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Radionuklidna terapija nevroendokrinih neoplazem : diplomsko delo
ID Misson, Lara (Avtor), ID Rep, Sebastijan (Mentor) Več o mentorju... Povezava se odpre v novem oknu, ID Ležaič, Luka (Komentor), ID Matjašič, Alenka (Recenzent)

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Izvleček
Uvod: Nevroendokrine neoplazme so redki raki, ki izvirajo iz nevroendokrinih celic, organov in celic difuznega endokrinega sistema. Somatostatinski receptorji omogočajo ciljno terapijo z radionuklidi. Radionuklidna terapija nevroendokrinih neoplazem (NEN) je ciljna terapija, ker se tumorske celice vežejo na somatostatinske receptorje, na katere se vežejo radionuklidi. Dandanes sta v klinični uporabi 90Y in 177Lu. Na začetku je bil v uporabi samo 90Y, z razvijanjem terapije, pa so ugotovili, da ima 90Y določeno toksičnost za posameznika. Preko razvijanja terapije so za klinično uporabo uvedli radionuklid 177Lu, kateri se iz do sedaj izvedenih študij kaže kot manj toksičen. Namen: Namen diplomskega dela je s sistematičnim pregledom literature predstaviti, kaj je radionuklidna terapija nevroendokrinih neoplazem in katere različne terapevtske radionuklide uporabljamo v nuklearni medicini. Namen je tudi predstaviti in opisati, kateri radionuklidi so še danes uspešno in najbolj uporabljeni, ter katere so razlike med njimi. Metode dela: Pri pisanju diplomskega dela smo uporabili deskriptivno metodo, in sicer sistematični pregled literature. Strokovne članke smo našli na različnih podatkovnih bazah, kot Mendeley, PubMed, ScienceDirect, Google Učenjak, Journal of Nuclear Medicine (JNM) in SpringerLink. Iskanje in pregled literature je potekalo od oktobra 2024 do marca 2025. Rezultati: Rezultati so prikazani v dveh delih. V prvem delu je shematsko prikazan potek pregleda literature, analiza in izbira strokovnih člankov. V drugem delu smo natančno preučili izbrane strokovne članke glede na: lastnost vzorca, namen in ugotovitve. Izbrana literatura vključuje študije delane na pacientih in miših v kliničnem okolju in laboratorijskem okolju. Analiza člankov je pokazala, da je radionuklidna terapija NEN še vedno v razvoju. Njena učinkovitost je zanesljiva in ima pozitivne rezultate na različne oblike NEN. Razprava in zaključek: Na podlagi raziskav smo ugotovili, da je radionuklidna terapija nevroendokrinih neoplazem v nenehnem napredovanju. Zaradi vezave na somatostatinske receptorje je varna in učinkovita terapija različnih tipov NEN. Glavna radionuklida v klinični uporabi sta 90Y in 177Lu, možna je tudi kombinirana terapija teh. Glavna razlika med njima je toksičnost, ki jo lahko povzročata v določenih tkivih. Za zmanjšanje toksičnosti in kot zaščita ledvic se lahko uporablja aminokisline.

Jezik:Slovenski jezik
Ključne besede:diplomska dela, radiološka tehnologija, nevroendokrine neoplazme (NEN), somatostatinski receptorji, peptidno receptorsko radionuklidno zdravljenje, radionuklidi, 90Y, 177Lu
Vrsta gradiva:Diplomsko delo/naloga
Tipologija:2.11 - Diplomsko delo
Organizacija:ZF - Zdravstvena fakulteta
Kraj izida:Ljubljana
Založnik:[L. Misson]
Leto izida:2025
Št. strani:25 str.
PID:20.500.12556/RUL-172952 Povezava se odpre v novem oknu
UDK:616-07
COBISS.SI-ID:248744707 Povezava se odpre v novem oknu
Datum objave v RUL:12.09.2025
Število ogledov:167
Število prenosov:19
Metapodatki:XML DC-XML DC-RDF
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Sekundarni jezik

Jezik:Angleški jezik
Naslov:Radionuclide therapy for neuroendocrine neoplasms : diploma work
Izvleček:
Introduction: Neuroendocrine neoplasms are rare cancers that originate from neuroendocrine cells, organs, and cells of the diffuse endocrine system. The expression of somatostatin receptors on tumor cells enables targeted radionuclide therapy. This form of therapy is considered targeted because tumor cells express somatostatin receptors, which can bind to radiolabelled compounds. Currently, the radionuclides90Y and 177Lu are in clinical use. Initially, only 90Y was used, but as the therapy evolved, it became evident that90Y could induce significant toxicity in some patients. As a result, 177Lu was introduced into clinical use, and has since demonstrated a more favourable toxicity profile in clinical studies. Purpose: The aim of the thesis is to present through a systematic literature review what is the radionuclide therapy for neuroendocrine neoplasms and with a focus on the therapeutic radionuclides used in nuclear medicine. Additionally, the thesis aims to identify the radionuclides that are currently the most effective and widely used in clinical practice, and to analyse the key differences between them. Methods: In writing this thesis, we used the descriptive method, specifically a systematic literature review. We found scientific articles in various databases such as Mendeley, PubMed, ScienceDirect, Google Scholar, Journal of Nuclear Medicine (JNM), and SpringerLink. The search and review of the literature took place from October 2024 to March 2025. Results: The results are presented in two parts. The first part schematically shows the process of the literature review, the analysis and selection of scientific articles. In the second part, we carefully examined the selected articles based on: sample characteristics, purpose, and findings. The selected literature includes studies conducted on patients and mice in both clinical and laboratory settings. The analysis of the articles showed that radionuclide therapy for NEN is still evolving. Its effectiveness is reliable and has shown positive results for various types of NEN. Discussion and conclusion: Based on research, we have found that radionuclide therapy for neuroendocrine neoplasms is continuously evolving. Owing to its affinity for somatostatin receptors, it represents a safe and effective treatment for various types of NEN. The main radionuclides used in clinical practice are 90Y and 177Lu, with combination therapy also being a viable option. The main difference between the two lies in the level of toxicity they may induce in certain tissues. To reduce this toxicity and protect the kidneys, amino acids can be administered.

Ključne besede:diploma theses, radiologic technology, neuroendocrine neoplasms (NEN), somatostatin receptors, peptide receptor radionuclide therapy, radionuclides, 90Y, 177Lu

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