostic tools, including advanced imaging techniques and biomarker identification, have improved the accuracy of GI-NET detection. These advancements enable clinicians to identify tumors at earlier stages, resulting in improved patient outcomes and contributing to market growth.

Launch of Emerging GI-NET Therapies

The expected launch of GI-NET therapies, such as ITM-11(n.c.a.177Lu-edotreotide) (ITM Solucin GmbH), CAM2029 (Camurus), RYZ101 (Actinium-225 DOTATATE) (Bristol Myers Squibb/RayzeBio), and others, is expected to change the market dynamics in the coming years.

Gastrointestinal Neuroendocrine Tumors Market Analysis

The treatment landscape for gastrointestinal neuroendocrine tumors continues to focus primarily on symptom management and disease control rather than achieving a cure. Somatostatin analogs, including SOMATULINE DEPOT and SANDOSTATIN LAR DEPOT, remain the standard of care for both functional and nonfunctional NETs, helping to suppress hormone production and slow tumor progression in well-differentiated cases. Radioligand therapies, such as LUTATHERA (¹⁷⁷Lu-DOTATATE), have broadened treatment options for somatostatin receptor–positive tumors by providing targeted therapy with demonstrated improvements in progression-free survival. Emerging radiopharmaceuticals, like ITM-11 (n.c.a. ¹⁷⁷Lu-edotreotide), show promise for enhanced tumor targeting and improved safety. Nevertheless, significant challenges persist, particularly in treating receptor-negative tumors, high-grade neuroendocrine carcinomas, and cases with extensive metastasis or resistance to first-line therapies.

There is a growing shift toward more precise, biologically informed treatment approaches. Next-generation somatostatin receptor modulators, such as CAM2029 and RYZ101, aim to enhance targeting and tolerability. Concurrent advances in diagnostic technologies, including gene expression assays such as the NETest and circulating tumor biomarkers, offer potential for earlier detection and real-time monitoring of disease. Collectively, these developments signal a move toward multimodal, mechanism-driven care that combines targeted radiotherapy, immunotherapy, and precision diagnostics. However, most of these therapies are still in early-phase trials, and no current treatment fully addresses aggressive or poorly differentiated NETs. Continued research is crucial for developing safer, more effective, and personalized strategies for managing this complex and often underappreciated group of tumors.

To know more about gastrointestinal neuroendocrine tumors treatment options, visit @ Approved Gastrointestinal Neuroendocrine Tumors Drugs

Gastrointestinal Neuroendocrine Tumors Competitive Landscape

Some of the GI-NET therapies in clinical trials include ITM-11 (n.c.a. 177Lu-edotreotide) (ITM Solucin GmbH), CAM2029 (Camurus), RYZ101 (Actinium-225 DOTATATE) (Bristol Myers Squibb/RayzeBio), and others.

ITM Solucin GmbH's ITM-11 (¹⁷⁷Lu-edotreotide) is an advanced targeted radionuclide therapy composed of two molecular parts: Edotreotide (DOTATOC), a somatostatin analog derived from octreotide, and EndolucinBeta, a no-carrier-added (n.c.a.) lutetium-177 chloride, a synthetic therapeutic radioisotope that emits low-energy beta particles. The therapy received orphan drug designation for the treatment of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) following positive Phase II clinical results, which showed significant clinical benefit characterized by low uptake in normal tissues and a high tumor-to-kidney ratio.

Currently, ITM-11 is being assessed in two pivotal Phase III trials, COMPETE (NCT03049189) and COMPOSE (NCT04919226). The COMPETE trial is investigating its efficacy in patients with Grade 1 and Grade 2 GEP-NETs, while COMPOSE is evaluating its potential in well-differentiated high-grade Grade 2 and Grade 3 GEP-NETs.

Meanwhile, Camurus' CAM2029 is a long-acting subcutaneous octreotide depot formulation in development for acromegaly, GEP-NET, and polycystic liver disease (PLD). The pivotal Phase III SORENTO study, a randomized, active-controlled trial, is assessing the efficacy and safety of CAM2029 in GEP-NET patients and is expected to conclude its randomized phase in early 2026. In parallel, preparations for the commercial launch of CAM2029 in GEP-NET are underway.

