Clinical Evaluation of Response to Octreotide and Chemotherapy in High-Grade Malignant Neuroendocrine Tumors and Promising In Vitro Preclinical Results with Pasireotide.
Kevin DoelloMaria Angeles ChicoFrancisco QuiñoneroRaúl OrtizJose Carlos PradosCristina MesasConsolación MelguizoPublished in: Medicina (Kaunas, Lithuania) (2024)
Background and Objectives : High-grade malignant neuroendocrine tumors (G3 NETs) and neuroendocrine carcinomas (NECs) are characterized by rapid proliferation, high metastatic capacity, and strong expression of somatostatin receptors (SSTRs). We aimed to analyze the presence of SSTRs in NET G3 and NEC, and to correlate their expression with the use of octreotide and pasireotide. Materials and Methods : For this purpose, we first performed a retrospective study of G3 NET and NEC patients, which included the determination of SSTR expression and response to octreotide treatment. Second, we selected the H69 small cell lung cancer cell line to determine the effect of octreotide and pasireotide. Results : Our results showed the traditional somatostatin analog (SSA) octreotide was ineffective in patients with NET G3 and NEC. On the other hand, RT-qPCR showed a high expression of SSTR2 and SSTR5 in H69 cells. Interestingly, while octreotide did not modify H69 cell proliferation, a strong inhibition of proliferation was detected with the use of pasireotide. Conclusions : In view of these results, a clinical trial in NET G3 and NEC patients using pasireotide is necessary to determine the usefulness of this drug in improving patient treatment.
Keyphrases
- neuroendocrine tumors
- high grade
- poor prognosis
- small cell lung cancer
- end stage renal disease
- clinical trial
- cell proliferation
- ejection fraction
- chronic kidney disease
- newly diagnosed
- peritoneal dialysis
- signaling pathway
- binding protein
- low grade
- prognostic factors
- clinical evaluation
- stem cells
- induced apoptosis
- mass spectrometry
- oxidative stress
- open label
- radiation therapy
- cell therapy
- replacement therapy
- sensitive detection
- drug induced
- molecularly imprinted