What is the mortality rate of grade 2 neuroendocrine tumors (NETs) compared to other types of cancer?

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Last updated: May 13, 2025View editorial policy

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From the Guidelines

Grade 2 neuroendocrine tumors have a relatively low mortality rate compared to many other cancers, with a 5-year survival rate of approximately 60-80%. While exact comparative statistics vary, this rate is more favorable than aggressive cancers like pancreatic, lung, or advanced colorectal cancer 1. The mortality rate for grade 2 neuroendocrine tumors depends on several factors including the primary tumor location, extent of metastasis, and patient characteristics. These tumors are classified as intermediate-grade based on their proliferation rate (Ki-67 index of 3-20%) and mitotic count, placing them between the slow-growing grade 1 and the aggressive grade 3 neuroendocrine neoplasms.

Key Factors Influencing Mortality Rate

  • Primary tumor location
  • Extent of metastasis
  • Patient characteristics

Treatment typically involves surgical resection when possible, followed by targeted therapies like somatostatin analogs (octreotide or lanreotide), peptide receptor radionuclide therapy, or in some cases, chemotherapy 1. The relatively lower mortality rate compared to other cancers reflects the often indolent nature of these tumors, though they can still progress and cause significant morbidity and mortality if not properly managed. According to the NCCN Guidelines, therapeutic options for locoregional advanced disease and distant metastasis include somatostatin analogs to regulate hormone secretion and tumor growth, hepatic-directed therapies for liver-predominant disease, molecularly targeted agents such as everolimus for antitumor effects, and cytotoxic chemotherapy 1.

Treatment Options

  • Surgical resection
  • Somatostatin analogs
  • Peptide receptor radionuclide therapy
  • Chemotherapy
  • Hepatic-directed therapies
  • Molecularly targeted agents like everolimus

Histopathologic assessment is important in determining prognosis and individualizing therapy, with the WHO classification of NETs providing a framework for understanding the behavior of these tumors 1. Overall, the management of grade 2 neuroendocrine tumors requires a multidisciplinary approach, taking into account the unique characteristics of each patient's disease.

From the Research

Comparison of Mortality Rates

  • The provided studies do not directly compare the mortality rates of grade 2 neuroendocrine tumors to other types of cancer 2, 3, 4, 5, 6.
  • However, the studies suggest that grade 2 neuroendocrine tumors have a distinct prognosis and clinical behavior compared to other grades of neuroendocrine tumors 3, 6.
  • A study published in 2021 found that well-differentiated high-grade neuroendocrine tumors (NET G3) have a poor prognosis, with a median overall survival of 14.2 months 4.
  • Another study published in 2020 found that the incorporation of histologic grade into the staging system for neuroendocrine tumors of the lung can better discriminate between stage categories and provide more accurate prognostic information 6.

Prognostic Factors

  • The Ki-67 index is a significant prognostic factor for grade 2 neuroendocrine tumors, with a cutoff of 10% identifying patients with significantly better outcomes in terms of progression-free survival 3.
  • Other prognostic factors for neuroendocrine tumors include tumor grade, stage at diagnosis, and absence of peptide receptor radionuclide therapy (PRRT) 3, 5.
  • Treatment outcomes for grade 2 neuroendocrine tumors vary depending on the treatment regimen, with capecitabine + temozolomide (CAPTEM) exhibiting clinically meaningful efficacy and disease control 5.

Treatment Options

  • Treatment options for grade 2 neuroendocrine tumors include CAPTEM, PRRT, Platinum-etoposide (EP), FOLFOX, and everolimus 5.
  • The choice of treatment depends on various factors, including tumor grade, stage, and patient characteristics 5.
  • Further studies are needed to determine the optimal treatment strategy for grade 2 neuroendocrine tumors 3, 5.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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