The anticipated launch of these emerging therapies are poised to transform the gastrointestinal neuroendocrine tumors market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the gastrointestinal neuroendocrine tumors market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth.

Discover more about therapy for gastrointestinal neuroendocrine tumors @ Gastrointestinal Neuroendocrine Tumors Clinical Trials 

Recent Developments in the Gastrointestinal Neuroendocrine Tumors Market

• InJune 2025, ITM Isotope Technologies Munich SE announced that they had presented data from their completed Phase III COMPETE trial in an oral presentation and Satellite Symposium at the Society of Nuclear Medicine and Molecular Imaging (SNMMI) annual meeting in Louisiana.
• In May 2025, Advanced Accelerator Applications, a Novartis Company, has decided to withdraw the Type II variation application to extend the indication of Lutathera, for the treatment of newly diagnosed, unresectable or metastatic, well-differentiated (Grade (G2) and G3), somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEPNETs) in adults.
• In March 2025, ITM Isotope Technologies Munich SE (ITM) presented positive topline data from its Phase III COMPETE trial in patients with Grade 1 or Grade 2 somatostatin receptor (SSTR)-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs) at the 22nd Annual European Neuroendocrine Tumor Society (ENETS) 2025.

What are Gastrointestinal Neuroendocrine Tumors?

Gastrointestinal neuroendocrine tumors (GI-NETs) are a distinct subtype of neuroendocrine tumors (NETs). Like other cancers, they are named based on their site of origin; for instance, a NET that begins in the gastrointestinal (GI) tract is referred to as a GI-NET, which represents the primary tumor. When it spreads to other organs, it is referred to as secondary cancer. GI-NETs typically develop in the GI tract, most commonly in the rectum, small intestine, or appendix. Common symptoms include abdominal pain, a noticeable lump under the skin, unusual fatigue, and weight loss.

The staging system for GI-NETs varies slightly depending on the site. Generally, it ranges from stage 1 to stage 4, with higher stages indicating more advanced and more difficult-to-treat disease. Some types may also have substages that describe the extent of cancer spread more precisely. GI-NETs can behave either indolently or aggressively. The World Health Organization (WHO) has developed a specific classification system for categorizing these tumors. While the exact cause remains unclear, several risk factors have been associated with GI-NETs, including pituitary adenomas, Von Hippel–Lindau (VHL) syndrome, and pheochromocytomas. These tumors often grow slowly, and in some cases, may remain stable for months or even years, meaning immediate treatment may not always be necessary.

Gastrointestinal Neuroendocrine Tumors Epidemiology Segmentation

The gastrointestinal neuroendocrine tumors epidemiology section provides insights into the historical and current gastrointestinal neuroendocrine tumors patient pool and forecasted trends for the leading markets. In the US, the overall incidence of GI-NETs was 4 cases per 100,000, with hindgut tumors being the most common. Hindgut, foregut, and midgut GI-NETs represented 60%, 30.4%, and 9.6% of cases, respectively.

The gastrointestinal neuroendocrine tumors market report proffers epidemiological analysis for the study period 2020–2034 in the leading markets, segmented into:

• Total Incident Cases of NETs
• Cases of NETs by Grade
• Stage-specific Cases of NETs
• Cases of NETs by Site
• Cases of NETs by Functional Status

Scope of the Gastrointestinal Neuroendocrine Tumors Market Report

• Therapeutic Assessment: Gastrointestinal Neuroendocrine Tumors current marketed and emerging therapies
• Gastrointestinal Neuroendocrine Tumors Market Dynamics: Key Market Forecast Assumptions of Emerging Gastrointestinal Neuroendocrine Tumors Drugs and Market Outlook
• Competitive Intelligence Analysis: SWOT analysis and Market entry strategies
• Unmet Needs, KOL's views, Analyst's views, Gastrointestinal Neuroendocrine Tumors Market Access and Reimbursement

Download the report to understand which factors are driving gastrointestinal neuroendocrine tumors therapeutics market trends @ Gastrointestinal Neuroendocrine Tumors Market Trends

Table of Contents

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