Neuroendocrine tumor (NET) diagnosis is challenging1

By the time patients with NETs reach you, ~60% already have metastatic disease, underscoring the need for timely, sensitive detection and localization2

NETs are rare,3 but their prevalence is rising.4 NETs comprise a heterogeneous group of tumors that arise from neuroendocrine cells throughout the body with varied, nonspecific symptoms.1,3

Patients saw an average of

6 HCPs

before diagnosis2

Patients required an average of

12 doctor visits

before final diagnosis2

There is typically a

5- to 7-year delay

from symptom onset to diagnosis5

Sensitive, accurate, and timely imaging can help you meet the challenges of NET diagnosis and inform treatment planning1

NETs overexpress somatostatin receptors (SSTRs), which can be targeted by radiopharmaceuticals for imaging and treatment.6

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References

  1. Johnbeck CB, Knigge U, Loft A, et al. Head-to-head comparison of 64Cu-DOTATATE and 68Ga-DOTATOC PET/CT: a prospective study of 59 patients with neuroendocrine tumors. J Nucl Med. 2017;58(3):451-457. doi:10.2967/jnumed.116.180430
  2. Singh S, Granberg D, Wolin E, et al. Patient-reported burden of a neuroendocrine tumor (NET) diagnosis: results from the first global survey of patients with NETs. J Glob Oncol. 2016;3(1):43-53. doi:10.1200/JGO.2015.002980
  3. Cuthbertson D, Shankland R, Srirajaskanthan R. Diagnosis and management of neuroendocrine tumours. Clin Med (Lond). 2023;23(2):119-124. doi:10.7861/clinmed.2023-0044
  4. Dasari A, Shen C, Halperin D, et al. Trends in the incidence, prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States. JAMA Oncol. 2017;3(10):1335-1342. doi:10.1001/jamaoncol.2017.0589
  5. Modlin IM, Oberg K, Chung DC, et al. Gastroenteropancreatic neuroendocrine tumours. Lancet Oncol. 2008;9(1):61-72. doi:10.1016/S1470-2045(07)70410-2
  6. Hope TA. Updates to the appropriate-use criteria for somatostatin receptor PET. J Nucl Med. 2020;61(12):1764. doi:10.2967/jnumed.120.257808